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        <title>Cryobiology via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Cryobiology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Cryobiology&t=Cryobiology&s=Search&f=source]]></link>
        <lastBuildDate>Mon, 06 Feb 2012 14:26:06 +0100</lastBuildDate>
        <item>
            <title>Evaluation of a low cost cryopreservation system on the biology of human amniotic fluid-derived mesenchymal stromal cells.</title>
            <link>http://www.medworm.com/index.php?rid=5638577&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22280955%26dopt%3DAbstract</link>
            <description>This study found that this cryopreservation protocol does not affect the biological properties of hAMSC. DISCUSSION: This shows that this protocol is a viable system for banking hAMSC, with the associated advantages that has a low cost in terms of expense, time and personnel involved and is easy to implement.
    PMID: 22280955 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638577</comments>
            <pubDate>Fri, 20 Jan 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Cryoprotective agent toxicity interactions in human articular chondrocytes.</title>
            <link>http://www.medworm.com/index.php?rid=5638579&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22274740%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Multiple-CPA solutions are less cytotoxic than single-CPA solutions of the same total concentration. PG was the most toxic CPA when used in combinations. The highest chondrocyte survival rates were obtained with the 6.0M DMSO-EG-Gy-Fm combination solution.
    PMID: 22274740 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638579</comments>
            <pubDate>Wed, 18 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5638579</guid>        </item>
        <item>
            <title>Effectiveness of human mesenchymal stem cells derived from bone marrow cryopreserved for 23-25years.</title>
            <link>http://www.medworm.com/index.php?rid=5638578&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22280954%26dopt%3DAbstract</link>
            <description>CONCLUSION: Using the methods described here, long-term (23-25years) cryopreserved human BMCs can be successfully cultivated to obtain MSCs that have good differentiation capabilities.
    PMID: 22280954 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638578</comments>
            <pubDate>Wed, 18 Jan 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Effect of vitrification on meiotic maturation and expression of genes in immature goat cumulus oocyte complexes.</title>
            <link>http://www.medworm.com/index.php?rid=5638576&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22280956%26dopt%3DAbstract</link>
            <description>In conclusion immature goat COCs vitrified using CT and HS showed that viability, maturation rates and expression of genes coding for oocyte secreted factors and apoptosis were similar to non-vitrified controls.
    PMID: 22280956 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638576</comments>
            <pubDate>Wed, 18 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5638576</guid>        </item>
        <item>
            <title>A case study on stress preconditioning of a Lactobacillus strain prior to freeze-drying.</title>
            <link>http://www.medworm.com/index.php?rid=5638580&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22266474%26dopt%3DAbstract</link>
            <description>This study characterized betaine formulations, with and without sucrose, and tested these with the model lactic acid bacteria Lactobacillus coryniformis Si3. Betaine alone did not act as a lyo-protectant and thus betaine import prior to freeze-drying should be avoided. Differences in protective agents were analyzed by calorimetry, which proved to be a suitable tool for evaluating the characteristics of the freeze-dried end products.
    PMID: 22266474 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638580</comments>
            <pubDate>Sun, 15 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5638580</guid>        </item>
        <item>
            <title>Mathematical optimization of procedures for cryoprotectant equilibration using toxicity cost function.</title>
            <link>http://www.medworm.com/index.php?rid=5620638&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22248796%26dopt%3DAbstract</link>
            <description>In this study, we have used previously published data to determine a toxicity cost function, a quantity that represents the cumulative damage caused by toxicity. We then used this cost function to define and numerically solve the optimal control problem for CPA equilibration, using human oocytes as representative cell type with high clinical relevance. The resulting toxicity-optimal procedures are predicted to yield significantly less toxicity than conventional stepwise procedures. In particular, our results show that toxicity is minimized during CPA addition by inducing the cell to swell to its maximum tolerable volume and then loading it with CPA while in the swollen state. This counterintuitive result is considerably different from the conventional stepwise strategy, which involves expo...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5620638</comments>
            <pubDate>Tue, 10 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5620638</guid>        </item>
        <item>
            <title>Different patterns of metabolic cryo-damage in domestic cat (Felis catus) and cheetah (Acinonyx jubatus) spermatozoa.</title>
            <link>http://www.medworm.com/index.php?rid=5577925&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22227231%26dopt%3DAbstract</link>
            <description>Authors: Terrell KA, Wildt DE, Anthony NM, Bavister BD, Leibo SP, Penfold LM, Marker LL, Crosier AE
    Abstract
    Felid spermatozoa are sensitive to cryopreservation-induced damage, but functional losses can be mitigated by post-thaw swim-up or density gradient processing methods that selectively recover motile or structurally-normal spermatozoa, respectively. Despite the importance of sperm energy production to achieving fertilization, there is little knowledge about the influence of cryopreservation or post-thaw processing on felid sperm metabolism. We conducted a comparative study of domestic cat and cheetah sperm metabolism after cryopreservation and post-thaw processing. We hypothesized that freezing/thawing impairs sperm metabolism and that swim-up, but not density gradient centri...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5577925</comments>
            <pubDate>Thu, 29 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5577925</guid>        </item>
        <item>
            <title>Use of liquid nitrogen during storage in a cell and tissue bank: Contamination risk and effect on the detectability of potential viral contaminants.</title>
            <link>http://www.medworm.com/index.php?rid=5577926&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22222678%26dopt%3DAbstract</link>
            <description>Authors: Mirabet V, Alvarez M, Solves P, Ocete D, Gimeno C
    Abstract
    Cryopreservation is widely used for banking cells and tissues intended for transplantation. Liquid nitrogen provides a very stable ultra-low temperature environment. Thus, it is used for longterm storage. Unlike the exhaustive microbiological monitoring of the environmental conditions during tissue processing, storage is not usually considered as a critical point of potential contamination risk in professional standards for cell and tissue banking. We have analysed the presence of microbial agents inside our nitrogen tanks. We have mainly detected environmental and water-borne bacteria and fungi. In addition, we have studied the effect of liquid nitrogen exposure on virus detectability. Only differences for hepatit...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5577926</comments>
            <pubDate>Wed, 28 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5577926</guid>        </item>
        <item>
            <title>Cytoskeletal proteins F-actin and β-dystrobrevin are altered by the cryopreservation process in bull sperm.</title>
            <link>http://www.medworm.com/index.php?rid=5559845&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22209823%26dopt%3DAbstract</link>
            <description>Authors: Felipe-Pérez YE, Valencia J, Juárez-Mosqueda ML, Pescador N, Roa-Espitia AL, Hernández-González EO
    Abstract
    The cryopreservation process has an important impact on sperm structure and physiology. The negative effects have been mainly observed on the plasma membrane, which is directly stabilized by the cytoskeleton. Since cytoskeleton proteins are osmosensitive and thermosensitive, the aim of this study was to evaluate the damage caused to the bull sperm cytoskeleton by cryopreservation (freezing-thawing). Fresh and frozen-thawed bull semen samples were exposed to a treatment with the neutral detergent Brij 36-T. Electron microscopy evidenced important damages at the sperm perinuclear theca after the protein extraction protocol; the perinuclear theca was partially solub...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5559845</comments>
            <pubDate>Mon, 26 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5559845</guid>        </item>
        <item>
            <title>Some comments on recent discussion of the Boyle van't Hoff relationship.</title>
            <link>http://www.medworm.com/index.php?rid=5559847&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22202670%26dopt%3DAbstract</link>
            <description>Authors: Benson JD
    Abstract
    The estimation of several cellular biophysical parameters must be made in order to mathematically predict optimal cryopreservation protocols. These parameters include total cell volume, osmotically inactive volume, cell surface area, and relative water and solute permeabilities. Recent attention has been paid to the determination of the osmotically inactive volume and, specifically, an argument was made suggesting that this volume was incorrectly determined in the literature [4]. Here we show that this assertion is false.
    PMID: 22202670 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5559847</comments>
            <pubDate>Tue, 20 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5559847</guid>        </item>
        <item>
            <title>The type and extent of injuries in vitrified mouse oocytes.</title>
            <link>http://www.medworm.com/index.php?rid=5559846&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22202671%26dopt%3DAbstract</link>
            <description>Authors: Liang Y, Ning FY, Du WJ, Wang CS, Piao SH, An TZ
    Abstract
    To improve the vitrification of mouse oocytes using straws, we attempted to estimate the type and extent of injuries during vitrification with a vitrification solution EAFS10/10. Injuries in oocytes were assessed based on cellular viability, the integrity of the plasma membrane, the status of the meiotic spindle/chromosomes, and morphological appearance. For morphologically normal oocytes, the ability to be fertilized and to develop into blastocysts was examined. Morphological assessment revealed 15% of oocytes to be injured by intracellular ice formed during vitrification, and 10% by osmotic swelling during removal of the cryoprotectant. When assessed by the status of spindles/chromosomes, the most sensitive criter...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5559846</comments>
            <pubDate>Mon, 19 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5559846</guid>        </item>
        <item>
            <title>Freezing injury: The special case of the sperm cell.</title>
            <link>http://www.medworm.com/index.php?rid=5548773&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22197768%26dopt%3DAbstract</link>
            <description>Authors: John Morris G, Acton E, Murray BJ, Fonseca F
    Abstract
    The cellular damage that spermatozoa encounter at rapid rates of cooling has often been attributed to the formation of intracellular ice although no convincing evidence of intracellular ice formation has ever been obtained. We demonstrate that the high intracellular protein content together with the osmotic shrinkage associated with extracellular ice formation leads to intracellular vitrification of spermatozoa during cooling. At rapid rates of cooling the cell damage to spermatozoa is a result of an osmotic imbalance encountered during thawing, not intracellular ice formation. The osmotic imbalance occurs at rapid cooling rates due to a diffusion limited ice crystallisation in the extracellular fluid, i.e. the amount o...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5548773</comments>
            <pubDate>Wed, 14 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5548773</guid>        </item>
        <item>
            <title>Trehalose transporter from African chironomid larvae improves desiccation tolerance of Chinese hamster ovary cells.</title>
            <link>http://www.medworm.com/index.php?rid=5533213&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22155480%26dopt%3DAbstract</link>
            <description>Authors: Chakraborty N, Menze MA, Elmoazzen H, Vu H, Yarmush ML, Hand SC, Toner M
    Abstract
    Dry preservation has been explored as an energy-efficient alternative to cryopreservation, but the high sensitivity of mammalian cells to desiccation stress has been one of the major hurdles in storing cells in the desiccated state. An important strategy to reduce desiccation sensitivity involves use of the disaccharide trehalose. Trehalose is known to improve desiccation tolerance in mammalian cells when present on both sides of the cell membrane. Because trehalose is membrane impermeant the development of desiccation strategies involving this promising sugar is hindered. We explored the potential of using a high-capacity trehalose transporter (TRET1) from the African chironomid Polypedilum ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5533213</comments>
            <pubDate>Sat, 03 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5533213</guid>        </item>
        <item>
            <title>Mathematical modeling of cryoprotectant addition and removal for the cryopreservation of engineered or natural tissues.</title>
            <link>http://www.medworm.com/index.php?rid=5533214&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22142903%26dopt%3DAbstract</link>
            <description>Authors: Lawson A, Mukherjee IN, Sambanis A
    Abstract
    Long-term storage of natural tissues or tissue-engineered constructs is critical to allow off-the-shelf availability. Vitrification is a method of cryopreservation that eliminates ice formation, as ice may be detrimental to the function of natural or bioartificial tissues. In order to achieve the vitreous state, high concentrations of CPAs must be added and later removed. The high concentrations may be deleterious to cells as the CPAs are cytotoxic and single-step addition or removal will result in excessive osmotic excursions and cell death. A previously described mathematical model accounting for the mass transfer of CPAs through the sample matrix and cell membrane was expanded to incorporate heat transfer and CPA cytotoxicity....</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5533214</comments>
            <pubDate>Mon, 28 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5533214</guid>        </item>
        <item>
            <title>Pulpal regeneration and root development after subcutaneous transplantation of cryopreserved immature teeth in rats.</title>
            <link>http://www.medworm.com/index.php?rid=5533215&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22138351%26dopt%3DAbstract</link>
            <description>Authors: Temmerman L, Vral A, Meire M, Verbeeck RM, Deschepper E, Dermaut LR, De Pauw GA
    Abstract
    The purpose of this in vivo study was to investigate revascularization and root growth after autotransplantation of cryopreserved immature teeth. Immature molar teeth were extracted in 4-week-old Wistar rats. In the test group, teeth were cryopreserved for 1week and transplanted subcutaneously to the abdomen. In the control group, teeth were transplanted subcutaneously immediately after extraction. Material was collected in test and control animals at intervals of 1, 2, 4 and 10weeks post-transplantation and histological and microradiographical examination was performed. Results showed that during the first weeks after transplantation, pulpal repair was similar in both groups although ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5533215</comments>
            <pubDate>Fri, 25 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5533215</guid>        </item>
        <item>
            <title>Development of 4-cell mouse embryos after re-vitrification.</title>
            <link>http://www.medworm.com/index.php?rid=5533217&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22127305%26dopt%3DAbstract</link>
            <description>Authors: Fathi R, Valojerdi MR, Yazdi PE, Ebrahimi B, Alipour H, Hassani F
    Abstract
    This paper reports studies on the effects of re-vitrification by the CPS (Closed Pulled Straw) method on the development of 4-cell stage mouse embryos. The procedure involved culturing 2-cell mouse embryos in G-1 medium until the 4-cell stage followed by the division of the normal 4-cell stage embryos into a control group (non-vitrified) and two experimental subgroups (vitrified and re-vitrified). Embryos in the vitrified subgroup were cryopreserved by the CPS vitrification method. In the second experimental subgroup (re-vitrified), embryos that were already vitrified were warmed and cryopreserved again by the same method. There was no significant reduction in the rate of blastocyst formation after ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5533217</comments>
            <pubDate>Wed, 23 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5533217</guid>        </item>
        <item>
            <title>Gene pathway analysis of the mechanism by which the Rho-associated kinase inhibitor Y-27632 inhibits apoptosis in isolated thawed human embryonic stem cells.</title>
            <link>http://www.medworm.com/index.php?rid=5533216&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22133891%26dopt%3DAbstract</link>
            <description>Authors: Ichikawa H, Nakata N, Abo Y, Shirasawa S, Yokoyama T, Yoshie S, Yue F, Tomotsune D, Sasaki K
    Abstract
    Cryopreservation is an essential technique in basic research and clinical applications of human embryonic stem (hES) cells. Cryopreserved hES cells are fragile and undergo post-thaw apoptosis. We performed gene pathway analysis on cryopreserved and thawed hES cells to examine the effect of Y-27632, a Rho-associated kinase (ROCK) inhibitor, on apoptosis and associated molecular events. Y-27632 was added to the cryopreservation solution and/or the post-thaw medium of two hES cell lines (KhES-1, KhES-3). Post-thaw apoptosis was recorded as a function of time using Giemsa staining and the terminal deoxynucleotidyl transferase dUTP nick end labeling assay. Apoptosis plateaued 1...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5533216</comments>
            <pubDate>Wed, 23 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5533216</guid>        </item>
        <item>
            <title>The effect of programmed cryopreservation on immunogenicity of bladder mucosa in New Zealand rabbits.</title>
            <link>http://www.medworm.com/index.php?rid=5533218&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22127304%26dopt%3DAbstract</link>
            <description>This study would provide theoretical support for the application of allogenic frozen-thawed bladder mucosa in the treatment of urethral stricture. Forty-two adult male New Zealand rabbits were used in this study. The immunogenicity was detected by mixed lymphocyte reaction using the allograft of bladder mucosa (fresh and frozen-thawed) and spleen lymphocytes. Twelve urethral stricture models were established in New Zealand rabbits for substitution urethroplasty using the allograft of bladder mucosa, which were divided into fresh and frozen-thawed group. Two weeks after operation, lymphocyte proliferation was detected in both blood and spleen of recipient rabbits. At the same time, immunohistochemical staining of urethral allograft was performed and the expression of CD3, CD4 and CD8 were o...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5533218</comments>
            <pubDate>Tue, 22 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5533218</guid>        </item>
        <item>
            <title>Structural integrity of collagen and elastin in SynerGraft® decellularized-cryopreserved human heart valves.</title>
            <link>http://www.medworm.com/index.php?rid=5455210&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22119932%26dopt%3DAbstract</link>
            <description>This study evaluates the effects of SG decellularization and subsequent cryopreservation on the extracellular matrix integrity of allograft heart valves. Human aortic and pulmonary valves were trisected, with one-third of each either left fresh (no further processing after dissection), decellularized, or decellularized and cryopreserved. Two-photon laser scanning confocal microscopy was used to visualize collagen and elastin in leaflets and conduits. The optimized percent laser transmission (OPLT) required for full dynamic range imaging of each site was determined, and changes in OPLT were used to infer changes in collagen and elastin signal intensity. Collagen fiber crimp period and collagen and elastin fiber diameter were measured in leaflet tissue. Statistically significant differences ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5455210</comments>
            <pubDate>Sat, 19 Nov 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5455210</guid>        </item>
        <item>
            <title>First results from conservation studies of chlorophyllous spores of the Royal fern (Osmunda regalis, Osmundaceae).</title>
            <link>http://www.medworm.com/index.php?rid=5379296&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22037613%26dopt%3DAbstract</link>
            <description>Authors: Magrini S, Scoppola A
    Abstract
    Pteridophytes spore banks are a promising ex situ conservation tool used to increase the chances of survival of ferns, in fact that large quantities of germplasm with high genetic variation can be conserved in a small space with low economic and technical costs. However, methods to maintain the viability of chlorophyllous spores during storage are less understood. The aim of this study was to investigate the influence of long term storage on the viability of Royal Fern spores, which were stored under different conditions derived from various combinations of temperature and degrees of hydration. Survival and germination tests were performed after 1 and 28months of storage. Our results showed the highest survival percentages for spores stored u...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379296</comments>
            <pubDate>Thu, 20 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379296</guid>        </item>
        <item>
            <title>Pinacidil enhances survival of cryopreserved human embryonic stem cells.</title>
            <link>http://www.medworm.com/index.php?rid=5379297&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22027383%26dopt%3DAbstract</link>
            <description>Authors: Barbaric I, Jones M, Buchner K, Baker D, Andrews PW, Moore HD
    Abstract
    Human embryonic stem cells (hESCs) can be maintained as undifferentiated cells in vitro and induced to differentiate into a variety of somatic cell types. Thus, hESCs provide a source of differentiated cell types that could be used to replace diseased cells of a tissue. The efficient cryopreservation of hESCs is important for establishing effective stem cell banks, however, conventional slow freezing methods usually lead to low rates of recovery after thawing cells and their replating in culture. We have established a method for recovering cryopreserved hESCs using pinacidil and compared it to a method that employs the ROCK inhibitor Y-27632. We show that pinacidil is similar to Y-27632 in promoting sur...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379297</comments>
            <pubDate>Mon, 17 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379297</guid>        </item>
        <item>
            <title>Cryopreservation of cartilage cell and tissue for biobanking.</title>
            <link>http://www.medworm.com/index.php?rid=5379299&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22020192%26dopt%3DAbstract</link>
            <description>In this study, we investigated the effect of vitrification and slow freezing on cartilage cell and tissue viability for biobanking. Firstly, primary adult cartilage cells (ACCs) and fetal cartilage cells (FCC) were cryopreserved by vitrification and slow freezing. Cells were vitrified after a two-step equilibration in a solution composed of ethylene glycol (EG), Ficoll and sucrose. For slow freezing three different cooling rates (0.5, 1 and 2°C/min) were tested in straws. Secondly, the tissues taken from articular cartilage were cryopreserved by vitrification and slow freezing (1°C/min). The results revealed no significant difference between the viability ratios, proliferative activity and GAG synthesis of cartilage cells which were cryopreserved by using vitrification or slow freezing m...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379299</comments>
            <pubDate>Wed, 12 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379299</guid>        </item>
        <item>
            <title>Cooling rate dependent biophysical and viability response shift with attachment state in human dermal fibroblast cells.</title>
            <link>http://www.medworm.com/index.php?rid=5379298&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22020295%26dopt%3DAbstract</link>
            <description>Authors: Choi J, Bischof JC
    Abstract
    While studies on the freezing of cells in suspension have been carried out extensively, corresponding studies with cells in the attached state and in tissue or tissue-equivalents are less developed. As attachment is a hallmark of the tissue state it is important to understand its impact on biophysics and viability to better apply freezing towards tissue preservation. The current study reports on observed biophysical response changes observed during freezing human dermal fibroblasts in suspension, attached cell, and fibrin tissue-equivalent models. Specifically, intracellular ice formation is shown to increase and dehydration is inferred to increase from suspension to attached systems. Biophysical model parameters fit to these experimental observ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379298</comments>
            <pubDate>Mon, 10 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379298</guid>        </item>
        <item>
            <title>Optimal temperature range for low-temperature preservation of dissociated neonatal rat cardiomyocytes.</title>
            <link>http://www.medworm.com/index.php?rid=5379300&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22005593%26dopt%3DAbstract</link>
            <description>In this study, we investigated the optimal temperature range for preserving dissociated cardiomyocytes for 72h while maintaining their normal growth and beating functions. Neonatal rat cardiomyocytes dissociated by collagenase and suspended in the culture medium were preserved at temperatures from -2 to 35°C for 72h. The cardiomyocytes preserved at temperatures below 20°C maintained the initial dispersed states, whereas they aggregated robustly at higher temperatures. The viability of the dispersed cells after preservation was more than 80%. After the preservation, the microscopic observations during the 7-days cultivation indicated that these dispersed cardiomyocytes grew normally to form a confluent monolayer, and beat spontaneously and regularly during culture, as did the fresh cells....</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5379300</comments>
            <pubDate>Sat, 08 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5379300</guid>        </item>
        <item>
            <title>Investigation of interleukin-1β release from cryopreserved blood stimulated with endotoxin.</title>
            <link>http://www.medworm.com/index.php?rid=5325670&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21996161%26dopt%3DAbstract</link>
            <description>Authors: Megha KB, Banerjee S, Mohanan PV
    Abstract
    The feasibility of an indigenously developed ELISA method to determine cytokine response to wide spectrum of pyrogenic stimuli utilizing fresh human whole blood is limited by the availability of healthy donors. The possibility of using cryopreservation of pooled human blood for detection of cytokine response to lipopolysaccharide is explored in this study. The effect of cryopreservation on blood parameters, cellular morphology and cytokine response were compared with that of the pooled fresh blood and cryopreserved blood from single and multiple donors. In vitro pyrogenic stimulation with 0.5 and 5EU of LPS was monitored on fresh and cryopreserved pooled blood from single and multiple donors. The release of IL-1β was quantitated b...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325670</comments>
            <pubDate>Sun, 02 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325670</guid>        </item>
        <item>
            <title>Osmotic challenge and expression of aquaporin 3 and Na/K ATPase genes in bovine embryos produced in vitro.</title>
            <link>http://www.medworm.com/index.php?rid=5325674&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21985766%26dopt%3DAbstract</link>
            <description>In conclusion, embryo ability to undergo shrinkage and swelling is influenced by medium used in a co-culture system and by embryo stage. Rehydrating ability of embryos after exposure to NaCl hypertonic medium is not associated with variations on expression of Aqp3 and ATPase1 genes, but the vitrification can alter gene expression of in vitro-fertilized bovine embryos produced in a co-culture system.
    PMID: 21985766 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325674</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325674</guid>        </item>
        <item>
            <title>In vitro maturation supplements affect developmental competence of bovine cumulus-oocyte complexes and embryo quality after vitrification.</title>
            <link>http://www.medworm.com/index.php?rid=5325673&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21985767%26dopt%3DAbstract</link>
            <description>We examined the impact of bovine oocyte in vitro maturation (IVM) conditions on subsequent embryo yield, quality and cryosurvival. Cumulus-oocyte complexes (COCs) were sampled for cytological and gene expression analysis after IVM in TCM199 supplemented with 10% fetal bovine serum (FBS), 4mg/ml of fatty-acid-free bovine serum albumin (FAFBSA), 4mg/ml of polyvinylpyrrolidone (PVP), FAFBSA with epidermal growth factor (EGF, 100ng/ml) and insulin-like growth factor 1 (IGF-I, 100ng/ml) (FAFBSAGF), PVP with EGF and IGF-I (PVPGF) or PVP with single strength BME and MEM amino acids (PVPAA). The remaining COCs were fertilized. On day 7 (IVF=day 0) quality 1 blastocysts were vitrified or analyzed for glucose transporter 1 (Glut-1) expression levels. The remaining blastocysts (days 7-9) were evaluat...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325673</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325673</guid>        </item>
        <item>
            <title>Post-implant evaluation of the anastomotic mechanical and geometrical coupling between human native arteries and arterial cryografts implanted in lower-limb Mechanical, histological and ultraestructural studies of implanted cryografts.</title>
            <link>http://www.medworm.com/index.php?rid=5325672&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21985768%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Post-implant cryograft remodeling improved native vessels/cryografts coupling. Cryografts would have mechanical and geometrical advantages over ePTFE. Anastomotic cryograft remodeling differed from that expected only due to haemodynamic factors. The structural properties of the remodeled cryografts contribute to explain their functional characteristics.
    PMID: 21985768 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325672</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325672</guid>        </item>
        <item>
            <title>Objective assessment of the cryoprotective effects of dimethylformamide for freezing goat semen.</title>
            <link>http://www.medworm.com/index.php?rid=5325671&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21985769%26dopt%3DAbstract</link>
            <description>In conclusion, dimethylformamide could be used as an alternative cryoprotectant for goat semen freezing. However it was showed that no benefits were derived by using dimethylformamide to replace glycerol at an equal 6% concentration.
    PMID: 21985769 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325671</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325671</guid>        </item>
        <item>
            <title>Polarcath cryoplasty enhances smooth muscle cell apoptosis in a rabbit iliac artery model: An experimental in vivo controlled study.</title>
            <link>http://www.medworm.com/index.php?rid=5325676&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21982952%26dopt%3DAbstract</link>
            <description>CONCLUSION: Cryoplasty demonstrated superior rates of SMC apoptosis at 30min and 72h and was associated to relatively low arterial injury and inflammation scores. An immediate second PolarCath inflation did not achieve superior apoptosis.
    PMID: 21982952 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325676</comments>
            <pubDate>Thu, 29 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325676</guid>        </item>
        <item>
            <title>Cryosurgery and rhTNF-α play synergistic effects on a rat cortex C6 glioma model.</title>
            <link>http://www.medworm.com/index.php?rid=5325675&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21982953%26dopt%3DAbstract</link>
            <description>Authors: Huang KM, Peng M, Feng YQ, Huang H, Tu HJ, Luo J, Zhang L, Yuan XH, Wang LC
    Abstract
    Glioma, a type of brain tumor originating from glioma cells, varies widely in aggressiveness and causes serious symptoms, but the treatments are limited. Studies have shown that cryosurgery has multiple effects on tumor treatments, and administration of human tumor necrosis factor-alpha (rhTNF-α) arguments the anti-tumor effect of cryotherapy in breast and prostate cancers. To test the hypothesis that cryosurgery and rhTNF-α play synergistic effects against brain tumors, we established a brain glioma model on rat cortex regions following different treatments: the G1 group was sham-operated; the G2 group was treated with cryosurgery; the G3 group was treated with rhTNF-α; and G4 group re...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5325675</comments>
            <pubDate>Thu, 29 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5325675</guid>        </item>
        <item>
            <title>Vitrification of in vitro produced goat blastocysts: Effects of oocyte donor age and development stage.</title>
            <link>http://www.medworm.com/index.php?rid=5296237&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21963380%26dopt%3DAbstract</link>
            <description>This study examines the effectiveness of the cryotop vitrification method for the cryopreservation of goat blastocysts. To determine the effects of embryo development stage and donor age on in vitro survival rates, good-quality blastocysts from adult and prepubertal goats were sorted into non-expanded, expanded, hatching and completely hatched. In vitro produced (IVP) blastocysts were derived from prepubertal goat oocytes by slicing of ovaries from slaughtered animals while adult goat oocytes were collected by the laparoscopic ovum pick up (LOPU) method. Blastocysts were vitrified/warmed using the cryotop technique. Survival rates were determined in terms of blastocoele re-expansion at 3 and 20h post-warming. For prepubertal goats, survival rates at 3h post-warming were significantly highe...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296237</comments>
            <pubDate>Thu, 22 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5296237</guid>        </item>
        <item>
            <title>Activity of bone morphogenetic protein-7 after treatment at various temperatures: Freezing vs. pasteurization vs. allograft.</title>
            <link>http://www.medworm.com/index.php?rid=5296236&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21963423%26dopt%3DAbstract</link>
            <description>Authors: Takata M, Sugimoto N, Yamamoto N, Shirai T, Hayashi K, Nishida H, Tanzawa Y, Kimura H, Miwa S, Takeuchi A, Tsuchiya H
    Abstract
    Insufficient bone union is the occasional complication of biomechanical reconstruction after malignant bone tumor resection using temperature treated tumor bearing bone; freezing, pasteurization, and autoclaving. Since bone morphogenetic protein (BMP) plays an important role in bone formation, we assessed the amount and activity of BMP preserved after several temperature treatments, including -196 and -73°C for 20min, 60 and 100°C for 30min, 60°C for 10h following -80°C for 12h as an allograft model, and 4°C as the control. The material extracted from the human femoral bone was treated, and the amount of BMP-7 was analyzed using an enzyme-link...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296236</comments>
            <pubDate>Mon, 19 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5296236</guid>        </item>
        <item>
            <title>Optimal developmental stage for vitrification of parthenogenetically activated porcine embryos.</title>
            <link>http://www.medworm.com/index.php?rid=5277090&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21945817%26dopt%3DAbstract</link>
            <description>The objective of this experiment was to determine the optimal developmental stage to vitrify in vitro cultured porcine parthenogenetically activated (PA) embryos. Embryos were vitrified by Cryotop on Day 4, 5 or 6 after oocyte activation (Day 0), and immediately after warming they were either time-lapse monitored for 24h or analyzed by differential staining. After warming, the embryos had to be cultured for at least 8h before their survival rates were stabilized. Both the survival rate at 8h and the hatching rate at 24h of Day 4 embryos were significant higher than those vitrified on Day 5 or 6 (P&amp;lt;0.05), no matter if they were morulae or blastocysts. These results demonstrate that porcine PA embryos can survive successfully after vitrification/warming, that the optimal time for vitrific...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5277090</comments>
            <pubDate>Fri, 16 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5277090</guid>        </item>
        <item>
            <title>Effects of dithioerythritol on ram semen after the freeze-thawing process.</title>
            <link>http://www.medworm.com/index.php?rid=5277089&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21945818%26dopt%3DAbstract</link>
            <description>Authors: Başpınar N, Coyan K, Bucak MN
    Abstract
    The aim of this study was to evaluate the effects of dithioerythritol added to cryopreservation extender on the post-thawed sperm parameters, lipid peroxidation and antioxidant activities of Merino ram sperm. Semen samples from 5 mature Merino rams (1 and 2years of age) were used in the study. Semen samples, which were diluted with a Tris-based extender containing 0.5, 1, and 2mM dithiothreitol and no antioxidant (control), were cooled to 5°C and frozen in 0.25ml French straws. Frozen straws were then thawed individually at 37°C for 20s in a water bath for evaluation. The addition of dithioerythritol at 0.5 and 2mM doses led to higher percentages of subjective motility (62.9±4.2% and 63.6±1.8%) compared to control (52.0±4.9%, P...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5277089</comments>
            <pubDate>Fri, 16 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5277089</guid>        </item>
        <item>
            <title>Loading solution prevents activation damage of human platelets before lyophilization.</title>
            <link>http://www.medworm.com/index.php?rid=5277088&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21945819%26dopt%3DAbstract</link>
            <description>Authors: Zhou J, Zhang C, Liu J, Fan L, Yang L
    Abstract
    The current study aims to optimize the compositions of platelet activation-inhibitors for a loading solution of lyophilizing protectants and to establish a series of perfect pretreatment methods for platelet lyophilization. The optimal combination of six kinds of inhibitors and loading solutions of lyophilizing protectants, including prostaglandin E1 (PGE1), adenosine, l-arginine, phyticacid, bivalirudin, and cilostazol, was analyzed using the orthogonal experimental design. The values of the expression rates of p-selectin (CD62p) and platelet membrane glyeoprotein (PAC-1), as well as of platelet and mean platelet volume (MPV), were selected as indices of platelet activation. The values of CD62p and Pac-1 induced by thrombin w...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5277088</comments>
            <pubDate>Fri, 16 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5277088</guid>        </item>
        <item>
            <title>Effective surface-based cryopreservation of human embryonic stem cells by vitrification.</title>
            <link>http://www.medworm.com/index.php?rid=5218470&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21910982%26dopt%3DAbstract</link>
            <description>Authors: Beier AF, Schulz JC, Dörr D, Katsen-Globa A, Sachinidis A, Hescheler J, Zimmermann H
    Abstract
    Human embryonic stem cells (hESCs) are candidates for many applications in the areas of regenerative medicine, tissue engineering, basic scientific research as well as pharmacology and toxicology. However, use of hESCs is limited by their sensitivity to freezing and thawing procedures. Hence, this emerging science needs new, reliable preservation methods for the long-term storage of large quantities of functional hESCs remaining pluripotent after post-thawing and culturing. Here, we present a highly efficient, surface based vitrification method for the cryopreservation of large numbers of adherent hESC colonies, using modified cell culture substrates. This technique results in mu...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218470</comments>
            <pubDate>Sat, 03 Sep 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218470</guid>        </item>
        <item>
            <title>Change of supercooling capability in solutions containing different kinds of ice nucleators by flavonol glycosides from deep supercooling xylem parenchyma cells in trees.</title>
            <link>http://www.medworm.com/index.php?rid=5218472&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21906586%26dopt%3DAbstract</link>
            <description>Authors: Kuwabara C, Kasuga J, Wang D, Fukushi Y, Arakawa K, Koyama T, Inada T, Fujikawa S
    Abstract
    Deep supercooling xylem parenchyma cells (XPCs) in Katsura tree contain flavonol glycosides with high supercooling-facilitating capability in solutions containing the ice nucleation bacterium (INB) Erwinia ananas, which is thought to have an important role in deep supercooling of XPCs. The present study, in order to further clarify the roles of these flavonol glycosides in deep supercooling of XPCs, the effects of these supercooling-facilitating (anti-ice nucleating) flavonol glycosides, kaempferol 3-O-β-d-glucopyranoside (K3Glc), kaempferol 7-O-β-d-glucopyranoside (K7Glc) and quercetin 3-O-β-d-glucopyranoside (Q3Glc), in buffered Milli-Q water (BMQW) containing different kinds of...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218472</comments>
            <pubDate>Sat, 27 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218472</guid>        </item>
        <item>
            <title>Production of channel catfish with sperm cryopreserved by rapid non-equilibrium cooling.</title>
            <link>http://www.medworm.com/index.php?rid=5218473&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21896271%26dopt%3DAbstract</link>
            <description>This report describes the feasibility of using vitrification for fish sperm. Vitrification can be used to preserve samples in the field and offers an alternative to conventional cryopreservation, although it has not been systematically studied for sperm of aquatic species. The overall goal of the project was to develop streamlined protocols that could be integrated into a standardized approach for vitrification of aquatic species germplasm. The objectives of the present study in channel catfish (Ictalurus punctatus) were to: (1) evaluate the acute toxicity of 5%, 10%, 20% and 30% methanol, N,N-dimethyl acetamide, dimethyl sulfoxide, 1,2-propanediol, and methyl glycol; (2) evaluate a range of devices commonly used for cryopreservation and vitrification of mammalian sperm; (3) compare vitrif...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218473</comments>
            <pubDate>Fri, 26 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218473</guid>        </item>
        <item>
            <title>Characterization of an antifreeze protein from the polar diatom Fragilariopsis cylindrus and its relevance in sea ice.</title>
            <link>http://www.medworm.com/index.php?rid=5218471&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21906587%26dopt%3DAbstract</link>
            <description>This study presents the AFP from F. cylindrus set in a molecular and crystallographic frame. Differential protein expression after exposure of the diatoms to environmentally relevant conditions underlined the importance of certain AFP isoforms in response to cold. Analyses of the recombinant AFP showed freezing point depression comparable to the activity of other moderate AFPs and further enhanced by salt (up to 0.9°C in low salinity buffer, 2.5°C at high salinity). However, unlike other moderate AFPs, its fastest growth direction is perpendicular to the c-axis. The protein also caused strong inhibition of recrystallization at concentrations of 1.2 and 0.12μM at low and high salinity, respectively. Observations of crystal habit modifications and pitting activity suggested binding of AFP...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218471</comments>
            <pubDate>Fri, 26 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218471</guid>        </item>
        <item>
            <title>Cryopreservation-induced alterations in protein tyrosine phosphorylation of spermatozoa from different portions of the boar ejaculate.</title>
            <link>http://www.medworm.com/index.php?rid=5218475&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21893053%26dopt%3DAbstract</link>
            <description>In conclusion, the study has shown that the cryopreservation process induced PTP in spermatozoa and their proportions were similar between portions of SRF.
    PMID: 21893053 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218475</comments>
            <pubDate>Wed, 24 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218475</guid>        </item>
        <item>
            <title>Development and subsequent cryotolerance of domestic cat embryos cultured in serum-free and serum-containing media.</title>
            <link>http://www.medworm.com/index.php?rid=5218474&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21893054%26dopt%3DAbstract</link>
            <description>The objectives of this study were to examine the effects of the presence or absence of serum during the in vitro culturing period of domestic cat embryos on their developmental potential into blastocysts as well as their tolerance to cryopreservation using a slow-freezing method. In vitro-fertilized cat oocytes were incubated in a modified synthetic oviduct fluid (mSOF) containing 4mg/mL bovine serum albumin (BSA) throughout culturing (BSA group) or in mSOF containing 4mg/mL BSA for the first 3days followed by mSOF containing 5% fetal bovine serum (FBS group). The developmental potential of the embryos to the blastocyst and expanded blastocyst stages was evaluated 7days after in vitro fertilization. The blastocysts were frozen-thawed by the slow-freezing method and cultured for 3days to ex...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218474</comments>
            <pubDate>Wed, 24 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218474</guid>        </item>
        <item>
            <title>Enhancement of supercooling capacity and survival by cold acclimation, rapid cold and heat hardening in Spodoptera exigua.</title>
            <link>http://www.medworm.com/index.php?rid=5218480&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21878325%26dopt%3DAbstract</link>
            <description>Authors: Zheng X, Cheng W, Wang X, Lei C
    Abstract
    Insects can increase their resistance to cold stress by prior exposure to non-lethal cold temperatures. Here, we investigated the supercooling capacity and survival of eggs, 3rd and 5th instar larvae, and pupae of Spodoptera exigua (Lepidoptera: Noctuidae) during CA, and responses to various pre-treatment protocols, including constant temperatures, thermoperiods, and RCH, RHH, RCH+RHH and RHH+RCH combined with thermoperiods. Only acclimated eggs demonstrated a significant decrease in SCP, from -20.7±0.3 to -22.9±0.3°C, among all experimental groups compared to non-acclimated stages. Survival increased by 17.5% for eggs, 40.0% and 13.3% for 3rd and 5th instar larvae, and by 20.0% for pupae after CA. Compared to controls, survival ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218480</comments>
            <pubDate>Tue, 23 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218480</guid>        </item>
        <item>
            <title>Assessment of two thawing processes of cryopreserved human sperm in pellets.</title>
            <link>http://www.medworm.com/index.php?rid=5218479&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21884688%26dopt%3DAbstract</link>
            <description>This study revealed a positive effect of the M2 thawing methodology on sperm parameters. The percentage of spermatozoa with fast-linear movement is increased (M1: 17.26% vs. M2: 28.05%, p&amp;lt;0.01), with higher viability (M1: 37.81% vs. M2: 40.15%, p&amp;lt;0.01) and less acrosome damage (M1: 40.44% vs. M2: 35.45%, p=0.02). We also detected an increase in the percentage of viable spermatozoa with low membrane lipid disorder (M1: 31.36% vs. M2: 33.17%, p=0.03) and a reduction in chromatin condensation (44.62 vs. 46.62 arbitrary units, p=0.02). Further studies will be necessary to evaluate the possible clinical applications.
    PMID: 21884688 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218479</comments>
            <pubDate>Tue, 23 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218479</guid>        </item>
        <item>
            <title>Effects of cooling rate, annealing time and biological antifreeze concentration on thermal hysteresis reading.</title>
            <link>http://www.medworm.com/index.php?rid=5218478&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21884689%26dopt%3DAbstract</link>
            <description>Authors: Kubota N
    Abstract
    Thermal hysteresis (TH) readings depend on the cooling rate, annealing time and the concentration of the biological antifreeze (AF) (i.e., antifreeze protein or antifreeze glycoprotein). Such time- and concentration-dependent TH readings are not true (or absolute) values. The true TH should be independent of time and AF concentration, and it should be a unique value for a given AF. Only the true TH can be used to assess the activity of an AF. A mathematical model is proposed to explain the time- and concentration-dependent behavior of AFs. The model assumes a reversible Langmuir adsorption mechanism for the AF molecules and the Kelvin effect to be applicable. A TH equation that correlates the TH reading with the cooling rate, annealing time and AF concent...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218478</comments>
            <pubDate>Tue, 23 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218478</guid>        </item>
        <item>
            <title>The effects of preservation procedures on amniotic membrane's ability to serve as a substrate for cultivation of endothelial cells.</title>
            <link>http://www.medworm.com/index.php?rid=5218477&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21884690%26dopt%3DAbstract</link>
            <description>Authors: Niknejad H, Deihim T, Solati-Hashjin M, Peirovi H
    Abstract
    Amniotic membrane (AM) has been used as a scaffold for the ex vivo expansion of different types of cells and a cell delivery matrix in regenerative medicine. Since the preservation procedures can influence the AM properties for experimental and clinical purposes, this study was established to investigate the feasibility of using the AM after different preservation methods to serve as substrates for endothelial cell expansion ex vivo. The effects of cryopreservation and lyophilization were evaluated on mechanical and histological characteristics of the AM, and the results were compared with the fresh AM. The ECM components of the basement membrane were well conserved in all groups. Although lyophilization resulted i...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218477</comments>
            <pubDate>Tue, 23 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218477</guid>        </item>
        <item>
            <title>Heterologous expression, refolding and functional characterization of two antifreeze proteins from Fragilariopsis cylindrus (Bacillariophyceae).</title>
            <link>http://www.medworm.com/index.php?rid=5218476&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21884691%26dopt%3DAbstract</link>
            <description>In this study we report the heterologous expression of two antifreeze protein isoforms from F. cylindrus in Escherichia coli. Refolding from inclusion bodies produced proteins functionally active with respect to crystal deformation, recrystallization inhibition and thermal hysteresis. We observed a reduction of activity in the presence of the pelB leader peptide in comparison with the GS-linked SUMO-tag. Activity was positively correlated to protein concentration and buffer salinity. Thermal hysteresis and crystal deformation habit suggest the affiliation of the proteins to the hyperactive group of AFPs. One isoform, carrying a signal peptide for secretion, produced a thermal hysteresis up to 1.53°C±0.53°C and ice crystals of hexagonal bipyramidal shape. The second isoform, which has a ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5218476</comments>
            <pubDate>Tue, 23 Aug 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5218476</guid>        </item>
        <item>
            <title>Effects of cooling and freezing on the motility of Ostrea edulis (L., 1758) spermatozoa after thawing.</title>
            <link>http://www.medworm.com/index.php?rid=5175011&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21856295%26dopt%3DAbstract</link>
            <description>Authors: Vitiello V, Carlino PA, Del Prete F, Langellotti AL, Sansone G
    Abstract
    The aim of this work was to evaluate the effects of temperature, cryoprotectant agents and freezing curves on sperm motility of Ostrea edulis. All phases of cryopreservation were studied (evaluation of semen motility pattern, choice of cryoprotectants and freezing rates) to restore after thawing the motility characteristics distinctive of fresh semen. To assess the temperature effects on sperm motility, semen was activated using four different temperatures (25, 18, 10 and 3°C). Sperm aliquots were maintained inactive at these temperatures for 1 and 3h, then activated with FSW at same temperature of conservation. Sperm was activated and incubated to 3°C with dimethylsulfoxide (M2SO), ethylene glycol (...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5175011</comments>
            <pubDate>Wed, 10 Aug 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5175011</guid>        </item>
        <item>
            <title>Effect of chilling on sox2, sox3 and sox19a gene expression in zebrafish (Danio rerio) embryos.</title>
            <link>http://www.medworm.com/index.php?rid=5141209&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21820425%26dopt%3DAbstract</link>
            <description>This study focused on the effect of chilling and subsequent warming on gene expression of sox2, sox3 and sox19a which play vital roles in the development of zebrafish embryos. A quantitative RT-PCR approach was used to investigate gene expression following chilling at 0°C for up to 180min. The effect on gene expression was also studied during a 180min warming period after chilling for 30 or 60min. There were significant decreases in sox2 (up to 4-fold) and sox3 (up to 3-fold) expressions following chilling. Significant increases in gene expressions of sox2 (up to 2-fold), sox3 (up to 33-fold) and sox19a (up to 25-fold) were observed during warming in the embryos that had been chilled for 30min. Similarly, significant increases were observed in sox2 (up to 3-fold) and sox3 (up to 2-fold) d...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5141209</comments>
            <pubDate>Wed, 27 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5141209</guid>        </item>
        <item>
            <title>Brassinosteroids regulate pectin methylesterase activity and AtPME41 expression in Arabidopsis under chilling stress.</title>
            <link>http://www.medworm.com/index.php?rid=5141210&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21819976%26dopt%3DAbstract</link>
            <description>Authors: Qu T, Liu R, Wang W, An L, Chen T, Liu G, Zhao Z
    Abstract
    Pectin methylesterases (PMEs) are important cell wall enzymes that may play important roles in plant chilling/freezing tolerance. We investigated the possible roles of brassinosteroids (BRs) in regulation of PMEs under chilling stress. Chilling stress or 24-epibrassinolide (eBL) treatments induced significant increases in PME activity in wild type (Col-0) seedlings of Arabidopsis. The chilling-stress-induced increases in PME activity were also found in bzr1-D mutant, a BZR1 stabilized mutant with a constitutively active BR signaling pathway, but not in bri1-116, a BR insensitive null allele of the BR receptor BRI1. The results suggest that the regulation of PME activity in Arabidopsis under chilling stress depends o...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5141210</comments>
            <pubDate>Tue, 26 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5141210</guid>        </item>
        <item>
            <title>Cryopreservation and quality control of mouse embryonic feeder cells.</title>
            <link>http://www.medworm.com/index.php?rid=5097620&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21810414%26dopt%3DAbstract</link>
            <description>Authors: Diekmann U, Spindler R, Wolkers WF, Glasmacher B, Müller T
    Stem cell research is a highly promising and rapidly progressing field inside regenerative medicine. Embryonic stem cells (ESCs), reprogrammed &quot;induced pluripotent&quot; cells (iPS), or lately protein induced pluripotent cells (piPS) share one inevitable factor: mouse embryonic feeder cells (MEFs), which are commonly used for ESC long term culture procedures and colony regeneration. These MEFs originate from different mouse strains, are inactivated by different methods and are differently cryopreserved. Incomprehensibly, there are to date no established quality control parameters for MEFs to insure consistency of ESC experiments and culture. Hence, in this work, we developed a bench-top quality control for embryonic feeder...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5097620</comments>
            <pubDate>Sat, 23 Jul 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">5097620</guid>        </item>
        <item>
            <title>Effects of cholesterol-loaded cyclodextrins on the quality of frozen-thawed equine epididymal sperm.</title>
            <link>http://www.medworm.com/index.php?rid=4956243&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21679702%26dopt%3DAbstract</link>
            <description>The objective of this study was to examine the effects of cholesterol loaded cyclodextrins (CLCs) on the quality of stallion epididymal sperm during cryopreservation. In experiment I, sperm were treated with different concentrations of CLCs: (1) 0mg (control), (2) 1.5mg, (3) 3mg, and (4) 6mg per 120×10(6) sperm. The sperm viability and amount of cholesterol were determined at 15, 30 and 45min after CLC treatment using viability markers (Ethidium homodimer-1 and Calcein AM) and gas chromatography, respectively. In experiment II, CLC treated sperm (1.5mg CLC per 120×10(6) sperm) were fixed and stained with filipin to examine the cholesterol distribution. In experiment III, sperm were treated with CLCs at concentrations of 1.5, 3.0, 6.0mg per 120×10(6) sperm for 15min, then equilibrated wi...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4956243</comments>
            <pubDate>Sun, 12 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4956243</guid>        </item>
        <item>
            <title>Osteogenic differentiation of GFP-labeled human umbilical cord blood derived mesenchymal stem cells after cryopreservation.</title>
            <link>http://www.medworm.com/index.php?rid=4956242&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21684270%26dopt%3DAbstract</link>
            <description>Authors: Liu G, Ye X, Zhu Y, Li Y, Sun J, Cui L, Cao Y
    The osteogenic capacity of human umbilical cord blood derived mesenchymal stem cells (UCB-MSCs) has been demonstrated both in vitro and in vivo. Therefore, cell labeling and storage are becoming necessary for researching the potential therapeutic use of UCB-MSCs for bone tissue engineering. The aim of this study was to determine the effect of cryopreservation on the osteogenic differentiation of green fluorescent protein (GFP)-marked UCB-MSCs in vitro. MSCs were isolated from full-term human UCB, expanded, transfected with the GFP gene, and then cryopreserved in liquid nitrogen for 4weeks. After thawing, cell surface antigen markers and osteogenic potential were analyzed, and the luminescence of these cells was observed by fluoresc...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4956242</comments>
            <pubDate>Sun, 12 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4956242</guid>        </item>
        <item>
            <title>Dopamine improves hypothermic machine preservation of the liver.</title>
            <link>http://www.medworm.com/index.php?rid=4907303&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21645501%26dopt%3DAbstract</link>
            <description>CONCLUSION: Efficiency of HMP might be increased by stimulating livers with dopamine during ex vivo preservation, limiting vascular side effects and improving functional recovery upon early reperfusion.
    PMID: 21645501 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4907303</comments>
            <pubDate>Sun, 29 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4907303</guid>        </item>
        <item>
            <title>Effective vitrification of human induced pluripotent stem cells using carboxylated ε-poly-l-lysine.</title>
            <link>http://www.medworm.com/index.php?rid=4907304&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21621529%26dopt%3DAbstract</link>
            <description>In this study, we developed a vitrification solution comprising ethylene glycol (EG) and sucrose as well as carboxylated ε-poly-l-lysine (PLL); this solution inhibited devitrification. Human iPS cells were vitrified in 200-μL vitrification solutions comprised 6.5M EG, 0.75M sucrose and 0 or 10%w/v carboxylated PLL with 65mol% of the amino groups converted to carboxyl groups [PLL (0.65)] in a cryovial by directly immersing in liquid nitrogen. After warming, attached colony and recovery rates of human iPS cells vitrified by adding PLL (0.65) were significantly higher than those for cells without PLL (0.65) and vitrification solution (DAP213: 2M dimethyl sulfoxide, 1M acetamide and 3M propylene glycol). Furthermore, even after warming at room temperature, attached colony and recovery rates ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4907304</comments>
            <pubDate>Thu, 19 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4907304</guid>        </item>
        <item>
            <title>Care during freeze-drying of bovine pericardium tissue to be used as a biomaterial: A comparative study.</title>
            <link>http://www.medworm.com/index.php?rid=4907306&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21619875%26dopt%3DAbstract</link>
            <description>This study was undertaken in order to study the effect of freeze-drying in the structure of BP. To perform this study BP samples were freeze-dried in two different types of freeze-dryers available in our laboratory: a laboratory freeze-dryer, in which it was not possible to control parameters and a pilot freeze-dryer, wherein all parameters during freezing and drying were controlled. After freeze-drying processes, samples were analyzed by SEM, Raman spectroscopy, tensile strength, water uptake tests and TEM. In summary, it has been demonstrated that damages occur in collagen fibers by the loss of bulk water of collagen structure implicating in a drastic decreasing of BP mechanical properties due to its structural alterations. Moreover, it was proven that the collagen fibrils suffered break...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4907306</comments>
            <pubDate>Mon, 16 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4907306</guid>        </item>
        <item>
            <title>Systematic parameter optimization of a Me(2)SO- and serum-free cryopreservation protocol for human mesenchymal stem cells.</title>
            <link>http://www.medworm.com/index.php?rid=4907305&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21620818%26dopt%3DAbstract</link>
            <description>Authors: Freimark D, Sehl C, Weber C, Hudel K, Czermak P, Hofmann N, Spindler R, Glasmacher B
    Human mesenchymal stem cells (hMSCs) have great potential for clinical therapy and regenerative medicine. One major challenge concerning their application is the development of an efficient cryopreservation protocol since current methods result in a poor viability and high differentiation rates. A high survival rate of cryopreserved cells requires an optimal cooling rate and the presence of cryoprotective agents (CPA) in sufficient concentrations. The most widely used CPA, dimethylsulfoxide (Me(2)SO), is toxic at high concentrations at temperatures &amp;gt;4°C and has harmful effects on the biological functionality of stem cell as well as on treated patients. Thus, this study investigates differe...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4907305</comments>
            <pubDate>Mon, 16 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4907305</guid>        </item>
        <item>
            <title>Cryopreservation of sperm from Atlantic halibut (Hippoglossus hippoglossus, L.) for commercial application.</title>
            <link>http://www.medworm.com/index.php?rid=4804257&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21549108%26dopt%3DAbstract</link>
            <description>Authors: Ding F, Lall SP, Li J, Lei J, Rommens M, Milley JE
    Development of Atlantic halibut (Hippoglossus hippoglossus) aquaculture will be enhanced with cryopreservation of halibut sperm by ensuring a reliable supply of sperm of desired quality and quantity. To assist in its commercial application, the cryopreservation of large volumes of halibut sperm was investigated. Three cryoprotectants were compared: dimethyl sulfoxide (DMSO), polyethylene glycol (PG) and glycerol (GLY) at two concentrations (10% or 15%). Two salt solutions, Hanks' balanced salt solution (HBSS) and 0.1M KHCO(3) with 0.125M sucrose solution (KS) were tested as diluents. Both factors were examined in 1.6mL volumes. A cryopreservation volume of 4mL and a low dilution ratio (1:1) were examined separately. Based on m...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4804257</comments>
            <pubDate>Wed, 27 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4804257</guid>        </item>
        <item>
            <title>The unfolded protein response in human corneal endothelial cells following hypothermic storage: Implications of a novel stress pathway.</title>
            <link>http://www.medworm.com/index.php?rid=4804256&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21549109%26dopt%3DAbstract</link>
            <description>Authors: Corwin WL, Baust JM, Baust JG, Van Buskirk RG
    Human corneal endothelial cells (HCEC) have become increasingly important for a range of eye disease treatment therapies. Accordingly, a more detailed understanding of the processing and preservation associated stresses experienced by corneal cells might contribute to improved therapeutic outcomes. To this end, the unfolded protein response (UPR) pathway was investigated as a potential mediator of corneal cell death in response to hypothermic storage. Once preservation-induced failure had begun in HCECs stored at 4°C, it was noted that necrosis accounted for the majority of cell death but with significant apoptotic involvement, peaking at several hours post-storage (4-8h). Western blot analysis demonstrated changes associated with...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4804256</comments>
            <pubDate>Wed, 27 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4804256</guid>        </item>
        <item>
            <title>Influence of intracellular trehalose concentration and pre-freeze cell volume on the cryosurvival of rapidly frozen human erythrocytes.</title>
            <link>http://www.medworm.com/index.php?rid=4804260&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21530502%26dopt%3DAbstract</link>
            <description>Authors: Lynch AL, Slater NK
    Significant interest exists in the application of trehalose, which has low permeability to the phospholipid bilayer, as a non-toxic intracellular cryopreservative for mammalian cells. Introduction of between 8±3mM and 266±22mM trehalose into human erythrocytes using the membrane permeabilizing polymer PP-50 allowed investigation of the relationship between intracellular trehalose concentration, pre-freeze cell volume, and cryosurvival. Cellular cryosurvival increased approximately linearly with pre-freeze cell volume up to the normal volume of fresh cells; diminished cell survival correlated with subnormal pre-freeze cell volume in some cases even at &amp;gt;100mM intracellular trehalose concentration. Uptake of &amp;gt;200mM trehalose in cells with near-normal c...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4804260</comments>
            <pubDate>Wed, 20 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4804260</guid>        </item>
        <item>
            <title>Intracellular ice formation and growth in MCF-7 cancer cells.</title>
            <link>http://www.medworm.com/index.php?rid=4804259&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21536022%26dopt%3DAbstract</link>
            <description>Authors: Yang G, Zhang A, Xu LX
    Direct cell injury in cryosurgery is highly related to intracellular ice formation (IIF) during tissue freezing and thawing. Mechanistic understanding of IIF in tumor cells is critical to the development of tumor cryo-ablation protocol. In aid of a high speed CMOS camera system, the events of IIF in MCF-7 cells have been studied using cryomicroscopy. Images of 'darkening' type IIF and recrystallization are compared between cells frozen with and without ice seeding. It is found that ice seeding has significant impact on the occurrence and growth of intracellular ice. Without ice seeding, IIF is observed to occur over a very small range of temperature (∼1°C). The crystal dendrites are indistinguishable, which is independent of the cooling rate. Ice crys...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4804259</comments>
            <pubDate>Wed, 20 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4804259</guid>        </item>
        <item>
            <title>Numerical simulation of cooling rates in vitrification systems used for oocyte cryopreservation.</title>
            <link>http://www.medworm.com/index.php?rid=4804258&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21540134%26dopt%3DAbstract</link>
            <description>Authors: Sansinena M, Santos MV, Zaritzky N, Chirife J
    Oocyte cryopreservation is of key importance in the preservation and propagation of germplasm. Interest in oocyte cryopreservation has increased in recent years due to the application of assisted reproductive technologies in farm animals such as in vitro fertilization, nuclear transfer and the need for the establishment of ova/gene banks worldwide. However, the cryopreservation of the female gamete has been met with limited success mainly due to its small surface-area:volume ratio. In the past decade, several vitrification devices such as open pulled straws (OPS), fine and ultra fine pipette tips, nylon loops and polyethylene films have been introduced in order to manipulate minimal volumes and achieve high cooling rates. However, ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4804258</comments>
            <pubDate>Wed, 20 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4804258</guid>        </item>
        <item>
            <title>Long-term cryopreservation of Greek fir embryogenic cell lines: Recovery, maturation and genetic fidelity.</title>
            <link>http://www.medworm.com/index.php?rid=4804262&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21521636%26dopt%3DAbstract</link>
            <description>Authors: Krajňáková J, Sutela S, Aronen T, Gömöry D, Vianello A, Häggman H
    In coniferous species, including Greek fir (Abies cephalonica Loud), the involvement of somatic embryo plants in breeding and reforestation programs is dependent on the success of long-term cryostorage of embryogenic cultures during clonal field testing. In the present study on Greek fir, we assayed the recovery, morphological characteristics and genetic fidelity of embryogenic cell lines 6 and 8 during proliferation and maturation after long-term cryostorage. Our results indicate successful recovery of both cell lines after 6years in cryostorage. In the maturation phase, both cell lines were capable of producing somatic embryos although some differences were detected among experiments. However, these chan...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4804262</comments>
            <pubDate>Sat, 16 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4804262</guid>        </item>
        <item>
            <title>Low cryoprotectant concentrations and fast cooling for nematode cryostorage.</title>
            <link>http://www.medworm.com/index.php?rid=4804261&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21524646%26dopt%3DAbstract</link>
            <description>In this study, we present a cryopreservation technique based on low, non-toxic concentrations of cryoprotectants (≈2-4M) combined with a rapid cooling rate in the liquid nitrogen phase (-196°C). Protocols for successfully cryopreserving the plant parasitic nematodes Globodera tabacum tabacum, Heterodera schachtii and Meloidogyne incognita were developed, as demonstrated by the high survival rates and reproducibility of cyst and root-knot nematode species post-cryostorage. This approach for effective cryopreservation of viable plant-parasitic nematodes was developed by inducing an &quot;apparent vitrification&quot; by rapid cooling of the microscopic samples in less than 2M of cryoprotectant. The extremely thin structure (15-20μm width, 350-400μm length) of these nematodes, in combination with a...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4804261</comments>
            <pubDate>Sat, 16 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4804261</guid>        </item>
        <item>
            <title>Full-term development of rats from oocytes fertilized in vitro using cryopreserved ejaculated sperm.</title>
            <link>http://www.medworm.com/index.php?rid=4804264&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21513706%26dopt%3DAbstract</link>
            <description>Authors: Seita Y, Fujiwara K, Takizawa A, Furukawa K, Inomata T, Ito J, Kashiwazaki N
    For preservation of rat spermatozoa, the general-purpose method requires that the male be sacrificed for collection of spermatozoa from the epididymides. However, it would be highly useful if the ejaculated spermatozoa could be successfully cryopreserved and the frozen-thawed spermatozoa used for in vitro fertilization, since this would allow the genetically valuable rats to be maintained alive rather than sacrificed. The aim of the present study was to clarify whether ejaculated rat spermatozoa could be successfully cryopreserved and fertilized in vitro. The motility and viability of frozen-thawed ejaculated spermatozoa were similar to those of frozen-thawed epididymal spermatozoa (around 10%). The p...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4804264</comments>
            <pubDate>Mon, 11 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4804264</guid>        </item>
        <item>
            <title>Effects of cysteine and ergothioneine on post-thawed Merino ram sperm and biochemical parameters.</title>
            <link>http://www.medworm.com/index.php?rid=4804263&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21513707%26dopt%3DAbstract</link>
            <description>Authors: Coyan K, Başpınar N, Bucak MN, Akalın PP
    The aim of the current study was to evaluate the effects of cysteine and ergothioneine on the post-thawed sperm parameters, lipid peroxidation and antioxidant activities. Semen samples from 5 mature Merino rams were used in the study. Semen samples, which were diluted with a Tris-based extender containing l-Cysteine and l-(+)-Ergothioneine and no antioxidant (control), were cooled to 5°C and frozen in 0.25ml French straws. Frozen straws were then thawed individually at 37°C for 20s in a water bath for evaluation. Ergothioneine at doses of 2 and 4mM increased percentages of subjective motility, VSL and VCL, compared to controls following the freeze-thawing (P&amp;lt;0.001). Ergothioneine at three different doses led to higher rates of p...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4804263</comments>
            <pubDate>Mon, 11 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4804263</guid>        </item>
        <item>
            <title>Manual cryopreservation of human alveolar periosteal tissue segments: Effects of pre-culture on recovery rate.</title>
            <link>http://www.medworm.com/index.php?rid=4697497&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21466797%26dopt%3DAbstract</link>
            <description>Authors: Kawase T, Kogami H, Nagata M, Uematsu K, Okuda K, Burns DM, Yoshie H
    Cultured human periosteal sheets constitute a promising grafting material for periodontal tissue regenerative therapy. However, preparation of these sheets usually requires six weeks or longer, and this lengthy commitment and delay limits both clinical applicability and availability. The aim of this study is to develop an efficient, practical, cost-effective cryopreservation method for periosteal tissue segments (PTSs). Human PTSs were aseptically excised from alveolar bone and pre-cultured in Medium 199 + 10% fetal bovine serum (FBS) for the indicated number of days before they were slowly frozen down to -75(o)C in a commercial freezing vessel using medium containing 10% dimethyl sulfoxide (Me(2)SO) and vari...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4697497</comments>
            <pubDate>Fri, 01 Apr 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4697497</guid>        </item>
        <item>
            <title>The effect of EIF dynamics on the cryopreservation process of a size distributed cell population.</title>
            <link>http://www.medworm.com/index.php?rid=4697498&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21463613%26dopt%3DAbstract</link>
            <description>Authors: Fadda S, Briesen H, Cincotti A
    Typical mathematical modelling of cryopreservation of cell suspensions assumes a thermodynamic equilibrium between the ice and liquid water in the extracellular solution. This work investigates the validity of this assumption by introducing a population balance approach for dynamic extracellular ice formation (EIF) in the absence of any cryo-protectant agent (CPA). The population balance model reflects nucleation and diffusion-limited growth in the suspending solution whose driving forces are evaluated in the relevant phase diagram - This population balance description of the extracellular compartment has been coupled to a model recently proposed in the literature [Fadda et al., AIChE Journal, 56, 2173-2185, (2010)], which is capable of quantitat...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4697498</comments>
            <pubDate>Thu, 31 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4697498</guid>        </item>
        <item>
            <title>Expression and characterization of an antifreeze protein from the perennial rye grass, Lolium perenne.</title>
            <link>http://www.medworm.com/index.php?rid=4697500&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21457707%26dopt%3DAbstract</link>
            <description>Authors: Lauersen KJ, Brown A, Middleton A, Davies PL, Walker VK
    Antifreeze proteins (AFP) are an evolutionarily diverse class of stress response products best known in certain metazoans that adopt a freeze-avoidance survival strategy. The perennial ryegrass, Lolium perenne (Lp), cannot avoid winter temperatures below the crystallization point and is thought to use its LpAFP in a freeze-tolerant strategy. In order to examine properties of LpAFP in relation to L. perenne's life history, cDNA cloning, recombinant protein characterization, ice-binding activities, gene copy number, and expression responses to low temperature were examined. Transcripts, encoded by only a few gene copies, appeared to increase in abundance after diploid plants were transferred to 4°C for 1-2days, and in para...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4697500</comments>
            <pubDate>Tue, 29 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4697500</guid>        </item>
        <item>
            <title>Two applications of the thermogram of the alcohol/water binary system with compositions of cryobiological interests.</title>
            <link>http://www.medworm.com/index.php?rid=4697499&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21458437%26dopt%3DAbstract</link>
            <description>Authors: Weng L, Li W, Zuo J
    Quantitative analyses of the bound water content in the alcohol aqueous solution and its osmotic behavior should be cryobiologically significant. This paper has presented two applications of the thermogram of the alcohol/water system recorded by differential scanning calorimeter (DSC). Both applications are: 1. generating the quantitative relationship between the bound water content and the solution composition; 2. calculating the osmotic virial coefficients for alcohols. Five alcohols including methanol, ethanol, ethylene glycol, propylene glycol and glycerol are investigated. In the present study, partial binary phase diagrams of these five alcohol solutions are determined in the first place. The bound water contents in these solutions are quantitatively ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4697499</comments>
            <pubDate>Tue, 29 Mar 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4697499</guid>        </item>
        <item>
            <title>Effects of cryopreservation with a newly-developed magnetic field programmed freezer on periodontal ligament cells and pulp tissues.</title>
            <link>http://www.medworm.com/index.php?rid=4638147&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21397593%26dopt%3DAbstract</link>
            <description>Authors: Abedini S, Kaku M, Kawata T, Koseki H, Kojima S, Sumi H, Motokawa M, Fujita T, Ohtani J, Ohwada N, Tanne K
    The purpose of this study was to evaluate the effects of long-term cryopreservation on the isolated human periodontal ligament cells (PDL) and pulp tissues. In the first part of study, 10 freshly extracted teeth were selected and divided into two groups. In the cryopreserved group, the teeth were frozen for 5years using a programmed freezer combined with a magnetic field, known as Cells Alive System &quot;CAS&quot;. As for the control group, freshly extracted teeth were used. In each group, extracted PDL tissues were cultured and gene expression and protein concentration of collagen type I, alkaline-phosphatase (ALP) and vascular endothelial growth factor (VEGF) was compared betwee...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4638147</comments>
            <pubDate>Thu, 17 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4638147</guid>        </item>
        <item>
            <title>Identification of two hydrophilins that contribute to the desiccation and freezing tolerance of yeast (Saccharomyces cerevisiae) cells.</title>
            <link>http://www.medworm.com/index.php?rid=4638146&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21420397%26dopt%3DAbstract</link>
            <description>Authors: Dang NX, Hincha DK
    Hydrophilins are a group of proteins that are present in all organisms and that have been defined as being highly hydrophilic and rich in glycine. They are assumed to play important roles in cellular dehydration tolerance. There are twelve genes in the yeast Saccharomyces cerevisiae that encode hydrophilins and most of these genes are stress responsive. However, the functional role of yeast hydrophilins, especially in desiccation and freezing tolerance, is largely unknown. Here, we selected six candidate hydrophilins for further analysis. All six proteins were predicted to be intrinsically disordered, i.e. to have no stable structure in solution. The contribution of these proteins to the desiccation and freezing tolerance of yeast was investigated in the res...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4638146</comments>
            <pubDate>Thu, 17 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4638146</guid>        </item>
        <item>
            <title>Amicus Plato, sed magis amica veritas: Plots must obey the laws they refer to and models shall describe biophysical reality!</title>
            <link>http://www.medworm.com/index.php?rid=4578995&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21376028%26dopt%3DAbstract</link>
            <description>Authors: Katkov II
    In the companion paper, we discussed in details proper linearization, calculation of the inactive osmotic volume, and analysis of the results on the Boyle- vant' Hoff plots. In this Letter, we briefly address some common errors and misconceptions in osmotic modeling and propose some approaches, namely: 1) inapplicability of the Kedem-Katchalsky formalism model in regards to the cryobiophysical reality, 2) calculation of the membrane hydraulic conductivity L(p) in the presence of permeable solutes, 3) proper linearization of the Arrhenius plots for the solute membrane permeability, 4) erroneous use of the term &quot;toxicity&quot; for the cryoprotective agents, and 5) advantages of the relativistic permeability approach (RP) developed by us vs. traditional (&quot;classic&quot;) 2-paramet...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4578995</comments>
            <pubDate>Tue, 01 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4578995</guid>        </item>
        <item>
            <title>On Proper Linearization, Construction and Analysis of the Boyle- van't Hoff Plots and Correct Calculation of the Osmotically Inactive Volume.</title>
            <link>http://www.medworm.com/index.php?rid=4578994&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21376029%26dopt%3DAbstract</link>
            <description>Authors: Katkov II
    The Boyle van't Hoff (BVH) law of physics has been widely used in cryobiology for calculation of the key osmotic parameters of cells and optimization of cryo-protocols. The proper use of linearization of the Boyle - vant'Hoff relationship for the osmotically inactive volume (v(b)) has been discussed in a rigorous way in (Katkov, Cryobiology, 2008, 57:142-149). Nevertheless, scientists in the field have been continuing to use inappropriate methods of linearization (and curve fitting) of the BVH data, plotting the BVH line and calculation of v(b). Here, we discuss the sources of incorrect linearization of the BVH relationship using concrete examples of recent publications, analyze the properties of the correct BVH line (which is unique for a given v(b)), provide approp...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4578994</comments>
            <pubDate>Tue, 01 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4578994</guid>        </item>
        <item>
            <title>Loss of Fertilization Potential of Desiccated Rhesus Macaque Spermatozoa Following Prolonged Storage.</title>
            <link>http://www.medworm.com/index.php?rid=4525420&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21349262%26dopt%3DAbstract</link>
            <description>This study demonstrates that while the vacuum dried spermatozoa were immotile and had compromised plasma membrane integrity, they were capable of fertilization using ICSI and could support embryo development to the morula stage.
    PMID: 21349262 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4525420</comments>
            <pubDate>Mon, 21 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4525420</guid>        </item>
        <item>
            <title>Cryobanking the genetic diversity in the critically endangered Iberian lynx (Lynx pardinus) from skin biopsies. Investigating the cryopreservation and culture ability of highly valuable explants and cells.</title>
            <link>http://www.medworm.com/index.php?rid=4525424&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21315706%26dopt%3DAbstract</link>
            <description>Authors: León-Quinto T, Simón MA, Sánchez A, Martín F, Soria B
    Cryobanking skin samples permit preserving a maximum of genetic representation from the population biodiversity. This is a relevant aspect for threatened species, potentially menaced by an epizooty and from which it is difficult to obtain gametes. As a first step for properly cryobanking skin samples of a given species, the optimal conditions of culture and freezing have to be studied by covering a broad range of possibilities. This paper presents, for the first time, a systematic study of such conditions for the Iberian lynx (Lynx pardinus). To that end, we have analyzed twenty different culture conditions and fifteen different freezing solutions for skin explants, as well as three freezing solutions for isolated cells...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4525424</comments>
            <pubDate>Sat, 19 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4525424</guid>        </item>
        <item>
            <title>Advances in the cryopreservation of sea-urchin embryos: Potential application in marine water quality assessment.</title>
            <link>http://www.medworm.com/index.php?rid=4525421&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21338597%26dopt%3DAbstract</link>
            <description>Authors: Bellas J, Paredes E
    Among the most widely used biological techniques in marine pollution assessment, the sea-urchin embryo-larval bioassay is in an advanced developmental stage. Cryopreservation might help to overcome the problem of the spawning seasonality and therefore strengthen the use of those embryo-larval bioassays. This work investigates different factors influencing cryopreservation of sea-urchin embryos, including the cooling rates and holding temperatures, the seeding, or the impact of plunging into liquid nitrogen. The blastula stage yielded better results than the fertilised egg, and the most effective cryoprotectants combination was dimethyl sulfoxide 1.5 M plus trehalose 0.04 M. The optimised protocol developed begins with an initial hold at 4°C for 2 min, foll...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4525421</comments>
            <pubDate>Fri, 18 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4525421</guid>        </item>
        <item>
            <title>Machine perfusion at 20°C reduces preservation damage to livers from non-heart beating donors.</title>
            <link>http://www.medworm.com/index.php?rid=4525423&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21315707%26dopt%3DAbstract</link>
            <description>Authors: Ferrigno A, Rizzo V, Boncompagni E, Bianchi A, Gringeri E, Neri D, Richelmi P, Freitas I, Cillo U, Vairetti M
    We previously reported that machine perfusion (MP) performed at 20°C enhanced the preservation of steatotic rat livers. Here, we tested whether rat livers retrieved 30min after cardiac arrest (NHBDs) were better protected by MP at 20°C than with cold storage. We compared the recovery of livers from NHBDs with organs obtained from heart beating donors (HBDs) preserved by cold storage. MP technique: livers were perfused for 6h with UW-G modified at 20°C. Cold storage: livers were perfused in situ and preserved with UW solution at 4°C for 6h. Both MP and cold storage preserved livers were reperfused with Krebs-Heinselet buffer (2h at 37°C). AST and LDH release and mi...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4525423</comments>
            <pubDate>Wed, 16 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4525423</guid>        </item>
        <item>
            <title>Cryopreservation of amniotic fluid-derived stem cells using natural cryoprotectants and low concentrations of dimethylsulfoxide.</title>
            <link>http://www.medworm.com/index.php?rid=4525422&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21335000%26dopt%3DAbstract</link>
            <description>In this study, we assessed the use of disaccharides, antioxidants and caspase inhibitors for cryopreservation of AFSCs in combination with a reduced concentration of Me(2)SO. The thawed cells were tested for viability with MTT assays and a growth curve was created to measure population doubling time. In addition, we performed flow cytometry analysis for cell surface antigens, RT-PCR for mRNA expression of stem cell markers, and assays to determine the myogenic differentiation potential of the cells. A statistically significant (p&amp;lt;0.05) increase in post-thawed cell viability in solutions containing trehalose, catalase and zVAD-fmk with 5% Me(2)SO was observed. The solutions containing trehalose and catalase with 5% or 2.5% (v/v) Me(2)SO produced results similar to those for the control (...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4525422</comments>
            <pubDate>Tue, 15 Feb 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4525422</guid>        </item>
        <item>
            <title>Evaluation of multi- and inter-disciplinary research - the no-peer problem.</title>
            <link>http://www.medworm.com/index.php?rid=4470808&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21277294%26dopt%3DAbstract</link>
            <description>Authors: Elliott JA
    
    PMID: 21277294 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4470808</comments>
            <pubDate>Fri, 28 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4470808</guid>        </item>
        <item>
            <title>Addition of oligosaccharide decreases the freezing lesions on human red blood cell membrane in the presence of dextran and glucose.</title>
            <link>http://www.medworm.com/index.php?rid=4470809&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21276438%26dopt%3DAbstract</link>
            <description>In conclusion, addition of oligosaccharide can efficiently reduce lesions of freezing on red blood cell membrane in the presence of glucose and dextran.
    PMID: 21276438 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4470809</comments>
            <pubDate>Wed, 26 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4470809</guid>        </item>
        <item>
            <title>Consequences of metaphase II oocyte cryopreservation on mRNA content.</title>
            <link>http://www.medworm.com/index.php?rid=4470811&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21272569%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Oocyte cryopreservation is associated with molecular injury associated with the decrease of stored mRNA. However the V/W protocol is more conservative than SF/RT resulting in a level of mRNA sufficient to maintain biologic functions in the subsequent fertilized oocyte.
    PMID: 21272569 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4470811</comments>
            <pubDate>Tue, 25 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4470811</guid>        </item>
        <item>
            <title>Galacto-oligosaccharides as protective molecules in the preservation of Lactobacillus delbrueckii subsp. bulgaricus.</title>
            <link>http://www.medworm.com/index.php?rid=4470810&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21272570%26dopt%3DAbstract</link>
            <description>Authors: Elizabeth Tymczyszyn E, Gerbino E, Illanes A, Gómez-Zavaglia A
    In this work, the protective capacity of galacto-oligosaccharides in the preservation of Lactobacillus delbrueckii subsp. bulgaricus CIDCA 333 was evaluated. Lactobacillus bulgaricus was freeze-dried or dried over silica gel in the presence of three commercial products containing galacto-oligosaccharides. The freeze-dried samples were stored at 5 and 25°C for different periods of time. After desiccation, freeze-drying or storage, samples were rehydrated and bacterial plate counts were determined. According to the results obtained, all galacto-oligosaccharides assays demonstrated to be highly efficient in the preservation of L. bulgaricus. The higher content of galacto-oligosaccharides in the commercial products w...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4470810</comments>
            <pubDate>Tue, 25 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4470810</guid>        </item>
        <item>
            <title>Cytotoxicity Effects of Cryoprotectants as Single-Component and Cocktail Vitrification Solutions.</title>
            <link>http://www.medworm.com/index.php?rid=4400858&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21262212%26dopt%3DAbstract</link>
            <description>In this study, we address these issues by determining the cytotoxicity kinetics for dimethylsulfoxide (Me(2)SO) and 1,2-propanediol (PD) on alginate-encapsulated βTC-tet mouse insulinomas for a range of concentrations and temperatures. Cytotoxicity kinetics were also determined for two cocktails, DPS (3M Me(2)SO + 3M PD + 0.5M sucrose) and PEG400 (1M Me(2)SO + 5M PD + 0.34 M poly(ethylene)glycol with M.W. of 400). PD was found to be more cytotoxic than Me(2)SO at higher concentrations and temperatures. This was reflected in PEG400 being more cytotoxic at room temperature than PEG400 at 4°C or DPS at either temperature. Addition of non-permeating solutes increased the cytotoxicity of cocktails. Furthermore, results indicate that CPA cytotoxicity may not be additive and that combining CPAs...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4400858</comments>
            <pubDate>Fri, 21 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4400858</guid>        </item>
        <item>
            <title>Development of a Cryopreservation Protocol for Testicular Interstitial Cells with the Account of Temperature Intervals for Controlled Cooling below -60°С</title>
            <link>http://www.medworm.com/index.php?rid=4400857&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21262213%26dopt%3DAbstract</link>
            <description>Authors: Gurina TM, Pakhomov AV, Kyryliuk AL, Bozhok GA
    A long course of anticancer therapy may lead to testicular steroidogenesis destruction. Cryopreservation of testicular interstitial cells (TIC) would be a strategy to protect hormonal and fertile potential of pre-pubertal boys treated with chemo- or radiotherapy. The aim of this research was to optimize protocols for freezing of TIC. Essential physical processes associated with the presence of dimethyl sulphoxide (Me2SO) in the cryoprotectant solution take place at the temperatures below -60°С. These processes are the eutectic crystallization at the stage of freezing and the recrystallization before the melting of the eutectic mixture at the stage of heating. Both of the processes affect the viability of the cells subjected to c...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4400857</comments>
            <pubDate>Fri, 21 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4400857</guid>        </item>
        <item>
            <title>Cryopreservation of buffy-coat-derived platelet concentrates in dimethyl sulfoxide and platelet additive solution.</title>
            <link>http://www.medworm.com/index.php?rid=4400859&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21241687%26dopt%3DAbstract</link>
            <description>Authors: Johnson LN, Winter KM, Reid S, Hartkopf-Theis T, Marks DC
    Platelets prepared in plasma can be frozen in 6% dimethyl sulfoxide (Me(2)SO) and stored for extended periods at -80°C. The aim of this study was to reduce the plasma present in the cryopreserved product, by substituting plasma with platelet additive solution (PAS; SSP+), whilst maintaining in vitro platelet quality. Buffy coat-derived pooled leukoreduced platelet concentrates were frozen in a mixture of SSP+, plasma and 6% Me(2)SO. The platelets were concentrated, to avoid post-thaw washing, and frozen at -80°C. The cryopreserved platelet units (n=9) were rapidly thawed at 37°C, reconstituted in 50% SSP+/plasma and stored at 22°C. Platelet recovery and quality were examined 1 and 24h post-thaw and compared to the p...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4400859</comments>
            <pubDate>Sat, 15 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4400859</guid>        </item>
        <item>
            <title>Characterization of a novel β-helix antifreeze protein from the desert beetle Anatolica polita.</title>
            <link>http://www.medworm.com/index.php?rid=4400860&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21232534%26dopt%3DAbstract</link>
            <description>In this study, a novel antifreeze protein gene from the desert beetle Anatolica polita (named as Apafp752) was expressed in a high level in Escherichia coli strain BL21 (DE3). An approximately 30kDa fusion protein thioredoxin (Trx)-ApAFP752 was purified through Ni-NTA affinity chromatography and gel filtration chromatography. The activity of the purified fusion protein Trx-ApAFP752 was analyzed by thermal hysteresis activity (THA) and cryoprotection assay. The results suggested that Trx-ApAFP752 conferred freeze resistance on bacterium in a concentration- and time-dependent manner and the cryoprotective effect increased under alkaline conditions. Circular Dichroism (CD) spectrum analysis showed that the recombinant protein of ApAFP752 possessing β-sheet as the main structure was stable un...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4400860</comments>
            <pubDate>Tue, 11 Jan 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4400860</guid>        </item>
        <item>
            <title>The advantages of Low Density Lipoproteins in the cryopreservation of bull semen.</title>
            <link>http://www.medworm.com/index.php?rid=4337591&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21199643%26dopt%3DAbstract</link>
            <description>In conclusion, sperm cryopreserved in the extender containing 8% LDL in place of egg yolk exhibited the greatest percentages of post-thaw sperm motility, acrosome integrity and membrane integrity, in comparison with the control, and favored the highest antioxidant activities of CAT, GSH-Px and GSH in comparison with other groups. The replacement of egg yolk by LDL in the composition of extenders was beneficial for bull sperm cryopreservation.
    PMID: 21199643 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4337591</comments>
            <pubDate>Fri, 31 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4337591</guid>        </item>
        <item>
            <title>High-throughput cryopreservation of spermatozoa of blue catfish (Ictalurus furcatus): Establishment of an approach for commercial-scale processing.</title>
            <link>http://www.medworm.com/index.php?rid=4337592&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21176772%26dopt%3DAbstract</link>
            <description>This study demonstrates that the protocol established for high-throughput cryopreservation of blue catfish sperm can provide commercially relevant quantities and quality of sperm with stable fertility for hybrid catfish production and provides a model for establishment of commercial-scale approaches for other aquatic species.
    PMID: 21176772 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4337592</comments>
            <pubDate>Sun, 19 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4337592</guid>        </item>
        <item>
            <title>Meiotic maturation of vitrified immature chousingha (Tetracerus quadricorni) oocytes recovered postmortem.</title>
            <link>http://www.medworm.com/index.php?rid=4276449&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21168399%26dopt%3DAbstract</link>
            <description>The objective of this study was to assess the in vitro meiotic maturation of chousingha (four-horned antelope) oocytes following vitrification using open pulled straw (OPS) method. The average number of oocytes recovered per ovary was 65.2. The proportion of oocytes that matured was significantly lower in vitrified oocytes (29.4%) when compared with fresh oocytes (69.3%). The study provides evidence that it is possible to cryopreserve immature oocytes by vitrification collected from the ovaries of chousingha at postmortem and also demonstrates that these cryopreserved oocytes retain their potential to undergo in vitro meiotic maturation.
    PMID: 21168399 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4276449</comments>
            <pubDate>Thu, 16 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4276449</guid>        </item>
        <item>
            <title>Hypothermia protects H9c2 cardiomyocytes from H(2)O(2) induced apoptosis.</title>
            <link>http://www.medworm.com/index.php?rid=4276448&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21168400%26dopt%3DAbstract</link>
            <description>In conclusion, we could demonstrate that hypothermia protects cardiomyocytes during oxidative stress by preventing apoptosis via inhibiting mitochondrial dysfunction and DNA damage.
    PMID: 21168400 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4276448</comments>
            <pubDate>Thu, 16 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4276448</guid>        </item>
        <item>
            <title>Sperm cryopreservation of the critically endangered olive barb (sarpunti) Puntius sarana (Hamilton, 1822).</title>
            <link>http://www.medworm.com/index.php?rid=4276447&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21168401%26dopt%3DAbstract</link>
            <description>Authors: Nahiduzzaman M, Hassan MM, Khanam UH, Mamun SN, Hossain MA, Tiersch TR
    The present study focused on development of a sperm cryopreservation protocol for the critically endangered olive barb Puntius sarana (Hamilton, 1822) collected from two stocks within Bangladesh and reared in the Fisheries Field Laboratory, Bangladesh Agricultural University (BAU). The sperm were collected in Alsever's solution prepared at 296 mOsmol kg(-1). Sperm were activated with distilled water (24 mOsmol kg(-1)) to characterize motility. Maximum motility (90%) was observed within 15 s after activation, and sperm remained motile for 35 s. Sperm activation was evaluated in different osmolalities and motility was completely inhibited when osmolality of the extender was ⩾ 287 mOsmol kg(-1). To evaluate ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4276447</comments>
            <pubDate>Thu, 16 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4276447</guid>        </item>
        <item>
            <title>Low temperature survival in different life stages of the Iberian slug, Arion lusitanicus.</title>
            <link>http://www.medworm.com/index.php?rid=4276446&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21168402%26dopt%3DAbstract</link>
            <description>Authors: Slotsbo S, Hansen LM, Holmstrup M
    The slug Arion lusitanicus Mabille (Gastropoda: Pulmonata: Arionidae) is an invasive species which has spread to most parts of Europe. The area of origin is unknown, but A. lusitanicus seems to cope well with the local conditions in the countries to which it has migrated. It spreads rapidly, occurs often in high densities and has become a serious pest in most European countries. Therefore there is an urgent need for better knowledge of the ecophysiology of Arion lusitanicus, such as the influence of climatic conditions, in order to develop prognostic models and strategies for novel pest management practises. The aim of our study was to investigate the influence of subzero temperatures in relation to winter survival. A. lusitanicus is shown to ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4276446</comments>
            <pubDate>Thu, 16 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4276446</guid>        </item>
        <item>
            <title>Reduced glutathione content in human sperm is decreased after cryopreservation. Effect of the addition of reduced glutathione to the freezing and thawing extenders.</title>
            <link>http://www.medworm.com/index.php?rid=4276450&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21156167%26dopt%3DAbstract</link>
            <description>In conclusion, the antioxidant defensive capacity of the GSH is severely altered by the freeze-thawing process. The addition of GSH to the freezing and thawing extender could be of partial and limited benefit in improving the function of frozen human spermatozoa.
    PMID: 21156167 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4276450</comments>
            <pubDate>Sat, 11 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4276450</guid>        </item>
        <item>
            <title>The disruption in actin-perinuclear theca interactions are related with changes induced by cryopreservation observed on sperm chromatin nuclear decondensation of boar semen.</title>
            <link>http://www.medworm.com/index.php?rid=4276451&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21145884%26dopt%3DAbstract</link>
            <description>Authors: Gutiérrez-Pérez O, Juárez-Mosqueda ML, Mota D, Trujillo ME
    The perinuclear theca (PT) is a cytoskeletal structure that surrounds the mammal sperm nucleus which must be disrupted once the sperm has penetrated the oocyte to permit normal chromatin decondensation and formation of male pronucleus. F-actin is a thermo sensitive protein found in the equatorial segment which is involved in the stability of PT. It has been reported that cryopreservation induces alterations in nuclear decondensation of spermatozoa, which have been interpreted as an over condensation. The aims of the present study were identified the presence of changes in sperm sPT integrity of frozen-thawed boar spermatozoa and its effect in sperm nuclei decondensation; and whether changes in the actin cytoskeleton...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4276451</comments>
            <pubDate>Thu, 09 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4276451</guid>        </item>
        <item>
            <title>Cryobiological properties of immature zebrafish oocytes assessed by their ability to be fertilized and develop into hatching embryos.</title>
            <link>http://www.medworm.com/index.php?rid=4218132&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21114971%26dopt%3DAbstract</link>
            <description>Authors: Seki S, Kouya T, Tsuchiya R, Valdez Jr DM, Jin B, Koshimoto C, Kasai M, Edashige K
    As a step to develop a cryopreservation method for zebrafish oocytes, we investigated the cryobiological properties of immature oocytes at stage III by examining their ability to mature and to develop into hatching embryos after fertilization. When oocytes were chilled at -5 °C for 30 min, the maturation rate decreased, but the rates of fertilization and hatching were not significantly different from those of controls. When oocytes were exposed to hypotonic solutions for 60 min at 25 °C, the rates of maturation, fertilization, and hatching decreased in a solution with 0.16 Osm/kg or below. When oocytes were exposed to hypertonic solutions (containing sucrose) at 25 °C for 30 min, the maturati...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4218132</comments>
            <pubDate>Fri, 26 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4218132</guid>        </item>
        <item>
            <title>Effect of cryopreservation on fish sperm subpopulations.</title>
            <link>http://www.medworm.com/index.php?rid=4218145&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21112321%26dopt%3DAbstract</link>
            <description>Authors: Beirão J, Cabrita E, Pérez-Cerezales S, Martínez-Páramo S, Herráez MP
    The evaluation of the motility data obtained with a CASA system, applying a Two-Step Cluster analysis, identified in seabream sperm 3 different sperm subpopulations that correlated differently with embryo hatching rates. Hence, we designed an experiment to understand the effect of the application of different cryopreservation protocols in these sperm motility-based subpopulations. We analyzed Sparus aurata frozen/thawed semen motility 15, 30, 45 and 60 seconds after activation, using CASA software. Different protocols were applied for cryopreservation: three different cryoprotectants (Dimethyl Sulfoxide (Me(2)SO), Ethylene Glycol (EG) and Propylene Glycol (PG)) each at two different concentrations and t...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4218145</comments>
            <pubDate>Thu, 25 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4218145</guid>        </item>
        <item>
            <title>Frozen-thawed rhesus sperm retain normal morphology and highly progressive motility but exhibit sharply reduced efficiency in penetrating cervical mucus and hyualuronic acid gel.</title>
            <link>http://www.medworm.com/index.php?rid=4218138&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21112322%26dopt%3DAbstract</link>
            <description>Authors: Tollner TL, Dong Q, Vandevoort CA
    The preservation of the genetic diversity of captive populations of rhesus monkeys is critical to the future of biomedical research. Cryopreservation of rhesus macaque sperm is relatively simple to perform, yields high post-thaw motility, and theoretically, provides via artificial insemination (AI) a way to easily transfer genetics among colonies of animals. In the interest of optimizing semen cryopreservation methods for use with vaginal AI, we evaluated the ability of frozen-thawed rhesus sperm to penetrate periovulatory cervical mucus (CM). Motile sperm concentration of pre-freeze (&quot;fresh&quot;) and post-thawed (&quot;thawed&quot;) samples from 5 different males were normalized for both computer assisted sperm motion analysis and CM penetration experiment...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4218138</comments>
            <pubDate>Thu, 25 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4218138</guid>        </item>
        <item>
            <title>Survival of mouse oocytes after being cooled in a vitrification solution to -196°C at 95° to 70,000°C/min and warmed at 610° to 118,000°C/min: A new paradigm for cryopreservation by vitrification.</title>
            <link>http://www.medworm.com/index.php?rid=4166187&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21055397%26dopt%3DAbstract</link>
            <description>Authors: Mazur P, Seki S
    There is great interest in achieving reproducibly high survivals of mammalian oocytes (especially human) after cryopreservation, but the results to date have not matched the interest. A prime cause of cell death is the formation of more than trace amounts of intracellular ice, and one strategy to avoid it is vitrification. In vitrification procedures, cells are loaded with high concentrations of glass-inducing solutes and cooled to -196°C at rates high enough to presumably induce the glassy state. In the last decade, several devices have been developed to achieve very high cooling rates. Nearly all in the field have assumed that the cooling rate is the critical factor. The purpose of our study was to test that assumption by examining the consequences of coolin...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4166187</comments>
            <pubDate>Tue, 02 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4166187</guid>        </item>
        <item>
            <title>Incorporation of DMSO and dextran-40 into a gelatin/alginate hydrogel for controlled assembled cell cryopreservation.</title>
            <link>http://www.medworm.com/index.php?rid=4166186&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21055398%26dopt%3DAbstract</link>
            <description>Authors: Wang X, Xu H
    A new cell cryopreservation strategy for cell-assembling constructs was proposed. With this strategy, different concentrations of dimethysulfoxide (DMSO) and dextran-40 were directly incorporated into the cell/gelatin/alginate systems, prototyped according to a predesigned structure, cryopreserved at -80°C for 10 days and followed a thawing process at 17°C. The rheological properties, bonding water contents and melting points of the gelatin/alginate hydrogel systems were changed with the addition of different amounts of DMSO. The microscopy analysis, (3-[4,5-dimethylthiazol-2-yl]-2, 5-diphenyl tetrasodium bromide (MTT) and hematoxylin and eosin (HE) staining indicated that the cell numbers were progressively in a selected DMSO concentration range. With DMSO 5% (...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4166186</comments>
            <pubDate>Tue, 02 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4166186</guid>        </item>
        <item>
            <title>Response of the cell membrane-cytoskeleton complex to osmotic and freeze/thaw stresses.</title>
            <link>http://www.medworm.com/index.php?rid=4166185&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21055399%26dopt%3DAbstract</link>
            <description>This study shows that both the membrane and cytoskeleton, as a system, are involved in the osmotic and freeze/thaw-induced responses of the mammalian cells.
    PMID: 21055399 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4166185</comments>
            <pubDate>Tue, 02 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4166185</guid>        </item>
        <item>
            <title>On freeze-thaw sequence of vital organ of assuming the cryoablation for malignant lung tumors by using cryoprobe as heat source.</title>
            <link>http://www.medworm.com/index.php?rid=4139582&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21036162%26dopt%3DAbstract</link>
            <description>Authors: Nakatsuka S, Yashiro H, Inoue M, Kuribayashi S, Kawamura M, Izumi Y, Tsukada N, Yamauchi Y, Hashimoto K, Iwata K, Nagasawa T, Lin YS
    Regarding cryoablation for the malignant lung tumors, multiple trials of the freeze-thaw process have been made, and we considered it necessary to view and analyze the freeze-thaw process as a freeze-thaw sequence. We caused the sequence in a porcine lung in vivo by using an acicular, cylindrical stainless-steel probe as the heat source for the freeze-thaw sequence and cooling to -150°C with super high-pressure argon gas by causing the Joule-Thompson effect phenomenon at the tip of the probe. In this experiment, we examined the sequence by measuring the temperature and using the isothermal curve and the freezing function. As a result, it was dem...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4139582</comments>
            <pubDate>Fri, 29 Oct 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4139582</guid>        </item>
        <item>
            <title>MDM2-related responses in 3T3-L1 adipocytes exposed to cooling and subsequent rewarming.</title>
            <link>http://www.medworm.com/index.php?rid=4139583&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21034728%26dopt%3DAbstract</link>
            <description>Authors: Ohsaka Y, Nishino H
    Insulin-like growth factor-I and insulin induce the production of phospho-Ser-166 MDM2, a target of Akt, and influence the formation of the MDM2 complex. The glycolipid hormone insulin differentially activates phosphatidylinositol 3-kinase (PI3K)/Akt pathways in 3T3-L1 (L1) adipocytes incubated at 19°C. Responses of L1 adipocytes to different temperature changes and their regulatory mechanisms are poorly understood. We exposed L1 adipocytes to cooling and subsequent rewarming in the presence or absence of wortmannin, a PI3K inhibitor, or mithramycin A, a transcription inhibitor, and examined the induction of phospho-Ser-166 MDM2 and MDM2 and the subcellular formation of the MDM2 complex using western blot analysis. Exposure to 28 and 18°C induced phospho-...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4139583</comments>
            <pubDate>Tue, 26 Oct 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4139583</guid>        </item>
        <item>
            <title>Ice restructuring inhibition activities in antifreeze proteins with distinct differences in thermal hysteresis.</title>
            <link>http://www.medworm.com/index.php?rid=4123238&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20977900%26dopt%3DAbstract</link>
            <description>Authors: Yu SO, Brown A, Middleton AJ, Tomczak MM, Walker VK, Davies PL
    Antifreeze proteins (AFPs) share two related properties: the ability to depress the freezing temperature below the melting point of ice (thermal hysteresis; TH); and the ability to inhibit the restructuring of ice into larger crystals. Since the 'hyperactive' AFPs, which have been more recently discovered, show an order of magnitude more TH than previously characterized AFPs, we have now determined their activities in ice restructuring inhibition (IrI) assays. IrI activities of three TH-hyperactive AFPs and three less TH-active AFPs varied over an 8-fold range. There was no obvious correlation between high TH activity and high IrI activity. However, the use of mutant AFPs demonstrated that severe disruption of ice-...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4123238</comments>
            <pubDate>Sat, 23 Oct 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4123238</guid>        </item>
        <item>
            <title>Melting Point Equations for the Ternary System Water/Sodium Chloride/Ethylene Glycol Revisited.</title>
            <link>http://www.medworm.com/index.php?rid=4088296&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20955693%26dopt%3DAbstract</link>
            <description>Authors: Benson JD, Bagchi A, Han X, Critser JK, Woods EJ
    Partial phase diagrams are of considerable utility in the development of optimized cryobiological procedures. Recent theoretical predictions of the melting points of ternary solutions of interest to cryobiology have caused us to re-examine measurments that our group made for the ethylene-glycol-sodium chloride-water phase diagram. Here we revisit our previous experiments by measuring melting points at five ethylene-glycol to sodium chloride ratios (R values; R=5, 10, 15, 30, and 45) and five levels of concentration for each ratio. Melting points were averaged from three measurements and plotted as a function of total solute concentration for each R value studied. The new measurements differed from our original experimental value...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4088296</comments>
            <pubDate>Thu, 14 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4088296</guid>        </item>
        <item>
            <title>Dehydration improves cryopreservation of coconut (Cocos nucifera L.).</title>
            <link>http://www.medworm.com/index.php?rid=4088295&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20959171%26dopt%3DAbstract</link>
            <description>Authors: Sisunandar , Sopade PA, Samosir YM, Rival A, Adkins SW
    Cryopreservation of coconut can be used as a strategy to back up the establishment of living collections which are expensive to maintain and are under constant threat from biotic and abiotic factors. Unfortunately, cryopreservation protocols still need to be developed that are capable of producing a sizeable number of field-grown plants. Therefore, we report on the development of an improved cryopreservation protocol which can be used on a wide range of coconut cultivars. The cryopreservation of zygotic embryos and their recovery to soil-growing plants was achieved through the application of four optimised steps viz.: (i) rapid dehydration; (ii) rapid cooling; (iii) rapid warming and recovery in vitro and (iv) acclimatisat...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4088295</comments>
            <pubDate>Thu, 14 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4088295</guid>        </item>
        <item>
            <title>The Effect of Cysteine and Glutathione on Sperm and Oxidative Stress Parameters of Post-Thawed Bull Semen.</title>
            <link>http://www.medworm.com/index.php?rid=4088297&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20951122%26dopt%3DAbstract</link>
            <description>Authors: Tuncer PB, Bucak MN, Büyükleblebici S, Sarıözkan S, Yeni D, Eken A, Akalın PP, Kinet H, Avdatek F, Fidan AF, Gündoğan M
    The aim of this study was to determine the effects of antioxidants such as reduced glutathione (GSH) and cysteine in Laiciphose(®) extender on semen parameters, fertilizing ability, lipid peroxidation (LPO) level and glutathione peroxidise (GPx) activity of post-thawed bull semen. Totally 54 ejaculates of three bulls were used in the study. Five groups, namely; GSH (0.5 and 2 mM), cysteine (5 and 10 mM) and control group, were conducted to test the antioxidants in Laiciphose(®). Insemination doses were processed that each 0.25-ml straw contained 15 x 10(6) sperm. The addition of antioxidants did not present any significant effect on the percentages o...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4088297</comments>
            <pubDate>Tue, 12 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4088297</guid>        </item>
        <item>
            <title>Pre-Conditioning Cryosurgery: Cellular and Molecular Mechanisms and Dynamics of TNF-α Enhanced Cryotherapy in an in vivo Prostate Cancer Model System.</title>
            <link>http://www.medworm.com/index.php?rid=4077279&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20940007%26dopt%3DAbstract</link>
            <description>Authors: Jiang J, Goel R, Schmechel S, Vercellotti G, Forster C, Bischof J
    Cryosurgery is increasingly being used to treat prostate cancer; however, a major limitation is local recurrence of disease within the previously frozen tissue. We have recently demonstrated that tumor necrosis factor alpha (TNF-α), given 4 hours prior to cryosurgery can yield complete destruction of prostate cancer within a cryosurgical iceball. The present work continues the investigation of the cellular and molecular mechanisms and dynamics of TNF-α enhancement on cryosurgery. In vivo prostate tumor (LNCaP Pro 5) was grown in a dorsal skin fold chamber (DSFC) on a male nude mouse. Intravital imaging, thermography, and post-sacrifice histology and immunohistochemistry were used to assess iceball location and...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4077279</comments>
            <pubDate>Fri, 08 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4077279</guid>        </item>
        <item>
            <title>Cryoprotectant agent toxicity in porcine articular chondrocytes.</title>
            <link>http://www.medworm.com/index.php?rid=4077278&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20940008%26dopt%3DAbstract</link>
            <description>This study was designed to determine the order of toxicity of five commonly used cryoprotectant agents as well as interactions that occur between them. Isolated porcine articular chondrocytes were exposed to individual cryoprotectant agents and combinations of these agents at 1M and 3M concentrations for 5 minutes and 120 minutes. Cell viability was determined using membrane integrity dyes and a metabolic activity assay. Subsequently, a regression analysis based study was undertaken to extract the maximum amount of information from this data. Results of this study demonstrated that all 1M solutions were minimally toxic. The 3M solutions demonstrated varying toxicity after 120 minutes. Ethylene glycol and glycerol were less toxic than propylene glycol, dimethyl sulfoxide, and formamide. Com...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4077278</comments>
            <pubDate>Fri, 08 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4077278</guid>        </item>
        <item>
            <title>Cryosolvent interaction with cellular actin using 3T3-LI cells as a model system.</title>
            <link>http://www.medworm.com/index.php?rid=4062183&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20937267%26dopt%3DAbstract</link>
            <description>Authors: Tian P, Legge M
    Previous immunolocalisation studies using intact cells have identified modification of the cytoskeleton by cryoprotectants. In the present study we have used a proteomics approach to directly resolve the interactive effects of 3T3-LI cells exposed to two cryoprotectants, dimethyl sulphoxide (Me(2)SO) and 1,2-propanediol (PROH) in 5,10, 20 and 50 (v/v) per cent solutions respectively. Two-dimensional protein electrophoresis and western blot analysis of the cell extracts identified a range of immunoreactive actin fragments with varying molecular weights and isoelectric points at all cryoprotectant concentrations. The addition of either 10mM L-cysteine or reduced glutathione to the cells prior to cryprotectant exposure modified the actin fragmentation. In this pre...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4062183</comments>
            <pubDate>Thu, 07 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4062183</guid>        </item>
        <item>
            <title>Cryopreservation of sperm from seven-band grouper, Epinephelus septemfasciatus.</title>
            <link>http://www.medworm.com/index.php?rid=4003515&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20869362%26dopt%3DAbstract</link>
            <description>Authors: Koh IC, Yokoi KI, Tsuji M, Tsuchihashi Y, Ohta H
    In the present study, we examined methods for the cryopreservation of Epinephelus septemfasciatus spermatozoa. The percent motility, average path velocity, and linearity of movement (LIN) of fresh and corresponding post-thaw sperm were evaluated. Sperm motility was investigated using computer-assisted sperm analysis. Five percent dimethyl sulphoxide (Me(2)SO) with 95% fetal bovine serum (FBS) was the most successful cryoprotectant diluent with a comparative post-thaw motility of 77.6 Â± 8.5%; 5% dimethyl formamide was also effective. Fetal bovine serum was significantly better as an extender when compared with artificial seminal plasma, glucose, and trehalose solution. Sperm tolerated a wide range of cooling rates (from 27.1 t...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4003515</comments>
            <pubDate>Tue, 21 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4003515</guid>        </item>
        <item>
            <title>Immunoregulatory effects of freeze injured whole tumour cells on human dendritic cells using an in vitro cryotherapy model.</title>
            <link>http://www.medworm.com/index.php?rid=4003793&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20863822%26dopt%3DAbstract</link>
            <description>The objective of this study is to assess the immunological effects of cryotreated whole tumour cells on dendritic cells (DC) maturation and function using an in vitro model.Prostate cancer cells were cooled using Endocare cryo-system to mimic temperatures achieved during clinical cryotherapy. Human DC were prepared from cluster of differentiation (CD) 14 monocytes and matured with lipopolysaccharide (LPS). Cryotreated cancer cells were added to DC on day 3. On day 7, DC were harvested and phenotyped. Cytokine gene expression was assessed using real time quantitative polymerase chain reaction (RT-PCR). Functional activity of DC was assessed in allogenic mixed lymphocyte reaction (MLR) and the molecular changes using gene microarray technology.There was statistically significant upregulation...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4003793</comments>
            <pubDate>Sun, 19 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4003793</guid>        </item>
        <item>
            <title>Comparing the effects of Dextran 70 and Hydroxyethyl starch in an intestinal storage solution.</title>
            <link>http://www.medworm.com/index.php?rid=4003586&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20863823%26dopt%3DAbstract</link>
            <description>CONCLUSION: The results of this study challenge the idea that oncotic support is not a fundamental requirement of static organ storage. Furthermore, our data suggests that HES is an effective oncotic agent for use in our intraluminal nutrient-rich preservation solution, while Dextran 70 is not.
    PMID: 20863823 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4003586</comments>
            <pubDate>Sun, 19 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4003586</guid>        </item>
        <item>
            <title>Effect of centrifugation and sugar supplementation on the semen cryopreservation of captive collared peccaries (Tauassu tajacu).</title>
            <link>http://www.medworm.com/index.php?rid=4003876&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20858475%26dopt%3DAbstract</link>
            <description>In conclusion, it is not recommended to centrifuge the ejaculates from collared peccaries prior to conducting the cryopreservative procedures using a Tris-based extender supplemented with fructose or glucose.
    PMID: 20858475 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4003876</comments>
            <pubDate>Fri, 17 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4003876</guid>        </item>
        <item>
            <title>Effects of antioxidants on post-thawed bovine sperm and oxidative stress parameters: Antioxidants protect DNA integrity against cryodamage.</title>
            <link>http://www.medworm.com/index.php?rid=3981417&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20833164%26dopt%3DAbstract</link>
            <description>This study was conducted to determine the effects of methionine, inositol and carnitine on sperm (sperm motility, abnormality, DNA integrity and in vivo fertility) and oxidative stres parameters (lipid peroxidation, total glutathione and antioxidant potential levels) of bovine semen after the freeze-thawing process. Nine ejaculates, collected with the aid of an artificial vagina twice a week from each Simmental bovine, were included in the study. Each ejaculate, splitted into seven equal groups and diluted in Tris-based extender containing methionine (2.5 and 7.5 mM), carnitine (2.5 and 7.5 mM), inositol (2.5 and 7.5 mM) and no additive (control), was cooled to 5Â°C and then frozen in 0.25 ml French straws. Frozen straws were then thawed individually at 37Â°C for 20 sec in a water bath...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3981417</comments>
            <pubDate>Wed, 08 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3981417</guid>        </item>
        <item>
            <title>Cryopreservation and Ultrasounds: Why dig up the past?</title>
            <link>http://www.medworm.com/index.php?rid=3954715&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20826129%26dopt%3DAbstract</link>
            <description>Authors: Olmo A, Risco R
    
    PMID: 20826129 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3954715</comments>
            <pubDate>Thu, 02 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3954715</guid>        </item>
        <item>
            <title>Optimizing the concentration of hydroxyethylstarch in a novel intestinal-specific preservation solution.</title>
            <link>http://www.medworm.com/index.php?rid=3899865&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20727872%26dopt%3DAbstract</link>
            <description>Conclusion Our data suggests that when employing an intraluminal preservation solution for static organ storage, oncotic support is a fundamental requirement; 5% HES is optimal.
    PMID: 20727872 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3899865</comments>
            <pubDate>Tue, 17 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3899865</guid>        </item>
        <item>
            <title>Cryopreservation of human failed maturation oocytes shows that vitrification gives superior outcomes to slow cooling.</title>
            <link>http://www.medworm.com/index.php?rid=3899864&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20727873%26dopt%3DAbstract</link>
            <description>In conclusion, for oocytes that had failed to mature, vitrification gave better survival, maturation, fertilization and also cleavage rates than the slow cooling protocols. Four cells embryos were obtained only from vitrified in vitro matured MI oocytes.
    PMID: 20727873 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3899864</comments>
            <pubDate>Tue, 17 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3899864</guid>        </item>
        <item>
            <title>Investigation of the use of Pulse Tube in cell cryopreservation systems.</title>
            <link>http://www.medworm.com/index.php?rid=3853924&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20691677%26dopt%3DAbstract</link>
            <description>In this study, the power to be dissipated is calculated individualizing the trend of temperature on the Pulse Tube cold head and inside the cell test tubes. The control system is not based on an historical series of data so it can be used in different operative conditions. The obtained temperature curve is in good agreement with the theoretical values, with errors within those accepted by commercial systems. The Pulse Tube cryorefrigerator may represent a valid alternative solution to programmable liquid nitrogen freezer, especially where nitrogen's supply is difficult or extremely expensive.
    PMID: 20691677 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3853924</comments>
            <pubDate>Tue, 03 Aug 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3853924</guid>        </item>
        <item>
            <title>Lyophilized somatic cells direct embryonic development after whole cell intracytoplasmic injection into pig oocytes.</title>
            <link>http://www.medworm.com/index.php?rid=3853932&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20691649%26dopt%3DAbstract</link>
            <description>In conclusion, our results suggest that lyophilized somatic cells can direct embryonic development up to blastocyst stage after WCICI into pig oocytes. Treatment of embryos, produced from lyophilized somatic cells, with TSA can further increase their in vitro developmental potential.
    PMID: 20691649 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3853932</comments>
            <pubDate>Wed, 28 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3853932</guid>        </item>
        <item>
            <title>Effect of long-term cryopreservation on physiological characteristics, antioxidant activities and lipid peroxidation of red seabream (Pagrus major) sperm.</title>
            <link>http://www.medworm.com/index.php?rid=3791606&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20654607%26dopt%3DAbstract</link>
            <description>Authors: Chen YK, Liu QH, Li J, Xiao ZZ, Xu SH, Shi XH, Ma DY
    The aim of this study was to determine the effect of long-term cryopreservation on physiological characteristics, the antioxidant activities and lipid peroxidation of red seabream sperm which were respectively cryopreserved with 15% dimethylsulfoxide (Me(2)SO) for 1 month, 13 months, 26 months, 48 months and 73 months. The motility and fertility of post-thaw sperm decreased with the storage time going on. The highest motility (87.67+/-2.52%) was obtained in sperm cryopreserved for 1 month and the lowest (50.67+/-5.31%) was in sperm for 73 months. There were no significant differences (P &amp;lt; 0.05) in fertilization rates of sperm cryopreserved for 1 month (71.33+/-8.84%), 13 months (69.22+/-1.02%) and 26 months (60.33+/-2.33%...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3791606</comments>
            <pubDate>Mon, 19 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3791606</guid>        </item>
        <item>
            <title>Evaluation of Cryoprotectant and Cooling Rate for Sperm Cryopreservation in the Euryhaline Fish Medaka Oryzias latipes.</title>
            <link>http://www.medworm.com/index.php?rid=3791605&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20654608%26dopt%3DAbstract</link>
            <description>The objectives were to: 1) evaluate the acute toxicity of methanol, 2-methoxyethanol (ME), dimethyl sulfoxide (Me(2)SO), N, N- dimethylacetamide (DMA), N, N,-dimethyl formamide (DMF), and glycerol with concentrations of 5, 10, and 15% for 60 min of incubation at 4 degrees C; 2) evaluate cooling rates from 5 to 25 degrees C/min for freezing and their interaction with cryoprotectants, and 3) test fertility of thawed sperm cryopreserved with selected cryoprotectants and associated cooling rates. Evaluation of cryoprotectant toxicity showed that methanol and ME (5 and 10%) did not change the sperm motility after 30 min; Me(2)SO, DMA, and DMF (10 and 15%) and glycerol (5, 10 and 15%) significantly decreased the motility of sperm within 1 min after mixing. Based on these results, methanol and ME...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3791605</comments>
            <pubDate>Mon, 19 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3791605</guid>        </item>
        <item>
            <title>Kinetics of osmotic water flow across cell membranes in non-ideal solutions during freezing and thawing.</title>
            <link>http://www.medworm.com/index.php?rid=3791604&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20654609%26dopt%3DAbstract</link>
            <description>This study demonstrates that our experimental data-based method is a valid one with clear physical interpretations, convenient expressions and a more extensive application room than traditional ones.
    PMID: 20654609 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3791604</comments>
            <pubDate>Mon, 19 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3791604</guid>        </item>
        <item>
            <title>Freezability of Iberian ibex (Capra pyrenaica) spermatozoa according to the glycerolization temperature and plasma testosterone concentration.</title>
            <link>http://www.medworm.com/index.php?rid=3791603&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20654610%26dopt%3DAbstract</link>
            <description>Authors: Coloma MA, GÃ³mez-Brunet A, VelÃ¡zquez R, Toledano-DÃ­az A, LÃ³pez-SebastiÃ¡n A, Santiago-Moreno J
    Ibex spermatozoa can be successfully frozen using glycerolated media. However, no information is available regarding the most effective method of glycerol addition in this species. The aim of the present work was to evaluate the effect of the glycerolization temperature on the response to freezing-thawing of ibex spermatozoa collected by electroejaculation. The effect of the interaction glycerolization temperature x plasma testosterone concentration was also evaluated. The spermatozoa used in this work came from six adult ibexes maintained in captivity. Each ejaculate was divided into two aliquots in a Tris-egg yolk-based medium. One fraction was subjected to single ste...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3791603</comments>
            <pubDate>Mon, 19 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3791603</guid>        </item>
        <item>
            <title>Cryopreservation of Atlantic cod Gadus morhua L. spermatozoa: effects of extender composition and freezing rate on sperm motility, velocity and morphology.</title>
            <link>http://www.medworm.com/index.php?rid=3776929&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20638376%26dopt%3DAbstract</link>
            <description>Authors: Butts IA, Litvak MK, Kaspar V, Trippel EA
    Broodstock selection programs are currently underway for Atlantic cod (Gadus morhua). To complement and further these selection programs we need to develop sperm cryopreservation procedures. This will allow genomic DNA from males from selected individuals or stocks to be frozen and conserved in perpetuity. In our study we used a full factorial ANOVA design to examine the effects of diluent (Mounib's sucrose-based diluent, Hanks' Balanced Salt Solution, Mounib's sucrose-based diluent + hen's egg yolk, and Hanks' Balanced Salt Solution + hen's egg yolk), cryoprotectant (propylene glycol, dimethyl sulphoxide, and glycerol), and freezing rate (-2.5, -5.0, -7.5, and -10.0 degrees C/min) on motility of cod frozen-thawed sperm. Sperm velocity...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3776929</comments>
            <pubDate>Wed, 14 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3776929</guid>        </item>
        <item>
            <title>The use of cryomicroscopy in guppy sperm freezing.</title>
            <link>http://www.medworm.com/index.php?rid=3776928&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20638377%26dopt%3DAbstract</link>
            <description>Authors: Wang X, Wang F, Wu X, Zhao X, Liu J, Huang C, Dong Q
    The present study employed cryomicroscopy to derive an optimal sperm freezing protocol for guppy (Poecilia reticulata) sperm. Evaluation criteria during the freezing-thawing process were assessed for nucleation temperature (Tn), temperature when more than 50% of sperm display bending midpiece (Tb), temperature when more than 80% of sperm stop moving (Tm), thawing temperature (Tt), and post-thaw motility. We compared four different cryoprotectants: 5% N-dimethyl formamide (DMF), 6% methanol (MEOH), 10% dimethyl sulfoxide (DMSO), and 14% glycerol, as well as glycerol at different concentrations of 7-50%; cooling and rewarming rates ranged from 5 to 100 degrees C/min. The protocol that yielded the highest post-thaw motility was...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3776928</comments>
            <pubDate>Wed, 14 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3776928</guid>        </item>
        <item>
            <title>Simple, Inexpensive Attainment and Measurement of Very High Cooling and Warming Rates.</title>
            <link>http://www.medworm.com/index.php?rid=3733564&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20599881%26dopt%3DAbstract</link>
            <description>Authors: Kleinhans FW, Seki S, Mazur P
    We have developed a simple, inexpensive system (&amp;lt; $300 US) for measuring cooling and warming rates of small ( approximately 0.1 mul) aqueous samples at rates as high as 10(5) degrees C/min. The measurement system itself, can track rates approaching one million degrees C/min. For temperature sensing, a Type T thermocouple with 50 mum wire was used. The thermocouple output voltage was read with an inexpensive USB based digital oscilloscope interfaced to a laptop computer, and the raw data were processed with MS Excel.
    PMID: 20599881 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3733564</comments>
            <pubDate>Thu, 01 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3733564</guid>        </item>
        <item>
            <title>Morphology of Hypoxia Following Cryoablation in a Prostate Cancer Murine Model: Its Relationship to Necrosis, Apoptosis and, Microvessel Density.</title>
            <link>http://www.medworm.com/index.php?rid=3733563&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20599882%26dopt%3DAbstract</link>
            <description>Authors: Kimura M, Rabbani Z, Mouraviev V, Tsivian M, Vujaskovic Z, Satoh T, Baba S, Baust JM, Baust JG, Polascik TJ
    The aim of this study is to investigate the tumor tissue changes in terms of hypoxia and demonstrate its relationship to vascularity and apoptosis following therapeutic cryoablation in a prostate tumor murine model. Total 67 male C57BL/J6 mice were assigned into sham-operation group and cryoablation group. Murine prostate tumors (RM-9) were inoculated subcutaneously in a right hind leg and treated with cryotherapy. Of 30 mice, tumor volumes were measured for 12 days following operation. Of 37 mice, tumor tissues were harvested in 24 hours following operation, and histological/molecular changes were analyzed. Hematoxylin and eosin or immunohistochemical staining were util...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3733563</comments>
            <pubDate>Thu, 01 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3733563</guid>        </item>
        <item>
            <title>Antioxidant supplementation improves boar sperm characteristics and fertility after cryopreservation: Comparison between cysteine and rosemary (Rosmarinus officinalis).</title>
            <link>http://www.medworm.com/index.php?rid=3733562&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20599883%26dopt%3DAbstract</link>
            <description>The objective of the study was to determine the effect of antioxidant addition to the freezing extender on boar semen qualities and fertility capacity. Ejaculates were collected from a previously selected boar and semen samples were processed using the straw freezing procedure. In experiment 1, semen samples were cryopreserved in lactose-egg yolk solution supplemented with various concentrations of cysteine (0,5and10mM) to determinate a cysteine concentration capable of producing a protective effect during cryopreservation. Semen quality (total motility, progressive motility, viability, acrosome integrity and hypoosmotic swelling test) was evaluated after freezing and thawing and then every hour for 3 h. In experiment 2, ejaculates were cryopreserved with lactose-egg yolk extender with or ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3733562</comments>
            <pubDate>Thu, 01 Jul 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3733562</guid>        </item>
        <item>
            <title>Intracellular ice formation in confluent monolayers of human dental stem cells and membrane damage.</title>
            <link>http://www.medworm.com/index.php?rid=3733561&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20599884%26dopt%3DAbstract</link>
            <description>The objective was to examine the effects of IIF on post-thaw viability of both confluent monolayers and suspensions of DPSCs. Confluent DPSC monolayers were assessed for the expression of gap junction protein Connexin-43. IIF was induced on the cryostage and in the methanol bath at different subzero temperatures. Membrane integrity and colony forming ability were assessed post-thaw. Confluent DPSC monolayers expressed Connexin-43. In cell suspensions, 85.9+/-1.7% of cells were damaged after 100% IIF. In cell monolayers, after 100% IIF, only 25.5+/-5.5% and 14.8+/-3.3% of cells were damaged on the cryostage and in the methanol bath respectively. However, DPSC monolayers exposed to 100% IIF showed no colony forming ability. We conclude that confluent monolayers of DPSCs express the gap junct...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3733561</comments>
            <pubDate>Mon, 21 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3733561</guid>        </item>
        <item>
            <title>Freezing in the Antarctic limpet, Nacella concinna.</title>
            <link>http://www.medworm.com/index.php?rid=3733560&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20599885%26dopt%3DAbstract</link>
            <description>Authors: Hawes TC, Worland MR, Bale JS
    The process of organismal freezing in the Antarctic limpet, Nacella concinna, is complicated by molluscan biology. Internal ice formation is, in particular, mediated by two factors: (a) the provision of an inoculative target for ice formation in the exposed mucus-secreting foot; and (b) osmoconformity to the marine environment. With regard to the first, direct observations of the independent freezing of pedal mucus support the hypothesis that internal ice formation is delayed by the mucal film. As to the second, ice nucleation parametrics of organismal tissue (head, midgut, gonad, foot) and mucus in both inter- and subtidal populations were characterized by high melting points (range = -4.61 to -6.29 degrees C), with only c.50% of a given sample o...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3733560</comments>
            <pubDate>Fri, 18 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3733560</guid>        </item>
        <item>
            <title>Thermodynamic analysis of intracellular ice recrystallization in mouse oocytes.</title>
            <link>http://www.medworm.com/index.php?rid=3733559&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20599886%26dopt%3DAbstract</link>
            <description>This report is expected to evoke interests in applying thermodynamics to the investigation of the intracellular ice formation.
    PMID: 20599886 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3733559</comments>
            <pubDate>Wed, 16 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3733559</guid>        </item>
        <item>
            <title>Direct Concentration Measurements of the Unfrozen Portion of Solutions under Freezing.</title>
            <link>http://www.medworm.com/index.php?rid=3733558&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20599887%26dopt%3DAbstract</link>
            <description>Authors: Chen HH, Clarke DM
    Phase diagrams of solutions consisting of cryoprotective agents (CPA) are very useful in cryobiology research. Those diagrams depict the points of solution concentrations at corresponding temperatures: one of essential inputs that can be utilized to compute the volume response of cell under freezing process. However, generating such plots is costly and time-consuming. A direct method is proposed in this study to determine the solution concentration of unfrozen parts at multiple subzero temperatures. Measurements of binary solutions, composed of water and sodium chloride, were performed and compared with published data. Ternary solutions, consisting of water, sodium chloride and dimethyl sulfoxide, were also measured. The uniqueness and advantage achieved thr...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3733558</comments>
            <pubDate>Wed, 16 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3733558</guid>        </item>
        <item>
            <title>Cryotherapy of the liver: a histological review.</title>
            <link>http://www.medworm.com/index.php?rid=3733557&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20599888%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: : Lesions obtained after cryotherapy seem similar and behave as those obtained after other techniques of liver ablation. However, controversial areas still exist and include the optimum number of freeze thaw cycles, the place of inflow occlusion, the potential corrupting effects of intra-lesional or proximal blood vessels on ablation morphology. The influence of these factors on the local recurrences are still not fully understood.
    PMID: 20599888 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3733557</comments>
            <pubDate>Wed, 16 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3733557</guid>        </item>
        <item>
            <title>Effects of Cholesterol-Loaded Cyclodextrin during Freezing Step of Cryopreservation with TCGY Extender Containing Bovine Serum Albumin on Quality of Goat Spermatozoa.</title>
            <link>http://www.medworm.com/index.php?rid=3691278&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20561514%26dopt%3DAbstract</link>
            <description>Authors: Amidi F, Farshad A, Khor AK
    The susceptibility of mammalian spermatozoa to cold shock and freezing damage is due to changes in membrane lipid composition, particularly cholesterol depletion in plasma membrane during cryopreservation. The aim of this study was to investigate the effects of different concentrations of cholesterol-loaded cyclodextrin (CLC) and bovine serum albumin (BSA) on the cryopreservation of goat spermatozoa in Tris-citrate egg yolk extender. Semen was collected from four mature goats and divided into seven aliquots prior to cryopreservation .The first aliquot remained untreated and was mixed with TCG, the second aliquot was mixed with TCG and egg yolk (TCGY), third aliquot was mixed with TCGY and 2.5% BSA (TCGYB) and other aliquots were mixed with TCGYB con...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3691278</comments>
            <pubDate>Mon, 14 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3691278</guid>        </item>
        <item>
            <title>Statistical prediction of the vitrifiability and glass stability of multi-component cryoprotective agent solutions.</title>
            <link>http://www.medworm.com/index.php?rid=3691279&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20558152%26dopt%3DAbstract</link>
            <description>This study was designed to determine the vitrifyability and glass stability of solutions containing combinations of commonly used CPAs and to document CPA interactions that occur. One hundred and sixty-four multi-CPA combination solutions of 6-9M were evaluated for vitrifyability and glass stability using direct visualization after immersion in liquid nitrogen for 30 minutes and upon warming. Binary and ordinal logistic regression analysis was used to statistically analyze each CPA for its ability to vitrify and its effect on glass stability in multi-component CPA solutions. Propylene glycol has the greatest incremental contribution to vitrification while formamide had the least contribution. A threshold was established whereby the ability of a solution to vitrify could be determined by ca...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3691279</comments>
            <pubDate>Sun, 13 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3691279</guid>        </item>
        <item>
            <title>Membrane permeability parameters for freezing of stallion sperm as determined by Fourier transform infrared spectroscopy.</title>
            <link>http://www.medworm.com/index.php?rid=3691280&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20553897%26dopt%3DAbstract</link>
            <description>We describe a method to determine membrane hydraulic permeability parameters (E(Lp), Lpg) at subzero temperatures from membrane phase behavior data. In order to do this, it was assumed that the measured freezing-induced shift in wavenumber position of the symmetric CH(2) stretching band arising from the lipid acyl chains is proportional to cellular dehydration. Membrane permeability parameters were also determined by analyzing the H(2)O-bending and -libration combination band, which yielded higher values for both E(Lp) and Lpg as compared to lipid band analysis. These differences likely reflect differences between transport of free and membrane-bound water. FTIR allows for direct assessment of membrane properties at subzero temperatures in intact cells. The derived biophysical membrane par...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3691280</comments>
            <pubDate>Mon, 07 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3691280</guid>        </item>
        <item>
            <title>Dehydrating phospholipid vesicles measured in real-time using ATR Fourier transform infrared spectroscopy.</title>
            <link>http://www.medworm.com/index.php?rid=3691277&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20566369%26dopt%3DAbstract</link>
            <description>In this study, Fourier transform infrared spectroscopy with an attenuated total reflection accessory was used to investigate the influence of trehalose on the dehydration kinetics and residual water content of egg phosphatidylcholine liposomes in real time under controlled relative humidity conditions. In the absence of trehalose, the lipids displayed a transition to a more ordered gel phase upon drying. The membrane conformational disorder in the dried state was found to decrease with decreasing relative humidity. Even at a relative humidity as high as 94% the conformational disorder of the lipid acyl chains decreased after evaporation of the bulk water. The presence of trehalose affects the rate of water removal from the system and the lipid phase behavior. The rate of water removal is d...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3691277</comments>
            <pubDate>Mon, 07 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3691277</guid>        </item>
        <item>
            <title>Mitochondria and Membrane Cryoinjury in Micropatterned Cells: Effects of Cell-Cell Interactions.</title>
            <link>http://www.medworm.com/index.php?rid=3691276&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20570671%26dopt%3DAbstract</link>
            <description>Authors: Tchir J, Acker JP
    The maintenance of cell membrane integrity is an absolute minimum criterion for the selection of a successful cryopreservation process; however, it is often used as the sole determinant of cell &quot;viability&quot;. Membrane stresses and strains that develop with cell volume fluctuations are only one component of the overall cellular response to freezing. Damage to organelles resulting from excessive concentration of intracellular solutes and/or the alternation of molecular signalling events may affect post-thaw outcomes. As the low temperature response of cells is affected by the presence of cell-cell interactions, the cryopreservation of tissues and tissue model systems would benefit from a more detailed understanding of the sites and mechanisms of cryoinjury. The p...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3691276</comments>
            <pubDate>Wed, 02 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3691276</guid>        </item>
        <item>
            <title>The effect of raffinose and methionine on frozen/thawed Angora buck (Capra hircus ancryrensis) semen quality, lipid peroxidation and antioxidant enzyme activities.</title>
            <link>http://www.medworm.com/index.php?rid=3626121&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20515679%26dopt%3DAbstract</link>
            <description>In conclusion, methionine and raffinose play a cryoprotective role against sperm CASA motility, acrosome abnormality and DNA damage. Raffinose 5 mM exhibited antioxidative properties, decreasing MDA levels. Further studies are required to obtain more concrete results on the characterization of microscopic parameters and antioxidant activities in cryopreserved goat sperm with different additives.
    PMID: 20515679 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3626121</comments>
            <pubDate>Fri, 28 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3626121</guid>        </item>
        <item>
            <title>Metabolic preconditioning of cells with AICAR-riboside: Improved cryopreservation and cell-type specific impacts on energetics and proliferation.</title>
            <link>http://www.medworm.com/index.php?rid=3626123&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20510224%26dopt%3DAbstract</link>
            <description>Authors: Menze MA, Chakraborty N, Clavenna M, Banerjee M, Liu XH, Toner M, Hand SC
    In species whose evolutionary history has provided natural tolerance to dehydration and freezing, metabolic depression is often a pre-requisite for survival. We tested the hypothesis that preconditioning of mammalian cells with 5-aminoimidazole-4-carboxamide-1-b-D-ribofuranoside (AICAR) to achieve metabolic depression will promote greater survivorship during cryopreservation. AICAR is used extensively to stimulate AMP-activated protein kinase (AMPK), which can result in downregulation of biosynthetic processes. We showed that the metabolic interconversion of AICAR was cell-type dependent. Accumulation of 5-aminoimidazole-4-carboxamide-1b-D-ribofuranosyl-5'-monophosphate (ZMP), as well as other metabolite...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3626123</comments>
            <pubDate>Mon, 24 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3626123</guid>        </item>
        <item>
            <title>Bovine oocyte vitrification using the Cryotop method Effect of cumulus cells and vitrification protocol on survival and subsequent development.</title>
            <link>http://www.medworm.com/index.php?rid=3626122&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20510225%26dopt%3DAbstract</link>
            <description>In conclusion, cumulus-enclosed GV bovine oocytes survived vitrification and subsequently developed at higher rates than MII oocytes using Cryotop method and conventional IVF procedure. Theoretical analysis of permeability characteristics and tolerance limits could not explain the low developmental competence of vitrified oocytes.
    PMID: 20510225 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3626122</comments>
            <pubDate>Sun, 23 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3626122</guid>        </item>
        <item>
            <title>Cryopreservation of periodontal ligament cells with magnetic field for tooth banking.</title>
            <link>http://www.medworm.com/index.php?rid=3578540&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20478291%26dopt%3DAbstract</link>
            <description>Authors: Kaku M, Kamada H, Kawata T, Koseki H, Abedini S, Kojima S, Motokawa M, Fujita T, Ohtani J, Tsuka N, Matsuda Y, Sunagawa H, Hernandes RA, Ohwada N, Tanne K
    The purpose of this study was to establish a long-term tooth cryopreservation method that can be used for tooth autotransplantation. Human periodontal ligament (PDL) cells were frozen in 10% dimethyl sulfoxide (Me2SO) using a programmed freezer with a magnetic field. Cells were cryopreserved for 7 days at -150 degrees C. Immediately after thawing, the number of surviving cells was counted and the cells were cultured; cultured cells were examined after 48 h. Results indicated that a 0.01mT of a magnetic field, a 15-min hold-time, and a plunging temperature of -30 degrees C led to the greatest survival rate of PDL cells. Based...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3578540</comments>
            <pubDate>Thu, 13 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3578540</guid>        </item>
        <item>
            <title>Investigating cryoinjury using simulations and experiments: 2. TF-1 cells during graded freezing (interrupted slow cooling without hold time).</title>
            <link>http://www.medworm.com/index.php?rid=3578541&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20471968%26dopt%3DAbstract</link>
            <description>Authors: Ross-Rodriguez LU, Elliott JA, McGann LE
    Cryopreservation plays a key role in the long-term storage of native and engineered cells and tissues for research and clinical applications. The survival of cells and tissues after freezing and thawing depends on the ability of the cells to withstand a variety of stresses imposed by the cryopreservation protocol. A better understanding of the nature and kinetics of cellular responses to temperature-induced conditions is required to minimize cryoinjury. An interrupted freezing procedure that allows dissection of cryoinjury was used to investigate the progressive damage that occurs to cells during cryopreservation using slow cooling. Simulations of cellular osmotic responses were used to provide interpretation linking states of the cell ...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3578541</comments>
            <pubDate>Wed, 12 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3578541</guid>        </item>
        <item>
            <title>Investigating cryoinjury using simulations and experiments: 1. TF-1 cells during two-step freezing (rapid cooling interrupted with a hold time).</title>
            <link>http://www.medworm.com/index.php?rid=3578542&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20471379%26dopt%3DAbstract</link>
            <description>This study also demonstrates why high cell recovery after cryopreservation could be achieved in the absence of traditional cryoprotectants.
    PMID: 20471379 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3578542</comments>
            <pubDate>Tue, 11 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3578542</guid>        </item>
        <item>
            <title>Membrane permeability characteristics of bovine oocytes and development of a step-wise cryoprotectant adding and diluting protocol.</title>
            <link>http://www.medworm.com/index.php?rid=3578543&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20470768%26dopt%3DAbstract</link>
            <description>In this study, experiments were performed to determine these characteristics for immature (germinal vesicle, GV) and in vitro matured (metaphase II, MII) bovine oocytes within 4 degrees C to 37 degrees C, and a new step-wise adding and diluting protocol for ethylene glycol (EG) was developed and verified. Osmotically inactive volumes (Vb) of GV and MII oocytes were calculated to be 16.1% and 26.1%. The membrane permeability of the oocytes to water (Lp) in the presence of EG were between 0.08-0.18 and 0.14-0.28mum/min/atm, and the membrane permeability of the oocytes to solutes (Ps) were between 0.0011-0.0038 and 0.0029-0.0061cm/min for GV and MII oocytes, respectively. The activation energies (Ea) for Lp and Ps in the presence of EG were 3.68 and 6.84kcal/mole for GV oocyte, while 3.62 and...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3578543</comments>
            <pubDate>Mon, 10 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3578543</guid>        </item>
        <item>
            <title>Determination of the quaternary phase diagram of the water-ethylene glycol-sucrose-NaCl system and a comparison between two theoretical methods for synthetic phase diagrams.</title>
            <link>http://www.medworm.com/index.php?rid=3545806&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20447385%26dopt%3DAbstract</link>
            <description>In this study, an auto-sampler differential scanning calorimeter (DSC) was used to determine the quaternary phase diagram of the water-ethylene glycol-sucrose-NaCl system. To improve the accuracy of melting point measurement, a &quot;mass redemption&quot; method was also applied for the DSC technique. Base on the analyses of these experimental data, a comparison was made between the two practical approaches to generate phase diagrams of multi-solute solutions from those of single-solute solutions: the summation of cubic polynomial melting point equations versus the use of osmotic virial equations with cross coefficients. The calculated values of the model standard deviations suggested that both methods are satisfactory for characterizing this quaternary system.
    PMID: 20447385 [PubMed - as suppli...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3545806</comments>
            <pubDate>Sun, 02 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3545806</guid>        </item>
        <item>
            <title>Cryopreservation of anoxygenic phototrophic Fe(II)-oxidizing bacteria.</title>
            <link>http://www.medworm.com/index.php?rid=3530618&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20433824%26dopt%3DAbstract</link>
            <description>Authors: Hegler F, Kappler A
    Preservation and storage of microbial stock cultures is desirable since the risk of contamination or loss of living cultures is immanent while over long periods mutations accumulate. Generally, it is rather difficult to preserve photosynthetic bacteria due to their sensitive photosynthetic membranes [1]. Phototrophic Fe(II)-oxidizing bacteria face an additional challenge; since they are exposed to light and Fe(II) during growth, they have to cope with radicals from Fenton-reactions of Fe(II)-species, light and water. Therefore, phototrophic Fe(II)-oxidizing strains are thought to be especially susceptible to genetic modifications. Here we provide a simple and fast protocol using glycerol as cryo-protectant to cryopreserve three strains of anoxygenic phototr...</description>
            <author>Cryobiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3530618</comments>
            <pubDate>Mon, 26 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3530618</guid>        </item>
        <item>
            <title>Gaseous persufflation with carbon monoxide during ischemia protects the isolated liver and enhances energetic recovery.</title>
            <link>http://www.medworm.com/index.php?rid=3524740&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20430019%26dopt%3DAbstract</link>
            <description>CONCLUSION: : Viability of cold stored liver grafts can be notably augmented by gaseous ex vivo application of low dose CO to the isolated organ.
    PMID: 20430019 [PubMed - as supplied by publisher] (Source: Cryobiology)</description>
            <author>Cryobiology</author>
            <type>journals</type>
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            <pubDate>Sun, 25 Apr 2010 23:00:00 +0100</pubDate>
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            <title>Use of Dynamic Mechanical Analysis (DMA) to determine critical transition temperatures in frozen biomaterials intended for lyophilization.</title>
            <link>http://www.medworm.com/index.php?rid=3524739&amp;cid=s_35487_62_f&amp;fid=35487&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20430020%26dopt%3DAbstract</link>
            <description>Authors: Gearing J, Malik KP, Matejtschuk P
    Dynamic Mechanical Analysis is widely used to determine glass transitions in solid state materials. However, here we demonstrate the application of DMA for the determination of glass transitions (Tg') in the frozen liquid state by means of a steel sample pocket. The use of the pocket allows frozen material to be analysed and glass transition events demonstrated. In addition, it allows weak glass transitions to be detected clearly in some complex formulations where they can be obscured by eutectic and other strong thermal events when other methods such as DSC or DTA are used. Classical excipients (trehalose, lactose, dextran) were analysed and shown to give reproducible Tg' values, though with values slightly higher than those obtained by DSC....</description>
            <author>Cryobiology</author>
            <type>journals</type>
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            <pubDate>Sun, 25 Apr 2010 23:00:00 +0100</pubDate>
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