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        <title>Cell Proliferation 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 'Cell Proliferation' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Cell+Proliferation&t=Cell+Proliferation&s=Search&f=source]]></link>
        <lastBuildDate>Tue, 07 Feb 2012 08:48:53 +0100</lastBuildDate>
        <item>
            <title>Basic fibroblast growth factor modulates cell cycle of human umbilical cord‐derived mesenchymal stem cells</title>
            <link>http://www.medworm.com/index.php?rid=5665139&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2012.00808.x</link>
            <description>ConclusionOur study showed that bFGF supplementation of UC‐MSC culture enhanced the cells' growth kinetics without compromising their nature. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5665139</comments>
            <pubDate>Wed, 01 Feb 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Inhibition of sphingosine kinase 1 suppresses proliferation of glioma cells under hypoxia by attenuating activity of extracellular signal‐regulated kinase</title>
            <link>http://www.medworm.com/index.php?rid=5645120&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2012.00807.x</link>
            <description>Conclusions:  SphK1 and SphK2 are involved in proliferation of glioma cells in hypoxic conditions through distinct signalling pathways. SphK1, but not SphK2, promotes cell population expansion in hypoxic conditions by activating ERK. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5645120</comments>
            <pubDate>Wed, 01 Feb 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5645120</guid>        </item>
        <item>
            <title>Effects of Wnt/β‐catenin signalling on proliferation and differentiation of apical papilla stem cells</title>
            <link>http://www.medworm.com/index.php?rid=5645122&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2012.00806.x</link>
            <description>Conclusion:  Our results suggest that canonical Wnt/β‐catenin signalling promotes proliferation and odonto/osteogenic differentiation of SCAP. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5645122</comments>
            <pubDate>Mon, 30 Jan 2012 05:00:00 +0100</pubDate>
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        <item>
            <title>Pluripotency of a polyploid H1 (ES) cell system without leukaemia inhibitory factor</title>
            <link>http://www.medworm.com/index.php?rid=5645121&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00805.x</link>
            <description>Conclusion:  Polyploid H1 (ES) cells retained pluripotency in vitro, without LIF with nanog over‐expression. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5645121</comments>
            <pubDate>Mon, 30 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5645121</guid>        </item>
        <item>
            <title>Proliferation and differentiation potential of cryopreserved human skin‐derived precursors</title>
            <link>http://www.medworm.com/index.php?rid=5618252&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00803.x</link>
            <description>Conclusions:  Results revealed that in only 5% DMSO, hSKPs could be cryopreserved for long‐term storage with considerable survival and proliferation levels, without losing multipotency. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5618252</comments>
            <pubDate>Sun, 22 Jan 2012 14:33:52 +0100</pubDate>
            <guid isPermaLink="false">5618252</guid>        </item>
        <item>
            <title>Fat pad‐derived mesenchymal stem cells as a potential source for cell‐based adipose tissue repair strategies</title>
            <link>http://www.medworm.com/index.php?rid=5618253&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00804.x</link>
            <description>Discussion:  These results indicate that the cells maintained their proliferation rate, and continued expressing mesenchymal stem‐cell markers and pericyte marker 3G5 at late passages. These results also show that the cells were capable of adipogenic differentiation and thus could be a promising source for regeneration and replacement of adipose tissue in reconstructive surgery. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5618253</comments>
            <pubDate>Fri, 20 Jan 2012 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5618253</guid>        </item>
        <item>
            <title>Mechanical stretch inhibits adipogenesis and stimulates osteogenesis of adipose stem cells</title>
            <link>http://www.medworm.com/index.php?rid=5579192&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00802.x</link>
            <description>In this study, rat adipose stem cells (ASCs) were isolated and cultured in adipogenic or normal medium. Their exposure to cyclic mechanical stretch (2000 με, 1 Hz) in the presence of adipogenic medium decreased mRNA and protein level of PPAR‐γ, and increased Runx2 mRNA and protein levels as well as Pref‐1 mRNA level, compared to static samples. ASCs cultured in normal medium without adipogenic induction did not show any significant change in mRNA expression of PPAR‐γ, Runx2, nor Pref‐1 irrespective of mechanical loading. Stretching induced phosphorylation of extracellular signal‐regulated protein kinases 1 and 2 (ERK1/2) during the induction period. It was concluded that mechanical stretch inhibited adipogenesis and stimulated osteogenesis of these ASCs in the presence of...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5579192</comments>
            <pubDate>Thu, 12 Jan 2012 12:41:44 +0100</pubDate>
            <guid isPermaLink="false">5579192</guid>        </item>
        <item>
            <title>A new development of triterpene acid‐containing extracts from Viscum album L. displays synergistic induction of apoptosis in acute lymphoblastic leukaemia</title>
            <link>http://www.medworm.com/index.php?rid=5570496&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00801.x</link>
            <description>Conclusion:  Here for the first time, we have demonstrated that either solubilized triterpene acids or lectins and combinations thereof, induce dose‐dependent apoptosis in the ALL cell line NALM‐6 via caspase‐8 and ‐9 dependent pathways. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5570496</comments>
            <pubDate>Sat, 07 Jan 2012 20:57:37 +0100</pubDate>
            <guid isPermaLink="false">5570496</guid>        </item>
        <item>
            <title>Astragalus membranaceus lectin (AML) induces caspase‐dependent apoptosis in human leukemia cells</title>
            <link>http://www.medworm.com/index.php?rid=5513622&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00800.x</link>
            <description>Conclusions:  Our results suggest that AML could act as a potential anti‐cancer drug. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5513622</comments>
            <pubDate>Fri, 16 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5513622</guid>        </item>
        <item>
            <title>Human AB serum for generation of mesenchymal stem cells from human chorionic villi: comparison with other source and other media including platelet lysate</title>
            <link>http://www.medworm.com/index.php?rid=5502615&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00799.x</link>
            <description>Conclusions:  Our results indicate that CV would be an optimal source of MSCs with high expansion potential in a HS propagation system and immunoregulatory capacity of T and B lymphocytes. More than 90% of CV samples achieved large‐scale expansion in HS, which is encouraging for potential clinical applications of these cells. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5502615</comments>
            <pubDate>Wed, 14 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5502615</guid>        </item>
        <item>
            <title>Effect of sesquiterpene lactone coronopilin on leukaemia cell population growth, cell type‐specific induction of apoptosis and mitotic catastrophe</title>
            <link>http://www.medworm.com/index.php?rid=5502614&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00796.x</link>
            <description>Conclusions:  This study demonstrated that coronopilin efficiently inhibited leukaemia cell population growth by triggering cell type‐specific responses. Moreover, coronopilin‐mediated cell population expansion inhibition was specific to neoplastic cells, as normal white blood cell viability was not significantly affected. Thus, coronopilin may represent an interesting new chemical scaffold upon which to develop new anti‐leukaemic agents. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5502614</comments>
            <pubDate>Wed, 14 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5502614</guid>        </item>
        <item>
            <title>Neuroprotective effects of a new skin care formulation following ultraviolet exposure</title>
            <link>http://www.medworm.com/index.php?rid=5502617&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00795.x</link>
            <description>Conclusions:  Our new skincare formulation obtained from E. purpurea provides important neuroprotective effects of UV irradiation and could be used together with SPFs to prevent chronic deleterious effects of solar exposure. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5502617</comments>
            <pubDate>Tue, 13 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5502617</guid>        </item>
        <item>
            <title>MicroRNA‐494 suppresses cell proliferation and induces senescence in A549 lung cancer cells</title>
            <link>http://www.medworm.com/index.php?rid=5502616&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00798.x</link>
            <description>Conclusions:  Taken together, IGF2BP1 and its downstream target IGF2 could be a crucial axis for miR‐494 in regulation of the destiny of A549 cells. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5502616</comments>
            <pubDate>Tue, 13 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5502616</guid>        </item>
        <item>
            <title>Cachrys pungens Jan inhibits human melanoma cell proliferation through photo‐induced cytotoxic activity</title>
            <link>http://www.medworm.com/index.php?rid=5484789&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00791.x</link>
            <description>Conclusions:  Plant‐derived natural compounds are an important source for development of cancer‐fighting drugs. This study has demonstrated strong phototoxic activity of the coumarin fraction of C. pungens, a plant which, to our knowledge, has never been studied before. This investigation offers a new perspective for developing other formulations potentially useful in photodynamic therapy for treatment of non‐melanoma skin cancers as well as melanomas. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5484789</comments>
            <pubDate>Wed, 07 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5484789</guid>        </item>
        <item>
            <title>Overexpression of Id3 induces apoptosis of A549 human lung adenocarcinoma cells</title>
            <link>http://www.medworm.com/index.php?rid=5484788&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00792.x</link>
            <description>Conclusion:  Overexpression of Id3 triggered apoptosis in A549 human lung adenocarcinoma cells, implicating Id3 in negative control of tumour growth. These Id3‐induced pro‐apoptotic signalling pathways require further study, but this preliminary investigation suggests that Id3 regulation could be exploited in anti‐tumour therapies. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5484788</comments>
            <pubDate>Wed, 07 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5484788</guid>        </item>
        <item>
            <title>Psidium guajava L. anti‐neoplastic effects: induction of apoptosis and cell differentiation</title>
            <link>http://www.medworm.com/index.php?rid=5513621&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00797.x</link>
            <description>Conclusions:  Our findings showed that P. guajava L. extract was able to exert anti‐cancer activity on cultures in vitro and ex vivo, supporting the hypothesis of its anti malignant pro‐apoptotic modulation. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5513621</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5513621</guid>        </item>
        <item>
            <title>Improving the time‐machine: estimating date of birth of grade II gliomas</title>
            <link>http://www.medworm.com/index.php?rid=5502613&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00790.x</link>
            <description>AbstractObjectives:  Here we present a model aiming to provide an estimate of time from tumour genesis, for grade II gliomas. The model is based on a differential equation describing the diffusion–proliferation process. We have applied our model to situations where tumour diameter was shown to increase linearly with time, with characteristic diametric velocity.Materials and methods:  We have performed numerical simulations to analyse data, on patients with grade II gliomas and to extract information concerning time of tumour biological onset, as well as radiology and distribution of model parameters.Results and conclusions:  We show that the estimate of tumour onset obtained from extrapolation using a constant velocity assumption, always underestimates biological tumour age, and th...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5502613</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5502613</guid>        </item>
        <item>
            <title>Involvement of transcription factor p53 and leptin in control of porcine ovarian granulosa cell functions</title>
            <link>http://www.medworm.com/index.php?rid=5484787&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00793.x</link>
            <description>AbstractThe aim of our in vitro experiments was to examine the role of transcription factor p53 and the metabolic hormone leptin, in controlling basic functions (proliferation, apoptosis and secretory activity) of ovarian cells, as well as involvement of p53 in mediating or modulating actions of leptin, on ovarian cells. Porcine ovarian granulosa cells, transfected and non‐transfected with a gene construct encoding p53, were cultured with leptin (at concentrations of 0, 1, 10 or 100 ng/ml). Accumulation of p53 and of apoptosis‐related (bax) and proliferation‐related (PCNA, cyclin B1) substances was evaluated by SDS–PAGE‐western blotting. Secretion of progesterone (P4) was measured by RIA. Transfection with the p53 gene construct promoted accumulation of this transcription facto...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5484787</comments>
            <pubDate>Thu, 01 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5484787</guid>        </item>
        <item>
            <title>Resveratrol enhances the cytotoxic profile of docetaxel and doxorubicin in solid tumour cell lines in vitro</title>
            <link>http://www.medworm.com/index.php?rid=5332855&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00783.x</link>
            <description>Conclusion:  Resveratrol potentiates cytotoxic properties of both cancer drugs used in the study through increasing their intracellular level due to p‐glycoprotein inhibition and downregulation of mdr1 gene. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332855</comments>
            <pubDate>Thu, 20 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332855</guid>        </item>
        <item>
            <title>Epidermal regeneration by ent‐16α, 17‐dihydroxy‐kauran‐19‐oic acid isolated from Siegesbeckia pubescens</title>
            <link>http://www.medworm.com/index.php?rid=5312251&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00786.x</link>
            <description>Conclusion:  Collectively, these results indicate that DHK regenerates epidermal tissue mainly through EGFR phosphorylation. As DHK has diverse advantages over recombinant growth factors for commercialization (that is long‐term stability and skin permeability), DHK might be applied to wound‐healing agents and to a basic materials used in cosmetics. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5312251</comments>
            <pubDate>Wed, 12 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5312251</guid>        </item>
        <item>
            <title>Loss of macrophage migration inhibitory factor impairs the growth properties of human HeLa cervical cancer cells</title>
            <link>http://www.medworm.com/index.php?rid=5312250&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00787.x</link>
            <description>Conclusion:  MIF plays a pivotal role in proliferation and tumourigenesis of human HeLa cervical carcinoma cells, and may represent a promising therapeutic target for cancer intervention. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5312250</comments>
            <pubDate>Wed, 12 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5312250</guid>        </item>
        <item>
            <title>Activation, isolation, identification and culture of hepatic stem cells from porcine liver tissues</title>
            <link>http://www.medworm.com/index.php?rid=5312252&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00781.x</link>
            <description>AbstractObjectives:  Utility of hepatic stem cells could provide a novel solution to the severe shortage of human donor livers, for treatment of liver‐related diseases, due to their ability to proliferate and differentiate into functional hepatocytes. Porcine liver tissues also offer an alternative source from human donor livers. However, morphology, phenotype, successful isolation and culture of porcine hepatic stem cells still require much investigation.Materials and methods:  In the present study, we performed partial hepatectomy to activate hepatic oval cells and developed a procedure utilizing enzymatic digestion and density gradient centrifugation to isolate and purify oval cells derived from porcine livers. We identified ovoid cells by their morphological characteristics and p...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5312252</comments>
            <pubDate>Tue, 11 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5312252</guid>        </item>
        <item>
            <title>Chromosomal stability during ex vivo expansion of UCB CD34+ cells</title>
            <link>http://www.medworm.com/index.php?rid=5282880&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00779.x</link>
            <description>Conclusions: Ex vivo expansion could lead to occurrence of chromosomal abnormality, although here it did not produce excessive proliferative advantage of the expended cells. Importantly, chromosomal alteration seemed not to be inheritable and unlikely to result in malignant transformation. However, further in‐depth evaluation of potential clinical risks of chromosomal abnormality is warranted. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5282880</comments>
            <pubDate>Tue, 04 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5282880</guid>        </item>
        <item>
            <title>Wnt and SHH in prostate cancer: trouble mongers occupy the TRAIL towards apoptosis</title>
            <link>http://www.medworm.com/index.php?rid=5282879&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00784.x</link>
            <description>AbstractProstate cancer is a serious molecular disorder that arises because of reduction in tumour suppressors and overexpression of oncogenes. The malignant cells survive within the context of a three‐dimensional microenvironment in which they are exposed to mechanical and physical cues. These signals are, nonetheless, deregulated through perturbations to mechanotransduction, from the nanoscale level to the tissue level. Increasingly sophisticated interpretations have uncovered significant contributions of signal transduction cascades in governing prostate cancer progression. To dismantle the major determinants that lie beneath disruption of spatiotemporal patterns of activity, crosstalk between various signalling cascades and their opposing and promoting effects on TRAIL‐mediated act...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5282879</comments>
            <pubDate>Tue, 04 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5282879</guid>        </item>
        <item>
            <title>Notch signalling pathway in tooth development and adult dental cells</title>
            <link>http://www.medworm.com/index.php?rid=5282878&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00780.x</link>
            <description>AbstractNotch signalling is a highly conserved intercellular signal transfer mechanism that includes canonical and non‐canonical pathways. It regulates differentiation and proliferation of stem/progenitor cells by means of para‐inducing effects. Expression and activation of Notch signalling factors (receptors and ligands) are critical not only for development of the dental germ but also for regeneration of injured tissue associated with mature teeth. Notch signalling plays key roles in differentiation of odontoblasts and osteoblasts, calcification of tooth hard tissue, formation of cusp patterns and generation of tooth roots. After tooth eruption, Notch signalling can also be triggered in dental stem cells of the pulp, where it induces them to differentiate into odontoblasts, thus gene...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5282878</comments>
            <pubDate>Tue, 04 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5282878</guid>        </item>
        <item>
            <title>Chitosan enhances mineralization during osteoblast differentiation of human bone marrow‐derived mesenchymal stem cells, by upregulating the associated genes</title>
            <link>http://www.medworm.com/index.php?rid=5332854&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00788.x</link>
            <description>Conclusions:  We demonstrate for the first time that chitosan enhanced mineralization by upregulating the associated genes. Thus, the study may help clinical situations promoting use of chitosan in bone mineralization, necessary for healing non‐union fractures and more. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5332854</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5332854</guid>        </item>
        <item>
            <title>In vitro effects of an in silico‐modelled 17β‐estradiol derivative in combination with dichloroacetic acid on MCF‐7 and MCF‐12A cells</title>
            <link>http://www.medworm.com/index.php?rid=5312249&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00789.x</link>
            <description>Conclusions:  These results demonstrate that the novel 17β‐oestradiol derivative C9, in combination with DCA is a potent anti‐proliferation treatment, with properties of selectivity towards tumourigenic cells. Thus, this warrants further studies as a potential combination chemotherapeutic agent for further cancer cell lines. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5312249</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5312249</guid>        </item>
        <item>
            <title>γ‐Tocotrienol inhibits HGF‐dependent mitogenesis and Met activation in highly malignant mammary tumour cells</title>
            <link>http://www.medworm.com/index.php?rid=5282877&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00785.x</link>
            <description>AbstractObjectives:  Aberrant Met signalling is associated with aggressive cancer cell phenotypes. γ‐tocotrienol displays potent anti‐cancer activity that is associated with suppression of HER/ErbB receptor signalling. Experiments were conducted to investigate the effects of γ‐tocotrienol treatment on HGF‐dependent +SA mammary tumour cell proliferation, upon Met activation.Materials and methods:  The +SA cells were maintained in serum‐free defined media containing 10 ng/ml HGF as the mitogen. Cell viability was determined using the MTT assay, western blot analysis was used to measure protein expression, and Met expression and activation were determined using immunofluorescent staining.Results and conclusions:  Treatment with γ‐tocotrienol or Met inhibitor, SU11274, s...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5282877</comments>
            <pubDate>Sat, 01 Oct 2011 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">5282877</guid>        </item>
        <item>
            <title>Proliferation of dental follicle‐derived cell populations in heat‐stress conditions</title>
            <link>http://www.medworm.com/index.php?rid=5247766&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00778.x</link>
            <description>Conclusion:  Stem cells appear to be more tolerant to heat stress than non‐stem cells. Incubation of a heterogeneous cell population in heat‐stress conditions resulted in increased stem cell numbers. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5247766</comments>
            <pubDate>Sat, 24 Sep 2011 02:02:26 +0100</pubDate>
            <guid isPermaLink="false">5247766</guid>        </item>
        <item>
            <title>Effects of 4‐nonylphenol on proliferation of AGS gastric cells</title>
            <link>http://www.medworm.com/index.php?rid=5247761&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00774.x</link>
            <description>Conclusions:  The results reported suggest that gastric cells can be useful as screening population for appropriate study of developmental toxicity. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5247761</comments>
            <pubDate>Sat, 24 Sep 2011 02:02:25 +0100</pubDate>
            <guid isPermaLink="false">5247761</guid>        </item>
        <item>
            <title>Expansion of human embryonic stem cells: a comparative study</title>
            <link>http://www.medworm.com/index.php?rid=5247760&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00773.x</link>
            <description>Conclusion:  Use of Cell Dissociation Solution, combined with slow adaptation protocol, allows a fast switch from the mechanical passaging technique to a single‐cell split technique, generating stable and robust hESC cell lines, which allow for large scale expansion of hESC for TE purposes. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5247760</comments>
            <pubDate>Sat, 24 Sep 2011 02:02:23 +0100</pubDate>
            <guid isPermaLink="false">5247760</guid>        </item>
        <item>
            <title>Ethyl acetate extract and its major constituent, isorhamnetin 3‐O‐rutinoside, from Nitraria retusa leaves, promote apoptosis of human myelogenous erythroleukaemia cells</title>
            <link>http://www.medworm.com/index.php?rid=5247757&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00772.x</link>
            <description>Conclusion:  Our results strongly suggest the involvement of the extrinsic pathway of apoptosis in cells treated by both the original EA extract and its major component, I3‐O‐R. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5247757</comments>
            <pubDate>Sat, 24 Sep 2011 02:02:21 +0100</pubDate>
            <guid isPermaLink="false">5247757</guid>        </item>
        <item>
            <title>Cholesterol synthesis‐related enzyme oxidosqualene cyclase is required to maintain self‐renewal in primary erythroid progenitors</title>
            <link>http://www.medworm.com/index.php?rid=5247755&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00771.x</link>
            <description>Conclusions:  Taken together, our results suggest that OSC/LSS expression and activity are required to maintain cell self‐renewal and may be involved in the self‐renewal versus differentiation/apoptosis decision making, by keeping cells in a self‐renewal state. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5247755</comments>
            <pubDate>Sat, 24 Sep 2011 02:02:19 +0100</pubDate>
            <guid isPermaLink="false">5247755</guid>        </item>
        <item>
            <title>Importance of Sox2 in maintenance of cell proliferation and multipotency of mesenchymal stem cells in low‐density culture</title>
            <link>http://www.medworm.com/index.php?rid=5247754&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00770.x</link>
            <description>This study has aimed to repopulate ‘primitive’ cells from late‐passage mesenchymal stem cells (MSCs) of poor multipotentiality and low cell proliferation rate, by simply altering plating density.Materials and methods:  Effects of low density culture compared t high density culture on late‐passage bone marrow (BM)‐derived MSCs and pluripotency markers of multipotentiality were investigated. Cell proliferation, gene expression, RNA interference and differentiation potential were assayed.Results and conclusions:  We repopulated ‘primitive’ cells by replating late‐passage MSCs at low density (17 cells/cm2) regardless of donor age. Repopulated MSCs from low‐density culture were smaller cells with spindle shaped morphology compared to MSCs from high‐density culture. The...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5247754</comments>
            <pubDate>Sat, 24 Sep 2011 02:02:17 +0100</pubDate>
            <guid isPermaLink="false">5247754</guid>        </item>
        <item>
            <title>Dose‐specific effects of tumor necrosis factor alpha on osteogenic differentiation of mesenchymal stem cells</title>
            <link>http://www.medworm.com/index.php?rid=5247753&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00769.x</link>
            <description>Conclusions:  The binding of TNF‐α to its receptors results in the activation of multiple signaling pathways, which actively interact with each other to regulate the differentiation, proliferation, survival and apoptosis of MSCs. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5247753</comments>
            <pubDate>Sat, 24 Sep 2011 02:02:15 +0100</pubDate>
            <guid isPermaLink="false">5247753</guid>        </item>
        <item>
            <title>Spontaneous and induced osteoclastogenic behaviour of human peripheral blood mononuclear cells and their CD14+ and CD14− cell fractions</title>
            <link>http://www.medworm.com/index.php?rid=5247752&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00768.x</link>
            <description>Conclusions:  Results show that although osteoclastic precursors reside in the CD14+ cell subpopulation, other populations (such as CD14− cells) derived from PBMC, have the ability to modulate osteoclastogenesis positively. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5247752</comments>
            <pubDate>Sat, 24 Sep 2011 02:02:14 +0100</pubDate>
            <guid isPermaLink="false">5247752</guid>        </item>
        <item>
            <title>3‐O‐methylfunicone, from Penicillium pinophilum, is a selective inhibitor of breast cancer stem cells</title>
            <link>http://www.medworm.com/index.php?rid=5247748&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00766.x</link>
            <description>AbstractObjectives:  Cancer stem cells make up a subpopulation of cells within tumours that drive tumour initiation, growth and recurrence. They are resistant to many current types of cancer treatment, causing failure of such therapeutic approaches, including chemotherapy and radiotherapy. In the study described here, anti‐proliferative effects of 3‐O‐methylfunicone (OMF), a metabolite from Penicillium pinophilum, were investigated on human breast cancer MCF‐7 cells and cancer stem cells selected as mammospheres derived from MCF‐7s.Materials and methods:  Stemness markers were analysed on isolated mammospheres showing positive expression of CD24, CD29, CD44, CD133, CD184 and CD338. Cell proliferation and apoptosis were analysed by flow cytometry and RT‐PCR. Cell colony form...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5247748</comments>
            <pubDate>Sat, 24 Sep 2011 02:02:12 +0100</pubDate>
            <guid isPermaLink="false">5247748</guid>        </item>
        <item>
            <title>Monitoring the fidelity of mitotic chromosome segregation by the spindle assembly checkpoint</title>
            <link>http://www.medworm.com/index.php?rid=5247747&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00767.x</link>
            <description>AbstractAccurate chromosome segregation relies on activity of the spindle assembly checkpoint, a surveillance mechanism that prevents premature anaphase onset until all chromosomes are properly attached to the mitotic spindle apparatus and aligned at the metaphase plate. Defects in this mechanism contribute to chromosome instability and aneuploidy, a hallmark of malignant cells. Here, we review the molecular mechanisms of activation and silencing of the spindle assembly checkpoint and its relationship to tumourigenesis. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5247747</comments>
            <pubDate>Sat, 24 Sep 2011 02:02:10 +0100</pubDate>
            <guid isPermaLink="false">5247747</guid>        </item>
        <item>
            <title>Effects of enamel matrix proteins on proliferation, differentiation and attachment of human alveolar osteoblasts</title>
            <link>http://www.medworm.com/index.php?rid=4975526&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00762.x</link>
            <description>Conclusions:  These results indicate that EMPs may inhibit osteoblastic differentiation and attachment to prevent ankylosis and allow other cell types to regenerate periodontal tissues. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4975526</comments>
            <pubDate>Tue, 28 Jun 2011 22:44:43 +0100</pubDate>
            <guid isPermaLink="false">4975526</guid>        </item>
        <item>
            <title>Effects of tumour necrosis factor‐alpha on activity and nitric oxide synthase of endothelial progenitor cells from peripheral blood</title>
            <link>http://www.medworm.com/index.php?rid=4975525&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00764.x</link>
            <description>AbstractThe aim of this investigation was to determine whether tumour necrosis factor‐alpha (TNF‐α) has any effect on endothelial progenitor cells (EPCs). Total mononuclear cells were isolated from peripheral blood by Ficoll density gradient centrifugation, and then the cells were plated on fibronectin‐coated culture dishes. After 7 days culture, attached cells were stimulated with tumour necrosis factor‐α (final concentrations: 0, 10, 20, 50 and 100 mg/l) for 0, 6, 12, 24 and 48 h. EPCs were characterized as adherent cells double positive for DiLDL‐uptake and lectin binding, by direct fluorescence staining. EPC proliferation and migration were assayed using the MTT assay and modified Boyden chamber assay, respectively. EPC adhesion assay was performed by re‐plating tho...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4975525</comments>
            <pubDate>Tue, 28 Jun 2011 22:44:42 +0100</pubDate>
            <guid isPermaLink="false">4975525</guid>        </item>
        <item>
            <title>Regulation of pre‐adipocyte proliferation and apoptosis by the small leucine‐rich proteoglycans, biglycan and decorin</title>
            <link>http://www.medworm.com/index.php?rid=4975524&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00763.x</link>
            <description>AbstractEvidence for a functional role for extracellular matrix (ECM) proteins in adipose tissue is demonstrated in dynamic changes in expression of ECM genes during adipocyte differentiation and in obesity. Components of the ECM may regulate adipose cell number expansion by restricting pre‐adipocyte proliferation, regulating apoptosis and inhibiting adipogenesis. Although pre‐adipocytes express multiple proteoglycans, their role in pre‐adipocyte proliferation up to now has remained unknown. The study described here was conducted to characterize roles of small leucine‐rich proteoglycans (SLRPs) in adipocyte proliferation. Pre‐adipocytes were seeded on plates coated with biglycan and decorin and were allowed to differentiate. In addition, pre‐adipocytes were incubated on plates ...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4975524</comments>
            <pubDate>Tue, 28 Jun 2011 22:44:41 +0100</pubDate>
            <guid isPermaLink="false">4975524</guid>        </item>
        <item>
            <title>RNAi‐mediated inhibition of the desmosomal cadherin (desmoglein 3) impairs epithelial cell proliferation</title>
            <link>http://www.medworm.com/index.php?rid=4975523&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00765.x</link>
            <description>Conclusion:  These findings suggest that Dsg3 depletion by RNAi reduces cell proliferation, which is likely to be secondary to a defect in cell–cell adhesion, an essential function required for cell differentiation and morphogenesis. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4975523</comments>
            <pubDate>Tue, 28 Jun 2011 22:44:39 +0100</pubDate>
            <guid isPermaLink="false">4975523</guid>        </item>
        <item>
            <title>CXCL13 mediates prostate cancer cell proliferation through JNK signalling and invasion through ERK activation</title>
            <link>http://www.medworm.com/index.php?rid=4902051&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00757.x</link>
            <description>Conclusions:  Our results show CXCL13‐mediated PCa cell invasion requires Akt and ERK1/2 activation and suggests a new role for DOCK2 in proliferation of hormone‐refractory CXCR5‐positive PCa cells. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4902051</comments>
            <pubDate>Sun, 05 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4902051</guid>        </item>
        <item>
            <title>Size‐sieved subpopulations of mesenchymal stem cells from intervascular and perivascular equine umbilical cord matrix</title>
            <link>http://www.medworm.com/index.php?rid=4902050&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00759.x</link>
            <description>Conclusions:  Here, cells from UCM represented an intermediate stage between pluripotent embryonic and adult stem cells. Size‐sieving can be used to isolate more rapidly proliferating cell populations. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4902050</comments>
            <pubDate>Sun, 05 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4902050</guid>        </item>
        <item>
            <title>Two novel aspirin analogues show selective cytotoxicity in primary chronic lymphocytic leukaemia cells that is associated with dual inhibition of Rel A and COX‐2</title>
            <link>http://www.medworm.com/index.php?rid=4902049&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00760.x</link>
            <description>Conclusions:  Our results demonstrate therapeutic potential of 4HBZ and are consistent with a mechanism involving suppression of Rel A nuclear translocation and inhibition of COX‐2 transcription. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4902049</comments>
            <pubDate>Sun, 05 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4902049</guid>        </item>
        <item>
            <title>Serine palmitoyltransferase inhibitor myriocin induces growth inhibition of B16F10 melanoma cells through G2/M phase arrest</title>
            <link>http://www.medworm.com/index.php?rid=4902048&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00761.x</link>
            <description>Conclusions:  Our results suggest that inhibition of sphingolipid synthesis by myriocin in melanoma cells may inhibit expression of cdc25C or activate expression of p53 and p21waf1/cip1, followed by inhibition of cyclin B1 and cdc2, resulting in G2/M arrest of the cell cycle and cell population growth inhibition. Thus, modulation of sphingolipid metabolism by myriocin may be a potential target of mechanism‐based therapy for this type of skin cancer. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4902048</comments>
            <pubDate>Sun, 05 Jun 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4902048</guid>        </item>
        <item>
            <title>Cholesterol esters as growth regulators of lymphocytic leukaemia cells</title>
            <link>http://www.medworm.com/index.php?rid=4902047&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00758.x</link>
            <description>AbstractObjective:  Alterations in plasma lipid profile and in intracellular cholesterol homoeostasis have been described in various malignancies; however, significance of these alterations, if any, in cancer biology is not clear. The aim of the present study was to investigate a possible correlation between alterations in cholesterol metabolism and expansion of leukaemia cell numbers.Materials and methods:  Lipid profiles in plasma and in primary leukaemia cells isolated from patients with acute or chronic lymphocytic leukaemia (ALL and CLL) were studied.Results and conclusions:  Decreased levels of HDL‐C were observed in plasma of leukaemic patients, levels of total cholesterol, LDL‐C, triglycerides and phospholipids were unchanged or only slightly increased. As compared to nor...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4902047</comments>
            <pubDate>Tue, 31 May 2011 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4902047</guid>        </item>
        <item>
            <title>Cyclin‐dependent kinase inhibitor 3 (CDKN3) novel cell cycle computational network between human non‐malignancy associated hepatitis/cirrhosis and hepatocellular carcinoma (HCC) transformation</title>
            <link>http://www.medworm.com/index.php?rid=4758554&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00752.x</link>
            <description>AbstractThe relationship of cyclin‐dependent kinase inhibitor 3 (CDKN3) with tumours has previously been presented in a number of publications. However, the molecular network and interpretation of CDKN3 through the cell cycle between non‐malignancy associated hepatitis/cirrhosis and hepatocellular carcinoma (HCC) have remained to be elucidated. Here, we have constructed and analysed significant high expression gene CDKN3 activated and inhibited cell cycle networks from 25 HCC versus 25 non‐malignancy associated hepatitis/cirrhosis patients (viral infection HCV or HBV) in GEO Dataset GSE10140‐10141, by combination of a gene regulatory network inference method based on linear programming, and decomposition procedure using CapitalBio MAS 3.0 software, based on integration of public da...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4758554</comments>
            <pubDate>Thu, 28 Apr 2011 07:44:43 +0100</pubDate>
            <guid isPermaLink="false">4758554</guid>        </item>
        <item>
            <title>Induction of apoptosis in human lymphoblastoid cells by kaempferol 3‐O‐β‐isorhamninoside and rhamnocitrin 3‐O‐β‐isorhamninoside from Rhamnus alaternus L. (Rhamnaceae)</title>
            <link>http://www.medworm.com/index.php?rid=4758553&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00749.x</link>
            <description>Conclusion:  We have demonstrated that K3O‐ir and R3O‐ir induce apoptosis in human lymphoblastoid cells by the extrinsic pathway of apoptosis. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4758553</comments>
            <pubDate>Thu, 28 Apr 2011 07:44:42 +0100</pubDate>
            <guid isPermaLink="false">4758553</guid>        </item>
        <item>
            <title>Ectopic study of tissue‐engineered bone complex with enamel matrix proteins, bone marrow stromal cells in porous calcium phosphate cement scaffolds, in nude mice</title>
            <link>http://www.medworm.com/index.php?rid=4758552&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00750.x</link>
            <description>Conclusions:  EMPs promoted osteogenic differentiation of pBMSCs, and the tissue‐engineered complex of EMPs, pBMSCs and CPC scaffold may be a valuable alternative to be used in periodontal bone tissue engineering and regeneration. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4758552</comments>
            <pubDate>Thu, 28 Apr 2011 07:44:41 +0100</pubDate>
            <guid isPermaLink="false">4758552</guid>        </item>
        <item>
            <title>Paracrine‐mediated differentiation and activation of human haematopoietic osteoclast precursor cells by skin and gingival fibroblasts</title>
            <link>http://www.medworm.com/index.php?rid=4758551&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00751.x</link>
            <description>Conclusions:  Fibroblasts are able to induce osteoclastogenesis by paracrine mechanisms, and age and anatomical location affect this ability. Other factors produced by fibroblasts, in addition to M‐CSF and RANKL, appear to contribute to observed osteoclastogenic potential. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4758551</comments>
            <pubDate>Thu, 28 Apr 2011 07:44:40 +0100</pubDate>
            <guid isPermaLink="false">4758551</guid>        </item>
        <item>
            <title>Insulin‐like growth factor 2 enhances insulinogenic differentiation of human eyelid adipose stem cells via the insulin receptor</title>
            <link>http://www.medworm.com/index.php?rid=4758550&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00755.x</link>
            <description>Conclusions:  From these results, it is suggested that IGF1 might inhibit insulinogenic differentiation of HEAC, whereas IGF2 enhances differentiation, and that enhancement of IGF2 appeared to be mediated via IR. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4758550</comments>
            <pubDate>Thu, 28 Apr 2011 07:44:40 +0100</pubDate>
            <guid isPermaLink="false">4758550</guid>        </item>
        <item>
            <title>Towards expansion of human hair follicle stem cells in vitro</title>
            <link>http://www.medworm.com/index.php?rid=4758549&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00754.x</link>
            <description>Conclusions:  This study demonstrates the possibility of culturing human hair follicle stem cells without causing any significant changes to phenotypes of the cells. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4758549</comments>
            <pubDate>Thu, 28 Apr 2011 07:44:39 +0100</pubDate>
            <guid isPermaLink="false">4758549</guid>        </item>
        <item>
            <title>In vitro study of enhanced osteogenesis induced by HIF‐1α‐transduced bone marrow stem cells</title>
            <link>http://www.medworm.com/index.php?rid=4758548&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00747.x</link>
            <description>Conclusions:  These results indicate that Lenti‐HIF‐1α can induce BMSC overexpression levels of angiogenic and osteogenic genes in vitro in the normoxic state. Further study will be focused on whether HIF‐1α can also improve bone repair in vivo. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4758548</comments>
            <pubDate>Thu, 28 Apr 2011 07:44:38 +0100</pubDate>
            <guid isPermaLink="false">4758548</guid>        </item>
        <item>
            <title>Proliferation of germ cells and somatic cells in first trimester human embryonic gonads as indicated by S and S+G2+M phase fractions</title>
            <link>http://www.medworm.com/index.php?rid=4758547&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00748.x</link>
            <description>Conclusions:  Cell proliferation as indicated by S and SG2M fractions could be estimated specifically for primordial germ and somatic cells. Estimation of total number of germ and somatic cells was not feasible. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4758547</comments>
            <pubDate>Thu, 28 Apr 2011 07:44:37 +0100</pubDate>
            <guid isPermaLink="false">4758547</guid>        </item>
        <item>
            <title>A model for random genetic damage directing selection of diploid or aneuploid tumours</title>
            <link>http://www.medworm.com/index.php?rid=4758546&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00746.x</link>
            <description>Conclusion:  Random loss of cell survival/replication genes was calculated to be low enough for colon stem cells with APC gene mutations to ‘select’ LOH and derivative chromosome combinations favouring tumour cell proliferation. However, cell survival/replication gene loss was calculated to be too high for colonic stem cells lacking MMR genes to survive chromosomal instability, explaining why MMR mutations only produce tumours with diploid chromosome cells. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4758546</comments>
            <pubDate>Thu, 28 Apr 2011 07:44:36 +0100</pubDate>
            <guid isPermaLink="false">4758546</guid>        </item>
        <item>
            <title>Cdc2: a monopotent or pluripotent CDK?</title>
            <link>http://www.medworm.com/index.php?rid=4758545&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00753.x</link>
            <description>AbstractCell cycle progression is controlled by both extracellular and intracellular signalling molecules. It has been generally believed that cdc2/CDK1 only control G2‐M transition in mammalian and many other higher eukaryotic cells. Accumulating evidence shows that cdc2 not only promotes G2‐M transition but is also capable of regulating G1 progress and G1‐S transition via association with multiple interphase cyclins; cdc2 activity can be inhibited by p21 and p27, two traditional G1 CDK inhibitors. In addition, cdc2‐cyclin B controls pronuclear union in interphase fertilized eggs. These data suggest that cdc2 may be a pluripotent CDK. Although mechanisms responsible for the multiple functions of cdc2 remain to be further investigated, interactions of cdc2 with pRb and with several...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4758545</comments>
            <pubDate>Thu, 28 Apr 2011 07:44:35 +0100</pubDate>
            <guid isPermaLink="false">4758545</guid>        </item>
        <item>
            <title>Mathematical model of the role of intercellular signalling in intercellular cooperation during tumorigenesis</title>
            <link>http://www.medworm.com/index.php?rid=4591848&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00739.x</link>
            <description>AbstractObjectives:  Intercellular cooperation has been hypothesized to enhance cell proliferation during cancer metastasis through autocrine signalling cascades and mathematical models can provide valuable insights into underlying mechanisms of metastatic tumorigenesis. Here, we present a model that incorporates signal‐stimulated cell proliferation, and investigate influences of diffusion‐driven heterogeneity in signal concentration on proliferation dynamics.Materials and methods:  Our model incorporates signal production through both autocrine and paracrine pathways, and signal diffusion and loss for a metastasizing cell population at a host site. We use the signalling pathway of IL‐6 for illustration where this signalling species forms an intermediate complex with its receptor...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4591848</comments>
            <pubDate>Wed, 16 Mar 2011 00:23:07 +0100</pubDate>
            <guid isPermaLink="false">4591848</guid>        </item>
        <item>
            <title>Immobilization of thrombocytes on PCL nanofibres enhances chondrocyte proliferation in vitro</title>
            <link>http://www.medworm.com/index.php?rid=4591847&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00737.x</link>
            <description>Conclusions:  These simply functionalized scaffolds present new possibilities for nanofibre applications, as smart cell scaffolds equipped with a GF delivery tool. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4591847</comments>
            <pubDate>Wed, 16 Mar 2011 00:23:06 +0100</pubDate>
            <guid isPermaLink="false">4591847</guid>        </item>
        <item>
            <title>EGFR is involved in control of gastric cell proliferation through activation of MAPK and Src signalling pathways in early‐weaned rats</title>
            <link>http://www.medworm.com/index.php?rid=4591846&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00733.x</link>
            <description>Conclusions:  EGFR is part of the mechanism that regulates cell proliferation in rat gastric mucosa during early weaning. We suggest that such responses might depend on activation of MAPK and/or Src signalling pathways and regulation of p21 levels. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4591846</comments>
            <pubDate>Wed, 16 Mar 2011 00:23:06 +0100</pubDate>
            <guid isPermaLink="false">4591846</guid>        </item>
        <item>
            <title>Mithramycin reduces expression of fibro‐proliferative mRNAs in human gingival fibroblasts</title>
            <link>http://www.medworm.com/index.php?rid=4591845&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00738.x</link>
            <description>AbstractFibrosis is characterized by loss of normal structure and function of a tissue or organ resulting from excessive fibroblast proliferation and extracellular matrix production. Currently, there is no efficient treatment for fibrosis. Herein, we test effects of the drug mithramycin, which targets the Sp1 family of transcription factors, on mRNA expression by human gingival fibroblasts. Mithramycin reduced expression of connective tissue growth factor and type I collagen mRNAs. Microarray profiling revealed that mithramycin selectively blocked expression of cell proliferation and transforming growth factor‐beta (TGF‐β) signalling clusters. These microarray data were validated using real‐time polymerase chain reaction and western blot analyses. Mithramycin suppressed expression o...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4591845</comments>
            <pubDate>Wed, 16 Mar 2011 00:23:05 +0100</pubDate>
            <guid isPermaLink="false">4591845</guid>        </item>
        <item>
            <title>Influence of proline‐rich inositol polyphosphate 5‐phosphatase, on early development of fertilized mouse eggs, via inhibition of phosphorylation of Akt</title>
            <link>http://www.medworm.com/index.php?rid=4591844&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00743.x</link>
            <description>Conclusions:  Our data suggest, for the first time, that PIPP may affect development of fertilized mouse eggs by inhibition of level of phosphorylated Akt at Ser473 and subsequent inhibition of downstream signal cascades. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4591844</comments>
            <pubDate>Wed, 16 Mar 2011 00:23:04 +0100</pubDate>
            <guid isPermaLink="false">4591844</guid>        </item>
        <item>
            <title>Phosphorylation at serine 482 affects stability of NF90 and its functional role in mitosis</title>
            <link>http://www.medworm.com/index.php?rid=4591843&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00742.x</link>
            <description>Conclusions:  Phosphorylation at S482 is important for NF90 stability and in regulating its functional role during mitosis. Based on the sequence surrounding S482, mitotic kinase PLK1 is a strong candidate for the enzyme that phosphorylates NF90 at this site. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4591843</comments>
            <pubDate>Wed, 16 Mar 2011 00:23:03 +0100</pubDate>
            <guid isPermaLink="false">4591843</guid>        </item>
        <item>
            <title>Anti‐tumour and anti‐angiogenetic effects of zoledronic acid on human non‐small‐cell lung cancer cell line</title>
            <link>http://www.medworm.com/index.php?rid=4591842&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00745.x</link>
            <description>Conclusion:  Taken together, these results support a possible anti‐cancer and anti‐angiogenetic activity of Zol. Our data may not only provide a basis for the clinical use of this drug as preventive agent of bone metastases but also suggest that Zol deserves attention as an anti‐cancer agent in non‐small‐cell lung cancer. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4591842</comments>
            <pubDate>Wed, 16 Mar 2011 00:23:02 +0100</pubDate>
            <guid isPermaLink="false">4591842</guid>        </item>
        <item>
            <title>Inhibition of metastasis‐associated gene 1 expression affects proliferation and osteogenic differentiation of immortalized human mesenchymal stem cells</title>
            <link>http://www.medworm.com/index.php?rid=4591841&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00735.x</link>
            <description>Conclusions:  Our data collectively suggest that endogenously produced MTA1 constrains osteogenic differentiation of MSCs and that targeting of this molecule may provide a novel strategy for enhancing bone regeneration. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4591841</comments>
            <pubDate>Wed, 16 Mar 2011 00:23:02 +0100</pubDate>
            <guid isPermaLink="false">4591841</guid>        </item>
        <item>
            <title>Mesenchymal differentiation propensity of a human embryonic stem cell line</title>
            <link>http://www.medworm.com/index.php?rid=4591840&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00744.x</link>
            <description>Conclusions:  The data presented suggest that the KCL‐002 hES cell line is pluripotent and harbours a bias in basal differentiation tendencies towards mesodermal and mesenchymal lineage cells. Characterizing innate differentiation propensities of hES cell lines is important for understanding heterogeneity between different cell lines and for further studies aimed at deriving specific lineages from hES cells. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4591840</comments>
            <pubDate>Wed, 16 Mar 2011 00:23:01 +0100</pubDate>
            <guid isPermaLink="false">4591840</guid>        </item>
        <item>
            <title>DNA‐unstable decaploid mouse H1 (ES) cells established from DNA‐stable pentaploid H1 (ES) cells polyploidized using demecolcine</title>
            <link>http://www.medworm.com/index.php?rid=4591839&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2011.00734.x</link>
            <description>Conclusion:  In the pentaploid–decaploid transition of H1 cells, cell cycle parameters and pluripotency were retained, but morphology and DNA stability were altered. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4591839</comments>
            <pubDate>Wed, 16 Mar 2011 00:23:00 +0100</pubDate>
            <guid isPermaLink="false">4591839</guid>        </item>
        <item>
            <title>Erratum</title>
            <link>http://www.medworm.com/index.php?rid=4298543&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00741.x</link>
            <description>(Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298543</comments>
            <pubDate>Thu, 30 Dec 2010 10:48:45 +0100</pubDate>
            <guid isPermaLink="false">4298543</guid>        </item>
        <item>
            <title>In vitro mesenchymal stem cell differentiation after mechanical stimulation</title>
            <link>http://www.medworm.com/index.php?rid=4298541&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00740.x</link>
            <description>Conclusions:  These experiments confirmed that MSC cell fate choice depends on minute, cell‐derived forces. Applied force could assist in commercial manufacture of cultured bio‐engineered prostheses for regenerative medicine as it mimics tissue stresses and constitutes a good model for development of tissue substitutes. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298541</comments>
            <pubDate>Thu, 30 Dec 2010 10:48:43 +0100</pubDate>
            <guid isPermaLink="false">4298541</guid>        </item>
        <item>
            <title>Adipose‐derived stem cells for clinical applications: a review</title>
            <link>http://www.medworm.com/index.php?rid=4298540&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00736.x</link>
            <description>AbstractThe use of stem cells derived from adipose tissue as an autologous and self‐replenishing source for a variety of differentiated cell phenotypes, provides a great deal of promise for reconstructive surgery. In this article, we review available literature encompassing methods of extraction of pluripotent adipose stem cells (ASCs) from lipoaspirate locations, their storage, options for culture, growth and differentiation, cryopreservation and its effect on stem cell survival and proliferation, and new technologies involving biomaterials and scaffolds. We will conclude by assessing potential avenues for developing this incredibly promising field. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298540</comments>
            <pubDate>Thu, 30 Dec 2010 10:48:43 +0100</pubDate>
            <guid isPermaLink="false">4298540</guid>        </item>
        <item>
            <title>Effect of long‐term culture of mouse embryonic stem cells under low oxygen concentration as well as on glycosaminoglycan hyaluronan on cell proliferation and differentiation</title>
            <link>http://www.medworm.com/index.php?rid=4298539&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00732.x</link>
            <description>Conclusions:  Our data suggest that hypoxia is not necessary for maintaining pluripotency of mES cells and appeared to be detrimental during ES differentiation. Moreover, HA may offer a valuable alternative for long‐term culture of mES cells in vitro. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298539</comments>
            <pubDate>Thu, 30 Dec 2010 10:48:42 +0100</pubDate>
            <guid isPermaLink="false">4298539</guid>        </item>
        <item>
            <title>Early spontaneous immortalization and loss of plasticity of rabbit bone marrow mesenchymal stem cells</title>
            <link>http://www.medworm.com/index.php?rid=4298538&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00731.x</link>
            <description>In this study, we have examined growth kinetics, morphological changes, differentiation potential and chromosomal abnormalities, as well as tumour formation potential of rabbit BM‐MSC in long‐term culture.Results and conclusion:  We found that shortly after isolation, proliferation rate of rabbit BM‐MSC decreases until they enter a dormant phase. During this period of quiescence, the cells are large and multinucleate. After some weeks of dormancy we found that several small mononuclear cells originated from each large multinucleate cell. These newly formed cells proliferated rapidly but had inferior differentiation potential. Although they were immortal, they did not have the capability for tumour formation in soft agar assay or in nude mice. This is the first report of spontaneous...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298538</comments>
            <pubDate>Thu, 30 Dec 2010 10:48:41 +0100</pubDate>
            <guid isPermaLink="false">4298538</guid>        </item>
        <item>
            <title>MicroRNA signatures associated with immortalization of EBV‐transformed lymphoblastoid cell lines and their clinical traits</title>
            <link>http://www.medworm.com/index.php?rid=4298537&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00717.x</link>
            <description>Conclusion:  Microarray data showed that nine miRNAs (miR‐20b*, miR‐28‐5p, miR‐99a, miR‐125b, miR‐151‐3p, miR‐151:9.1, miR‐216a, miR‐223* and miR‐1296) were differentially expressed in most LCLs during long‐term culture. In particular, miR‐125b was up‐regulated in all the tested late‐passage LCLs. miR‐99a, miR‐125b, miR‐216a and miR‐1296 were putative negative regulators of RASGRP3, GPR160, PRKCH and XAF1, respectively, which were found to be differentially expressed in LCLs during long‐term culture in a previous study. Linear regression analysis showed that miR‐200a and miR‐296‐3p correlated with triglyceride and HbA1C levels, respectively, suggesting that miRNA signatures of LCLs could provide information on the donor’s health. In conclus...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298537</comments>
            <pubDate>Thu, 30 Dec 2010 10:48:40 +0100</pubDate>
            <guid isPermaLink="false">4298537</guid>        </item>
        <item>
            <title>Extracellular transglutaminase 2 has a role in cell adhesion, whereas intracellular transglutaminase 2 is involved in regulation of endothelial cell proliferation and apoptosis</title>
            <link>http://www.medworm.com/index.php?rid=4298536&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00716.x</link>
            <description>Conclusion:  We conclude that TG2 loss in endothelial cells causes reduction in cell number as a result of cell cycle arrest, flaws in adhesion and induction of apoptosis. Our results imply that reduction in cell number and increased apoptosis in response to TG2 silencing is independent of the cell adhesion process. Altogether, our findings underline the significance of TG2 in endothelial cell cycle progression and cell survival, in vitro. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298536</comments>
            <pubDate>Thu, 30 Dec 2010 10:48:39 +0100</pubDate>
            <guid isPermaLink="false">4298536</guid>        </item>
        <item>
            <title>Fibrin acts as biomimetic niche inducing both differentiation and stem cell marker expression of early human endothelial progenitor cells</title>
            <link>http://www.medworm.com/index.php?rid=4298534&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00715.x</link>
            <description>Conclusion:  Fibrin is a suitable matrix for EPC growth, differentiation and angiogenesis capability, suggesting that fibrin gel may be very useful for regenerative medicine. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298534</comments>
            <pubDate>Thu, 30 Dec 2010 10:48:39 +0100</pubDate>
            <guid isPermaLink="false">4298534</guid>        </item>
        <item>
            <title>Characterization of immortalized mesenchymal stem cells derived from foetal porcine pancreas</title>
            <link>http://www.medworm.com/index.php?rid=4298533&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00714.x</link>
            <description>In this study, we isolated and established an immortalized mesenchymal stem cell (MSC) line derived from foetal porcine pancreas, by transfecting human telomerase reverse transcriptase (hTERT) and called these immortalized pancreatic mesenchymal stem cells (iPMSCs). The iPMSCs have been cultured for more than 80 passages and have capacity to differentiate into neurons, cardiomyocytes, germ cells and islet‐like cells, analysed by morphology, RT‐PCR, western blotting, immunofluorescence, immunocytochemistry and transplantation assay. Islets derived from iPMSCs reversed hyperglycaemia in streptozotocin‐induced diabetic mice and secreted insulin and C‐peptide in vitro. These results demonstrated that iPMSCs might provide unlimited resources for islet replacement therapy and models for ...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298533</comments>
            <pubDate>Thu, 30 Dec 2010 10:48:38 +0100</pubDate>
            <guid isPermaLink="false">4298533</guid>        </item>
        <item>
            <title>Foe turned friend: multiple functional roles attributable to hyper‐activating stem cell factor receptor mutant in regeneration of the haematopoietic cell compartment</title>
            <link>http://www.medworm.com/index.php?rid=4298532&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00713.x</link>
            <description>Conclusion:  These results suggest that recruitment of the hyper‐activating variant of c‐kit (Kitmu) lead to early recovery of the bone marrow of lethally irradiated mice. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4298532</comments>
            <pubDate>Thu, 30 Dec 2010 10:48:37 +0100</pubDate>
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            <title>Anaphase‐promoting complex/cyclosome controls HEC1 stability</title>
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            <description>Conclusion:  APC/C‐Cdh1 controls stability of HEC1, ensuring normal cell cycle progression. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
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            <pubDate>Thu, 30 Dec 2010 10:48:36 +0100</pubDate>
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            <title>Experimental analysis and modelling of in vitro HUVECs proliferation in the presence of various types of drugs</title>
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            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
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            <pubDate>Sat, 30 Oct 2010 03:51:48 +0100</pubDate>
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            <title>Schwann‐like cell differentiation of rat adipose‐derived stem cells by indirect co‐culture with Schwann cells in vitro</title>
            <link>http://www.medworm.com/index.php?rid=4118205&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00710.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
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            <pubDate>Sat, 30 Oct 2010 03:51:47 +0100</pubDate>
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            <title>Genistein and daidzein repress adipogenic differentiation of human adipose tissue‐derived mesenchymal stem cells via Wnt/β‐catenin signalling or lipolysis</title>
            <link>http://www.medworm.com/index.php?rid=4118204&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00709.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
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            <pubDate>Sat, 30 Oct 2010 03:51:47 +0100</pubDate>
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            <title>Identification of tyrosine‐nitrated proteins in HT22 hippocampal cells during glutamate‐induced oxidative stress</title>
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            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
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            <pubDate>Sat, 30 Oct 2010 03:51:46 +0100</pubDate>
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            <title>Chromatin‐bound PCNA as S‐phase marker in mononuclear blood cells of patients with acute lymphoblastic leukaemia or multiple myeloma</title>
            <link>http://www.medworm.com/index.php?rid=4118202&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00707.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
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            <pubDate>Sat, 30 Oct 2010 03:51:46 +0100</pubDate>
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            <title>Normal red blood cells partially decrease diepoxybutane‐induced chromosome breakage in cultured lymphocytes from Fanconi anaemia patients</title>
            <link>http://www.medworm.com/index.php?rid=4118201&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00706.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4118201</comments>
            <pubDate>Sat, 30 Oct 2010 03:51:45 +0100</pubDate>
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            <title>Assessment of cell proliferation and muscular structure following surgical tongue volume reduction in pigs</title>
            <link>http://www.medworm.com/index.php?rid=4118200&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00705.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
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            <pubDate>Sat, 30 Oct 2010 03:51:45 +0100</pubDate>
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            <title>Improved procedure for the measurement of telomere length in whole cells by PNA probe and flow cytometry</title>
            <link>http://www.medworm.com/index.php?rid=4118199&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00704.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4118199</comments>
            <pubDate>Sat, 30 Oct 2010 03:51:44 +0100</pubDate>
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            <title>Coupled mathematical model of tumorigenesis and angiogenesis in vascular tumours</title>
            <link>http://www.medworm.com/index.php?rid=4118198&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00703.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4118198</comments>
            <pubDate>Sat, 30 Oct 2010 03:51:44 +0100</pubDate>
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            <title>Ion channels in volume regulation of clonal kidney cells</title>
            <link>http://www.medworm.com/index.php?rid=4118197&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00702.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4118197</comments>
            <pubDate>Sat, 30 Oct 2010 03:51:43 +0100</pubDate>
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        <item>
            <title>Proteomic analysis of 3T3‐L1 preadipocytes having a higher cell proliferation rate after treatment with low‐molecular‐weight silk fibroin peptides</title>
            <link>http://www.medworm.com/index.php?rid=3914809&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00701.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3914809</comments>
            <pubDate>Tue, 31 Aug 2010 05:20:52 +0100</pubDate>
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            <title>17β‐oestradiol acts as a negative modulator of insulin‐induced lactotroph cell proliferation through oestrogen receptor alpha, via nitric oxide/guanylyl cyclase/cGMP</title>
            <link>http://www.medworm.com/index.php?rid=3914808&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00700.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3914808</comments>
            <pubDate>Tue, 31 Aug 2010 05:20:51 +0100</pubDate>
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            <title>Two‐fold elevation of expression of FoxM1 transcription factor in mouse embryonic fibroblasts enhances cell cycle checkpoint activity by stimulating p21 and Chk1 transcription</title>
            <link>http://www.medworm.com/index.php?rid=3914807&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00699.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3914807</comments>
            <pubDate>Tue, 31 Aug 2010 05:20:51 +0100</pubDate>
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            <title>Combination of photodynamic therapy with aspirin in human‐derived lung adenocarcinoma cells affects proteasome activity and induces apoptosis</title>
            <link>http://www.medworm.com/index.php?rid=3914806&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00698.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3914806</comments>
            <pubDate>Tue, 31 Aug 2010 05:20:50 +0100</pubDate>
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            <title>Chloroform extract from Moricandia arvensis inhibits growth of B16‐F0 melanoma cells and promotes differentiation in vitro</title>
            <link>http://www.medworm.com/index.php?rid=3914805&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00697.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3914805</comments>
            <pubDate>Tue, 31 Aug 2010 05:20:50 +0100</pubDate>
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            <title>The role of inhibitor of DNA‐binding (Id1) in hyperproliferation of keratinocytes: the pathological basis for middle ear cholesteatoma from chronic otitis media</title>
            <link>http://www.medworm.com/index.php?rid=3914804&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00695.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3914804</comments>
            <pubDate>Tue, 31 Aug 2010 05:20:49 +0100</pubDate>
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            <title>Cell proliferation of human bone marrow mesenchymal stem cells on biodegradable microcarriers enhances in vitro differentiation potential</title>
            <link>http://www.medworm.com/index.php?rid=3914803&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00694.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3914803</comments>
            <pubDate>Tue, 31 Aug 2010 05:20:49 +0100</pubDate>
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            <title>Culture and in vitro hepatogenic differentiation of placenta‐derived stem cells, using placental extract as an alternative to serum</title>
            <link>http://www.medworm.com/index.php?rid=3914802&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00693.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3914802</comments>
            <pubDate>Tue, 31 Aug 2010 05:20:48 +0100</pubDate>
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            <title>Differentiation of bone marrow‐derived mesenchymal stem cells into hepatocyte‐like cells in an alginate scaffold</title>
            <link>http://www.medworm.com/index.php?rid=3914801&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00692.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3914801</comments>
            <pubDate>Tue, 31 Aug 2010 05:20:48 +0100</pubDate>
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            <title>Age-related changes in biological characteristics of human alveolar osteoblasts</title>
            <link>http://www.medworm.com/index.php?rid=3822718&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00696.x</link>
            <description>Conclusions: Comparison of biological characteristics of AOBs from young adult women with those from elderly women in vitro revealed differences in proliferative capacity and bone formation functions, which decreased with aging. These data indicate that aging may play an important role in pathogenesis of human AOBs loss. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3822718</comments>
            <pubDate>Wed, 04 Aug 2010 23:00:00 +0100</pubDate>
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            <title>Age‐related changes in biological characteristics of human alveolar osteoblasts</title>
            <link>http://www.medworm.com/index.php?rid=3885193&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00696.x</link>
            <description>(Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3885193</comments>
            <pubDate>Sat, 31 Jul 2010 23:00:00 +0100</pubDate>
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            <title>Long‐term proliferation and characterization of human spermatogonial stem cells obtained from obstructive and non‐obstructive azoospermia under exogenous feeder‐free culture conditions</title>
            <link>http://www.medworm.com/index.php?rid=3844627&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00691.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3844627</comments>
            <pubDate>Sat, 31 Jul 2010 23:00:00 +0100</pubDate>
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            <title>Differential proteome and phosphoproteome signatures in human T‐lymphoblast cells induced by sirolimus</title>
            <link>http://www.medworm.com/index.php?rid=3844626&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00690.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3844626</comments>
            <pubDate>Sat, 31 Jul 2010 23:00:00 +0100</pubDate>
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            <title>Inhibition of cell proliferation by CD44: Akt is inactivated and EGR‐1 is down‐regulated</title>
            <link>http://www.medworm.com/index.php?rid=3844625&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00689.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3844625</comments>
            <pubDate>Sat, 31 Jul 2010 23:00:00 +0100</pubDate>
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            <title>Expression phenotype changes of EBV‐transformed lymphoblastoid cell lines during long‐term subculture and its clinical significance</title>
            <link>http://www.medworm.com/index.php?rid=3844624&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00687.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3844624</comments>
            <pubDate>Sat, 31 Jul 2010 23:00:00 +0100</pubDate>
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            <title>Spontaneous immortalization of neural crest‐derived corneal progenitor cells after chromosomal aberration</title>
            <link>http://www.medworm.com/index.php?rid=3844623&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00686.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3844623</comments>
            <pubDate>Sat, 31 Jul 2010 23:00:00 +0100</pubDate>
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            <title>p53‐dependent G1 arrest in 1st or 2nd cell cycle may protect human cancer cells from cell death after treatment with ionizing radiation and Chk1 inhibitors</title>
            <link>http://www.medworm.com/index.php?rid=3844622&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00685.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3844622</comments>
            <pubDate>Sat, 31 Jul 2010 23:00:00 +0100</pubDate>
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            <title>MEK/ERK and p38 MAPK regulate chondrogenesis of rat bone marrow mesenchymal stem cells through delicate interaction with TGF‐β1/Smads pathway</title>
            <link>http://www.medworm.com/index.php?rid=3844621&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00682.x</link>
            <description>Abstract (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3844621</comments>
            <pubDate>Sat, 31 Jul 2010 23:00:00 +0100</pubDate>
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            <title>MEK/ERK and p38 MAPK regulate chondrogenesis of rat bone marrow mesenchymal stem cells through delicate interaction with TGF-&amp;#x03B2;1/Smads pathway</title>
            <link>http://www.medworm.com/index.php?rid=3713938&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00682.x</link>
            <description>Conclusions: MAPK subtypes seemed to regulate chondrogenesis with a delicate balance, interacting with the TGF-[beta]1/Smads signalling pathway. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3713938</comments>
            <pubDate>Thu, 01 Jul 2010 07:56:23 +0100</pubDate>
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            <title>Optimization of culture conditions for endothelial progenitor cells from porcine bone marrow in vitro</title>
            <link>http://www.medworm.com/index.php?rid=3713947&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00688.x</link>
            <description>Objectives: The aim of this study was to determine an optimal culture method for porcine bone marrow-derived endothelial progenitor cells (EPCs).Materials and methods: Mononuclear cells (MNCs) were isolated by density centrifugation and differentiated into EPCs in in vitro. At first-passage, EPCs were cultured at different cell densities (5 × 103, 1 × 104, 2 × 104 or 5 × 104/cm2) and in basic medium (EGM, medium 199, DMEM or 1640) supplemented with FBS (2%, 5%, 10% or 20%) and different combinations of cytokines (VEGF, VEGF + bFGF, VEGF + bFGF + EGF, or VEGF + bFGF + EGF + IGF), the experiment being based on L64 (421) orthogonal design.Results and conclusions: This demonstrated that the optimal culture method for our EPCs displayed higher expansion and migration rates as compared to ot...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3713947</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
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            <title>Long-term proliferation and characterization of human spermatogonial stem cells obtained from obstructive and non-obstructive azoospermia under exogenous feeder-free culture conditions</title>
            <link>http://www.medworm.com/index.php?rid=3713946&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00691.x</link>
            <description>Conclusion: These finding may support the idea that in vitro propagation of SSCs could be a useful tool for infertility treatment and study of reproductive biology. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3713946</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3713946</guid>        </item>
        <item>
            <title>Differential proteome and phosphoproteome signatures in human T-lymphoblast cells induced by sirolimus</title>
            <link>http://www.medworm.com/index.php?rid=3713945&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00690.x</link>
            <description>Conclusions: We report for the first time the simultaneous early influence of SRL on phosphorylation status and on protein expression in the total proteome of CCRF-CEM T lymphoblasts and predict that 56% of the proteins interact with each other, highlighting significance of these results. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3713945</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3713945</guid>        </item>
        <item>
            <title>Inhibition of cell proliferation by CD44: Akt is inactivated and EGR-1 is down-regulated</title>
            <link>http://www.medworm.com/index.php?rid=3713944&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00689.x</link>
            <description>Conclusion: Our results suggest a novel pathway by which CD44 inactivates Akt, down-regulates EGR-1 expression and inhibits cell proliferation. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3713944</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3713944</guid>        </item>
        <item>
            <title>Expression phenotype changes of EBV-transformed lymphoblastoid cell lines during long-term subculture and its clinical significance</title>
            <link>http://www.medworm.com/index.php?rid=3713943&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00687.x</link>
            <description>Conclusion: Our results showed that LCLs acquired expression phenotype changes involving expression of NF-[kappa]B pathway- and carcinogenesis-related genes during long-term subculture. These differentially expressed genes can be considered to be a gene signature of LCL immortalization or EBV-induced carcinogenesis. Clinical trait-associated expression phenotypes should prove useful in the discovery of new candidate genes for particular traits. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3713943</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3713943</guid>        </item>
        <item>
            <title>Spontaneous immortalization of neural crest-derived corneal progenitor cells after chromosomal aberration</title>
            <link>http://www.medworm.com/index.php?rid=3713942&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00686.x</link>
            <description>Conclusions: MCCs immortalize spontaneously after extensive cell culture, but still demonstrate stem cell-like qualities. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3713942</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3713942</guid>        </item>
        <item>
            <title>p53-dependent G1 arrest in 1st or 2nd cell cycle may protect human cancer cells from cell death after treatment with ionizing radiation and Chk1 inhibitors</title>
            <link>http://www.medworm.com/index.php?rid=3713941&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00685.x</link>
            <description>Conclusion: Our results suggest that p53-dependent G1 arrest in both 1st and 2nd cell cycles may protect human cancer cells from cell death after treatment with IR and Chk1 inhibitors. However, a challenge for future clinical use will be that different cancers display different intrinsic sensitivity to such inhibitors. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3713941</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3713941</guid>        </item>
        <item>
            <title>Curcumin disrupts meiotic and mitotic divisions via spindle impairment and inhibition of CDK1 activity</title>
            <link>http://www.medworm.com/index.php?rid=3713940&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00684.x</link>
            <description>Objectives: Curcumin, a natural compound, is a potent anti-cancer agent, which inhibits cell division and/or induces cell death. It is believed that normal cells are less sensitive to curcumin than malignant cells; however, the mechanism(s) responsible for curcumin's effect on normal cells are poorly understood. The aim of this study was to verify the hypothesis that curcumin affects normal cell division by influencing microtubule stability, using mouse oocyte and early embryo model systems.Materials and methods: Maturating mouse oocytes and two-cell embryos were treated with different concentrations of curcumin (10[ndash]50 [mu]m), and meiotic resumption and mitotic cleavage were analysed. Spindle and chromatin structure were visualized using confocal microscopy. In addition, acetylation ...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3713940</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3713940</guid>        </item>
        <item>
            <title>Oscillations in growth of multicellular tumour spheroids: a revisited quantitative analysis</title>
            <link>http://www.medworm.com/index.php?rid=3713939&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00683.x</link>
            <description>Conclusions: Biological mechanisms, which can be directly responsible for observed oscillations, are proposed, which relates also to recent work on related topics. Further investigations, both at experimental and at modelling levels, are also suggested. Finally, from a methodological point of view, results obtained represent further confirmation of applicability and usefulness of the PUN approach. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3713939</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3713939</guid>        </item>
        <item>
            <title>Differences between karyotypically normal and abnormal human embryonic stem cells</title>
            <link>http://www.medworm.com/index.php?rid=3515180&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00669.x</link>
            <description>Conclusion: Karyotypically abnormal chHES-3 cells had a more developed capacity for proliferation, resistance to apoptosis and less genetic stability compared to normal chHES-3 cells and may be an excellent model for studying and characterizing initial stages that determine transition of embryonic stem cells into cancer stem cells. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515180</comments>
            <pubDate>Thu, 29 Apr 2010 15:53:40 +0100</pubDate>
            <guid isPermaLink="false">3515180</guid>        </item>
        <item>
            <title>Neutropenia dynamics in a case of T-LGL lymphoproliferation illustrate rapid turnover of granulocyte progenitors</title>
            <link>http://www.medworm.com/index.php?rid=3515190&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00678.x</link>
            <description>Conclusion: These findings illustrate how the deleterious effect of T-LGL on neutrophils is balanced, over periods of years, by pulses of compensatory neutrophil production, potentially accounting for the commonly observed prolonged indolent course of the disease. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515190</comments>
            <pubDate>Tue, 27 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3515190</guid>        </item>
        <item>
            <title>Epidermal kinetic alterations required to generate the psoriatic phenotype: a reappraisal</title>
            <link>http://www.medworm.com/index.php?rid=3515189&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00672.x</link>
            <description>Objectives: Although there have been major advances in understanding immunopathogenesis of psoriasis, the basic processes causing psoriatic morphology remain to be identified.Materials and methods: Our group has designed a systematic review of studies (1962[ndash]2009) on keratinocyte kinetics in psoriasis. We obtained data from MEDLINE, PubMed, Current Contents, reference lists and specialist textbooks. A general equation for evolution of the differentiated epidermis has been analysed. Necessary conditions for observed qualitative change in homeostasis between normal skin and established psoriatic lesions were determined.Results and discussion: Increase in the number of cell divisions (or imbalance in symmetric division rates of committed progenitor cells) and/or decrease in physiological...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515189</comments>
            <pubDate>Tue, 27 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3515189</guid>        </item>
        <item>
            <title>Global gene expression reveals a set of new genes involved in the modification of cells during erythroid differentiation</title>
            <link>http://www.medworm.com/index.php?rid=3515188&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00679.x</link>
            <description>Conclusions: The results of this study amplify previously published data and may contribute to comprehension of erythroid differentiation and identification of new target genes involved in some erythroid concerning diseases. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515188</comments>
            <pubDate>Tue, 27 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3515188</guid>        </item>
        <item>
            <title>Expansion of mouse sertoli cells on microcarriers</title>
            <link>http://www.medworm.com/index.php?rid=3515187&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00677.x</link>
            <description>Conclusion: Data obtained in this study demonstrate the vast potential of this stirred culture system for efficient, reproducible and cost-effective expansion of SCs in vitro. The system has advantages over static culture, which has major obstacles such as lower cell density, is time-consuming and susceptible to contamination. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515187</comments>
            <pubDate>Tue, 27 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3515187</guid>        </item>
        <item>
            <title>Cell proliferation and cell cycle alterations in oesophageal p53-mutated cancer cells treated with cisplatin in combination with photodynamic therapy</title>
            <link>http://www.medworm.com/index.php?rid=3515186&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00673.x</link>
            <description>Conclusions: Our results show that low CDDP doses (0.25[ndash]1 [mu]m) induce cell mortality and cell cycle perturbation, which were more evident when given in combination with PDT, but in contrast to work of other authors no synergistic activity was found. Apoptosis occurred via intrinsic pathways in treated cells, although it did not represent the predominant mode of cell death. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515186</comments>
            <pubDate>Tue, 27 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3515186</guid>        </item>
        <item>
            <title>Soluble factors from ASCs effectively direct control of chondrogenic fate</title>
            <link>http://www.medworm.com/index.php?rid=3515185&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00680.x</link>
            <description>Conclusion: ASC CM-derived TGF-[beta]1-induced chondrogenic differentiation of ASCs resulted in significant reduction in chondrogenic activity after inhibition of the p38 pathway, revealing involvement of this MAPK pathway in TGF-[beta]1 signalling. On the other hand, TGF-[beta]1 signalling also led to SMAD activation that could directly increase chondrogenic activity of ASCs. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515185</comments>
            <pubDate>Tue, 27 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3515185</guid>        </item>
        <item>
            <title>Isolation of therapeutically functional mouse bone marrow mesenchymal stem cells within 3&amp;nbsp;h by an effective single-step plastic-adherent method</title>
            <link>http://www.medworm.com/index.php?rid=3515184&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00674.x</link>
            <description>Conclusions: We have developed a simple and economical method that effectively isolates HC-free, therapeutically functional mMSCs from bone marrow cell adherent cultures. These cells are suitable for various mechanistic and therapeutic studies in the mouse model. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515184</comments>
            <pubDate>Tue, 27 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3515184</guid>        </item>
        <item>
            <title>Mouse sarcoma L1 cell line holoclones have a stemness signature</title>
            <link>http://www.medworm.com/index.php?rid=3515183&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00671.x</link>
            <description>Accumulating data suggest that cancers contain a fraction of cells called cancer stem cells (CSCs), that may be responsible for upkeep and relapses of disease. In experimental settings, CSCs are regarded as most effective at tumour initiation in in vivo assays. Since the first isolation of cancer stem cells from acute myeloid leukaemia in 1994, cancer stem cells have been identified in human solid tumours and they have also been found in the established cell lines, based on ability of CSCs to form in vitro colonies of a specific morphology, called holoclones. Our study examined the ability of a mouse sarcoma cell line, derived from a lung metastasis of a BALB/c mouse and established as a stably growing line (L1), to produce holoclones in vitro. We aimed to verify a stemness signature of th...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515183</comments>
            <pubDate>Tue, 27 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3515183</guid>        </item>
        <item>
            <title>Multilineage differentiation of dental follicle cells and the roles of Runx2 over-expression in enhancing osteoblast/cementoblast-related gene expression in dental follicle cells</title>
            <link>http://www.medworm.com/index.php?rid=3515182&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00670.x</link>
            <description>Conclusions: Multipotent DFCs can be induced to differentiate towards osteoblasts, adipocytes or chondrocytes in vitro. Runx2 over-expression up-regulated expression levels of osteoblast/cementoblast-related genes and in vitro enhanced osteogenic differentiation of DFCs. In addition, mutant Runx2-induced changes in DFCs were more prominent than those induced by full-length Runx2. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515182</comments>
            <pubDate>Tue, 27 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3515182</guid>        </item>
        <item>
            <title>Induction of bone formation by transforming growth factor-&amp;#x03B2;2 in the non-human primate Papio ursinus and its modulation by skeletal muscle responding stem cells</title>
            <link>http://www.medworm.com/index.php?rid=3515181&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00675.x</link>
            <description>Conclusions: In Papio ursinus, in marked contrast to rodents and lagomorphs, hTGF-[beta]2 induced large corticalized and vascularized ossicles by day 30 after implantation into the rectus abdominis muscle. This striated muscle contains responding stem cells that enhance the bone induction cascade of hTGF-[beta]2. Induction of bone formation by hTGF-[beta]2 in the non-human primate Papio ursinus may occur as a result of expression of bone morphogenetic proteins on heterotopic implantation of hTGF-[beta]2; the bone induction cascade initiated by mammalian TGF-[beta] proteins in Papio ursinus needs to be re-evaluated for novel molecular therapeutics for induction of bone formation in clinical contexts. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3515181</comments>
            <pubDate>Tue, 27 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3515181</guid>        </item>
        <item>
            <title>Proliferation of myofibroblasts in the stroma of renal oncocytoma</title>
            <link>http://www.medworm.com/index.php?rid=3471628&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00681.x</link>
            <description>Conclusions: Renal oncocytomas were composed of two independent compartments: benign oncocytes and pronounced fibrotic stroma, which consisted of proliferating myofibroblasts (SMA- and MIB-1-positive) which were associated with excessive deposition of extracellular matrix (periodic acid Schiff-component, collagen I-, collagen III- and fibronectin-positive, and desmin- and human caldesmon-negative). (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3471628</comments>
            <pubDate>Wed, 14 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3471628</guid>        </item>
        <item>
            <title>In vitro ovine articular chondrocyte proliferation: experiments and modelling</title>
            <link>http://www.medworm.com/index.php?rid=3471629&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00676.x</link>
            <description>This study focuses on analysis of in vitro cultures of chondrocytes from ovine articular cartilage. Isolated cells were seeded in Petri dishes, then expanded to confluence and phenotypically characterized by flow cytometry. The sigmoidal temporal profile of total counts was obtained by classic haemocytometry and corresponding cell size distributions were measured electronically using a Coulter Counter. A mathematical model recently proposed (1) was adopted for quantitative interpretation of these experimental data. The model is based on a 1-D (that is, mass-structured), single-staged population balance approach capable of taking into account contact inhibition at confluence. The model's parameters were determined by fitting measured total cell counts and size distributions. Model reliabili...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3471629</comments>
            <pubDate>Tue, 13 Apr 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3471629</guid>        </item>
        <item>
            <title>Oestrogen-related receptor alpha inverse agonist XCT-790 arrests A549 lung cancer cell population growth by inducing mitochondrial reactive oxygen species production</title>
            <link>http://www.medworm.com/index.php?rid=3311450&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00659.x</link>
            <description>Conclusions: ERR[alpha] affects cell cycle mechanisms through modulating mitochondrial mass and function. Dysregulation of this essential pathway leads to elevation in mitochondrial ROS production, which in turn modulates activities of tumour suppressors, resulting in cell cycle arrest. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311450</comments>
            <pubDate>Fri, 26 Feb 2010 16:58:07 +0100</pubDate>
            <guid isPermaLink="false">3311450</guid>        </item>
        <item>
            <title>Recombinant human midkine stimulates proliferation of articular chondrocytes</title>
            <link>http://www.medworm.com/index.php?rid=3311458&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00668.x</link>
            <description>Conclusion: Our results demonstrate that rhMK stimulates proliferation of primary articular chondrocytes in vitro and in vivo. The results of this study warrant further examination of rhMK for treatment of animal models of articular cartilage defects. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311458</comments>
            <pubDate>Fri, 26 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3311458</guid>        </item>
        <item>
            <title>Feasibility of using cryopreserved lymphoblastoid cells to diagnose some lysosomal storage diseases</title>
            <link>http://www.medworm.com/index.php?rid=3311457&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00660.x</link>
            <description>The Epstein[ndash]Barr virus (EBV) is utilized as a tool in the study of cellular biology because of its capacity to transform B-lymphocytes. For this reason, EBV is used in conservation of human B-lymphocytes for long periods for subsequent evaluation of lysosomal hydrolase activity. Lymphoblastoid cell lines have several advantages for use over other cell types, such as prompt availability and possibility to develop, characterize and standardize cell banks, to test effects of promising pharmaceutical reagents. The study below presents biochemical data that demonstrate validity of lymphoblastoid cell lines for diagnosis of GM1-gangliosidosis, Gaucher, Fabry and Pompe diseases and mucopolysaccharidosis type I. Cultures were prepared from peripheral blood, collected from 25 normal subjects ...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311457</comments>
            <pubDate>Fri, 26 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3311457</guid>        </item>
        <item>
            <title>Establishment and biological characterization of fibroblast cell line from the Langshan chicken</title>
            <link>http://www.medworm.com/index.php?rid=3311456&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00666.x</link>
            <description>Conclusion: The cell line met each of the quality control standards required for the American Type Culture Collection. It had not only preserved the genetic resources of the important Langshan chicken at the cellular level, but also provided valuable material for genomic, post-genomic and somatic cell cloning research and other applications. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311456</comments>
            <pubDate>Fri, 26 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3311456</guid>        </item>
        <item>
            <title>&amp;#x03B3;-secretase inhibitor induces adipogenesis of adipose-derived stem cells by regulation of Notch and PPAR-&amp;#x03B3;</title>
            <link>http://www.medworm.com/index.php?rid=3311455&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00661.x</link>
            <description>Conclusions: We conclude that blocking Notch signalling with DAPT enhances adipogenesis of differentiated mASCs at an early stage. It may be due to depression of DLK-1/Pref-1 and promotion of de-PPAR-[gamma] activation, which work through inhibition of Notch-2-Hes-1 pathway by DAPT. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311455</comments>
            <pubDate>Fri, 26 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3311455</guid>        </item>
        <item>
            <title>Analysis of radiation-induced changes to human melanoma cultures using a mathematical model</title>
            <link>http://www.medworm.com/index.php?rid=3311454&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00667.x</link>
            <description>Conclusions: The results, combined with existing data from clonogenic survival assays, support the hypothesis that a dominant effect of radiation in these melanoma lines is the induction of long-term cell cycle arrest. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311454</comments>
            <pubDate>Fri, 26 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3311454</guid>        </item>
        <item>
            <title>Microplate spectrophotometry for high-throughput screening of cytotoxic molecules</title>
            <link>http://www.medworm.com/index.php?rid=3311453&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00665.x</link>
            <description>Conclusions: Microplate spectrophotometry is a robust and sensitive method to monitor growth of animal cell populations both in the absence and in the presence of cytotoxic drugs. This method implements existing technologies and can be fully automated. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311453</comments>
            <pubDate>Fri, 26 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3311453</guid>        </item>
        <item>
            <title>Evaluation of Ki-67 and Bcl-2 antigen expression in breast carcinomas of women treated with raloxifene</title>
            <link>http://www.medworm.com/index.php?rid=3311452&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00664.x</link>
            <description>Conclusions: Raloxifene treatment significantly reduced Ki-67 antigen expression and increased Bcl-2 expression in breast carcinomas of post-menopausal women. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311452</comments>
            <pubDate>Fri, 26 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3311452</guid>        </item>
        <item>
            <title>3-O-Methylfunicone, a metabolite produced by Penicillium pinophilum, modulates ERK1/2 activity, affecting cell motility of human mesothelioma cells</title>
            <link>http://www.medworm.com/index.php?rid=3311451&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2010.00663.x</link>
            <description>Conclusion: OMF may have potential as a naturally derived anti-tumour drug for treatment of mesothelioma. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3311451</comments>
            <pubDate>Fri, 26 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3311451</guid>        </item>
        <item>
            <title>Apigenin induces apoptosis via downregulation of S-phase kinase-associated protein 2-mediated induction of p27Kip1 in primary effusion lymphoma cells</title>
            <link>http://www.medworm.com/index.php?rid=3171697&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00662.x</link>
            <description>Conclusions: Altogether, these data suggest a novel function for apigenin, acting as a suppressor of AKT/PKB pathway in PEL cells, and raise the possibility that this agent may have a future therapeutic role in PEL and possibly other malignancies with constitutive activation of the AKT/PKB pathway. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3171697</comments>
            <pubDate>Thu, 14 Jan 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3171697</guid>        </item>
        <item>
            <title>Blunting effect of hypoxia on the proliferation and differentiation of human primary and rat L6 myoblasts is not counteracted by Epo</title>
            <link>http://www.medworm.com/index.php?rid=3124443&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00648.x</link>
            <description>Conclusions: The data show that exposure to hypoxic conditions (1% O2) of rat and human myoblasts altered their proliferation and differentiation processes. They also show that Epo is not an efficient growth factor to counteract this deleterious effect. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3124443</comments>
            <pubDate>Mon, 28 Dec 2009 16:15:36 +0100</pubDate>
            <guid isPermaLink="false">3124443</guid>        </item>
        <item>
            <title>DNER modulates adipogenesis of human adipose tissue-derived mesenchymal stem cells via regulation of cell proliferation</title>
            <link>http://www.medworm.com/index.php?rid=3124444&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00650.x</link>
            <description>Conclusions: These results indicate that DNER knockdown in hAMSC accelerated onset of adipogenic differentiation by bypassing mitotic clonal expansion during the early stages of adipogenesis. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3124444</comments>
            <pubDate>Sun, 27 Dec 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3124444</guid>        </item>
        <item>
            <title>Targeted therapy of spinal cord glioma with a genetically modified Salmonella typhimurium</title>
            <link>http://www.medworm.com/index.php?rid=3007905&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00652.x</link>
            <description>Conclusions: These results suggest that S. typhimurium A1-R monotherapy can effectively treat spinal cord glioma. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3007905</comments>
            <pubDate>Thu, 19 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3007905</guid>        </item>
        <item>
            <title>Sub-millimolar concentration of the novel phenol-based compound, 2-hydroxy benzoate zinc, induces apoptosis in human HT-1080 fibrosarcoma cells</title>
            <link>http://www.medworm.com/index.php?rid=3003622&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00658.x</link>
            <description>Conclusions: These results demonstrate that the novel phenolic compound 2HBZ is a potent apoptosis-inducing agent in HT-1080 cells and warrants further investigation as a potential chemotherapeutic agent in primary cancer cell models. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3003622</comments>
            <pubDate>Wed, 18 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3003622</guid>        </item>
        <item>
            <title>The role of scaffold proteins in JNK signalling</title>
            <link>http://www.medworm.com/index.php?rid=3003625&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00654.x</link>
            <description>This paper summarises how scaffold proteins affects and regulate the JNK signalling pathway. We believe that some of these scaffold proteins, by virtue of their anchoring and catalytic properties contribute to a high degree of specificity of intra cellular signalling pathways that regulate the progression through the cell cycle. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3003625</comments>
            <pubDate>Tue, 17 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3003625</guid>        </item>
        <item>
            <title>Anti-proliferative effects of &amp;#x03B3;-tocotrienol on mammary tumour cells are associated with suppression of cell cycle progression</title>
            <link>http://www.medworm.com/index.php?rid=3003624&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00657.x</link>
            <description>Objectives: Previous studies have shown that [gamma]-tocotrienol induces potent anti-proliferative effects on +SA mammary tumour cells in culture; here, investigations have been conducted to determine its effects on intracellular signalling proteins involved in regulating cell cycle progression.Materials and methods: +SA cells were maintained in mitogen-free defined media containing 0 or 4 [mu]m[gamma]-tocotrienol, for 48 h to synchronize cell cycle in G0 phase, and then they were exposed to 100 ng/ml EGF to initiate cell cycle progression. Whole cell lysates were collected at various time points from each treatment group and were prepared for Western blot analysis.Results and conclusions: Treatment with 4 [mu]m[gamma]-tocotrienol significantly inhibited +SA cell proliferation over a 4-day...</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3003624</comments>
            <pubDate>Tue, 17 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3003624</guid>        </item>
        <item>
            <title>Cellular responses and expression profiling of human bone marrow stromal cells stimulated with enamel matrix proteins in vitro</title>
            <link>http://www.medworm.com/index.php?rid=3003623&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00656.x</link>
            <description>Conclusions: EMPs promoted cell proliferation and differentiation and gene expression profiles of HBMSCs were affected. This may help elucidation of mechanisms involved in promoting regeneration of periodontal tissues by EMPs. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3003623</comments>
            <pubDate>Tue, 17 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3003623</guid>        </item>
        <item>
            <title>Involvement of fibroblast growth factor 18 in dedifferentiation of cultured human chondrocytes</title>
            <link>http://www.medworm.com/index.php?rid=2977107&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00655.x</link>
            <description>Conclusion: FGF18 seems to play a role in maintenance of chondrocyte properties, although its expression was rather high in dedifferentiated chondrocytes. Upregulation of FGF18 in dedifferentiated chondrocytes implied that it may be a marker of dedifferentiation. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2977107</comments>
            <pubDate>Tue, 10 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">2977107</guid>        </item>
        <item>
            <title>Heparin regulates colon cancer cell growth through p38 mitogen-activated protein kinase signalling</title>
            <link>http://www.medworm.com/index.php?rid=2912056&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00649.x</link>
            <description>Conclusions: This study demonstrates that an extracellular glycosaminoglycan, heparin, finely modulates expression of genes crucial to cell cycle regulation through specific activation of p38 MAP kinase to stimulate colon cancer cell growth. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2912056</comments>
            <pubDate>Tue, 20 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2912056</guid>        </item>
        <item>
            <title>Expression and role of Oct3/4, Nanog and Sox2 in regeneration of rat tracheal epithelium</title>
            <link>http://www.medworm.com/index.php?rid=2912055&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00653.x</link>
            <description>Conclusions: G0 phase cells with resistance to 5-FU damage expressed Oct3/4, Nanog and Sox2. This indicated that these cells were undifferentiated, but had the ability to terminally differentiate into downstream-type cells. They possessed stem cell properties. The results are consistent with Oct3/4, Nanog and Sox2-expressing cells being considered as tracheal stem cells. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2912055</comments>
            <pubDate>Tue, 20 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2912055</guid>        </item>
        <item>
            <title>Effect of syndecan-1 overexpression on mesenchymal tumour cell proliferation with focus on different functional domains</title>
            <link>http://www.medworm.com/index.php?rid=2890460&amp;cid=s_32058_171_f&amp;fid=32058&amp;url=http%3A%2F%2Fdx.doi.org%2F10.1111%252Fj.1365-2184.2009.00651.x</link>
            <description>Conclusions: Both full-length and truncated syndecan-1 inhibited proliferation of the mesenchymal tumour cells, providing new insights into the importance for cancer growth of different functional domains of this proteoglycan. (Source: Cell Proliferation)</description>
            <author>Cell Proliferation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2890460</comments>
            <pubDate>Tue, 13 Oct 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2890460</guid>        </item>
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