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        <title>MedWorm: Chemistry</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 headlines from journals and sites in the Chemistry category.</description>
        <link><![CDATA[http://www.medworm.com/rss/index.php/Chemistry/59/]]></link>
        <lastBuildDate>Sat, 20 Mar 2010 15:57:28 +0100</lastBuildDate>
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            <title>Synform issue 2010/4</title>
            <link>http://www.medworm.com/index.php?rid=3385015&amp;cid=d_59_59_f&amp;fid=36597&amp;url=http%3A%2F%2Fwww.thieme-connect.com%2FDOI%2FDOI10.1055%2Fs-0029-1219633</link>
            <description>Synthesis 2010; 2010: A33-A38DOI: 10.1055/s-0029-1219633© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.Get connected:Table of contents (Source: Synthesis)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Synthesis</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 15:56:54 +0100</pubDate>
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            <title>Selective Synthesis of Allenes and Alkynes through Ligand-Controlled, Palladium-Catalyzed Decarboxylative Hydrogenolysis of Propargylic Formates</title>
            <link>http://www.medworm.com/index.php?rid=3384996&amp;cid=d_59_59_f&amp;fid=30096&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fol100405k%3Fai%3D52a%26af%3DR</link>
            <description>Organic Letters, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Organic Letters)</description>
            <author>Organic Letters</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 10:08:06 +0100</pubDate>
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            <title>(Py)2Co(CH2SiMe3)2 As an Easily Accessible Source of “CoR2”</title>
            <link>http://www.medworm.com/index.php?rid=3385065&amp;cid=d_59_59_f&amp;fid=37607&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fom901045s%3Fai%3D55g%26af%3DR</link>
            <description>Organometallics, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Organometallics)</description>
            <author>Organometallics</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 10:07:55 +0100</pubDate>
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            <title>Structure of the Ethylammonium Nitrate Surface: An X-ray Reflectivity and Vibrational Sum Frequency Spectroscopy Study</title>
            <link>http://www.medworm.com/index.php?rid=3385052&amp;cid=d_59_59_f&amp;fid=37606&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fla904697g%3Fai%3D517%26af%3DR</link>
            <description>Langmuir, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Langmuir)</description>
            <author>Langmuir</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385052</comments>
            <pubDate>Sat, 20 Mar 2010 10:07:19 +0100</pubDate>
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            <title>Erratum: Length-Dependent Optical Effects in Single Walled Carbon Nanotubes</title>
            <link>http://www.medworm.com/index.php?rid=3384990&amp;cid=d_59_59_f&amp;fid=30095&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fjp101959e%3Fai%3D519%26af%3DR</link>
            <description>The Journal of Physical Chemistry B, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Journal of Physical Chemistry B)</description>
            <author>Journal of Physical Chemistry B</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3384990</comments>
            <pubDate>Sat, 20 Mar 2010 10:06:15 +0100</pubDate>
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            <title>Modeling the Rovibrationally Excited C2H4OH Radicals from the Photodissociation of 2-Bromoethanol at 193 nm</title>
            <link>http://www.medworm.com/index.php?rid=3384983&amp;cid=d_59_59_f&amp;fid=30094&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fjp911739a%3Fai%3D51r%26af%3DR</link>
            <description>The Journal of Physical Chemistry A, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Journal of Physical Chemistry A)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Journal of Physical Chemistry A</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 10:06:03 +0100</pubDate>
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            <title>Zinc Chloride Promoted Formal Oxidative Coupling of Aromatic Aldehydes and Isocyanides to α-Ketoamides</title>
            <link>http://www.medworm.com/index.php?rid=3384977&amp;cid=d_59_59_f&amp;fid=30093&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fjo100302y%3Fai%3D55h%26af%3DR</link>
            <description>The Journal of Organic Chemistry, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: The Journal of Organic Chemistry)</description>
            <author>The Journal of Organic Chemistry</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 10:05:42 +0100</pubDate>
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            <title>(1S)-1,5-Anhydro-1-[5-(4-ethoxybenzyl)-2-methoxy-4-methylphenyl]-1-thio-d-glucitol (TS-071) is a Potent, Selective Sodium-Dependent Glucose Cotransporter 2 (SGLT2) Inhibitor for Type 2 Diabetes Treatment</title>
            <link>http://www.medworm.com/index.php?rid=3384999&amp;cid=d_59_59_f&amp;fid=32526&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fjm901893x%3Fai%3D55a%26af%3DR</link>
            <description>Journal of Medicinal Chemistry, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Journal of Medicinal Chemistry)</description>
            <author>Journal of Medicinal Chemistry</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 10:05:20 +0100</pubDate>
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            <title>Bonding in Classical and Nonclassical Transition Metal Carbonyls: The Interacting Quantum Atoms Perspective</title>
            <link>http://www.medworm.com/index.php?rid=3384974&amp;cid=d_59_59_f&amp;fid=30092&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fct9006629%3Fai%3D557%26af%3DR</link>
            <description>Journal of Chemical Theory and Computation, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Journal of Chemical Theory and Computation)</description>
            <author>Journal of Chemical Theory and Computation</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 10:05:14 +0100</pubDate>
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            <title>Enantioselective Alkenylation via Nickel-Catalyzed Cross-Coupling with Organozirconium Reagents</title>
            <link>http://www.medworm.com/index.php?rid=3384960&amp;cid=d_59_59_f&amp;fid=30090&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fja1017046%3Fai%3D1jm%26af%3DR</link>
            <description>Journal of the American Chemical Society, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Journal of the American Chemical Society)</description>
            <author>Journal of the American Chemical Society</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 10:03:32 +0100</pubDate>
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            <title>Synthesis, Structure, and Electrochemistry of the Dicluster Molecular Pincer [Pt3(μ-PBut2)3(CO)2]2(μ-1′,1′′′-diethynylbiferrocene)</title>
            <link>http://www.medworm.com/index.php?rid=3384953&amp;cid=d_59_59_f&amp;fid=30089&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fic9014459%3Fai%3D551%26af%3DR</link>
            <description>Inorganic Chemistry, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Inorganic Chemistry)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Inorganic Chemistry</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 10:03:04 +0100</pubDate>
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            <title>Erratum: Transition Metal-Catalyzed Direct Arylation of Substrates with Activated sp3-Hybridized C−H Bonds and Some of Their Synthetic Equivalents with Aryl Halides or Pseudohalides</title>
            <link>http://www.medworm.com/index.php?rid=3384952&amp;cid=d_59_59_f&amp;fid=30088&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fcr100067x%3Fai%3D54p%26af%3DR</link>
            <description>Chemical Reviews, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Chemical Reviews)</description>
            <author>Chemical Reviews</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 10:01:56 +0100</pubDate>
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            <title>Kinetics of Chemical Degradation in Monoclonal Antibodies: Relationship between Rates at the Molecular and Peptide Levels</title>
            <link>http://www.medworm.com/index.php?rid=3384950&amp;cid=d_59_59_f&amp;fid=30087&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fac902752e%3Fai%3D54k%26af%3DR</link>
            <description>Analytical Chemistry, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Analytical Chemistry)</description>
            <author>Analytical Chemistry</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 10:01:06 +0100</pubDate>
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            <title>This Day in Science History - March 20 - Mayer and Conservation of Energy</title>
            <link>http://www.medworm.com/index.php?rid=3385070&amp;cid=d_59_59_f&amp;fid=38289&amp;url=http%3A%2F%2Fchemistry.about.com%2Fb%2F2010%2F03%2F20%2Fthis-day-in-science-history-march-20-mayer-and-conservation-of-energy.htm</link>
            <description>March 20th marks the passing of Julius Robert von Mayer. Mayer was a German physician who had a hobby of studying physics. Most of his work centered around how energy was transferred from one form to another. He was one of the first to recognize that plants converted light into chemical energy, and the process of oxidation was the primary source of energy in living creatures. He also outlined the earliest versions of what would become the first law of thermodynamics by writing &quot;Energy is neither created nor destroyed&quot;.
He attempted to publish his ideas as conservation of force, but had several basic errors due to his lack of formal physics training and was largely ignored. James Joule published his work a year later describing the conservation of energy and mechanical equivalent of heat an...</description>
            <author>About.com Chemistry</author>
            <type>consumer</type>
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            <pubDate>Sat, 20 Mar 2010 00:05:11 +0100</pubDate>
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            <title>Savannah's Nuclear Bomb</title>
            <link>http://www.medworm.com/index.php?rid=3385069&amp;cid=d_59_59_f&amp;fid=38289&amp;url=http%3A%2F%2Fchemistry.about.com%2Fb%2F2010%2F03%2F20%2Fsavannahs-nuclear-bomb.htm</link>
            <description>About.com is holding a meeting in Savannah this weekend so I suspect my coworkers would be interested to know that there is a live nuclear bomb off the Georgia coast. In February 1958 a B-47 bomber on a training mission out of Homestead Air Force Base in Florida had a collision with an F-86. The pilot of the F-86 parachuted to safety and the fighter jet crashed. The B-47 also sustained damage. The crew requested and received permission to jettison the 7,600 pound Mark 15 bomb it was carrying so that the aircraft could more safely land at Hunter Air Force Base. The bomb was lost somewhere in Wassaw Sound off the shores of Tybee Island, where it remains to this day, probably sunk in 5-12 feet of muck at the bottom of the sound. This puts it in shallow water just off the coast of Savannah, cl...</description>
            <author>About.com Chemistry</author>
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
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            <title>4-Iodoanilinium perchlorate</title>
            <link>http://www.medworm.com/index.php?rid=3385051&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Ffi2083</link>
            <description>In the crystal structure of the title compound, C6H7IN+·ClO4−, the ions are connected in a three-dimensional hydrogen-bonded network via N—H...O hydrogen bonds. (Source: Acta Crystallographica Section E)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
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            <title>3-(1,3-Benzodioxol-5-yl)-3H-benzo[f]isobenzofuran-1-one</title>
            <link>http://www.medworm.com/index.php?rid=3385050&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fci5047</link>
            <description>In the title compound, C19H12O4, the dioxole ring adopts a flattened envelope conformation with the methylene C at the flap [deviation = 0.104 (2) Å]. The benzene ring of the benzodioxole ring system makes a dihedral angle of 76.45 (5)° with the planar [maximum deviation = 0.016 (1) Å] 3H-benzo[f]isobenzofuran-1-one ring system. In the crystal structure, the molecules are linked into C(5) chains running along the b axis by intermolecular C—H...O hydrogen bonds. In addition, C—H...π interactions are observed. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
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            <title>Methyl 3-(4-methoxyphenyl)-1-methyl-1,2,3,3a,4,11b-hexahydrobenzo[f]chromeno[4,3-b]pyrrole-3a-carboxylate</title>
            <link>http://www.medworm.com/index.php?rid=3385049&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fbt5203</link>
            <description>In the title compound, C25H25NO4, the pyrrolidine ring exhibits an envelope conformation and the tetrahydropyran ring exhibits a half-chair conformation. The crystal structure is stabilized by intermolecular C–H...π interactions. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
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            <title>N′-(2-Hydroxy-4-methoxybenzylidene)isonicotinohydrazide</title>
            <link>http://www.medworm.com/index.php?rid=3385048&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fbx2271</link>
            <description>The title compound, C14H13N3O3, was synthesized by the condensation reaction of 2-hydroxy-4-methoxybenzaldehyde with isonicotinohydrazide in a methanol solution. The molecule of the compound displays a trans configuration with respect to the C=N and C—N bonds. The dihedral angle between the benzene and the pyridine rings is 27.3 (2)°. In the crystal, molecules are linked by N—H...N interactions into zigzag chains with graph-set notation C(7) along [010]. An intramolecular O—H...N hydrogen bond is observed. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
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            <title>N-(2-Chlorophenyl)-3-methylbenzamide</title>
            <link>http://www.medworm.com/index.php?rid=3385047&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fbt5219</link>
            <description>In the title compound, C14H12ClNO, the N—H bond is anti to the carbonyl bond and the two aromatic rings make a dihedral angle of 5.4 (2)°. In the crystal, intermolecular N—H...O hydrogen bonds connect the molecules into chains running along the b axis. The chains are interconnected through short Cl...Cl contacts [3.279 (1) Å]. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
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            <title>11-(2-Oxopyrrolidin-1-ylmethyl)-1,2,3,4,5,6,11,11a-octahydropyrido[2,1-b]quinazolin-6-one dihydrate</title>
            <link>http://www.medworm.com/index.php?rid=3385046&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fbq2200</link>
            <description>In the crystal structure of the title compound, C17H21N3O2·2H2O, water molecules are mutually O—H...O hydrogen bonded and form infinite chains propagating along the b axis. Neighboring chains are linked by the quinazoline molecules by means of O—H...O=C hydrogen bonds, forming a two–dimensional network. (Source: Acta Crystallographica Section E)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
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            <title>Sodium N,2-dichlorobenzenesulfonamidate sesquihydrate</title>
            <link>http://www.medworm.com/index.php?rid=3385045&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fbx2268</link>
            <description>In the title compound, Na+·C6H4Cl2NO2S−·1.5H2O, one of the water molecules lies on a twofold axis. There is no interaction between the N atom and the sodium ion. The sodium ion exhibits a pseudo-octahedral coordination defined by three water O atoms and three sulfonyl O atoms from three different anions. The S—N distance of 1.588 (2) Å is consistent with an S=N double bond. The crystal structure is stabilized by O—H...N and O—H...Cl hydrogen bonds. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385045</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385045</guid>        </item>
        <item>
            <title>Ethyl (2E)-2-(hydroxyimino)propanoate</title>
            <link>http://www.medworm.com/index.php?rid=3385044&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fbq2193</link>
            <description>The molecule of the title compound, C5H9NO3, is essentially planar [the maximum deviation for a non-H atom from the mean plane is 0.021 (3) Å] due to the π-conjugation of the hydroxyimino and carbonyl groups, which are trans to each other; ab initio calculations in vacuo at the DFT (B3LYP/6–311G**++) level of theory confirmed that E conformer is indeed the lowest in energy. The packing in crystal structure is influenced by strong intermolecular O—H...N hydrogen-bonding interactions between oxime groups and also by π-stacking of the molecules due to the carbonyl and oxime group orbital overlap [interplanar distance between adjacent molecules = 3.143 (4) Å]. Jointly, these factors afford infinite 6.32 Å thick molecular sheets, where the plane of each molecule is perpendicu...</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385044</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385044</guid>        </item>
        <item>
            <title>5-Chloro-3-ethylsulfinyl-2-(4-fluorophenyl)-7-methyl-1-benzofuran</title>
            <link>http://www.medworm.com/index.php?rid=3385043&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fvm2020</link>
            <description>In the title compound, C17H14ClFO2S, the 4-fluorophenyl ring is rotated slightly out of the benzofuran plane, as indicated by the dihedral angle of 8.32 (5)°. The crystal structure features a short Cl...O contact [3.092 (1) Å]. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385043</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385043</guid>        </item>
        <item>
            <title>3-(3-Chlorobenzoyl)-4-hydroxy-2H-1,2-benzothiazine 1,1-dioxide</title>
            <link>http://www.medworm.com/index.php?rid=3385042&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fpk2231</link>
            <description>In the title compound, C15H10ClNO4S, the heterocyclic thiazine ring adopts a half-chair conformation with the S and N atoms displaced by 0.476 (5) and 0.227 (5) Å, respectively, on opposite sides of the mean plane formed by the remaining ring atoms. The structure is stabilized by intermolecular N—H...O and C—H...O hydrogen bonds. In addition, intramolecular O—H...O and C—H...N interactions are also present. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385042</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385042</guid>        </item>
        <item>
            <title>2,2,2-Tribromo-N-(2-methylphenyl)acetamide</title>
            <link>http://www.medworm.com/index.php?rid=3385041&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fpk2229</link>
            <description>The asymmetric unit of the title compound, C9H8Br3NO, contains two independent molecules. Intramolecular N—H...Br hydrogen bonds are present in both molecules. In the crystal, molecules are packed into columnar chains by intermolecular N—H...O hydrogen bonds. (Source: Acta Crystallographica Section E)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385041</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385041</guid>        </item>
        <item>
            <title>(E)-2-[1-(3-Amino-4-chlorophenylimino)ethyl]-4-bromophenol</title>
            <link>http://www.medworm.com/index.php?rid=3385040&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Ftk2641</link>
            <description>The title Schiff base compound, C14H12BrClN2O, exists in an E configuration with respect to the central C=N double bond. The amino group adopts a pyramidal configuration. The dihedral angle between the two benzene rings is 76.88 (10)° and an intramolecular O—H...N hydrogen bond forms a six-membered ring, generating an S(6) ring motif. In the crystal structure, molecules are linked into chains along [010] via N—H...O hydrogen bonds. The presence of π–π interactions [centroid–centroid distance = 3.6244 (12) Å] further stabilizes the crystal structure. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385040</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385040</guid>        </item>
        <item>
            <title>2-[2-(2,6-Dichloroanilino)phenyl]-N-[(2S)-2-methyl-3-oxo-8-phenyl-1-thia-4-azaspiro[4.5]dec-4-yl]acetamide</title>
            <link>http://www.medworm.com/index.php?rid=3385039&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fbt5217</link>
            <description>In the title compound, C29H29Cl2N3O2S, the phenyl ring is disordered over two orientations with occupancies of 0.55 (3) and 0.45 (3). The molecular packing in the crystal is stabilized by intermolecular N—H...O interactions, linking the molecules into infinite chains along the c axis. In addition, there are weak C—H...S and C—H...π interactions. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385039</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385039</guid>        </item>
        <item>
            <title>N-(2,4-Dimethylphenyl)succinimide</title>
            <link>http://www.medworm.com/index.php?rid=3385038&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fvm2021</link>
            <description>In the title compound, C12H13NO2, the dihedral angle between the benzene ring and the imide segment is 85.7 (1)°. In the crystal, the molecules are packed into zigzag chains parallel to the a axis. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385038</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385038</guid>        </item>
        <item>
            <title>Absolute configuration of isoeichlerialactone</title>
            <link>http://www.medworm.com/index.php?rid=3385037&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Frz2425</link>
            <description>The title seco-dammarane triterpenoid, C27H42O4 (systematic name: 3-{(3S,3aR,5aR,6S,7S,9aR,9bR)-6,9a,9b-trimethyl-3-[(R)-2-methyl-5-oxotetrahydrofuran-2-yl]-7-(prop-1-en-2-yl)dodecahydro-1H-cyclopenta[a]naphthalen-6-yl}propanoic acid), has been isolated for the first time from the seeds of Aglaia forbesii. The molecule has three fused rings and all rings are in trans-fused. The two cyclohexane rings are in standard chair conformations and the cyclopentane ring adopts an envelope conformation. Its absolute configuration was determined by the refinement of the Flack parameter to 0.26 (17). In the crystal, molecules are linked into chains along [010] by O—H...O hydrogen bonds. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385037</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385037</guid>        </item>
        <item>
            <title>2-[4-Acetyl-5-(biphenyl-4-yl)-4,5-dihydro-1,3,4-oxadiazol-2-yl]phenyl acetate</title>
            <link>http://www.medworm.com/index.php?rid=3385036&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fpv2264</link>
            <description>In the title molecule, C24H20N2O4, the five-membered oxadiazole ring is nearly planar (r.m.s. deviation = 0.053 Å) and the phenyl ring of the biphenyl unit attached to it forms a dihedral angle of 73.2 (1)°; the other phenyl ring is close to coplanar with the oxadiazole ring [dihedral angle = 6.2 (2)°]. (Source: Acta Crystallographica Section E)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385036</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385036</guid>        </item>
        <item>
            <title>3-Chloro-N-(4-hydroxy-3-methoxybenzyl)-2,2-dimethylpropanamide</title>
            <link>http://www.medworm.com/index.php?rid=3385035&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fxu2733</link>
            <description>In the molecular structure of the title compound, C13H18ClNO3, the amide group is nearly perpendicular to the benzene ring, making a dihedral angle of 85.66 (9)°. The C=O bond distance of 1.242 (3) Å and the C—N bond distance of 1.333 (3) Å suggest electron delocalization in the amide fragment. Intermolecular O—H...O and N—H...O hydrogen bonding helps to stabilize the crystal structure. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385035</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385035</guid>        </item>
        <item>
            <title>N′-(2,4-Dichlorobenzylidene)-3-methoxybenzohydrazide</title>
            <link>http://www.medworm.com/index.php?rid=3385034&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fsj2748</link>
            <description>There are two independent molecules in the asymmetric unit of the title compound, C15H12Cl2N2O2. The dihedral angle between the two benzene rings is 27.6 (4)° in one molecule and 16.4 (4)° in the other. Both molecules adopt an E configuration about the C=N bonds. In the crystal structure, molecules are linked through intermolecular N—H...O hydrogen bonds, forming chains in the a-axis direction. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385034</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385034</guid>        </item>
        <item>
            <title>(E)-1-(4-Methylphenyl)ethanone [8-(trifluoromethyl)quinolin-4-yl]hydrazone</title>
            <link>http://www.medworm.com/index.php?rid=3385033&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fdn2546</link>
            <description>In the title compound, C19H16F3N3, the dihedral angle between the naphthalene and quinoline ring systems is 14.58 (8)°. The hydrazone C—N—N=C—C chain is in an extended conformation and its mean plane is nearly coplanar with the quinoline plane [dihedral angle = 3.45 (9)°]. The bond angles within the phenyl ring show the almost additive influence of the two para substituents. In the crystal, weak π–π [centroid–centroid distances = 3.779 (2) and 3.718 (1) Å] and C—H...F directional interactions join the molecules into centrosymmetric dimers, which are further connected into infinite zigzag chains propagating along a. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385033</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385033</guid>        </item>
        <item>
            <title>(8-Bromo-2,7-dimethoxy-1-naphthyl)(4-chlorophenyl)methanone</title>
            <link>http://www.medworm.com/index.php?rid=3385032&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fis2530</link>
            <description>In the title compound, C19H14BrClO3, the naphthalene ring system and the benzene ring make a dihedral angle of 77.36 (10)°. The conformation around the central C=O group is such that the C=O bond vector forms a larger angle to the plane of the naphthalene ring system than to the plane of the benzene ring, viz. 75.73 (15)° versus 2.33 (17)°. In the crystal structure, a π–π interaction is formed between naphthalene ring systems, with a centroid–centroid distance of 3.8363 (14) Å and a lateral offset of 1.606 Å. Intermolecular C—H...Br and C—H...O hydrogen bonds and a C—H...π contact are present in the crystal structure. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385032</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385032</guid>        </item>
        <item>
            <title>5,11,17,23-Tetrabromo-25,26,27,28-tetrakis(4-tolylsulfonyloxy)-2,8,14,20-tetrathiacalix[4]arene dichloromethane solvate</title>
            <link>http://www.medworm.com/index.php?rid=3385031&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fbg2335</link>
            <description>In the crystal structure of the title compound, C52H36Br4O12S8·CH2Cl2, the thiacalix[4]arene unit adopts a 1,3-alternate conformation with an intramolecular C—H...O hydrogen bond and four C—H...π interactions, with the four 4-MeC6H4SO3 groups located alternately above and below the virtual plane (R) defined by the four bridging S atoms. The benzene ring of each 4-MeC6H4SO3 unit is nearly perpendicular to one of the two neighboring phenol rings with interplanar angles varying from 72.97 (13) to 78.70 (13)°, while the dihedral angles between the plane (R) and the phenol rings range from 83.04 (7) to 84.30 (9)°. In the supramolecular structure, a solvent-bridged dimer composed of two main molecules is formed by four intermolecular C—H...O hydrogen bonds and locally creates a...&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385031</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385031</guid>        </item>
        <item>
            <title>N′-Benzoyl-N,N-diethylthiourea: a monoclinic polymorph</title>
            <link>http://www.medworm.com/index.php?rid=3385030&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fhb5361</link>
            <description>In the crystal of the title compound, C12H16N2OS, inversion dimers linked by pairs of N—H...S hydrogen bonds occur, generating R22(8) loops. The molecules are also linked by weak C—H...O hydrogen bonds. The structure is isostructural with that of N′-benzoyl-N,N-diethylselenourea [Bruce et al. (2007). New J. Chem. 31, 1647–1653]. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385030</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385030</guid>        </item>
        <item>
            <title>N-[4-(N-Cyclohexylsulfamoyl)phenyl]acetamide</title>
            <link>http://www.medworm.com/index.php?rid=3385029&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fhb5359</link>
            <description>In the title compound, C14H20N2O3S, the cyclohexyl ring adopts a chair conformation: the four coplanar C atoms of this ring make a dihedral angle of 64.8 (2)° with the benzene ring. In the molecule, an intramolecular C—H...O contact generates an S(6) ring motif. In the crystal structure, molecules are linked via intermolecular N—H...O hydrogen bonds into two-dimensional layers propagating in (100). (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385029</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385029</guid>        </item>
        <item>
            <title>(E)-5-Benzyl-1-methyl-N-nitro-1,3,5-triazinan-2-imine</title>
            <link>http://www.medworm.com/index.php?rid=3385028&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fis2529</link>
            <description>In the title compound, C11H15N5O2, the 1,3,5-triazine ring exhibits a half-chair conformation. An intramolecular N—H...O interaction occurs. In the crystal structure, molecules are connected by intermolecular C—H...O and N—H...N hydrogen bonds, forming a zigzag chain along the b axis. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385028</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385028</guid>        </item>
        <item>
            <title>N-Butyl-4-methyl-6-phenylpyrimidin-2-amine</title>
            <link>http://www.medworm.com/index.php?rid=3385027&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fsj2745</link>
            <description>In the title compound, C15H19N3, the pyrimidine ring is approximately planar [maximum deviation = 0.007 (1) Å] and forms a dihedral angle of 3.15 (6)° with the benzene ring. In the crystal packing, intermolecular N—H...N hydrogen bonds link pairs of neighbouring molecules into dimers with R22(6) ring motifs. These dimers are stacked along the b axis. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385027</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385027</guid>        </item>
        <item>
            <title>Bis[μ-2,2′-dimethyl-1,1′-(oxydiethylene)bis(1H-benzimidazole)-κ2N3:N3′]bis[bis(4-methoxybenzoato-κ2O,O′)cadmium(II)]</title>
            <link>http://www.medworm.com/index.php?rid=3385026&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Flx2137</link>
            <description>The title complex, [Cd2(C8H7O3)4(C20H22N4O)2], forms a dimer of the paddle-wheel type, located on a crystallographic inversion centre. The CdII ion is hexacoordinated by four carboxylate O atoms [Cd...O = 2.280 (2)–2.404 (2) Å] from two chelating 4-methoxybenzoate anions, and two N atoms [Cd...N = 2.313 (2) and 2.332 (2) Å] from one chelating 2,2′-dimethyl-3,3′-(oxydiethylene)bis(1H-benzimidazole) ligand. In the crystal, molecules are linked by a weak intermolecular C—H...O hydrogen bond and an intermolecular C—H...π interaction. (Source: Acta Crystallographica Section E)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385026</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385026</guid>        </item>
        <item>
            <title>[(Z)-O-Isopropyl N-phenylthiocarbamato-κS](tricyclohexylphosphine-κP)gold(I)</title>
            <link>http://www.medworm.com/index.php?rid=3385025&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fez2204</link>
            <description>The Au atom in the title compound, [Au(C10H12NOS)(C18H33P)], is coordinated within an S,P-donor set that defines a slightly distorted linear geometry [S—Au—P = 174.54 (2)°], with the distortion due in part to a close intramolecular Au...O contact [3.1702 (16) Å]. In the crystal structure, molecules are arranged into supramolecular chains along the b axis mediated by C—H...O interactions. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385025</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385025</guid>        </item>
        <item>
            <title>(meso-5,7,7,12,14,14-Hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene)copper(II) bis[O,O′-bis(4-methylphenyl) dithiophosphate]</title>
            <link>http://www.medworm.com/index.php?rid=3385024&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fdn2547</link>
            <description>The title compound, [Cu(C16H32N4)](C14H14O2PS2)2 or [Cu(trans[14]dien)][S2P(OC6H4Me-4)2]2, where trans[14]dien is meso-5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene, was obtained by the reaction of [Cu(trans[14]dien)](ClO4)2 and [(C2H5)2NH]2 [S2P(OC6H4Me-4)2]2. The CuII atom lies on a centre of inversion and possesses a relatively undistorted square-planar coordination arrangement with four N atoms of the macrocyclic tetramine trans[14]dien [Cu—N = 1.9716 (19) and 2.0075 (19) Å]. The two uncoordinated [(4-MeC6H4O)2PS2]− groups act as counter-ions to balance the charge and interact with the [Cu(trans[14]dien)]2+ complex cation through N—H...S hydrogen bonds. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385024</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385024</guid>        </item>
        <item>
            <title>catena-Poly[sodium-di-μ-aqua-sodium-bis[μ-2,2,2-trichloro-N-(dimorpholinophosphoryl)acetamide]]</title>
            <link>http://www.medworm.com/index.php?rid=3385023&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fjh2135</link>
            <description>The title compound, [Na2(C10H16Cl3N3O4P)2(H2O)2]n, can be considered as a two-dimensional coordination polymer in which one-dimensional chains are connected to each other by intermolecular C—H...O hydrogen bonds involving the water molecules. The NaI ion is five-coordinated in a distorted trigonal-bipyramidal geometry. The connection between the two NaI ions is facilitated by the two μ-O atoms of the carbonyl group of the 2,2,2-trichloro-N-(dimorpholinophosphoryl)acetamide (CAPh) ligand. A bridging coordination of the CAPh ligand via the carbonyl O atom is observed for the first time. The bridging water molecules form intermolecular O—H...O hydrogen bonds with the O atoms of the morpholine rings and the phosphoryl groups of neighboring CAPh molecules. (Source: Acta Crystallographica S...</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385023</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385023</guid>        </item>
        <item>
            <title>Diacridinium hexachloridoplatinate(IV) dihydrate</title>
            <link>http://www.medworm.com/index.php?rid=3385022&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fya2119</link>
            <description>The asymmetric unit of the title compound, (C13H10N)2[PtCl6]·2H2O, contains a protonated acridine cation, one half of a [PtCl6]2− dianionic complex and a solvent water molecule. The octahedral [PtCl6]2− dianion is located on an inversion centre. π–π interactions between neighboring acridinium cations produce stacks along the a axis; the shortest distance between the centroids of the six-membered rings within the cations is 3.553 (9) Å. In the crystal, two independent intermolecular O—H...Cl hydrogen bonds, both involving the same Cl atom of the anion as acceptor, give rise to chains also running along the a axis; in addition each water molecule, as a hydrogen-bond acceptor, is linked to the acridinium N—H group. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385022</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385022</guid>        </item>
        <item>
            <title>Substitutional disorder in the ionic diorganoantimony halide adduct [bromido/chlorido(0.33/0.67)][2-(dimethylaminomethyl)phenyl][2-(dimethylammoniomethyl)phenyl]antimony(III) 0.75-bromide 0.25-chloride</title>
            <link>http://www.medworm.com/index.php?rid=3385021&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fzb2001</link>
            <description>The title complex, [SbBr0.33Cl0.67(C9H13N)(C9H12N)]Br0.75Cl0.25, exhibits substitutional disorder of both halogen atoms in the asymmetric unit, however, with different occupancies. Thus, the halogen atom bonded to Sb has 0.67 (4) occupancy for Cl and 0.33 (4) for Br, while the anionic halogen atom shows 0.75 (4) occupancy for Br and 0.25 (4) for Cl. An N—H...Cl/Br hydrogen bond is established between the cation and the halide anion. The coordination geometry of the Sb center in the cation is distorted pseudo-trigonal-bipyramidal as a result of the strong intramolecular N→Sb coordination trans to the Sb—Cl/Br bond. The pendant arm on the second ligand is twisted away from the metal center. The compound crystallizes as a racemate, i.e. a mixture of (RN2,CSb1) and (SN2,ASb1) iso...&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385021</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385021</guid>        </item>
        <item>
            <title>Hexaaquamagnesium(II) bis[4-(3-ethoxy-2-hydroxybenzylideneamino)-3-methylbenzenesulfonate]</title>
            <link>http://www.medworm.com/index.php?rid=3385020&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fhb5354</link>
            <description>In the title compound, [Mg(H2O)6](C16H16NO5S)2, the Mg2+ ion (site symmetry 2) adopts an almost regular octahedral coordination geometry. The anion is stabilized by an intramolecular O—H...N hydrogen bond, generating an S(6) ring, and the dihedral angle between the aromatic rings is 41.02 (7)°. In the crystal, the cations and anions are linked by O—H...O hydrogen bonds, generating sheets lying parallel to (100). (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385020</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385020</guid>        </item>
        <item>
            <title>[(Z)-O-Isopropyl N-(m-tolyl)thiocarbamato-κS](tricyclohexylphosphine-κP)gold(I)</title>
            <link>http://www.medworm.com/index.php?rid=3385019&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fhg2660</link>
            <description>The Au atom in the title compound, [Au(C11H14NOS)(C18H33P)], is coordinated within an S,P-donor set that defines a slightly distorted linear geometry [S—Au—P = 174.73 (3)°], with the distortion due in part to a close intramolecular Au...O contact [3.060 (3) Å]. In the crystal structure, molecules are arranged in layers in the bc plane with the primary connections between the arrays being of the type C—H...π. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385019</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385019</guid>        </item>
        <item>
            <title>[(Z)-O-Isopropyl N-(4-chlorophenyl)thiocarbamato-κS](tricyclohexylphosphine-κP)gold(I)</title>
            <link>http://www.medworm.com/index.php?rid=3385018&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fhg2659</link>
            <description>The Au atom in the title compound, [Au(C10H11ClNOS)(C18H33P)], is coordinated within an S,P-donor set that defines a slightly distorted linear geometry [S—Au—P = 172.45 (5)°], with the distortion due in part to a close intramolecular Au...O contact [3.134 (3) Å]. (Source: Acta Crystallographica Section E)</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385018</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385018</guid>        </item>
        <item>
            <title>A new crystal modification of diammonium hydrogen phosphate, (NH4)2(HPO4)</title>
            <link>http://www.medworm.com/index.php?rid=3385017&amp;cid=d_59_59_f&amp;fid=37343&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fbr2137</link>
            <description>The addition of hexafluoridophosphate salts (ammonium, silver, thallium or potassium) is usually used to precipitate complex cations from aqueous solutions. It has long been known that PF6− is sensitive towards hydrolysis under acidic conditions [Gebala &amp; Jones (1969). J. Inorg. Nucl. Chem. 31, 771–776; Plakhotnyk et al. (2005). J. Fluorine Chem. 126, 27–31]. During the course of our investigation into coinage metal complexes of diphosphine ligands, we used ammonium hexafluoridophosphate in order to crystallize [Ag(diphosphine)2]PF6 complexes. From these solutions we always obtained needle-like crystals which turned out to be the title compound, 2NH4+·HPO42−. It was received as the hydrolysis product of NH4PF6. The crystals are a new modification of diammonium hydrogen phosphate. ...</description>
            <author>Acta Crystallographica Section E</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385017</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385017</guid>        </item>
        <item>
            <title>Benzene-1,4-diboronic acid–4,4′-bipyridine–water (1/2/2)</title>
            <link>http://www.medworm.com/index.php?rid=3385016&amp;cid=d_59_59_f&amp;fid=37341&amp;url=http%3A%2F%2Fscripts.iucr.org%2Fcgi-bin%2Fpaper%3Fdn3139</link>
            <description>In the presence of water, benzene-1,4-diboronic acid (1,4-bdba) and 4,4′-bipyridine (4,4′-bpy) form a cocrystal of composition (1,4-bdba)(4,4′-bpy)2(H2O)2, in which the molecular components are organized in two, so far unknown, cyclophane-type hydrogen-bonding patterns. The asymmetric unit of the title compound, C6H8B2O4·2C10H8N2·2H2O, contains two 4,4′-bpy, two water molecules and two halves of 1,4-bdba molecules arranged around crystallographic inversion centers. The occurrence of O—H...O and O—H...N hydrogen bonds involving the water molecules and all O atoms of boronic acid gives rise to a two-dimensional hydrogen-bonded layer structure that develops parallel to the (01\overline{4}) plane. This supramolecular organization is reinforced by π–π interactions between symm...&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Acta Crystallographica Section C</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385016</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385016</guid>        </item>
        <item>
            <title>Active sites of stoichiometric cerium oxide cations (CemO2m+) probed by reactions with carbon monoxide and small hydrocarbon molecules</title>
            <link>http://www.medworm.com/index.php?rid=3385014&amp;cid=d_59_59_f&amp;fid=33812&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Db925294k%26RSS%3D1</link>
            <description>Xiao-Nan Wu, Yan-Xia Zhao, Wei Xue, Zhe-Chen Wang, Sheng-Gui He, Xun-Lei Ding 
(Paper from Phys. Chem. Chem. Phys.)
Xiao-Nan Wu, Phys. Chem. Chem. Phys., 2010, DOI: 10.1039/b925294k
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            <author>RSC - Phys. Chem. Chem. Phys. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385014</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385014</guid>        </item>
        <item>
            <title>Oxidative heme protein-mediated nitroxyl (HNO) generation</title>
            <link>http://www.medworm.com/index.php?rid=3385012&amp;cid=d_59_59_f&amp;fid=33801&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Dc000980f%26RSS%3D1</link>
            <description>Julie A. Reisz, Erika Bechtold, S. Bruce King 
(Perspective from Dalton Trans.)
Julie A. Reisz, Dalton Trans., 2010, DOI: 10.1039/c000980f
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            <author>RSC - Dalton Trans. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385012</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385012</guid>        </item>
        <item>
            <title>Novel class of functionalized ionic liquids with grafted CMPO-moieties for actinides and rare-earth elements recovery</title>
            <link>http://www.medworm.com/index.php?rid=3385011&amp;cid=d_59_59_f&amp;fid=33801&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Db926377b%26RSS%3D1</link>
            <description>Irina L. Odinets, Elena V. Sharova, Oleg I. Artyshin, Konstantin A. Lyssenko, Yulia V. Nelyubina, Galina V. Myasoedova, Nadezhda P. Molochnikova, Elena A. Zakharchenro 
(Paper from Dalton Trans.)
Irina L. Odinets, Dalton Trans., 2010, DOI: 10.1039/b926377b
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            <author>RSC - Dalton Trans. latest articles</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3385011</comments>
            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385011</guid>        </item>
        <item>
            <title>Macrocyclic phosphazane ligands</title>
            <link>http://www.medworm.com/index.php?rid=3385010&amp;cid=d_59_59_f&amp;fid=33801&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Db926428k%26RSS%3D1</link>
            <description>Silvia Gonzalez Calera, Dominic S. Wright 
(Perspective from Dalton Trans.)
Silvia Gonzalez Calera, Dalton Trans., 2010, DOI: 10.1039/b926428k
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            <author>RSC - Dalton Trans. latest articles</author>
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385010</guid>        </item>
        <item>
            <title>A new Cu(i) coordination polymer with the CdSO4 structure type prepared via biphasic solvothermal reaction</title>
            <link>http://www.medworm.com/index.php?rid=3385009&amp;cid=d_59_59_f&amp;fid=33799&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Db919342c%26RSS%3D1</link>
            <description>Tuoping Hu, Haiyan He, Fangna Dai, Xiaoliang Zhao, Daofeng Sun 
(Communication from CrystEngComm)
Tuoping Hu, CrystEngComm, 2010, DOI: 10.1039/b919342c
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The content of this RSS Feed (c) The Royal Society of Chemistry (Source: RSC - CrystEngComm latest articles)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>RSC - CrystEngComm latest articles</author>
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385009</guid>        </item>
        <item>
            <title>Crystallization of unidirectionally oriented fibrous calcium carbonate on thermo-responsive polymer brush matrices</title>
            <link>http://www.medworm.com/index.php?rid=3385008&amp;cid=d_59_59_f&amp;fid=33799&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Db923049a%26RSS%3D1</link>
            <description>Surjith Kumar, Takahiro Ito, Yuki Yanagihara, Yuya Oaki, Tatsuya Nishimura, Takashi Kato 
(Communication from CrystEngComm)
Surjith Kumar, CrystEngComm, 2010, DOI: 10.1039/b923049a
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385008</guid>        </item>
        <item>
            <title>Exploring the limits of 73Ge solid-state NMR spectroscopy at ultrahigh magnetic field</title>
            <link>http://www.medworm.com/index.php?rid=3385006&amp;cid=d_59_59_f&amp;fid=33798&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Db926071d%26RSS%3D1</link>
            <description>Andre Sutrisno, Margaret A. Hanson, Paul A. Rupar, Victor V. Terskikh, Kim M. Baines, Yining Huang 
(Communication from Chem. Commun.)
Andre Sutrisno, Chem. Commun., 2010, DOI: 10.1039/b926071d
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            <pubDate>Sat, 20 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3385006</guid>        </item>
        <item>
            <title>Fluorescence detection for DNA using hybridization chain reaction with enzyme-amplification</title>
            <link>http://www.medworm.com/index.php?rid=3385005&amp;cid=d_59_59_f&amp;fid=33798&amp;url=http%3A%2F%2Fxlink.rsc.org%2F%3FDOI%3Dc000166j%26RSS%3D1</link>
            <description>Shuyan Niu, Yu Jiang, Shusheng Zhang 
(Communication from Chem. Commun.)
Shuyan Niu, Chem. Commun., 2010, DOI: 10.1039/c000166j
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Victor Chechik, Chem. Commun., 2010, DOI: 10.1039/c001703e
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        <comments>http://www.medworm.com/rss/comments.php?id=3384975</comments>
            <pubDate>Fri, 19 Mar 2010 14:18:18 +0100</pubDate>
            <guid isPermaLink="false">3384975</guid>        </item>
        <item>
            <title>Efficient Parallel Decomposition of Dynamical Sampling in Glass-Forming Materials Based on an “On the Fly” Definition of Metabasins</title>
            <link>http://www.medworm.com/index.php?rid=3384976&amp;cid=d_59_59_f&amp;fid=30092&amp;url=http%3A%2F%2Fpubs.acs.org%2Fdoi%2Fabs%2F10.1021%2Fct9004245%3Fai%3D557%26af%3DR</link>
            <description>Journal of Chemical Theory and Computation, Volume 0, Issue 0, Articles ASAP (As Soon As Publishable). (Source: Journal of Chemical Theory and Computation)</description>
            <author>Journal of Chemical Theory and Computation</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3384976</comments>
            <pubDate>Fri, 19 Mar 2010 14:17:13 +0100</pubDate>
            <guid isPermaLink="false">3384976</guid>        </item>
        <item>
            <title>GET with the Complex{diamondsuit}: Crystal Structure of Get4-Get5 Complex and Its Interactions with Sgt2, Get3, and Ydj1 [Papers Of The Week]</title>
            <link>http://www.medworm.com/index.php?rid=3381983&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2Fe99925%3Frss%3D1</link>
            <description>(Source: Journal of Biological Chemistry)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381983</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381983</guid>        </item>
        <item>
            <title>Hydrophobic Side Chain Dynamics of a Glutamate Receptor Ligand Binding Domain [Neurobiology]</title>
            <link>http://www.medworm.com/index.php?rid=3381982&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10154%3Frss%3D1</link>
            <description>Ionotropic glutamate receptors are ligand-gated ion channels that mediate much of the fast excitatory neurotransmission in the central nervous system. The extracellular ligand binding core (S1S2) of the GluR2 subtype of ionotropic glutamate receptors can be produced as a soluble protein with properties essentially identical to the corresponding domain in the intact, membrane-bound protein. Using a variety of biophysical techniques, much has been learned about the structure and dynamics of S1S2 and the relationship between its ligand-induced conformational changes and the function of the receptor. It is clear that dynamic processes are essential to the function of ionotropic glutamate receptors. We have isotopically labeled side chain methyls of GluR2 S1S2 and used NMR spectroscopy to study...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381982</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381982</guid>        </item>
        <item>
            <title>Ginkgolide X Is a Potent Antagonist of Anionic Cys-loop Receptors with a Unique Selectivity Profile at Glycine Receptors [Protein Structure and Folding]</title>
            <link>http://www.medworm.com/index.php?rid=3381981&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10141%3Frss%3D1</link>
            <description>The novel ginkgolide analog ginkgolide X was characterized functionally at human glycine and -aminobutyric acid type A receptors (GlyRs and GABAARs, respectively) in the fluorescence-based FLIPRTM Membrane Potential assay. The compound inhibited the signaling of all GABAAR subtypes included in the study with high nanomolar/low micromolar IC50 values, except the 1 receptor at which it was a significantly weaker antagonist. Ginkgolide X also displayed high nanomolar/low micromolar IC50 values at the homomeric 1 and 2 GlyRs, whereas it was inactive at the heteromeric 1&amp;beta; and 2&amp;beta; subtypes at concentrations up to 300 &amp;micro;m. Thus, the functional properties of the compound were significantly different from those of the naturally occurring ginkgolides A, B, C, J, and M but similar to th...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381981</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381981</guid>        </item>
        <item>
            <title>Structure and Filament Dynamics of the pSK41 Actin-like ParM Protein: IMPLICATIONS FOR PLASMID DNA SEGREGATION [Dna and Chromosomes]</title>
            <link>http://www.medworm.com/index.php?rid=3381980&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10130%3Frss%3D1</link>
            <description>Type II plasmid partition systems utilize ParM NTPases in coordination with a centromere-binding protein called ParR to mediate accurate DNA segregation, a process critical for plasmid retention. The Staphylococcus aureus pSK41 plasmid is a medically important plasmid that confers resistance to multiple antibiotics, disinfectants, and antiseptics. In the first step of partition, the pSK41 ParR binds its DNA centromere to form a superhelical partition complex that recruits ParM, which then mediates plasmid separation. pSK41 ParM is homologous to R1 ParM, a known actin homologue, suggesting that it may also form filaments to drive partition. To gain insight into the partition function of ParM, we examined its ability to form filaments and determined the crystal structure of apoParM to 1.95 &amp;...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381980</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381980</guid>        </item>
        <item>
            <title>Src Kinase Phosphorylates RUNX3 at Tyrosine Residues and Localizes the Protein in the Cytoplasm [Molecular Bases Of Disease]</title>
            <link>http://www.medworm.com/index.php?rid=3381979&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10122%3Frss%3D1</link>
            <description>In this study, we found that the overexpression of Src results in the tyrosine phosphorylation and cytoplasmic localization of RUNX3. We also found that the tyrosine residues of endogenous RUNX3 are phosphorylated and that the protein is localized in the cytoplasm in Src-activated cancer cell lines. We further showed that the knockdown of Src by small interfering RNA, or the inhibition of Src kinase activity by a chemical inhibitor, causes the re-localization of RUNX3 to the nucleus. Collectively, our results demonstrate that the tyrosine phosphorylation of RUNX3 by activated Src is associated with the cytoplasmic localization of RUNX3 in gastric and breast cancers. (Source: Journal of Biological Chemistry)</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381979</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381979</guid>        </item>
        <item>
            <title>Gated Access to the Pore of a P2X Receptor: STRUCTURAL IMPLICATIONS FOR CLOSED-OPEN TRANSITIONS [Molecular Biophysics]</title>
            <link>http://www.medworm.com/index.php?rid=3381978&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10110%3Frss%3D1</link>
            <description>In this study, we quantified gated access to Cd2+ at substituted cysteines in TM2 of P2X2 receptors in the open and closed states. Our data for the closed state are consistent with the zebrafish P2X4.1 structure, with isoleucines and threonines (Ile-332 and Thr-336) positioned one helical turn apart lining the channel wall on approach to the gate. Our data for the open state reveal gated access to deeper parts of the pore (Thr-339, Val-343, Asp-349, and Leu-353), suggesting the closed channel gate is between Thr-336 and Thr-339. We also found unexpected interactions between native Cys-348 and D349C that result in tight Cd2+ binding deep within the intracellular vestibule in the open state. Interpreted with a P2X2 receptor structural model of the closed state, our data suggest that the chan...&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381978</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381978</guid>        </item>
        <item>
            <title>CB1 Cannabinoid Receptors Increase Neuronal Precursor Proliferation through AKT/Glycogen Synthase Kinase-3{beta}/{beta}-Catenin Signaling [Signal Transduction]</title>
            <link>http://www.medworm.com/index.php?rid=3381977&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10098%3Frss%3D1</link>
            <description>The endocannabinoid system is involved in the regulation of many physiological effects in the central and peripheral nervous system. Recent findings have demonstrated the presence of a functional endocannabinoid system within neuronal progenitors located in the hippocampus and ventricular/subventricular zone that participates in the regulation of cell proliferation. It is presently unknown whether the endocannabinoid system exerts a widespread effect on neuronal precursors from different neurogenic regions, and very little is known about the signaling by which it regulates neuronal precursor proliferation. Herein, we demonstrate the presence of cannabinoid CB1 receptors in granule cell precursors (GCPs) during early cerebellar development. Activation of CB1 receptors by HU-210 promoted GCP...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381977</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381977</guid>        </item>
        <item>
            <title>Structure of the DNA-bound BRCA1 C-terminal Region from Human Replication Factor C p140 and Model of the Protein-DNA Complex [Dna and Chromosomes]</title>
            <link>http://www.medworm.com/index.php?rid=3381976&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10087%3Frss%3D1</link>
            <description>BRCA1 C-terminal domain (BRCT)-containing proteins are found widely throughout the animal and bacteria kingdoms where they are exclusively involved in cell cycle regulation and DNA metabolism. Whereas most BRCT domains are involved in protein-protein interactions, a small subset has bona fide DNA binding activity. Here, we present the solution structure of the BRCT region of the large subunit of replication factor C bound to DNA and a model of the structure-specific complex with 5'-phosphorylated double-stranded DNA. The replication factor C BRCT domain possesses a large basic patch on one face, which includes residues that are structurally conserved and ligate the phosphate in phosphopeptide binding BRCT domains. An extra -helix at the N terminus, which is required for DNA binding, insert...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381976</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381976</guid>        </item>
        <item>
            <title>Stefin B Interacts with Histones and Cathepsin L in the Nucleus [Enzymology]</title>
            <link>http://www.medworm.com/index.php?rid=3381975&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10078%3Frss%3D1</link>
            <description>Stefin B (cystatin B) is an endogenous inhibitor of cysteine proteinases localized in the nucleus and the cytosol. Loss-of-function mutations in the stefin B gene (CSTB) gene were reported in patients with Unverricht-Lundborg disease (EPM1). We have identified an interaction between stefin B and nucleosomes, specifically with histones H2A.Z, H2B, and H3. In synchronized T98G cells, stefin B co-immunoprecipitated with histone H3, predominantly in the G1 phase of the cell cycle. Stefin B-deficient mouse embryonic fibroblasts entered S phase earlier than wild type mouse embryonic fibroblasts. In contrast, increased expression of stefin B in the nucleus delayed cell cycle progression in T98G cells. The delay in cell cycle progression was associated with the inhibition of cathepsin L in the nuc...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381975</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381975</guid>        </item>
        <item>
            <title>Histone Deacetylase Inhibitors Activate NF-{kappa}B in Human Leukemia Cells through an ATM/NEMO-related Pathway [Signal Transduction]</title>
            <link>http://www.medworm.com/index.php?rid=3381974&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10064%3Frss%3D1</link>
            <description>Mechanisms underlying histone deacetylase inhibitor (HDACI)-mediated NF-B activation were investigated in human leukemia cells. Exposure of U937 and other leukemia cells to LBH-589 induced reactive oxygen species (ROS) followed by single strand (XRCC1) and double strand (-H2AX) DNA breaks. Notably, LBH-589 lethality was markedly attenuated by small interfering RNA (siRNA) knockdown of the DNA damage-linked histone, H1.2. LBH-589 triggered p65/RelA activation, NF-B-dependent induction of Mn-SOD2, and ROS elimination. Interference with LBH-589-mediated NF-B activation (e.g. in IB super-repressor transfected cells) diminished HDACI-mediated Mn-SOD2 induction and increased ROS accumulation, DNA damage, and apoptosis. The Mn-SOD2 mimetic TBAP (manganese(III)-tetrakis 4-benzoic acid porphyrin) p...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381974</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381974</guid>        </item>
        <item>
            <title>Regulation of Microtubule Dynamics through Phosphorylation on Stathmin by Epstein-Barr Virus Kinase BGLF4 [Protein Synthesis and Degradation]</title>
            <link>http://www.medworm.com/index.php?rid=3381973&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10053%3Frss%3D1</link>
            <description>In conclusion, we have shown that a viral Ser/Thr kinase can directly modulate the activity of stathmin and this contributes to alteration of cellular MT dynamics and then may modulate the associated cellular processes. (Source: Journal of Biological Chemistry)&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381973</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381973</guid>        </item>
        <item>
            <title>Revelation of p53-independent Function of MTA1 in DNA Damage Response via Modulation of the p21WAF1-Proliferating Cell Nuclear Antigen Pathway [Cell Biology]</title>
            <link>http://www.medworm.com/index.php?rid=3381972&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10044%3Frss%3D1</link>
            <description>Although metastasis-associated protein 1 (MTA1), a component of the nucleosome remodeling and deacetylase (NuRD) complex, is a DNA-damage response protein and regulates p53-dependent DNA repair, it remains unknown whether MTA1 also participates in p53-independent DNA damage response. Here, we provide evidence that MTA1 is a p53-independent transcriptional corepressor of p21WAF1, and the underlying mechanism involves recruitment of MTA1-histone deacetylase 2 (HDAC2) complexes onto two selective regions of the p21WAF1 promoter. Accordingly, MTA1 depletion, despite its effect on p53 down-regulation, superinduces p21WAF1, increases p21WAF1 binding to proliferating cell nuclear antigen (PCNA), and decreases the nuclear accumulation of PCNA in response to ionizing radiation. In support of a p53-...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381972</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381972</guid>        </item>
        <item>
            <title>Pro-hormone Secretogranin II Regulates Dense Core Secretory Granule Biogenesis in Catecholaminergic Cells [Cell Biology]</title>
            <link>http://www.medworm.com/index.php?rid=3381971&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10030%3Frss%3D1</link>
            <description>Processes underlying the formation of dense core secretory granules (DCGs) of neuroendocrine cells are poorly understood. Here, we present evidence that DCG biogenesis is dependent on the secretory protein secretogranin (Sg) II, a member of the granin family of pro-hormone cargo of DCGs in neuroendocrine cells. Depletion of SgII expression in PC12 cells leads to a decrease in both the number and size of DCGs and impairs DCG trafficking of other regulated hormones. Expression of SgII fusion proteins in a secretory-deficient PC12 variant rescues a regulated secretory pathway. SgII-containing dense core vesicles share morphological and physical properties with bona fide DCGs, are competent for regulated exocytosis, and maintain an acidic luminal pH through the V-type H+-translocating ATPase. ...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381971</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381971</guid>        </item>
        <item>
            <title>Physical Interaction of Jab1 with Human Serotonin 6 G-protein-coupled Receptor and Their Possible Roles in Cell Survival [Signal Transduction]</title>
            <link>http://www.medworm.com/index.php?rid=3381970&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10016%3Frss%3D1</link>
            <description>The 5-HT6 receptor (5-HT6R) is one of the most recently cloned serotonin receptors, and it plays important roles in Alzheimer disease, depression, and learning and memory disorders. However, unlike the other serotonin receptors, the cellular mechanisms of 5-HT6R are poorly elucidated relative to its significance in human brain diseases. Here, using a yeast two-hybrid assay, we found that the human 5-HT6R interacts with Jun activation domain-binding protein-1 (Jab1). We also confirmed a physical interaction between 5-HT6R and Jab1 using glutathione S-transferase pulldown, fluorescence resonance energy transfer, co-immunoprecipitation, and immunocyto(histo)chemistry assays. The manipulation of Jab1 expression using Jab1 small interference RNA decreased 5-HT6R-mediated activity and cell membr...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381970</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381970</guid>        </item>
        <item>
            <title>Recessive COL6A2 C-globular Missense Mutations in Ullrich Congenital Muscular Dystrophy: ROLE OF THE C2a SPLICE VARIANT [Molecular Bases Of Disease]</title>
            <link>http://www.medworm.com/index.php?rid=3381969&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F10005%3Frss%3D1</link>
            <description>Ullrich congenital muscular dystrophy (UCMD) is a disabling and life-threatening disorder resulting from either recessive or dominant mutations in genes encoding collagen VI. Although the majority of the recessive UCMD cases have frameshift or nonsense mutations in COL6A1, COL6A2, or COL6A3, recessive structural mutations in the COL6A2 C-globular region are emerging also. However, the underlying molecular mechanisms have remained elusive. Here we identified a homozygous COL6A2 E624K mutation (C1 subdomain) and a homozygous COL6A2 R876S mutation (C2 subdomain) in two UCMD patients. The consequences of the mutations were investigated using fibroblasts from patients and cells stably transfected with the mutant constructs. In contrast to expectations based on the clinical severity of these two...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381969</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381969</guid>        </item>
        <item>
            <title>Podocyte Injury Induces Nuclear Translocation of WTIP via Microtubule-dependent Transport [Molecular Bases Of Disease]</title>
            <link>http://www.medworm.com/index.php?rid=3381968&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9995%3Frss%3D1</link>
            <description>Podocyte structural and transcriptional phenotype plasticity characterizes glomerular injury. Transcriptional activity of WT1 (Wilm's tumor 1) is required for normal podocyte structure and is repressed by the podocyte adherens junction protein, WTIP (WT1 interacting protein). Here we show that WTIP translocated into podocyte nuclei in lipopolysaccharide (LPS)-treated mice, a model of transient nephrotic syndrome. Cultured podocytes, which stably expressed an epitope-tagged WTIP, were treated with LPS. Imaging and cellular fractionation studies demonstrated that WTIP translocated from podocyte cell contacts into nuclei within 6 h and relocalized to cell contacts within 24 h after LPS treatment. LPS-stimulated WTIP nuclear translocation required JNK activity, which assembled a multiprotein c...&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381968</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381968</guid>        </item>
        <item>
            <title>A Conformational Switch in the Scaffolding Protein NHERF1 Controls Autoinhibition and Complex Formation [Protein Structure and Folding]</title>
            <link>http://www.medworm.com/index.php?rid=3381967&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9981%3Frss%3D1</link>
            <description>The mammalian Na+/H+ exchange regulatory factor 1 (NHERF1) is a multidomain scaffolding protein essential for regulating the intracellular trafficking and macromolecular assembly of transmembrane ion channels and receptors. NHERF1 consists of tandem PDZ-1, PDZ-2 domains that interact with the cytoplasmic domains of membrane proteins and a C-terminal (CT) domain that binds the membrane-cytoskeleton linker protein ezrin. NHERF1 is held in an autoinhibited state through intramolecular interactions between PDZ2 and the CT domain that also includes a C-terminal PDZ-binding motif (-SNL). We have determined the structures of the isolated and tandem PDZ2CT domains by high resolution NMR using small angle x-ray scattering as constraints. The PDZ2CT structure shows weak intramolecular interactions b...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381967</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381967</guid>        </item>
        <item>
            <title>Global Conformational Change Associated with the Two-step Reaction Catalyzed by Escherichia coli Lipoate-Protein Ligase A [Protein Structure and Folding]</title>
            <link>http://www.medworm.com/index.php?rid=3381966&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9971%3Frss%3D1</link>
            <description>Lipoate-protein ligase A (LplA) catalyzes the attachment of lipoic acid to lipoate-dependent enzymes by a two-step reaction: first the lipoate adenylation reaction and, second, the lipoate transfer reaction. We previously determined the crystal structure of Escherichia coli LplA in its unliganded form and a binary complex with lipoic acid (Fujiwara, K., Toma, S., Okamura-Ikeda, K., Motokawa, Y., Nakagawa, A., and Taniguchi, H. (2005) J Biol. Chem. 280, 33645&amp;ndash;33651). Here, we report two new LplA structures, LplA&amp;middot;lipoyl-5'-AMP and LplA&amp;middot;octyl-5'-AMP&amp;middot;apoH-protein complexes, which represent the post-lipoate adenylation intermediate state and the pre-lipoate transfer intermediate state, respectively. These structures demonstrate three large scale conformational changes...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381966</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381966</guid>        </item>
        <item>
            <title>Crystal Structure of Get4-Get5 Complex and Its Interactions with Sgt2, Get3, and Ydj1 [Protein Structure and Folding]</title>
            <link>http://www.medworm.com/index.php?rid=3381965&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9962%3Frss%3D1</link>
            <description>Get3, Get4, and Get5 in Saccharomyces cerevisiae participate in the insertion of tail-anchored proteins into the endoplasmic reticulum membrane. We elucidated the interaction between Get4 and Get5 and investigated their interaction with Get3 and a tetratricopeptide repeat-containing protein, Sgt2. Based on co-immunoprecipitation and crystallographic studies, Get4 and Get5 formed a tight complex, suggesting that they constitute subunits of a larger complex. In contrast, although Get3 interacted physically with the Get4-Get5 complex, low amounts of Get3 co-precipitated with Get5, implying a transient interaction between Get3 and Get4-Get5. Sgt2 also interacted with Get5, although the amount of Sgt2 that co-precipitated with Get5 varied. Moreover, GET3, GET4, and GET5 interacted genetically w...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381965</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:05 +0100</pubDate>
            <guid isPermaLink="false">3381965</guid>        </item>
        <item>
            <title>Hyaluronan Mixed Esters of Butyric and Retinoic Acid Affording Myocardial Survival and Repair without Stem Cell Transplantation [Glycobiology and Extracellular Matrices]</title>
            <link>http://www.medworm.com/index.php?rid=3381964&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9949%3Frss%3D1</link>
            <description>In conclusion, efficient cardiac regenerative therapy can be afforded by HBR without the need of stem cell transplantation or vector-mediated gene delivery. (Source: Journal of Biological Chemistry)</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381964</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381964</guid>        </item>
        <item>
            <title>Akt Cys-310-targeted Inhibition by Hydroxylated Benzene Derivatives Is Tightly Linked to Their Immunosuppressive Effects [Cell Biology]</title>
            <link>http://www.medworm.com/index.php?rid=3381963&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9932%3Frss%3D1</link>
            <description>In this study we characterized Akt (protein kinase B)-targeted regulation by HQ and its derivatives, in suppressing inflammatory responses using cellular, molecular, biochemical, and immunopharmacological approaches. HQ down-regulated inflammatory responses such as NO production, surface levels of pattern recognition receptors, and cytokine gene expression with IC50 values that ranged from 5 to 10 &amp;micro;m. HQ inhibition was mediated by blocking NF-B activation via suppression of its translocation pathway, which is composed of Akt, IB kinase &amp;beta;, and IB. Of the targets in this pathway, HQ directly targeted and bound to the sulfhydryl group of Cys-310 of Akt and sequentially interrupted the phosphorylation of both Thr-308 and Ser-473 by mediation of &amp;beta;-mercaptoethanol, according to t...&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381963</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381963</guid>        </item>
        <item>
            <title>Secretin Occupies a Single Protomer of the Homodimeric Secretin Receptor Complex: INSIGHTS FROM PHOTOAFFINITY LABELING STUDIES USING DUAL SITES OF COVALENT ATTACHMENT [Protein Structure and Folding]</title>
            <link>http://www.medworm.com/index.php?rid=3381962&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9919%3Frss%3D1</link>
            <description>The secretin receptor, a prototypic family B G protein-coupled receptor, forms a constitutive homodimeric complex that is stable even in the presence of hormone. Recently, a model of this agonist-bound receptor was built based on high resolution structures reported for amino-terminal domains of other family members. Although this model provided the best solution for all extant data, including 10 photoaffinity labeling constraints, a new such constraint now obtained with a position 16 photolabile probe was inconsistent with this model. As the secretin receptor forms constitutive homodimers, we explored whether secretin might dock across both protomers of the complex, an observation that could also contribute to the negative cooperativity observed. To directly explore this, we prepared six s...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381962</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381962</guid>        </item>
        <item>
            <title>Neuropilin 1 Directly Interacts with Fer Kinase to Mediate Semaphorin 3A-induced Death of Cortical Neurons [Molecular Bases Of Disease]</title>
            <link>http://www.medworm.com/index.php?rid=3381961&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9908%3Frss%3D1</link>
            <description>Neuropilins (NRPs) are receptors for the major chemorepulsive axonal guidance cue semaphorins (Sema). The interaction of Sema3A/NRP1 during development leads to the collapse of growth cones. Here we show that Sema3A also induces death of cultured cortical neurons through NRP1. A specific NRP1 inhibitory peptide ameliorated Sema3A-evoked cortical axonal retraction and neuronal death. Moreover, Sema3A was also involved in cerebral ischemia-induced neuronal death. Expression levels of Sema3A and NRP1, but not NRP2, were significantly increased early during brain reperfusion following transient focal cerebral ischemia. NRP1 inhibitory peptide delivered to the ischemic brain was potently neuroprotective and prevented the loss of motor functions in mice. The integrity of the injected NRP1 inhibi...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381961</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381961</guid>        </item>
        <item>
            <title>Molecular Interfaces of the Galactose-binding Protein Tectonin Domains in Host-Pathogen Interaction [Molecular Biophysics]</title>
            <link>http://www.medworm.com/index.php?rid=3381960&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9898%3Frss%3D1</link>
            <description>&amp;beta;-Propeller proteins function in catalysis, protein-protein interaction, cell cycle regulation, and innate immunity. The galactose-binding protein (GBP) from the plasma of the horseshoe crab, Carcinoscorpius rotundicauda, is a &amp;beta;-propeller protein that functions in antimicrobial defense. Studies have shown that upon binding to Gram-negative bacterial lipopolysaccharide (LPS), GBP interacts with C-reactive protein (CRP) to form a pathogen-recognition complex, which helps to eliminate invading microbes. However, the molecular basis of interactions between GBP and LPS and how it interplays with CRP remain largely unknown. By homology modeling, we showed that GBP contains six &amp;beta;-propeller/Tectonin domains. Ligand docking indicated that Tectonin domains 6 to 1 likely contain the LP...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381960</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381960</guid>        </item>
        <item>
            <title>In Vitro and in Vivo Enhanced Generation of Human A9 Dopamine Neurons from Neural Stem Cells by Bcl-XL [Neurobiology]</title>
            <link>http://www.medworm.com/index.php?rid=3381959&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9881%3Frss%3D1</link>
            <description>Human neural stem cells derived from the ventral mesencephalon (VM) are powerful research tools and candidates for cell therapies in Parkinson disease. Previous studies with VM dopaminergic neuron (DAn) precursors indicated poor growth potential and unstable phenotypical properties. Using the model cell line hVM1 (human ventral mesencephalic neural stem cell line 1; a new human fetal VM stem cell line), we have found that Bcl-XL enhances the generation of DAn from VM human neural stem cells. Mechanistically, Bcl-XL not only exerts the expected antiapoptotic effect but also induces proneural (NGN2 and NEUROD1) and dopamine-related transcription factors, resulting in a high yield of DAn with the correct phenotype of substantia nigra pars compacta (SNpc). The expression of key genes directly ...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381959</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381959</guid>        </item>
        <item>
            <title>Low Density Subcellular Fractions Enhance Disease-specific Prion Protein Misfolding [Protein Structure and Folding]</title>
            <link>http://www.medworm.com/index.php?rid=3381958&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9868%3Frss%3D1</link>
            <description>The production of prion particles in vitro by amplification with or without exogenous seed typically results in infectivity titers less than those associated with PrPSc isolated ex vivo and highlights the potential role of co-factors that can catalyze disease-specific prion protein misfolding in vivo. We used a cell-free conversion assay previously shown to replicate many aspects of transmissible spongiform encephalopathy disease to investigate the cellular location of disease-specific co-factors using fractions derived from gradient centrifugation of a scrapie-susceptible cell line. Fractions from the low density region of the gradient doubled the efficiency of conversion of recombinant PrP. These fractions contain plasma membrane and cytoplasmic proteins, and conversion enhancement can b...&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381958</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381958</guid>        </item>
        <item>
            <title>Cul8/Rtt101 Forms a Variety of Protein Complexes That Regulate DNA Damage Response and Transcriptional Silencing [Protein Synthesis and Degradation]</title>
            <link>http://www.medworm.com/index.php?rid=3381957&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9858%3Frss%3D1</link>
            <description>The budding yeast, Saccharomyces cerevisiae, has three cullin proteins, which act as platforms for Cullin-based E3 ubiquitin ligases. Genetic evidence indicates that Cul8, together with Mms1, Mms22, and Esc4, is involved in the repair of DNA damage that can occur during DNA replication. Cul8 is thought to form a complex with these proteins, but the composition and the function of Cul8-based E3 ubiquitin ligases remain largely uncharacterized. Herein, we report a comprehensive biochemical analysis of Cul8 complexes. Cul8 was found to form a Cul8-Mms1-Mms22-Esc4 complex under physiological conditions, with Mms1 bridging Cul8 and Mms22 and Mms22 bridging Mms1 and Esc4. Domain analysis demonstrated that the N-terminal region of Mms1 and the C-terminal region of Mms22 are required for the Mms1-...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381957</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381957</guid>        </item>
        <item>
            <title>Functional Interaction of Phosphatase and Tensin Homologue (PTEN) with the E3 Ligase NEDD4-1 during Neuronal Response to Zinc [Protein Synthesis and Degradation]</title>
            <link>http://www.medworm.com/index.php?rid=3381956&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9847%3Frss%3D1</link>
            <description>This study demonstrates that NEDD4-1-mediated PTEN ubiquitination is crucial in the regulation of PI3K/Akt signaling by PTEN during the neuronal response to zinc, which may represent a common mechanism in neurodegeneration. (Source: Journal of Biological Chemistry)</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381956</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381956</guid>        </item>
        <item>
            <title>Nuclear Factor {kappa}B- and Specificity Protein 1-dependent p53-mediated Bi-directional Regulation of the Human Manganese Superoxide Dismutase Gene [Signal Transduction]</title>
            <link>http://www.medworm.com/index.php?rid=3381955&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9835%3Frss%3D1</link>
            <description>Tumor suppressor p53 is known to activate certain sets of genes while suppressing others. However, whether p53 can both activate and suppress the same gene is unclear. To address this question, concentration-dependent p53 effect on the manganese superoxide dismutase (MnSOD) gene was investigated. By transfecting p53 in PC-3 cells, we demonstrate that low concentrations of p53 increase while high concentrations suppress MnSOD expression. The physiological relevance of this effect was determined in vitro and in vivo using combined UVB-mediated activation and small interference RNA-mediated suppression of p53. Results were consistent with the bi-directional effect of p53 on MnSOD expression. MnSOD-promoter/enhancer analysis demonstrates that p53 is suppressive to the promoter activity regardl...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381955</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381955</guid>        </item>
        <item>
            <title>Altered Function of the SCN1A Voltage-gated Sodium Channel Leads to {gamma}-Aminobutyric Acid-ergic (GABAergic) Interneuron Abnormalities [Molecular Bases Of Disease]</title>
            <link>http://www.medworm.com/index.php?rid=3381954&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9823%3Frss%3D1</link>
            <description>Voltage-gated sodium channels are required for the initiation and propagation of action potentials. Mutations in the neuronal voltage-gated sodium channel SCN1A are associated with a growing number of disorders including generalized epilepsy with febrile seizures plus (GEFS+),7 severe myoclonic epilepsy of infancy, and familial hemiplegic migraine. To gain insight into the effect of SCN1A mutations on neuronal excitability, we introduced the human GEFS+ mutation SCN1A-R1648H into the orthologous mouse gene. Scn1aRH/RH mice homozygous for the R1648H mutation exhibit spontaneous generalized seizures and premature death between P16 and P26, whereas Scn1aRH/+ heterozygous mice exhibit infrequent spontaneous generalized seizures, reduced threshold and accelerated propagation of febrile seizures...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381954</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381954</guid>        </item>
        <item>
            <title>CDKN1C Negatively Regulates RNA Polymerase II C-terminal Domain Phosphorylation in an E2F1-dependent Manner [Cell Biology]</title>
            <link>http://www.medworm.com/index.php?rid=3381953&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9813%3Frss%3D1</link>
            <description>CDKN1C is a cyclin-dependent kinase inhibitor and is a candidate tumor suppressor gene. We previously found that the CDKN1C protein represses E2F1-driven transcription in an apparent negative feedback loop. Herein, we explore the mechanism by which CDKN1C represses transcription. We find that adenoviral-mediated overexpression of CDKN1C leads to a dramatic reduction in phosphorylation of the RNA polymerase II (pol II) C-terminal domain (CTD). RNA interference studies demonstrate that this activity is not an artifact of CDKN1C overexpression, because endogenous CDKN1C mediates an inhibition of RNA pol II CTD phosphorylation in HeLa cells upon treatment with dexamethasone. Surprisingly, we find that CDKN1C-mediated repression of RNA pol II phosphorylation is E2F1-dependent, suggesting that E...&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381953</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381953</guid>        </item>
        <item>
            <title>Last Step in the Conversion of Trehalose to Glycogen: A MYCOBACTERIAL ENZYME THAT TRANSFERS MALTOSE FROM MALTOSE 1-PHOSPHATE TO GLYCOGEN [Glycobiology and Extracellular Matrices]</title>
            <link>http://www.medworm.com/index.php?rid=3381952&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9803%3Frss%3D1</link>
            <description>We show that Mycobacterium smegmatis has an enzyme catalyzing transfer of maltose from [14C]maltose 1-phosphate to glycogen. This enzyme was purified 90-fold from crude extracts and characterized. Maltose transfer required addition of an acceptor. Liver, oyster, or mycobacterial glycogens were the best acceptors, whereas amylopectin had good activity, but amylose was a poor acceptor. Maltosaccharides inhibited the transfer of maltose from [14C]maltose-1-P to glycogen because they were also acceptors of maltose, and they caused production of larger sized radioactive maltosaccharides. When maltotetraose was the acceptor, over 90% of the 14C-labeled product was maltohexaose, and no radioactivity was in maltopentaose, demonstrating that maltose was transferred intact. Stoichiometry showed that...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381952</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381952</guid>        </item>
        <item>
            <title>Anti-inflammatory Compounds Parthenolide and Bay 11-7082 Are Direct Inhibitors of the Inflammasome [Immunology]</title>
            <link>http://www.medworm.com/index.php?rid=3381951&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9792%3Frss%3D1</link>
            <description>Activation of the inflammasome generates the pro-inflammatory cytokines interleukin-1&amp;beta; and -18, which are important mediators of inflammation. Abnormal activation of the inflammasome leads to many inflammatory diseases, including gout, silicosis, neurodegeneration, and genetically inherited periodic fever syndromes. Therefore, identification of small molecule inhibitors that target the inflammasome is an important step toward developing effective therapeutics for the treatment of inflammation. Here, we show that the herbal NF-B inhibitory compound parthenolide inhibits the activity of multiple inflammasomes in macrophages by directly inhibiting the protease activity of caspase-1. Additional investigations of other NF-B inhibitors revealed that the synthetic IB kinase-&amp;beta; inhibitor ...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381951</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381951</guid>        </item>
        <item>
            <title>Energy Restriction as an Antitumor Target of Thiazolidinediones [Metabolism]</title>
            <link>http://www.medworm.com/index.php?rid=3381950&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9780%3Frss%3D1</link>
            <description>Cancer cells gain growth advantages in the microenvironment by shifting cellular metabolism to aerobic glycolysis, the so-called Warburg effect. There is a growing interest in targeting aerobic glycolysis for cancer therapy by exploiting the differential susceptibility of malignant versus normal cells to glycolytic inhibition, of which the proof-of-concept is provided by the in vivo efficacy of dietary caloric restriction and natural product-based energy restriction-mimetic agents (ERMAs) such as resveratrol and 2-deoxyglucose in suppressing carcinogenesis in animal models. Here, we identified thiazolidinediones as a novel class of ERMAs in that they elicited hallmark cellular responses characteristic of energy restriction, including transient induction of Sirt1 (silent information regulat...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381950</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381950</guid>        </item>
        <item>
            <title>FKBP38 Protects Bcl-2 from Caspase-dependent Degradation [Protein Synthesis and Degradation]</title>
            <link>http://www.medworm.com/index.php?rid=3381949&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9770%3Frss%3D1</link>
            <description>The cellular processes that regulate Bcl-2 at the posttranslational levels are as important as those that regulate bcl-2 synthesis. Previously we demonstrated that the suppression of FK506-binding protein 38 (FKBP38) contributes to the instability of Bcl-2 or leaves Bcl-2 unprotected from degradation in an unknown mechanism. Here, we studied the underlying molecular mechanism mediating this process. We first showed that Bcl-2 binding-defective mutants of FKBP38 fail to accumulate Bcl-2 protein. We demonstrated that the FKBP38-mediated Bcl-2 stability is specific as the levels of other anti-apoptotic proteins such as Bcl-XL and Mcl-1 remained unaffected. FKBP38 enhanced the Bcl-2 stability under the blockade of de novo protein synthesis, indicating it is posttranslational. We showed that th...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381949</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381949</guid>        </item>
        <item>
            <title>Structure of RecJ Exonuclease Defines Its Specificity for Single-stranded DNA [Protein Structure and Folding]</title>
            <link>http://www.medworm.com/index.php?rid=3381948&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9762%3Frss%3D1</link>
            <description>RecJ is a single-stranded DNA (ssDNA)-specific 5'-3' exonuclease that plays an important role in DNA repair and recombination. To elucidate how RecJ achieves its high specificity for ssDNA, we determined the entire structures of RecJ both in a ligand-free form and in a complex with Mn2+ or Mg2+ by x-ray crystallography. The entire RecJ consists of four domains that form a molecule with an O-like structure. One of two newly identified domains had structural similarities to an oligonucleotide/oligosaccharide-binding (OB) fold. The OB fold domain alone could bind to DNA, indicating that this domain is a novel member of the OB fold superfamily. The truncated RecJ containing only the core domain exhibited much lower affinity for the ssDNA substrate compared with intact RecJ. These results suppo...&lt;div id=&quot;medworm&quot;&gt;&lt;p&gt;&lt;b&gt;&lt;i&gt;MedWorm Message:&lt;/i&gt;&lt;/b&gt; Get the very latest Swine Flu news via the MedWorm &lt;b&gt;&lt;a href=&quot;http://www.medworm.com/rss/search.php?qu=%2Bswine+%2B%28influenza+flu%29&amp;t=Swine+Flu&amp;f=infectiousdiseases&amp;r=Any&amp;o=d&quot; target =&quot;_self&quot;&gt;Swine Flu RSS news feed&lt;/a&gt;&lt;/b&gt; -  updated hourly from thousands of authoritative health and news sources.&lt;/p&gt;&lt;/div&gt;</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381948</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381948</guid>        </item>
        <item>
            <title>Pituitary Adenylate Cyclase-activating Polypeptide (PACAP)/PAC1HOP1 Receptor Activation Coordinates Multiple Neurotrophic Signaling Pathways: Akt ACTIVATION THROUGH PHOSPHATIDYLINOSITOL 3-KINASE {gamma} AND VESICLE ENDOCYTOSIS FOR NEURONAL SURVIVAL [Neurobiology]</title>
            <link>http://www.medworm.com/index.php?rid=3381947&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9749%3Frss%3D1</link>
            <description>MAPK and Akt pathways are predominant mediators of trophic signaling for many neuronal systems. Among the vasoactive intestinal peptide/secretin/glucagon family of related peptides, pituitary adenylate cyclase-activating polypeptide (PACAP) binding to specific PAC1 receptor isoforms can engage multiple signaling pathways and promote neuroprotection through mechanisms that are not well understood. Using a primary sympathetic neuronal system, the current studies demonstrate that PACAP activation of PAC1HOP1 receptors engages both MAPK and Akt neurotrophic pathways in an integrated program to facilitate neuronal survival after growth factor withdrawal. PACAP not only stimulated prosurvival ERK1/2 and ERK5 activation but also abrogated SAPK/JNK and p38 MAPK signaling in parallel. In contrast t...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381947</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381947</guid>        </item>
        <item>
            <title>Tobacco Calcium-dependent Protein Kinases Are Differentially Phosphorylated in Vivo as Part of a Kinase Cascade That Regulates Stress Response [Plant Biology]</title>
            <link>http://www.medworm.com/index.php?rid=3381946&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9740%3Frss%3D1</link>
            <description>In vivo phosphorylation sites of the tobacco calcium-dependent protein kinases NtCDPK2 and NtCDPK3 were determined in response to biotic or abiotic stress. Stress-inducible phosphorylation was exclusively located in the variable N termini, where both kinases were phosphorylated differentially despite 91% overall sequence identity. In NtCDPK2, serine 40 and threonine 65 were phosphorylated within 2 min after stress. Whereas Thr65 is subjected to intra-molecular in vivo autophosphorylation, Ser40 represents a target for a regulatory upstream protein kinase, and correct NtCDPK2 membrane localization is required for Ser40 phosphorylation. NtCDPK3 is phosphorylated at least at two sites in the N terminus by upstream kinase(s) upon stress stimulus, first at Ser54, a site not present in NtCDPK2, ...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381946</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381946</guid>        </item>
        <item>
            <title>Mutation of Actin Tyr-53 Alters the Conformations of the DNase I-binding Loop and the Nucleotide-binding Cleft [Protein Structure and Folding]</title>
            <link>http://www.medworm.com/index.php?rid=3381945&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9729%3Frss%3D1</link>
            <description>All but 11 of the 323 known actin sequences have Tyr at position 53, and the 11 exceptions have the conservative substitution Phe, which raises the following questions. What is the critical role(s) of Tyr-53, and, if it can be replaced by Phe, why has this happened so infrequently? We compared the properties of purified endogenous Dictyostelium actin and mutant constructs with Tyr-53 replaced by Phe, Ala, Glu, Trp, and Leu. The Y53F mutant did not differ significantly from endogenous actin in any of the properties assayed, but the Y53A and Y53E mutants differed substantially; affinity for DNase I was reduced, the rate of nucleotide exchange was increased, the critical concentration for polymerization was increased, filament elongation was inhibited, and polymerized actin was in the form of...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381945</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381945</guid>        </item>
        <item>
            <title>Inhibition of Lung Fluid Clearance and Epithelial Na+ Channels by Chlorine, Hypochlorous Acid, and Chloramines [Membrane Biology]</title>
            <link>http://www.medworm.com/index.php?rid=3381944&amp;cid=d_59_59_f&amp;fid=32070&amp;url=http%3A%2F%2Fwww.jbc.org%2Fcgi%2Fcontent%2Fshort%2F285%2F13%2F9716%3Frss%3D1</link>
            <description>We investigated the mechanisms by which chlorine (Cl2) and its reactive byproducts inhibit Na+-dependent alveolar fluid clearance (AFC) in vivo and the activity of amiloride-sensitive epithelial Na+ channels (ENaC) by measuring AFC in mice exposed to Cl2 (0&amp;ndash;500 ppm for 30 min) and Na+ and amiloride-sensitive currents (INa and Iamil, respectively) across Xenopus oocytes expressing human -, &amp;beta;-, and -ENaC incubated with HOCl (1&amp;ndash;2000 &amp;micro;m). Both Cl2 and HOCl-derived products decreased AFC in mice and whole cell and single channel INa in a dose-dependent manner; these effects were counteracted by serine proteases. Mass spectrometry analysis of the oocyte recording medium identified organic chloramines formed by the interaction of HOCl with HEPES (used as an extracellular bu...</description>
            <author>Journal of Biological Chemistry</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3381944</comments>
            <pubDate>Fri, 19 Mar 2010 13:36:04 +0100</pubDate>
            <guid isPermaLink="false">3381944</guid>        </item>
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