<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/css" href="http://www.antibodies-online.com/rss.css" ?><rss version="2.0"><channel><docs>You are viewing an RSS 2.0 feed. Visit http://blogs.law.harvard.edu/tech/rss to learn more.</docs><title>antibodies-online.com | News</title><category>New Antibodies</category><category>Research News</category><category>About antibodies-online.com</category><link>http://www.antibodies-online.com/news/0/All+Entries.htm</link><description>All Entries</description><language>en</language><copyright>2005-2008 antibodies-online GmbH</copyright><generator>antibodies-online GmbH RSS Feed</generator><webMaster>Alexander Golubowitsch &lt;news@antikoerper-online.de&gt;</webMaster><managingEditor>Tim Hiddemann &lt;news@antikoerper-online.de&gt;</managingEditor><lastBuildDate>Thu, 17 Jul 2008 12:05:00 +0200</lastBuildDate><pubDate>Thu, 24 Jul 2008 19:19:44 +0200</pubDate><ttl>720</ttl><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Thu, 17 Jul 2008 12:05:00 +0200</pubDate><title>New possibilities for manipulating Notch signalling</title><category>Research News</category><description>The &lt;a href=&quot;http://www.antibodies-online.com/antigen/N/4/&quot;&gt;Notch pathway&lt;/a&gt; is responsible for the correct development of many tissues and cell types. Recent findings link mutations and/or abnormal signalling of &lt;a href=&quot;http://www.antibodies-online.com/antigen/N/4/&quot;&gt;Notch receptors&lt;/a&gt; with the onset of human diseases. Therefore, the &lt;a href=&quot;http://www.antibodies-online.com/antigen/N/4/&quot;&gt;Notch pathway&lt;/a&gt; is a promising therapeutic target. Unfortunately, until recently, there have been no specific inhibitors and/or agonists for human Notch receptors (&lt;a href=&quot;http://www.antibodies-online.com/antigen/N/4/&quot;&gt;NOTCH1-4&lt;/a&gt;), leaving the potential unexplored.</description><link>http://www.antibodies-online.com/news/3/336/New+possibilities+for+manipulating+Notch+signalling.htm</link><guid>http://www.antibodies-online.com/news/3/336/New+possibilities+for+manipulating+Notch+signalling.htm</guid></item><item><author>Tim Hiddemann &lt;news@antikoerper-online.de&gt;</author><pubDate>Thu, 17 Jul 2008 11:56:00 +0200</pubDate><title>New supplier: Biovision</title><category>New Antibodies</category><description>&lt;a href=&quot;http://www.antibodies-online.com/supplier/Biovision/&quot;&gt;Biovision antibodies&lt;/a&gt; are now listed at antibodies-online.com. &lt;a href=&quot;http://www.antibodies-online.com/supplier/Biovision/&quot;&gt;»Show Biovision antibodies&lt;/a&gt;</description><guid>http://www.antibodies-online.com/news/2/340/New+supplier+Biovision.htm</guid></item><item><author>Tim Hiddemann &lt;news@antikoerper-online.de&gt;</author><pubDate>Thu, 17 Jul 2008 11:52:00 +0200</pubDate><title>New supplier: Lifespan antibodies at antibodies-online.com</title><category>New Antibodies</category><description>More than 34.000 &lt;a href=&quot;http://www.antibodies-online.com/supplier/Lifespan/&quot;&gt;Lifespan antibodies&lt;/a&gt; are now available at antibodies-online.com. &lt;a href=&quot;http://www.antibodies-online.com/supplier/Lifespan/&quot;&gt;»Show Lifespan-antibodies&lt;/a&gt;</description><guid>http://www.antibodies-online.com/news/2/339/New+supplier+Lifespan+antibodies+at+antibodiesonlinecom.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Tue, 01 Jul 2008 18:03:00 +0200</pubDate><title>Nutritional Control of Reproductive Status in Honeybees via DNA Methylation</title><category>Research News</category><description>Silencing the expression of DNA methyltransferase &lt;a href=&quot;http://www.antibodies-online.com/antigen/D/4/&quot;&gt;Dnmt3&lt;/a&gt; in newly hatched Apis larvae leads to a royal jelly-like effect on larva development. According to scientists from the Australian National University, the majority of larvae treated with &lt;a href=&quot;http://www.antibodies-online.com/antigen/D/4/&quot;&gt;Dnmt3&lt;/a&gt; siRNA grew up to be queens with fully developed ovaries. </description><link>http://www.antibodies-online.com/news/3/333/Nutritional+Control+of+Reproductive+Status+in+Honeybees+via+DNA+Methylation.htm</link><guid>http://www.antibodies-online.com/news/3/333/Nutritional+Control+of+Reproductive+Status+in+Honeybees+via+DNA+Methylation.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Tue, 01 Jul 2008 17:59:00 +0200</pubDate><title>Listeriolysin O allows Listeria monocytogenes replication in macrophage vacuoles</title><category>Research News</category><description>A recent study revealed that &lt;a href=&quot;http://www.antibodies-online.com/antigen/Listeria+monocytogenes/&quot;&gt;&lt;em&gt;Listeria monocytogenes&lt;/em&gt;&lt;/a&gt; can replicate in the vacuoles within &lt;a href=&quot;http://www.antibodies-online.com/antigen/Macrophages/&quot;&gt;macrophages&lt;/a&gt;. Cheryl L. Birmingham and her team from the University of Toronto in Canada observed the localisation of bacteria in large &lt;a href=&quot;http://www.antibodies-online.com/antigen/LAMP1/&quot;&gt;LAMP1+&lt;/a&gt; compartments that they denoted spacious Listeria-containing phagosomes (SLAPs). The SLAPs could also be seen &lt;em&gt;in vitro&lt;/em&gt;. They turned out to be non-acidic and non-degradative compartments that are generated in an autophagy-dependent manner.</description><link>http://www.antibodies-online.com/news/3/332/Listeriolysin+O+allows+Listeria+monocytogenes+replication+in+macrophage+vacuoles.htm</link><guid>http://www.antibodies-online.com/news/3/332/Listeriolysin+O+allows+Listeria+monocytogenes+replication+in+macrophage+vacuoles.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Tue, 01 Jul 2008 17:55:00 +0200</pubDate><title>Neurokinin 1 Receptor Antagonism as a Possible Therapy for Alcoholism</title><category>Research News</category><description>A lab group from the National Institutes of Health (USA) investigated the role of &lt;a href=&quot;http://www.antibodies-online.com/antigen/Neurokinin-1+Receptor+(NK1R)/&quot;&gt;neurokinin 1 receptor&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antigen/Neurokinin-1+Receptor+(NK1R)/&quot;&gt;NK1R&lt;/a&gt;) in alcohol dependence and treatment. &lt;a href=&quot;http://www.antibodies-online.com/antigen/Neurokinin-1+Receptor+(NK1R)/&quot;&gt;NK1R&lt;/a&gt; is a mediator of behavioural stress responses and the stress system of the brain and is an important factor for continued alcohol (ab)use and relapse.</description><link>http://www.antibodies-online.com/news/3/331/Neurokinin+1+Receptor+Antagonism+as+a+Possible+Therapy+for+Alcoholism.htm</link><guid>http://www.antibodies-online.com/news/3/331/Neurokinin+1+Receptor+Antagonism+as+a+Possible+Therapy+for+Alcoholism.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Tue, 01 Jul 2008 17:44:00 +0200</pubDate><title>Endogenous human microRNAs that suppress breast cancer metastasis</title><category>Research News</category><description>A set of microRNAs were discovered to be general regulators of cancer metastasis. Scientist from the Memorial Sloan-Kettering Cancer Center in New York (USA) now demonstrated, how restoring the expression of these microRNAs in malignant cells can suppress lung and bone metastasisation of human cancer cells &lt;em&gt;in vivo&lt;/em&gt;.</description><link>http://www.antibodies-online.com/news/3/329/Endogenous+human+microRNAs+that+suppress+breast+cancer+metastasis.htm</link><guid>http://www.antibodies-online.com/news/3/329/Endogenous+human+microRNAs+that+suppress+breast+cancer+metastasis.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Tue, 01 Jul 2008 17:40:00 +0200</pubDate><title>Reprogramming of human somatic cells to pluripotency with defined factors</title><category>Research News</category><description>In a recently published study, murine &lt;a href=&quot;http://www.antibodies-online.com/antigen/Fibroblast/&quot;&gt;fibroblasts&lt;/a&gt; were reprogrammed directly to pluripotency by ectopic expression of the transcription factors &lt;a href=&quot;http://www.antibodies-online.com/antibody/131129/Oct4/&quot;&gt;Oct4&lt;/a&gt;, &lt;a href=&quot;http://www.antibodies-online.com/antigen/SOX2/&quot;&gt;Sox2&lt;/a&gt;, &lt;a href=&quot;http://www.antibodies-online.com/antibody/183209/KLF4+Human/&quot;&gt;Klf4&lt;/a&gt; and &lt;a href=&quot;http://www.antibodies-online.com/antigen/Myc+Tag/&quot;&gt;Myc&lt;/a&gt;. </description><link>http://www.antibodies-online.com/news/3/328/Reprogramming+of+human+somatic+cells+to+pluripotency+with+defined+factors.htm</link><guid>http://www.antibodies-online.com/news/3/328/Reprogramming+of+human+somatic+cells+to+pluripotency+with+defined+factors.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Wed, 11 Jun 2008 21:01:00 +0200</pubDate><title>Defective tryptophan catabolism underlies inflammation in chronic granulomatous disease of mice</title><category>Research News</category><description>Chronic granulomatous disease (CGD) is an inherited disease, fatally impairing children&#039;s ability to survive infections. The cause is a lack of NADPH oxidase activity in the phagocytes that can not generate reactive oxygen species, most notably superoxide anion. Recurring bacterial and fungal infections are the consequences. Patients with CGD also suffer from chronic inflammatory conditions, most prominently granuloma formation in hollow viscera.</description><link>http://www.antibodies-online.com/news/3/327/Defective+tryptophan+catabolism+underlies+inflammation+in+chronic+granulomatous+disease+of+mice.htm</link><guid>http://www.antibodies-online.com/news/3/327/Defective+tryptophan+catabolism+underlies+inflammation+in+chronic+granulomatous+disease+of+mice.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Wed, 11 Jun 2008 20:59:00 +0200</pubDate><title>Association of Systemic Lupus Erythematosus with C8orf13-BLK and ITGAM-ITGAX</title><category>Research News</category><description>Two novel genetic loci associated with risk for systemic &lt;em&gt;lupus erythematosus&lt;/em&gt; were found by scientists of the company Genentech. One locus turned out to encode for a promoter-region allele associated with weaker expression of &lt;a href=&quot;http://www.antibodies-online.com/antigen/B+lymphoid+tyrosine+kinase+(BLK)/&quot;&gt;B lymphoid tyrosine kinase&lt;/a&gt; and stronger expression of C8orf13 (chromosome 8p23.1). Individuals carrying the risk allele also displayed altered levels of messenger RNA in their &lt;a href=&quot;http://www.antibodies-online.com/browse/antigen/B+Cell/&quot;&gt;B-cell&lt;/a&gt; lines. The second locus is on chromosome 16p11.22, close to the gene loci encoding for &lt;a href=&quot;http://www.antibodies-online.com/antigen/Integrin+alpha+M/&quot;&gt;integrin alpha M&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antigen/Integrin+alpha+M/&quot;&gt;ITGAM&lt;/a&gt;, or CD11b) and &lt;a href=&quot;http://www.antibodies-online.com/antigen/Integrin+alpha+X/&quot;&gt;integrin alpha X&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antigen/Integrin+alpha+X/&quot;&gt;ITGAX&lt;/a&gt;). </description><link>http://www.antibodies-online.com/news/3/326/Association+of+Systemic+Lupus+Erythematosus+with+C8orf13BLK+and+ITGAMITGAX.htm</link><guid>http://www.antibodies-online.com/news/3/326/Association+of+Systemic+Lupus+Erythematosus+with+C8orf13BLK+and+ITGAMITGAX.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Wed, 11 Jun 2008 20:55:00 +0200</pubDate><title>A Shared Docking Motif in TRF1 and TRF2 Used for Differential Recruitment of Telomeric Proteins</title><category>Research News</category><description>The binding of &lt;a href=&quot;http://www.antibodies-online.com/antigen/TRF1/&quot;&gt;TRF1&lt;/a&gt; and &lt;a href=&quot;http://www.antibodies-online.com/antigen/TRF2/&quot;&gt;TRF2&lt;/a&gt; to their shared binding partner &lt;a href=&quot;http://www.antibodies-online.com/antigen/Tin2/&quot;&gt;TIN2&lt;/a&gt; and other shelterin accessory factors takes place in two different ways. &lt;a href=&quot;http://www.antibodies-online.com/antigen/TRF1/&quot;&gt;TRF1&lt;/a&gt; binds to &lt;a href=&quot;http://www.antibodies-online.com/antigen/Tin2/&quot;&gt;TIN2&lt;/a&gt; through its TRF homology (TRFH) domain, which is also used for binding with shelterin-associated factor &lt;a href=&quot;http://www.antibodies-online.com/antigen/PINX1/&quot;&gt;PinX1&lt;/a&gt;. The &lt;a href=&quot;http://www.antibodies-online.com/antigen/Tin2/&quot;&gt;TIN2&lt;/a&gt; binding site of &lt;a href=&quot;http://www.antibodies-online.com/antigen/TRF2/&quot;&gt;TRF2&lt;/a&gt; lies outside the TRFH domain. Instead, the TRFH domain functions as docking site for shelterin accessory factor &lt;a href=&quot;http://www.antibodies-online.com/antigen/baculoviral+IAP+repeat-containing+6+%28apollon%29+%28BIRC6%29&quot;&gt;Apollo&lt;/a&gt;. Interestingly, &lt;a href=&quot;http://www.antibodies-online.com/antigen/baculoviral+IAP+repeat-containing+6+%28apollon%29+%28BIRC6%29&quot;&gt;Apollo&lt;/a&gt; and the &lt;a href=&quot;http://www.antibodies-online.com/antigen/TRF1/&quot;&gt;TRF1&lt;/a&gt; TRFH domain do not interact.&lt;/p&gt;
</description><link>http://www.antibodies-online.com/news/3/322/A+Shared+Docking+Motif+in+TRF1+and+TRF2+Used+for+Differential+Recruitment+of+Telomeric+Proteins.htm</link><guid>http://www.antibodies-online.com/news/3/322/A+Shared+Docking+Motif+in+TRF1+and+TRF2+Used+for+Differential+Recruitment+of+Telomeric+Proteins.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Wed, 11 Jun 2008 20:47:00 +0200</pubDate><title>Spine-Type-Specific Recruitment of Newly Synthesized AMPA Receptors with Learning</title><category>Research News</category><description>Learning-associated newly synthesized &lt;a href=&quot;http://www.antibodies-online.com/antigen/Glutamate+Receptor+1+(GluR1)/&quot;&gt;GluR1&lt;/a&gt; were selectively recruited to mushroom-type spines in adult hippocampal CA1 neurons 24 hours after fear conditioning, as the study conducted by the Institute for Childhood and Neglected Diseases demonstrates.&lt;br&gt;
The scientists analysed the dynamics of newly synthesized &lt;a href=&quot;http://www.antibodies-online.com/antigen/glutamate+receptor,+ionotropic,+AMPA+1+(GRIA1)/&quot;&gt;AMPA-type glutamate receptors&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antigen/glutamate+receptor,+ionotropic,+AMPA+1+(GRIA1)/&quot;&gt;AMPARs&lt;/a&gt;) in regard to learning. For this task they used transgenic mice expressing the &lt;a href=&quot;http://www.antibodies-online.com/antigen/Glutamate+Receptor+1+(GluR1)/&quot;&gt;GluR1&lt;/a&gt; subunit fused to &lt;a href=&quot;http://www.antibodies-online.com/antigen/GFP/&quot;&gt;green fluorescent protein&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antigen/GFP/&quot;&gt;GFP&lt;/a&gt;-&lt;a href=&quot;http://www.antibodies-online.com/antigen/Glutamate+Receptor+1+(GluR1)/&quot;&gt;GluR1&lt;/a&gt;). The fusion protein was under the control of the &lt;a href=&quot;http://www.antibodies-online.com/antigen/c-Fos/&quot;&gt;c-fos&lt;/a&gt; promoter.&lt;/p&gt;</description><link>http://www.antibodies-online.com/news/3/321/SpineTypeSpecific+Recruitment+of+Newly+Synthesized+AMPA+Receptors+with+Learning.htm</link><guid>http://www.antibodies-online.com/news/3/321/SpineTypeSpecific+Recruitment+of+Newly+Synthesized+AMPA+Receptors+with+Learning.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Wed, 11 Jun 2008 20:42:00 +0200</pubDate><title>Semaphorin and neuropilin co-expression in motoneuronssets axon sensitivity to environmental semaphorin sources during motor axon pathfinding</title><category>Research News</category><description>Overexpression of &lt;a href=&quot;http://www.antibodies-online.com/antigen/sema+domain,+immunoglobulin+domain+(Ig),+short+basic+domain,+secreted,+(semaphorin)+3A+(SEMA3A)/&quot;&gt;Semaphorin 3A&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antigen/sema+domain,+immunoglobulin+domain+(Ig),+short+basic+domain,+secreted,+(semaphorin)+3A+(SEMA3A)/&quot;&gt;Sema3A&lt;/a&gt;) causes defasciculation and excessive growth of motor axons into normally non-permissive territories, as a study conducted by scientist from the University of Lyon in France concludes. They also state that motoneuronal &lt;a href=&quot;http://www.antibodies-online.com/antigen/sema+domain,+immunoglobulin+domain+(Ig),+short+basic+domain,+secreted,+(semaphorin)+3A+(SEMA3A)/&quot;&gt;Sema3A&lt;/a&gt; is required for correct spinal nerve compaction and dorsal motor axon extension.</description><link>http://www.antibodies-online.com/news/3/330/Semaphorin+and+neuropilin+coexpression+in+motoneuronssets+axon+sensitivity+to+environmental+semaphorin+sources+during+motor+axon+pathfinding.htm</link><guid>http://www.antibodies-online.com/news/3/330/Semaphorin+and+neuropilin+coexpression+in+motoneuronssets+axon+sensitivity+to+environmental+semaphorin+sources+during+motor+axon+pathfinding.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Tue, 20 May 2008 17:18:00 +0200</pubDate><title>Hepatitis E Virus and Chronic Hepatitis in Organ Transplant Recipients</title><category>Research News</category><description>Scientists of the Centre Hospitalier Universitaire in Toulouse (France) identified 14 cases of acute &lt;a href=&quot;http://www.antibodies-online.com/antigen/Hepatitis+E+Virus/&quot;&gt;hepatitis E&lt;/a&gt; infections in patients with either liver transplants, kidney transplants or kidney and pancreas transplants.</description><link>http://www.antibodies-online.com/news/3/324/Hepatitis+E+Virus+and+Chronic+Hepatitis+in+Organ+Transplant+Recipients.htm</link><guid>http://www.antibodies-online.com/news/3/324/Hepatitis+E+Virus+and+Chronic+Hepatitis+in+Organ+Transplant+Recipients.htm</guid></item><item><author>Anna Lena Marwedel &lt;news@antikoerper-online.de&gt;</author><pubDate>Tue, 20 May 2008 17:16:00 +0200</pubDate><title>Hepatic Glucose Sensing via the CREB Coactivator CRTC2</title><category>Research News</category><description>A study conducted by the Salk Institute for Biological Studies recently showed that O-glycosyl transferase triggers hepatic gluconeogenesis through the O-glycosylation of the transducer of regulated &lt;a href=&quot;http://www.antibodies-online.com/antigen/CREB/&quot;&gt;CREB&lt;/a&gt; 2 (&lt;a href=&quot;http://www.antibodies-online.com/antigen/CREB/&quot;&gt;cAMP response element-binding protein&lt;/a&gt;, also called &lt;a href=&quot;http://www.antibodies-online.com/antigen/TORC2&quot;&gt;TORC2&lt;/a&gt; or &lt;a href=&quot;http://www.antibodies-online.com/antigen/CREB+regulated+transcription+coactivator+2+%28CRTC2%29&quot;&gt;CRTC2&lt;/a&gt;).</description><link>http://www.antibodies-online.com/news/3/323/Hepatic+Glucose+Sensing+via+the+CREB+Coactivator+CRTC2.htm</link><guid>http://www.antibodies-online.com/news/3/323/Hepatic+Glucose+Sensing+via+the+CREB+Coactivator+CRTC2.htm</guid></item></channel></rss>