<?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>http://blogs.law.harvard.edu/tech/rss</docs><title>antibodies-online.com | News | Research News</title><category>Research News</category><link>http://www.antibodies-online.com/news/3/Research+News.htm</link><description>Research News</description><language>en</language><copyright>2005-2008 antibodies-online GmbH</copyright><generator>antibodies-online GmbH RSS Feed</generator><webMaster>news@antikoerper-online.de (Alexander Golubowitsch)</webMaster><managingEditor>news@antikoerper-online.de (Tim Hiddemann)</managingEditor><lastBuildDate>Thu, 13 Nov 2008 14:09:00 +0100</lastBuildDate><pubDate>Tue, 02 Dec 2008 08:28:18 +0100</pubDate><ttl>720</ttl><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Thu, 13 Nov 2008 14:09:00 +0100</pubDate><title>Hepatocyte-specific ablation of Foxa2 alters bile acid homeostasis and results in endoplasmic reticulum stress</title><category>Research News</category><description>The winged helix transcription factor &lt;a href=&quot;http://www.antibodies-online.com/antigen/FOXA2+(forkhead+box+A2)+/+HNF3B/&quot;&gt;Foxa2&lt;/a&gt; is required for normal bile acid homeostasis, as a study conducted by Irina M. Bochkis and colleagues from the University of Pennsylvania (USA). The bile production in the liver is essential for the absorption of lipophilic nutrients. If the bile acid homeostasis is disrupted, cholestatic liver disease and endoplasmic reticulum (ER) stress can be the results.</description><link>http://www.antibodies-online.com/news/3/378/Hepatocytespecific+ablation+of+Foxa2+alters+bile+acid+homeostasis+and+results+in+endoplasmic+reticulum+stress.htm</link><guid>http://www.antibodies-online.com/news/3/378/Hepatocytespecific+ablation+of+Foxa2+alters+bile+acid+homeostasis+and+results+in+endoplasmic+reticulum+stress.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Thu, 13 Nov 2008 14:08:00 +0100</pubDate><title>Effective induction of high-titer antibodies by viral vector vaccines</title><category>Research News</category><description>A lab group from the University of Oxford discovered that a recombinant &lt;a href=&quot;http://www.antibodies-online.com/antigen/Adenovirus/&quot;&gt;adenovirus&lt;/a&gt;–poxvirus prime-boost immunisation regime which induces strong &lt;a href=&quot;http://www.antibodies-online.com/antigen/T-cell/&quot;&gt;T-cell&lt;/a&gt; immunogenicity is able to cause fulminant antigen-specific antibody responses. The scientists found a simple, complement-based adjuvant to support immunogenicity even more.</description><link>http://www.antibodies-online.com/news/3/377/Effective+induction+of+hightiter+antibodies+by+viral+vector+vaccines.htm</link><guid>http://www.antibodies-online.com/news/3/377/Effective+induction+of+hightiter+antibodies+by+viral+vector+vaccines.htm</guid></item><item><author>news@antikoerper-online.de (Tim Hiddemann)</author><pubDate>Mon, 03 Nov 2008 22:08:00 +0100</pubDate><title>Y-box-1 protein (Yb-1) and breast cancer: Prognostic factor and target for therapy</title><category>Research News</category><description>A research group at the University of British Columbia (Vancouver) led by Sandy Dunn underlined the potential of &lt;a href=&quot;http://www.antibodies-online.com/antibody/173291/YB1+Human/&quot;&gt;Y-box-1 (YB-1)&lt;/a&gt; for the prognosis and therapy of breast cancer in two recent publications.</description><link>http://www.antibodies-online.com/news/3/374/Ybox1+protein+Yb1+and+breast+cancer+Prognostic+factor+and+target+for+therapy.htm</link><guid>http://www.antibodies-online.com/news/3/374/Ybox1+protein+Yb1+and+breast+cancer+Prognostic+factor+and+target+for+therapy.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Tue, 28 Oct 2008 11:28:00 +0100</pubDate><title>NALP3 inflammasome is involved in the innate immune response to amyloid-beta</title><category>Research News</category><description>The inflammasome of cytoplasmic receptor &lt;a href=&quot;http://www.antibodies-online.com/antigen/NALP3/&quot;&gt;NALP3&lt;/a&gt; was identified by Annett Halle and her colleagues from the  University of Massachusetts (USA) as a sensor of &lt;a href=&quot;http://www.antibodies-online.com/antigen/Amyloid,+beta-/&quot;&gt;amyloid-β&lt;/a&gt; in a process in which &lt;a href=&quot;http://www.antibodies-online.com/antigen/Amyloid,+beta-/&quot;&gt;amyloid-β&lt;/a&gt; is phagocytosed, followed by lysosomal damage and the release of &lt;a href=&quot;http://www.antibodies-online.com/antigen/Cathepsin+B/&quot;&gt;cathepsin B&lt;/a&gt;.</description><link>http://www.antibodies-online.com/news/3/373/NALP3+inflammasome+is+involved+in+the+innate+immune+response+to+amyloidbeta.htm</link><guid>http://www.antibodies-online.com/news/3/373/NALP3+inflammasome+is+involved+in+the+innate+immune+response+to+amyloidbeta.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Tue, 28 Oct 2008 11:23:00 +0100</pubDate><title>Adenovirus Small e1a Alters Global Patterns of Histone Modification</title><category>Research News</category><description>A research team from the University of California recently showed that &lt;a href=&quot;http://www.antibodies-online.com/antibody/187759/Adenovirus+E1A/&quot;&gt;adenovirus small early region 1a&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antibody/187759/Adenovirus+E1A/&quot;&gt;e1a&lt;/a&gt;) protein interaction with &lt;a href=&quot;http://www.antibodies-online.com/antigen/p300/&quot;&gt;p300&lt;/a&gt; and &lt;a href=&quot;http://www.antibodies-online.com/antigen/CREB+Binding+Protein+(CBP)/&quot;&gt;CBP&lt;/a&gt; result in a threefold reduction of total cellular &lt;a href=&quot;http://www.antibodies-online.com/antibody/189410/Histone+H3+Acetyl+K18+body+Human/&quot;&gt;histone H3 lysine 18 acetylation&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antibody/189410/Histone+H3+Acetyl+K18+body+Human/&quot;&gt;H3K18&lt;/a&gt;). &lt;a href=&quot;http://www.antibodies-online.com/antigen/CREB+Binding+Protein+(CBP)/&quot;&gt;CBP&lt;/a&gt; and &lt;a href=&quot;http://www.antibodies-online.com/antigen/p300/&quot;&gt;p300&lt;/a&gt; seem to be essential for the reaction at this position because a specific hypoacetylation occurs at &lt;a href=&quot;http://www.antibodies-online.com/antibody/189410/Histone+H3+Acetyl+K18+body+Human/&quot;&gt;H3K18&lt;/a&gt; upon knockdown of their genes. &lt;a href=&quot;http://www.antibodies-online.com/antigen/SV40+T-antigen/&quot;&gt;The SV40 T antigen&lt;/a&gt; was also observed to trigger &lt;a href=&quot;http://www.antibodies-online.com/antibody/189410/Histone+H3+Acetyl+K18+body+Human/&quot;&gt;H3K18&lt;/a&gt; hypoacetylation.</description><link>http://www.antibodies-online.com/news/3/372/Adenovirus+Small+e1a+Alters+Global+Patterns+of+Histone+Modification.htm</link><guid>http://www.antibodies-online.com/news/3/372/Adenovirus+Small+e1a+Alters+Global+Patterns+of+Histone+Modification.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Tue, 28 Oct 2008 11:21:00 +0100</pubDate><title>Plant Immunity Requires Conformational Charges of NPR1 via S-Nitrosylation and Thioredoxins</title><category>Research News</category><description>&lt;a href=&quot;http://www.antibodies-online.com/antibody/221518/Atrial+Natriuretic+Peptide+Receptor+A+NPR1+Human/&quot;&gt;NPR1&lt;/a&gt; is regulated by the opposing action of  S-nitrosoglutathione and &lt;a href=&quot;http://www.antibodies-online.com/antibody/233997/Trx+Ab+Sampler+Kit+All+Species/&quot;&gt;thioredoxins&lt;/a&gt;, as Yasuomi Tada and colleagues from the Duke University (USA) report.</description><link>http://www.antibodies-online.com/news/3/371/Plant+Immunity+Requires+Conformational+Charges+of+NPR1+via+SNitrosylation+and+Thioredoxins.htm</link><guid>http://www.antibodies-online.com/news/3/371/Plant+Immunity+Requires+Conformational+Charges+of+NPR1+via+SNitrosylation+and+Thioredoxins.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Tue, 28 Oct 2008 11:13:00 +0100</pubDate><title>The Spread of Ras Activity Triggered by Activation of a Single Dendritic Spine</title><category>Research News</category><description>As scientists from the Watson School of Biological Sciences discovered, calcium ion-dependent synaptic signals in neurons can spread to couple multiple synapses on short stretches of dendrites. Individual dendritic spines segregate calcium ion accumulations from the dendrite and other spines. The accumulations were mediated by the &lt;a href=&quot;http://www.antibodies-online.com/antigen/N/4/&quot;&gt;N-methyl-D-aspartate&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antigen/N/4/&quot;&gt;NMDA&lt;/a&gt;) &lt;a href=&quot;http://www.antibodies-online.com/antigen/N/4/&quot;&gt;receptor&lt;/a&gt;.</description><link>http://www.antibodies-online.com/news/3/365/The+Spread+of+Ras+Activity+Triggered+by+Activation+of+a+Single+Dendritic+Spine.htm</link><guid>http://www.antibodies-online.com/news/3/365/The+Spread+of+Ras+Activity+Triggered+by+Activation+of+a+Single+Dendritic+Spine.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Thu, 09 Oct 2008 08:42:00 +0200</pubDate><title>Autophagy Is Essential for Preimplantation Development of Mouse Embryos</title><category>Research News</category><description>Autophagic degradation within early embryos seems to be essential for preimplantation development in mammals. A research group from the Tokyo Medical and Dental University, Japan analysed the degradation of maternal proteins in oocytes upon fertilisation.</description><link>http://www.antibodies-online.com/news/3/364/Autophagy+Is+Essential+for+Preimplantation+Development+of+Mouse+Embryos.htm</link><guid>http://www.antibodies-online.com/news/3/364/Autophagy+Is+Essential+for+Preimplantation+Development+of+Mouse+Embryos.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Thu, 09 Oct 2008 08:40:00 +0200</pubDate><title>Modulation of Gene Expression via Disruption of NF-kappa-B Signaling by a Bacterial Small Molecule</title><category>Research News</category><description>The bacterial N-3-oxo-dodecanoyl homoserine lactone (C12) selectively impairs the regulation of &lt;a href=&quot;http://www.antibodies-online.com/antigen/NF-kB+p65+(Rel+A)/&quot;&gt;NF-κ-B&lt;/a&gt; functions in activated mammalian cells, according to the data of a research group from The Scripps Research Institute (USA). The nuclear &lt;a href=&quot;http://www.antibodies-online.com/research-area/Transcription+Factors/&quot;&gt;transcription factor&lt;/a&gt; &lt;a href=&quot;http://www.antibodies-online.com/antigen/NF-kB+p65+(Rel+A)/&quot;&gt;NF-κ-B&lt;/a&gt; is indispensable for the defence of the body against invading microbial pathogens. Activation of &lt;a href=&quot;http://www.antibodies-online.com/antigen/NF-kB+p65+(Rel+A)/&quot;&gt;NF-κ-B&lt;/a&gt; controls the innate immune response, thus eradicating harmful pathogens.</description><link>http://www.antibodies-online.com/news/3/363/Modulation+of+Gene+Expression+via+Disruption+of+NFkappaB+Signaling+by+a+Bacterial+Small+Molecule.htm</link><guid>http://www.antibodies-online.com/news/3/363/Modulation+of+Gene+Expression+via+Disruption+of+NFkappaB+Signaling+by+a+Bacterial+Small+Molecule.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Thu, 09 Oct 2008 08:37:00 +0200</pubDate><title>Anomalous Type 17 Response to Viral Infection by CD8+ T Cells Lacking T-bet and Eomesodermin</title><category>Research News</category><description>&lt;a href=&quot;http://www.antibodies-online.com/antigen/CD8/&quot;&gt;CD8+ T cells&lt;/a&gt; that have defective &lt;a href=&quot;http://www.antibodies-online.com/research-area/Transcription+Factors/&quot;&gt;transcription factors&lt;/a&gt; &lt;a href=&quot;http://www.antibodies-online.com/antigen/T-bet/&quot;&gt;T-bet&lt;/a&gt; and &lt;a href=&quot;http://www.antibodies-online.com/antigen/eomesodermin+homolog+(Xenopus+laevis)+(EOMES)/&quot;&gt;eomesodermin&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antigen/eomesodermin+homolog+(Xenopus+laevis)+(EOMES)/&quot;&gt;Eomes&lt;/a&gt;) were shown to be unable to defend the body against &lt;a href=&quot;http://www.antibodies-online.com/antigen/LCMV/&quot;&gt;lymphocytic choriomeningitis viral&lt;/a&gt; infection, as a study conducted by the University of Pennsylvania demonstrates.</description><link>http://www.antibodies-online.com/news/3/361/Anomalous+Type+17+Response+to+Viral+Infection+by+CD8+T+Cells+Lacking+Tbet+and+Eomesodermin.htm</link><guid>http://www.antibodies-online.com/news/3/361/Anomalous+Type+17+Response+to+Viral+Infection+by+CD8+T+Cells+Lacking+Tbet+and+Eomesodermin.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Fri, 26 Sep 2008 10:14:00 +0200</pubDate><title>Eco1-Dependent Cohesin Acetylation During Establishment of Sister Chromatid Cohesion</title><category>Research News</category><description>Eco1 modifies &lt;a href=&quot;http://www.antibodies-online.com/antibody/131782/Cohesin+Scc1Rad21/&quot;&gt;cohesin&lt;/a&gt; to stabilise sister chromatid cohesion. This has been observed by scientists from the Cancer Research UK London Research Institute.
Sister chromosomes are bound to each other by chromosomal &lt;a href=&quot;http://www.antibodies-online.com/antibody/131782/Cohesin+Scc1Rad21/&quot;&gt;cohesin&lt;/a&gt; complexes ever since their synthesis in the S phase of mitosis. This is dependent on the acetyl transferase Eco1. Eco1 is associated with the replication fork but its way of function is yet unknown.</description><link>http://www.antibodies-online.com/news/3/360/Eco1Dependent+Cohesin+Acetylation+During+Establishment+of+Sister+Chromatid+Cohesion.htm</link><guid>http://www.antibodies-online.com/news/3/360/Eco1Dependent+Cohesin+Acetylation+During+Establishment+of+Sister+Chromatid+Cohesion.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Fri, 26 Sep 2008 10:11:00 +0200</pubDate><title>Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry</title><category>Research News</category><description>Subject of the study were families in which the parents were blood-related, which stresses the importance of heredity. The scientists analysed loci with large inherited homozygous deletions that were probably mutations. Among the genes affected by those deletions were &lt;a href=&quot;http://www.antibodies-online.com/antibody/172800/protocadherin+10+PCDH10+Human/&quot;&gt;PCDH10&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antibody/172800/protocadherin+10+PCDH10+Human/&quot;&gt;protocadherin 10&lt;/a&gt;) and DIA1 (deleted in autism1, or c3orf58). The expression intensity of these genes changed according to &lt;a href=&quot;http://www.antibodies-online.com/research-area/Neurology/&quot;&gt;neuronal&lt;/a&gt; activity, attributing thus to synaptic changes that underlie learning.
Some other genes, like NHE9 (Na+/H+ exchanger 9), were also observed to carry possible mutations in patients with unrelated parents.</description><link>http://www.antibodies-online.com/news/3/359/Identifying+Autism+Loci+and+Genes+by+Tracing+Recent+Shared+Ancestry.htm</link><guid>http://www.antibodies-online.com/news/3/359/Identifying+Autism+Loci+and+Genes+by+Tracing+Recent+Shared+Ancestry.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Fri, 26 Sep 2008 10:08:00 +0200</pubDate><title>Endothelins are vascular-derived axonal guidance cues for developing sympathetic neurons</title><category>Research News</category><description>Vascular-derived &lt;a href=&quot;http://www.antibodies-online.com/antigen/E/2/&quot;&gt;endothelins&lt;/a&gt; seem to be essential to axonal pathfinding and thus for the developing nervous system.</description><link>http://www.antibodies-online.com/news/3/358/Endothelins+are+vascularderived+axonal+guidance+cues+for+developing+sympathetic+neurons.htm</link><guid>http://www.antibodies-online.com/news/3/358/Endothelins+are+vascularderived+axonal+guidance+cues+for+developing+sympathetic+neurons.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Thu, 11 Sep 2008 14:01:00 +0200</pubDate><title>Transcription factor EBF restricts alternative lineage options and promotes B cell fate commitment independent of Pax5</title><category>Research News</category><description>In the absence of &lt;a href=&quot;http://www.antibodies-online.com/antigen/early+B-cell+factor+(EBF)/&quot;&gt;early B cell factor&lt;/a&gt; (&lt;a href=&quot;http://www.antibodies-online.com/antigen/early+B-cell+factor+(EBF)/&quot;&gt;EBF&lt;/a&gt;), &#039;expandable&#039; and clonal lymphoid progenitor cells seem to retain considerable myeloid potential. &lt;a href=&quot;http://www.antibodies-online.com/antigen/early+B-cell+factor+(EBF)/&quot;&gt;EBF&lt;/a&gt; is assumed to play a part in the lineage restriction and &lt;a href=&quot;http://www.antibodies-online.com/browse/antigen/B+Cell/&quot;&gt;B cell&lt;/a&gt; fate commitment that also require transcription factor &lt;a href=&quot;http://www.antibodies-online.com/antigen/PAX5/&quot;&gt;Pax5&lt;/a&gt;. &lt;a href=&quot;http://www.antibodies-online.com/antigen/early+B-cell+factor+(EBF)/&quot;&gt;EBF&lt;/a&gt; induces &lt;a href=&quot;http://www.antibodies-online.com/antigen/PAX5/&quot;&gt;Pax5&lt;/a&gt; and inhibits the expression of genes encoding for the transcription factors C/EBPalpha, PU.1 and &lt;a href=&quot;http://www.antibodies-online.com/antigen/inhibitor+of+DNA+binding+2,+dominant+negative+helix-loop-helix+protein+(ID2)/&quot;&gt;ID2&lt;/a&gt;.</description><link>http://www.antibodies-online.com/news/3/353/Transcription+factor+EBF+restricts+alternative+lineage+options+and+promotes+B+cell+fate+commitment+independent+of+Pax5.htm</link><guid>http://www.antibodies-online.com/news/3/353/Transcription+factor+EBF+restricts+alternative+lineage+options+and+promotes+B+cell+fate+commitment+independent+of+Pax5.htm</guid></item><item><author>news@antikoerper-online.de (Anna Lena Marwedel)</author><pubDate>Thu, 11 Sep 2008 13:59:00 +0200</pubDate><title>Smad3 and NFAT cooperate to induce Foxp3 expression through its enhancer</title><category>Research News</category><description>Scientists from the University of Pennsylvania generated a model system for analysing &lt;a href=&quot;http://www.antibodies-online.com/antigen/FOXP3/&quot;&gt;Foxp3&lt;/a&gt; induction and identified an enhancer element in this gene when they used their model system with primary &lt;a href=&quot;http://www.antibodies-online.com/browse/antigen/T-cell/&quot;&gt;T-cells&lt;/a&gt;.</description><link>http://www.antibodies-online.com/news/3/352/Smad3+and+NFAT+cooperate+to+induce+Foxp3+expression+through+its+enhancer.htm</link><guid>http://www.antibodies-online.com/news/3/352/Smad3+and+NFAT+cooperate+to+induce+Foxp3+expression+through+its+enhancer.htm</guid></item></channel></rss>