Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:18818690rdf:typepubmed:Citationlld:pubmed
pubmed-article:18818690lifeskim:mentionsumls-concept:C0025914lld:lifeskim
pubmed-article:18818690lifeskim:mentionsumls-concept:C0026809lld:lifeskim
pubmed-article:18818690lifeskim:mentionsumls-concept:C0812314lld:lifeskim
pubmed-article:18818690lifeskim:mentionsumls-concept:C0229671lld:lifeskim
pubmed-article:18818690lifeskim:mentionsumls-concept:C0020861lld:lifeskim
pubmed-article:18818690lifeskim:mentionsumls-concept:C0205245lld:lifeskim
pubmed-article:18818690lifeskim:mentionsumls-concept:C0441889lld:lifeskim
pubmed-article:18818690lifeskim:mentionsumls-concept:C2587213lld:lifeskim
pubmed-article:18818690lifeskim:mentionsumls-concept:C1332838lld:lifeskim
pubmed-article:18818690lifeskim:mentionsumls-concept:C0240795lld:lifeskim
pubmed-article:18818690pubmed:issue1lld:pubmed
pubmed-article:18818690pubmed:dateCreated2009-1-21lld:pubmed
pubmed-article:18818690pubmed:abstractTextNatural IgM are involved in numerous immunological functions but the genetic factors that control the homeostasis of its secretion and upholding remain unknown. Prompted by the finding that C57BL/6 mice had significantly lower serum levels of IgM when compared with BALB/c mice, we performed a genome-wide screen and found that the level of serum IgM was controlled by a QTL on chromosome 13 reaching the highest level of association at marker D13Mit266 (LOD score=3.54). This locus was named IgMSC1 and covered a region encompassing the interferon-regulatory factor 4 gene (Irf4). The number of splenic mature B cells in C57BL/6 did not differ from BALB/c mice but we found that low serum levels of IgM in C57BL/6 mice correlated with lower frequency of IgM-secreting cells in the spleen and in the peritoneal cavity. These results suggested that C57BL/6 mice have lower efficiency in late B-cell maturation, a process that is highly impaired in Irf4 knockout mice. In fact, we also found reduced Irf4 gene expression in B cells of C57BL/6 mice. Thus, we propose Irf4 as a candidate for the IgMSC1 locus, which controls IgM homeostatic levels at the level of B-cell terminal differentiation.lld:pubmed
pubmed-article:18818690pubmed:languageenglld:pubmed
pubmed-article:18818690pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18818690pubmed:citationSubsetIMlld:pubmed
pubmed-article:18818690pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18818690pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18818690pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18818690pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18818690pubmed:statusMEDLINElld:pubmed
pubmed-article:18818690pubmed:monthJanlld:pubmed
pubmed-article:18818690pubmed:issn1476-5470lld:pubmed
pubmed-article:18818690pubmed:authorpubmed-author:GarciaJJlld:pubmed
pubmed-article:18818690pubmed:authorpubmed-author:CoutinhoAAlld:pubmed
pubmed-article:18818690pubmed:authorpubmed-author:DemengeotJJlld:pubmed
pubmed-article:18818690pubmed:authorpubmed-author:AlmeidaPPlld:pubmed
pubmed-article:18818690pubmed:authorpubmed-author:RodoJJlld:pubmed
pubmed-article:18818690pubmed:authorpubmed-author:Penha-Gonçalv...lld:pubmed
pubmed-article:18818690pubmed:authorpubmed-author:Côrte-RealJJlld:pubmed
pubmed-article:18818690pubmed:issnTypeElectroniclld:pubmed
pubmed-article:18818690pubmed:volume10lld:pubmed
pubmed-article:18818690pubmed:ownerNLMlld:pubmed
pubmed-article:18818690pubmed:authorsCompleteYlld:pubmed
pubmed-article:18818690pubmed:pagination93-9lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:meshHeadingpubmed-meshheading:18818690...lld:pubmed
pubmed-article:18818690pubmed:year2009lld:pubmed
pubmed-article:18818690pubmed:articleTitleIrf4 is a positional and functional candidate gene for the control of serum IgM levels in the mouse.lld:pubmed
pubmed-article:18818690pubmed:affiliationInstituto Gulbenkian de Ciência, Oeiras, Portugal.lld:pubmed
pubmed-article:18818690pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:18818690pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
entrez-gene:16364entrezgene:pubmedpubmed-article:18818690lld:entrezgene
entrez-gene:62816entrezgene:pubmedpubmed-article:18818690lld:entrezgene
http://linkedlifedata.com/r...entrezgene:pubmedpubmed-article:18818690lld:entrezgene