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http://purl.uniprot.org/citations/28085150http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28085150http://www.w3.org/2000/01/rdf-schema#comment"The pro-survival proteins of the BCL-2 family regulate the survival of all cells, and genetic deletion models for these proteins have revealed which specific BCL-2 family member(s) is/are critical for the survival of particular cell types. A1 is a pro-survival BCL-2-like protein that is expressed predominantly in haematopoietic cells, and here we describe the characterisation of a novel mouse strain that lacks all three functional isoforms of A1 (A1-a, A1-b and A1-d). Surprisingly, complete loss of A1 caused only minor defects, with significant, although relatively small, decreases in γδTCR T cells, antigen-experienced conventional as well as regulatory CD4 T cells and conventional dendritic cells (cDCs). When examining these cell types in tissue culture, only cDC survival was significantly impaired by the loss of A1. Therefore, A1 appears to be a surprisingly redundant pro-survival protein in the haematopoietic system and other tissues, suggesting that its targeting in cancer may be readily tolerated."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.org/dc/terms/identifier"doi:10.1038/cdd.2016.156"xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Zhan Y."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Lew A.M."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Tai L."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Strasser A."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Villunger A."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Herold M.J."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Teh C.E."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Gray D.H."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Heinzel S."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Carrington E.M."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Tuzlak S."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/author"Schenk R.L."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/name"Cell Death Differ"xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/pages"534-545"xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/title"Characterisation of mice lacking all functional isoforms of the pro-survival BCL-2 family member A1 reveals minor defects in the haematopoietic compartment."xsd:string
http://purl.uniprot.org/citations/28085150http://purl.uniprot.org/core/volume"24"xsd:string
http://purl.uniprot.org/citations/28085150http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/28085150
http://purl.uniprot.org/citations/28085150http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/28085150
http://purl.uniprot.org/uniprot/#_O55177-mappedCitation-28085150http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28085150
http://purl.uniprot.org/uniprot/#_O55179-mappedCitation-28085150http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28085150
http://purl.uniprot.org/uniprot/#_Q07440-mappedCitation-28085150http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/28085150