منابع مشابه
BCL 2 L 11 ( BCL 2 - like 11 ( apoptosis facilitator ) )
Other names: BAM, BIM, BIM-alpha6, BIM-beta6, BIM-beta7, BOD, BimEL, BimL HGNC (Hugo): BCL2L11 Location: 2q13 Local order: According to GeneLoc and NCBI Map Viewer, genes flanking BCL2L11 in plus strand direction are: ACOXL 2q13 (acyl-Coenzyme A oxidase-like); PAFAH1P2 2q13 (platelet-activating factor acetylhydrolase, isoform Ib, pseudogene 2). Note: BCL2L11/BIM is a BH3-only protein from the B...
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Two major pathways for induction of apoptosis have been identified-intrinsic and extrinsic. The extrinsic pathway is represented by tumor necrosis factor family receptors, which utilize protein interaction modules known as death domains and death effector domains (DEDs) to assemble receptor signaling complexes that recruit and activate certain caspase-family cell death proteases, namely procasp...
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(Igaki et al., 2000) unveils the long anticipated, missing piece of the apoptosome in flies. On page 703 in this issue, in a paper by Colussi et al., Ku-mur, Richardson, and colleagues characterize the first Drosophila members of the Bcl-2 gene family whose function is important for programmed cell death (PCD). The founding member of this gene family was identified as the proto-oncogene upregul...
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The bcl-2 gene provides a window on the basic cellular machinery of apoptosis or programmed cell death, a process involved in virtually all biologic events in multicellular organisms, but particularly relevant to neoplasia and development. bcl-2 gene function supports cell survival and appears to lie at a nodal point in pathways leading to activation or execution of apoptosis. Carcinogenesis ma...
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Bcl-2 family proteins are key intracellular regulators of programmed cell death. Several recent discoveries demonstrate how these proteins interact with the molecular machinery that controls and executes the cell-death programme, and how they can themselves be regulated by extracellular survival signals.
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ژورنال
عنوان ژورنال: Papers on Anthropology
سال: 2013
ISSN: 1736-7646,1406-0140
DOI: 10.12697/poa.2013.22.07