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dc.creatorHART,STEPHEN M
dc.date2002-01-01
dc.date.accessioned2019-11-14T12:54:29Z
dc.date.available2019-11-14T12:54:29Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0716-97602002000200021
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/116600
dc.descriptionNuclear receptors comprise a family of transcription factors that regulate gene expression in a ligand dependent manner. They can activate or repress target genes by binding directly to DNA response elements as homo- or hetero-dimers or by binding to other classes of DNA-bound transcription factors. These activities have been linked to the formation of complexes with molecules that appear to serve as coactivators or corepressors, causing local modification of chromatin structure in order to regulate expression of their target genes. Several members of nuclear receptor family are directly associated with human malignancies including breast cancer, prostate cancer and leukaemia. The pathogenesis of each of these diseases is underpinned by the activities of a member of the superfamily; estrogen receptor-a (ERa) in breast cancer, androgen receptor (AR) in prostate cancer, and retinoic acid receptor a (RARa) in acute promyelocytic leukaemia
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dc.languageen
dc.publisherSociedad de Biología de Chile
dc.relation10.4067/S0716-97602002000200021
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceBiological Research v.35 n.2 2002
dc.titleModulation of nuclear receptor dependent transcription


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