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Transcriptional repression by nuclear hormone receptors

期刊

TRENDS IN ENDOCRINOLOGY AND METABOLISM
卷 11, 期 1, 页码 6-10

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ELSEVIER SCIENCE LONDON
DOI: 10.1016/S1043-2760(99)00215-5

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资金

  1. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R37DK043806, R01DK043806, R01DK045586] Funding Source: NIH RePORTER
  2. NIDDK NIH HHS [DK43806, DK45586] Funding Source: Medline

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Repression by nuclear receptor plays important roles in a cute promyelocytic leukemia and other diseases. nuclear receptor corepressor (N-CoR) and SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) are corepressor proteins whose modular structure facilitates receptor interaction as well as translation of repression signals involving histone deacetylation, alterations in chromatin structure and direct interactions with the basal transcription machinery. Interactions between nuclear receptors and corepressor complexes have multiple determinants. This allows regulation, and potentially therapeutic manipulation, of receptor, corepressor, cell-type and target-gene specificity.

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