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10.1096/fj.10-161612

http://scihub22266oqcxt.onion/10.1096/fj.10-161612
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20837776!3005421!20837776
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suck abstract from ncbi


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pmid20837776      FASEB+J 2011 ; 25 (1): 16-28
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  • Endothelin-1 gene regulation #MMPMID20837776
  • Stow LR; Jacobs ME; Wingo CS; Cain BD
  • FASEB J 2011[Jan]; 25 (1): 16-28 PMID20837776show ga
  • Over two decades of research have demonstrated that the peptide hormone endothelin-1 (ET-1) plays multiple, complex roles in cardiovascular, neural, pulmonary, reproductive, and renal physiology. Differential and tissue-specific production of ET-1 must be tightly regulated in order to preserve these biologically diverse actions. The primary mechanism thought to control ET-1 bioavailability is the rate of transcription from the ET-1 gene (edn1). Studies conducted on a variety of cell types have identified key transcription factors that govern edn1 expression. With few exceptions, the cis-acting elements bound by these factors have been mapped in the edn1 regulatory region. Recent evidence has revealed new roles for some factors originally believed to regulate edn1 in a tissue or hormone-specific manner. In addition, other mechanisms involved in epigenetic regulation and mRNA stability have emerged as important processes for regulated edn1 expression. The goal of this review is to provide a comprehensive overview of the specific factors and signaling systems that govern edn1 activity at the molecular level.
  • |*Gene Expression Regulation[MESH]
  • |Animals[MESH]
  • |Binding Sites/genetics[MESH]
  • |Endothelin-1/*genetics[MESH]
  • |Epigenomics[MESH]
  • |Humans[MESH]
  • |Protein Binding[MESH]
  • |RNA Stability[MESH]
  • |Regulatory Sequences, Nucleic Acid/*genetics[MESH]


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