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Heredity of Endothelin Secretion
Author(s) -
Elizabeth O. Lillie,
Manjula Mahata,
Srikrishna Khandrika,
Fangwen Rao,
Richard A. Bundey,
Gen Wen,
Yuqing Chen,
Laurent Taupenot,
Doug W. Smith,
Sushil K. Mahata,
Michael G. Ziegler,
Myles Cockburn,
Nicholas J. Schork,
Daniel T. O’Connor
Publication year - 2007
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.106.648345
Subject(s) - chromogranin a , umbilical vein , haplotype , endocrinology , medicine , allele , single nucleotide polymorphism , phenotype , gene , genetics , microbiology and biotechnology , biology , genotype , in vitro , immunohistochemistry
Endothelial dysfunction predisposes to vascular injury in association with hypertension. Endothelin (ET-1) is a potent vasoactive peptide that is synthesized and released by the vascular endothelium and is a marker of endothelial function. Chromogranin A (CHGA) regulates the storage and release of catecholamines and may have direct actions on the microvasculature. CHGA, a candidate gene for intermediate phenotypes that contribute to hypertension, shows a pattern of single nucleotide polymorphism variations that alter the expression and function of this gene both in vivo and in vitro.

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