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Human Molecular Genetics|June 23, 2007
An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertensionGen Wen, Jennifer Wessel, Weidong Zhou, et al.BMC Medical Genetics|March 13, 2016
Polymorphisms at the F12 and KLKB1 loci have significant trait association with activation of the renin-angiotensin systemNilima Biswas, Adam X Maihofer, Saiful Anam Mir, et al.Journal of Hypertension|August 9, 2012
Genes and environment: novel, functional polymorphism in the human cathepsin L (CTSL1) promoter disrupts a xenobiotic response element (XRE) to alter transcription and blood pressureNzali Mbewe-Campbell, Zhiyun Wei, Kuixing Zhang, et al.Diabetes, Obesity & Metabolism|October 10, 2006
Catecholamine storage vesicles and the metabolic syndrome: The role of the chromogranin A fragment pancreastatinKuixing Zhang, Fangwen Rao, Gen Wen, et al.American Journal of Hypertension|September 16, 2011
Genetic variation within a metabolic motif in the chromogranin a promoter: pleiotropic influence on cardiometabolic risk traits in twinsFangwen Rao, Stephane Chiron, Zhiyun Wei, et al.The Journal of Clinical Endocrinology and Metabolism|June 16, 2005
Pancreastatin: multiple actions on human intermediary metabolism in vivo, variation in disease, and naturally occurring functional genetic polymorphismDaniel T O'Connor, Peter E Cadman, Clayton Smiley, et al.American Journal of Nephrology|May 21, 2010
Progression of chronic kidney disease: Adrenergic genetic influence on glomerular filtration rate decline in hypertensive nephrosclerosisYuqing Chen, Michael S Lipkowitz, Rany M Salem, et al.Journal of Hypertension|December 17, 2009
Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressureYuqing Chen, Gen Wen, Fangwen Rao, et al.Plos One|January 7, 2014
Heritable influence of DBH on adrenergic and renal function: twin and disease studiesDalal N Pasha, Jason T Davis, Fangwen Rao, et al.The Journal of Clinical Investigation|August 25, 2007
Discovery of common human genetic variants of GTP cyclohydrolase 1 (GCH1) governing nitric oxide, autonomic activity, and cardiovascular riskLian Zhang, Fangwen Rao, Kuixing Zhang, et al.Pageof 7