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Jennifer Wessel

Showing results (31-40 of 64) with videos related to

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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.
Plos One|September 22, 2017
Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in KenyaTecla M Temu, Kathleen A Lane, Changyu Shen, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|August 26, 2010
Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependenceJennifer Wessel, Sarah M McDonald, David A Hinds, et al.
Hypertension (Dallas, Tex. : 1979)|March 14, 2007
Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphismFangwen Rao, Jennifer Wessel, Gen Wen, et al.
BMC Endocrine Disorders|January 30, 2016
A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humansKatharine R Clapham, Audrey Y Chu, Jennifer Wessel, 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.
The Journal of Pharmacology and Experimental Therapeutics|August 13, 2009
Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairsBrinda K Rana, Jennifer Wessel, Vafa Mahboubi, et al.
Circulation|August 19, 2007
Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivoFangwen Rao, Lian Zhang, Jennifer Wessel, et al.
Annals of the New York Academy of Sciences|January 6, 2009
Adrenergic polymorphism and the human stress responseFangwen Rao, Lian Zhang, Jennifer Wessel, et al.
Journal of Hypertension|January 11, 2007
C-reactive protein, an 'intermediate phenotype' for inflammation: human twin studies reveal heritability, association with blood pressure and the metabolic syndrome, and the influence of common polymorphism at catecholaminergic/beta-adrenergic pathway lociJennifer Wessel, Guillermo Moratorio, Fangwen Rao, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
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.
Plos One|September 22, 2017
Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in KenyaTecla M Temu, Kathleen A Lane, Changyu Shen, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|August 26, 2010
Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependenceJennifer Wessel, Sarah M McDonald, David A Hinds, et al.
Hypertension (Dallas, Tex. : 1979)|March 14, 2007
Renal albumin excretion: twin studies identify influences of heredity, environment, and adrenergic pathway polymorphismFangwen Rao, Jennifer Wessel, Gen Wen, et al.
BMC Endocrine Disorders|January 30, 2016
A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humansKatharine R Clapham, Audrey Y Chu, Jennifer Wessel, 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.
The Journal of Pharmacology and Experimental Therapeutics|August 13, 2009
Natural variation within the neuronal nicotinic acetylcholine receptor cluster on human chromosome 15q24: influence on heritable autonomic traits in twin pairsBrinda K Rana, Jennifer Wessel, Vafa Mahboubi, et al.
Circulation|August 19, 2007
Tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis: discovery of common human genetic variants governing transcription, autonomic activity, and blood pressure in vivoFangwen Rao, Lian Zhang, Jennifer Wessel, et al.
Annals of the New York Academy of Sciences|January 6, 2009
Adrenergic polymorphism and the human stress responseFangwen Rao, Lian Zhang, Jennifer Wessel, et al.
Journal of Hypertension|January 11, 2007
C-reactive protein, an 'intermediate phenotype' for inflammation: human twin studies reveal heritability, association with blood pressure and the metabolic syndrome, and the influence of common polymorphism at catecholaminergic/beta-adrenergic pathway lociJennifer Wessel, Guillermo Moratorio, Fangwen Rao, et al.
Pageof 7