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American Journal of Human Genetics
|
September 14, 2000
Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism
S M Fullerton, A G Clark, K M Weiss, et al.
The Pharmacogenomics Journal
|
February 13, 2013
Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans
J L Del-Aguila, A L Beitelshees, R M Cooper-Dehoff, et al.
Journal of Hypertension
|
February 24, 2001
Linkage of hypertension to chromosome 2q14-q23 in Chinese families
D L Zhu, H Y Wang, M M Xiong, et al.
International Journal of Obesity (2005)
|
October 12, 2011
The association of variants in the FTO gene with longitudinal body mass index profiles in non-Hispanic white children and adolescents
D M Hallman, V C Friedel, M A H Eissa, et al.
Circulation
|
June 17, 1997
Genetic variant showing a positive interaction with beta-blocking agents with a beneficial influence on lipoprotein lipase activity, HDL cholesterol, and triglyceride levels in coronary artery disease patients. The Ser447-stop substitution in the lipoprotein lipase gene. REGRESS Study Group
B E Groenemeijer, M D Hallman, P W Reymer, et al.
Clinical Pharmacology and Therapeutics
|
July 3, 2009
Hydrochlorothiazide and atenolol combination antihypertensive therapy: effects of drug initiation order
J A Johnson, Y Gong, K R Bailey, et al.
The Pharmacogenomics Journal
|
February 22, 2012
Association of chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression
J D Duarte, S T Turner, B Tran, et al.
Clinical Genetics
|
April 29, 1998
The Asn9 variant of lipoprotein lipase is associated with the -93G promoter mutation and an increased risk of coronary artery disease. The Regress Study Group
J J Kastelein, B E Groenemeyer, D M Hallman, et al.
Journal of Internal Medicine
|
March 12, 2014
Hydrochlorothiazide-induced hyperuricaemia in the pharmacogenomic evaluation of antihypertensive responses study
A G Vandell, C W McDonough, Y Gong, et al.
Journal of Thrombosis and Haemostasis : JTH
|
May 19, 2006
Association between patterns of nucleotide variation across the three fibrinogen genes and plasma fibrinogen levels: the Coronary Artery Risk Development in Young Adults (CARDIA) study
A P Reiner, C L Carty, C S Carlson, et al.
Page
of 18
Search research articles
Search
Showing results (151-160 of 174) with videos related to
Sort By:
Page
of 18
American Journal of Human Genetics
|
September 14, 2000
Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism
S M Fullerton, A G Clark, K M Weiss, et al.
The Pharmacogenomics Journal
|
February 13, 2013
Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans
J L Del-Aguila, A L Beitelshees, R M Cooper-Dehoff, et al.
Journal of Hypertension
|
February 24, 2001
Linkage of hypertension to chromosome 2q14-q23 in Chinese families
D L Zhu, H Y Wang, M M Xiong, et al.
International Journal of Obesity (2005)
|
October 12, 2011
The association of variants in the FTO gene with longitudinal body mass index profiles in non-Hispanic white children and adolescents
D M Hallman, V C Friedel, M A H Eissa, et al.
Circulation
|
June 17, 1997
Genetic variant showing a positive interaction with beta-blocking agents with a beneficial influence on lipoprotein lipase activity, HDL cholesterol, and triglyceride levels in coronary artery disease patients. The Ser447-stop substitution in the lipoprotein lipase gene. REGRESS Study Group
B E Groenemeijer, M D Hallman, P W Reymer, et al.
Clinical Pharmacology and Therapeutics
|
July 3, 2009
Hydrochlorothiazide and atenolol combination antihypertensive therapy: effects of drug initiation order
J A Johnson, Y Gong, K R Bailey, et al.
The Pharmacogenomics Journal
|
February 22, 2012
Association of chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression
J D Duarte, S T Turner, B Tran, et al.
Clinical Genetics
|
April 29, 1998
The Asn9 variant of lipoprotein lipase is associated with the -93G promoter mutation and an increased risk of coronary artery disease. The Regress Study Group
J J Kastelein, B E Groenemeyer, D M Hallman, et al.
Journal of Internal Medicine
|
March 12, 2014
Hydrochlorothiazide-induced hyperuricaemia in the pharmacogenomic evaluation of antihypertensive responses study
A G Vandell, C W McDonough, Y Gong, et al.
Journal of Thrombosis and Haemostasis : JTH
|
May 19, 2006
Association between patterns of nucleotide variation across the three fibrinogen genes and plasma fibrinogen levels: the Coronary Artery Risk Development in Young Adults (CARDIA) study
A P Reiner, C L Carty, C S Carlson, et al.
Page
of 18