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Circulation. Cardiovascular genetics

Showing results (371-380 of 961) with videos related to

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Circulation. Cardiovascular Genetics|February 4, 2010
Chylomicronemia with low postheparin lipoprotein lipase levels in the setting of GPIHBP1 defectsRemco Franssen, Stephen G Young, Frank Peelman, et al.
Circulation. Cardiovascular Genetics|February 4, 2010
Human tyrosine hydroxylase natural genetic variation: delineation of functional transcriptional control motifs disrupted in the proximal promoterKuixing Zhang, Lian Zhang, Fangwen Rao, et al.
Circulation. Cardiovascular Genetics|September 15, 2009
Genome-wide association studies for atherosclerotic vascular disease and its risk factorsKeyue Ding, Iftikhar J Kullo
Circulation. Cardiovascular Genetics|September 1, 2009
Quantitative trait locus analysis of neointimal formation in an intercross between C57BL/6 and C3H/HeJ apolipoprotein E-deficient miceZuobiao Yuan, Hong Pei, Drew J Roberts, et al.
Circulation. Cardiovascular Genetics|August 24, 2010
Novel nonmajor histocompatibility complex-linked loci from mouse chromosome 17 confer susceptibility to viral-mediated chronic autoimmune myocarditisMaya C Poffenberger, Iryna Shanina, Connie Aw, et al.
Circulation. Cardiovascular Genetics|June 17, 2010
Albuminuria risk in Hispanic populations: not so black and whitePaul E Drawz, Jeffrey R Schelling
Circulation. Cardiovascular Genetics|June 17, 2010
GWAS applied to heart failure: bigger will be better...eventuallyDennis M McNamara, Barry London
Circulation. Cardiovascular Genetics|September 2, 2011
Venous thromboembolism does not share strong familial susceptibility with ischemic stroke: a nationwide family study in SwedenBengt Zöller, Xinjun Li, Henrik Ohlsson, et al.
Circulation. Cardiovascular Genetics|September 2, 2011
Protein interaction-based genome-wide analysis of incident coronary heart diseaseMajken K Jensen, Tune H Pers, Piotr Dworzynski, et al.
Circulation. Cardiovascular Genetics|August 12, 2011
Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutationAlon Barsheshet, Arthur J Moss, Scott McNitt, et al.
Pageof 97

Showing results (371-380 of 961) with videos related to

Sort By:
Pageof 97
Circulation. Cardiovascular Genetics|February 4, 2010
Chylomicronemia with low postheparin lipoprotein lipase levels in the setting of GPIHBP1 defectsRemco Franssen, Stephen G Young, Frank Peelman, et al.
Circulation. Cardiovascular Genetics|February 4, 2010
Human tyrosine hydroxylase natural genetic variation: delineation of functional transcriptional control motifs disrupted in the proximal promoterKuixing Zhang, Lian Zhang, Fangwen Rao, et al.
Circulation. Cardiovascular Genetics|September 15, 2009
Genome-wide association studies for atherosclerotic vascular disease and its risk factorsKeyue Ding, Iftikhar J Kullo
Circulation. Cardiovascular Genetics|September 1, 2009
Quantitative trait locus analysis of neointimal formation in an intercross between C57BL/6 and C3H/HeJ apolipoprotein E-deficient miceZuobiao Yuan, Hong Pei, Drew J Roberts, et al.
Circulation. Cardiovascular Genetics|August 24, 2010
Novel nonmajor histocompatibility complex-linked loci from mouse chromosome 17 confer susceptibility to viral-mediated chronic autoimmune myocarditisMaya C Poffenberger, Iryna Shanina, Connie Aw, et al.
Circulation. Cardiovascular Genetics|June 17, 2010
Albuminuria risk in Hispanic populations: not so black and whitePaul E Drawz, Jeffrey R Schelling
Circulation. Cardiovascular Genetics|June 17, 2010
GWAS applied to heart failure: bigger will be better...eventuallyDennis M McNamara, Barry London
Circulation. Cardiovascular Genetics|September 2, 2011
Venous thromboembolism does not share strong familial susceptibility with ischemic stroke: a nationwide family study in SwedenBengt Zöller, Xinjun Li, Henrik Ohlsson, et al.
Circulation. Cardiovascular Genetics|September 2, 2011
Protein interaction-based genome-wide analysis of incident coronary heart diseaseMajken K Jensen, Tune H Pers, Piotr Dworzynski, et al.
Circulation. Cardiovascular Genetics|August 12, 2011
Risk of syncope in family members who are genotype-negative for a family-associated long-QT syndrome mutationAlon Barsheshet, Arthur J Moss, Scott McNitt, et al.
Pageof 97