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Circulation. Cardiovascular genetics

Showing results (441-450 of 645) with videos related to

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Circulation. Cardiovascular Genetics|June 7, 2012
Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndromeRyan S Friese, Chun Ye, Caroline M Nievergelt, et al.
Circulation. Cardiovascular Genetics|October 15, 2013
Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysisSahoko Ichihara, Ken Yamamoto, Hiroyuki Asano, et al.
Circulation. Cardiovascular Genetics|October 15, 2013
Association of neuroimmune guidance cue netrin-1 and its chemorepulsive receptor UNC5B with atherosclerotic plaque expression signatures and stability in human(s): Tampere Vascular Study (TVS)Niku Oksala, Jenita Pärssinen, Ilkka Seppälä, et al.
Circulation. Cardiovascular Genetics|June 4, 2013
Two chromosome 9p21 haplotype blocks distinguish between coronary artery disease and myocardial infarction riskMeng Fan, Sonny Dandona, Ruth McPherson, et al.
Circulation. Cardiovascular Genetics|April 26, 2013
Putting pleiotropy and selection into context defines a new paradigm for interpreting genetic dataIrene M Predazzi, Antonis Rokas, Amos Deinard, et al.
Circulation. Cardiovascular Genetics|July 19, 2013
Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite populationBrenda Gerull, Florian Kirchner, Jessica X Chong, et al.
Circulation. Cardiovascular Genetics|May 22, 2013
Comparison of echocardiographic and cardiac magnetic resonance imaging in hypertrophic cardiomyopathy sarcomere mutation carriers without left ventricular hypertrophyAnne Marie Valente, Neal K Lakdawala, Andrew J Powell, et al.
Circulation. Cardiovascular Genetics|July 16, 2014
Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology studyCara L Carty, Samsiddhi Bhattacharjee, Jeff Haessler, et al.
Circulation. Cardiovascular Genetics|September 25, 2014
Candidate pathway-based genome-wide association studies identify novel associations of genomic variants in the complement system associated with coronary artery diseaseChengqi Xu, Qin Yang, Hongbo Xiong, et al.
Circulation. Cardiovascular Genetics|November 12, 2013
Gene network and proteomic analyses of cardiac responses to pathological and physiological stressIgnat Drozdov, Athanasios Didangelos, Xiaoke Yin, et al.
Pageof 65

Showing results (441-450 of 645) with videos related to

Sort By:
Pageof 65
Circulation. Cardiovascular Genetics|June 7, 2012
Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndromeRyan S Friese, Chun Ye, Caroline M Nievergelt, et al.
Circulation. Cardiovascular Genetics|October 15, 2013
Identification of a glutamic acid repeat polymorphism of ALMS1 as a novel genetic risk marker for early-onset myocardial infarction by genome-wide linkage analysisSahoko Ichihara, Ken Yamamoto, Hiroyuki Asano, et al.
Circulation. Cardiovascular Genetics|October 15, 2013
Association of neuroimmune guidance cue netrin-1 and its chemorepulsive receptor UNC5B with atherosclerotic plaque expression signatures and stability in human(s): Tampere Vascular Study (TVS)Niku Oksala, Jenita Pärssinen, Ilkka Seppälä, et al.
Circulation. Cardiovascular Genetics|June 4, 2013
Two chromosome 9p21 haplotype blocks distinguish between coronary artery disease and myocardial infarction riskMeng Fan, Sonny Dandona, Ruth McPherson, et al.
Circulation. Cardiovascular Genetics|April 26, 2013
Putting pleiotropy and selection into context defines a new paradigm for interpreting genetic dataIrene M Predazzi, Antonis Rokas, Amos Deinard, et al.
Circulation. Cardiovascular Genetics|July 19, 2013
Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite populationBrenda Gerull, Florian Kirchner, Jessica X Chong, et al.
Circulation. Cardiovascular Genetics|May 22, 2013
Comparison of echocardiographic and cardiac magnetic resonance imaging in hypertrophic cardiomyopathy sarcomere mutation carriers without left ventricular hypertrophyAnne Marie Valente, Neal K Lakdawala, Andrew J Powell, et al.
Circulation. Cardiovascular Genetics|July 16, 2014
Analysis of metabolic syndrome components in >15 000 african americans identifies pleiotropic variants: results from the population architecture using genomics and epidemiology studyCara L Carty, Samsiddhi Bhattacharjee, Jeff Haessler, et al.
Circulation. Cardiovascular Genetics|September 25, 2014
Candidate pathway-based genome-wide association studies identify novel associations of genomic variants in the complement system associated with coronary artery diseaseChengqi Xu, Qin Yang, Hongbo Xiong, et al.
Circulation. Cardiovascular Genetics|November 12, 2013
Gene network and proteomic analyses of cardiac responses to pathological and physiological stressIgnat Drozdov, Athanasios Didangelos, Xiaoke Yin, et al.
Pageof 65