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Circulation. Cardiovascular Genetics
|
October 13, 2010
Endothelial, sympathetic, and cardiac function in inherited (6R)-L-erythro-5,6,7,8-tetrahydro-L-biopterin deficiency
Lila Mayahi, Lydia Mason, Katherine Bleasdale-Barr, et al.
Circulation. Cardiovascular Genetics
|
March 16, 2011
Common variation at the 11-β hydroxysteroid dehydrogenase type 1 gene is associated with left ventricular mass
Thahira J Rahman, Bongani M Mayosi, Darroch Hall, et al.
Circulation. Cardiovascular Genetics
|
April 16, 2011
A novel KCNJ2 nonsense mutation, S369X, impedes trafficking and causes a limited form of Andersen-Tawil syndrome
Takahiro Doi, Takeru Makiyama, Takeshi Morimoto, et al.
Circulation. Cardiovascular Genetics
|
April 16, 2011
Coronary artery endothelial transcriptome in vivo: identification of endoplasmic reticulum stress and enhanced reactive oxygen species by gene connectivity network analysis
Mete Civelek, Elisabetta Manduchi, Rebecca J Riley, et al.
Circulation. Cardiovascular Genetics
|
March 5, 2011
Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease
Yan Gong, Amber L Beitelshees, Rhonda M Cooper-DeHoff, et al.
Circulation. Cardiovascular Genetics
|
March 17, 2011
A complex double deletion in LMNA underlies progressive cardiac conduction disease, atrial arrhythmias, and sudden death
Roos F Marsman, Abdennasser Bardai, Alex V Postma, et al.
Circulation. Cardiovascular Genetics
|
April 23, 2015
Guiding Cardiac Conduction With GATA
Mona Nemer, Lara Gharibeh
Circulation. Cardiovascular Genetics
|
July 16, 2016
Mendelian Randomization Studies Do Not Support a Role for Vitamin D in Coronary Artery Disease
Despoina Manousaki, Lauren E Mokry, Stephanie Ross, et al.
Circulation. Cardiovascular Genetics
|
July 16, 2016
Genotype-Dependent Effects of Dalcetrapib on Cholesterol Efflux and Inflammation: Concordance With Clinical Outcomes
Jean-Claude Tardif, David Rhainds, Mathieu Brodeur, et al.
Circulation. Cardiovascular Genetics
|
July 16, 2016
Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease
Stephanie LaHaye, Don Corsmeier, Madhumita Basu, et al.
Page
of 97
Search research articles
Search
Showing results (21-30 of 961) with videos related to
Sort By:
Page
of 97
Circulation. Cardiovascular Genetics
|
October 13, 2010
Endothelial, sympathetic, and cardiac function in inherited (6R)-L-erythro-5,6,7,8-tetrahydro-L-biopterin deficiency
Lila Mayahi, Lydia Mason, Katherine Bleasdale-Barr, et al.
Circulation. Cardiovascular Genetics
|
March 16, 2011
Common variation at the 11-β hydroxysteroid dehydrogenase type 1 gene is associated with left ventricular mass
Thahira J Rahman, Bongani M Mayosi, Darroch Hall, et al.
Circulation. Cardiovascular Genetics
|
April 16, 2011
A novel KCNJ2 nonsense mutation, S369X, impedes trafficking and causes a limited form of Andersen-Tawil syndrome
Takahiro Doi, Takeru Makiyama, Takeshi Morimoto, et al.
Circulation. Cardiovascular Genetics
|
April 16, 2011
Coronary artery endothelial transcriptome in vivo: identification of endoplasmic reticulum stress and enhanced reactive oxygen species by gene connectivity network analysis
Mete Civelek, Elisabetta Manduchi, Rebecca J Riley, et al.
Circulation. Cardiovascular Genetics
|
March 5, 2011
Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease
Yan Gong, Amber L Beitelshees, Rhonda M Cooper-DeHoff, et al.
Circulation. Cardiovascular Genetics
|
March 17, 2011
A complex double deletion in LMNA underlies progressive cardiac conduction disease, atrial arrhythmias, and sudden death
Roos F Marsman, Abdennasser Bardai, Alex V Postma, et al.
Circulation. Cardiovascular Genetics
|
April 23, 2015
Guiding Cardiac Conduction With GATA
Mona Nemer, Lara Gharibeh
Circulation. Cardiovascular Genetics
|
July 16, 2016
Mendelian Randomization Studies Do Not Support a Role for Vitamin D in Coronary Artery Disease
Despoina Manousaki, Lauren E Mokry, Stephanie Ross, et al.
Circulation. Cardiovascular Genetics
|
July 16, 2016
Genotype-Dependent Effects of Dalcetrapib on Cholesterol Efflux and Inflammation: Concordance With Clinical Outcomes
Jean-Claude Tardif, David Rhainds, Mathieu Brodeur, et al.
Circulation. Cardiovascular Genetics
|
July 16, 2016
Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease
Stephanie LaHaye, Don Corsmeier, Madhumita Basu, et al.
Page
of 97