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Genetics of cardiovascular disease
Citations 371-380 of 490 total displayed.
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Past content
(since Jan 1999):
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- Articles
Primary Pulmonary Hypertension Is
Associated With Reduced Pulmonary Vascular Expression of Type
II Bone Morphogenetic Protein Receptor
- Carl Atkinson, Susan Stewart, Paul D. Upton, Rajiv Machado, Jennifer R. Thomson, Richard C. Trembath, and Nicholas W. Morrell
Circulation published March 25, 2002, doi:10.1161/01.CIR.0000012754.72951.3D
[Abstract]
- Basic Science Reports
Maternal Hypercholesterolemia During Pregnancy Promotes Early Atherogenesis in LDL Receptor-Deficient Mice and Alters Aortic Gene Expression Determined by Microarray
- Claudio Napoli, Filomena de Nigris, John S. Welch, Federico B. Calara, Robert O. Stuart, Christopher K. Glass, and Wulf Palinski
Circulation 2002;105:1360-1367; published online before print as doi:10.1161/01.CIR.0000013090.96919.FA
[Abstract]
[Full text]
- Clinical Investigations and Reports
Na+ Channel Mutation That Causes Both Brugada and Long-QT Syndrome Phenotypes: A Simulation Study of Mechanism
- Colleen E. Clancy and Yoram Rudy
Circulation 2002;105:1208-1213; published online before print as doi:10.1161/hc1002.105183
[Abstract]
[Full text]
- Basic Science Reports
Maternal Hypercholesterolemia During Pregnancy Promotes Early Atherogenesis in LDL Receptor–Deficient Mice and Alters Aortic Gene Expression Determined by Microarray
- Claudio Napoli, Filomena de Nigris, John S. Welch, Federico B. Calara, Robert O. Stuart, Christopher K. Glass, and Wulf Palinski
Circulation published February 25, 2002, doi:10.1161/01.CIR.0000013090.96919.FA
[Abstract]
[Full text]
- Articles
Peroxisome Proliferator-Activated Receptor
 Gene Variants Influence Progression of Coronary
Atherosclerosis and Risk of Coronary Artery
Disease
- David M. Flavell, Yalda Jamshidi, Emma Hawe, Inés Pineda Torra, Marja-Riitta Taskinen, M. Heikki Frick, Markku S. Nieminen, Y. Antero Kesäniemi, Amos Pasternack, Bart Staels, George Miller, Steve E. Humphries, Philippa J. Talmud, and Mikko Syvänne
Circulation published February 25, 2002, doi:10.1161/01.CIR.0000012145.80593.25
[Abstract]
- Clinical Investigations and Reports
Increased Risk of Arrhythmic Events in Long-QT Syndrome With Mutations in the Pore Region of the Human Ether-a-go-go–Related Gene Potassium Channel
- Arthur J. Moss, Wojciech Zareba, Elizabeth S. Kaufman, Eric Gartman, Derick R. Peterson, Jesaia Benhorin, Jeffrey A. Towbin, Mark T. Keating, Silvia G. Priori, Peter J. Schwartz, G. Michael Vincent, Jennifer L. Robinson, Mark L. Andrews, Changyong Feng, W. Jackson Hall, Aharon Medina, Li Zhang, and Zhiqing Wang
Circulation 2002;105:794-799; published online before print as doi:10.1161/hc0702.105124
[Abstract]
[Full text]
- Clinical Investigations and Reports
Fibrillin-1 Genotype Is Associated With Aortic Stiffness and Disease Severity in Patients With Coronary Artery Disease
- Tanya L. Medley, Timothy J. Cole, Christoph D. Gatzka, William Y.S. Wang, Anthony M. Dart, and Bronwyn A. Kingwell
Circulation 2002;105:810-815; published online before print as doi:10.1161/hc0702.104129
[Abstract]
[Full text]
- Articles
Na+ Channel Mutation
That Causes Both Brugada and Long-QT Syndrome
Phenotypes. A Simulation Study of
Mechanism
- Colleen E. Clancy and Yoram Rudy
Circulation published February 18, 2002, doi:10.1161/hc1002.105183
[Abstract]
- Clinical Investigations and Reports
Clinical and Molecular Heterogeneity in the Brugada Syndrome: A Novel Gene Locus on Chromosome 3
- Raul Weiss, M. Michael Barmada, Tuduy Nguyen, Jolene S. Seibel, Doris Cavlovich, Cari A. Kornblit, Adam Angelilli, Flordeliza Villanueva, Dennis M. McNamara, and Barry London
Circulation 2002;105:707-713; published online before print as doi:10.1161/hc0602.103618
[Abstract]
[Full text]
- Clinical Investigations and Reports
Metavinculin Mutations Alter Actin Interaction in Dilated Cardiomyopathy
- Timothy M. Olson, Susanne Illenberger, Nina Y. Kishimoto, Stefan Huttelmaier, Mark T. Keating, and Brigitte M. Jockusch
Circulation 2002;105:431-437, doi:10.1161/hc0402.102930
[Abstract]
[Full text]
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