Genetics of cardiovascular disease

Citations 401-410 of 492 total displayed.

Past content (since Jan 1999):

Clinical Investigations and Reports
Altered Growth Responses of Pulmonary Artery Smooth Muscle Cells From Patients With Primary Pulmonary Hypertension to Transforming Growth Factor-ß₁ and Bone Morphogenetic Proteins: Nicholas W. Morrell, Xudong Yang, Paul D. Upton, Karen B. Jourdan, Neal Morgan, Karen K. Sheares, and Richard C. Trembath
Circulation 2001;104:790-795, doi:10.1161/hc3201.094152 [Abstract] [Full text]

Clinical Investigations and Reports
Maternal and Paternal History of Myocardial Infarction and Risk of Cardiovascular Disease in Men and Women: Howard D. Sesso, I-Min Lee, J. Michael Gaziano, Kathryn M. Rexrode, Robert J. Glynn, and Julie E. Buring
Circulation 2001;104:393-398, doi:10.1161/hc2901.093115 [Abstract] [Full text]

Clinical Investigations and Reports
Platelet Glycoprotein IIIa Pl^A Polymorphism, Fibrinogen, and Platelet Aggregability: The Framingham Heart Study: DaLi Feng, Klaus Lindpaintner, Martin G. Larson, Christopher J. O’Donnell, Izabella Lipinska, Patrice A. Sutherland, Murray Mittleman, James E. Muller, Ralph B. D’Agostino, Daniel Levy, and Geoffrey H. Tofler
Circulation 2001;104:140-144 [Abstract] [Full text]

Clinical Investigations and Reports
Polymorphism in the ß₁-Adrenergic Receptor Gene and Hypertension: Kristina Bengtsson, Olle Melander, Marju Orho-Melander, Ulf Lindblad, Jonas Ranstam, Lennart Råstam, and Leif Groop
Circulation 2001;104:187-190 [Abstract] [Full text]

Clinical Investigations and Reports
Genetic and Environmental Contributions to Platelet Aggregation : The Framingham Heart Study: Christopher J. O’Donnell, Martin G. Larson, DaLi Feng, Patrice A. Sutherland, Klaus Lindpaintner, Richard H. Myers, Ralph A. D’Agostino, Daniel Levy, and Geoffrey H. Tofler
Circulation 2001;103:3051-3056 [Abstract] [Full text]

Basic Science Reports
Simvastatin Induces Regression of Cardiac Hypertrophy and Fibrosis and Improves Cardiac Function in a Transgenic Rabbit Model of Human Hypertrophic Cardiomyopathy: Rajnikant Patel, Sherif F. Nagueh, Natalie Tsybouleva, Maha Abdellatif, Silvia Lutucuta, Helen A. Kopelen, RDCS, Miguel A. Quinones, William A. Zoghbi, Mark L. Entman, Robert Roberts, and A. J. Marian
Circulation published June 25, 2001, doi:10.1161/hc2801.094031 [Abstract] [Full text]

Clinical Investigations and Reports
G20210A Prothrombin Gene Polymorphism and Prothrombin Activity in Subjects With or Without Angiographically Documented Coronary Artery Disease: Carla Russo, Domenico Girelli, Oliviero Olivieri, Patrizia Guarini, Franco Manzato, Francesca Pizzolo, Barbara Zaia, Alessandro Mazzucco, and Roberto Corrocher
Circulation 2001;103:2436-2440 [Abstract] [Full text]

Clinical Investigations and Reports
Sudden Cardiac Death, Genes, and Arrhythmogenesis : Consideration of New Population and Mechanistic Approaches From a National Heart, Lung, and Blood Institute Workshop, Part II: Peter M. Spooner, Christine Albert, Emelia J. Benjamin, Robin Boineau, Robert C. Elston, Alfred L. George, Jr, Xavier Jouven, Lewis H. Kuller, Jean W. MacCluer, Eduardo Marbán, James E. Muller, Peter J. Schwartz, David S. Siscovick, Russell P. Tracy, Wojciech Zareba, and Douglas P. Zipes
Circulation 2001;103:2447-2452 [Abstract] [Full text]

Clinical Investigations and Reports
Familial Thoracic Aortic Aneurysms and Dissections : Genetic Heterogeneity With a Major Locus Mapping to 5q13-14: Dongchuan Guo, Sumera Hasham, Shao-Qing Kuang, Carl J. Vaughan, Eric Boerwinkle, Hua Chen, Dianne Abuelo, Harry C. Dietz, Craig T. Basson, Sanjay S. Shete, and Dianna M. Milewicz
Circulation 2001;103:2461-2468 [Abstract] [Full text]

Clinical Investigations and Reports
Identification of a Chromosome 11q23.2-q24 Locus for Familial Aortic Aneurysm Disease, a Genetically Heterogeneous Disorder: Carl J. Vaughan, Mairead Casey, Jie He, Mark Veugelers, Kiersten Henderson, Dongchuan Guo, Robert Campagna, Mary J. Roman, Dianna M. Milewicz, Richard B. Devereux, and Craig T. Basson
Circulation 2001;103:2469-2475 [Abstract] [Full text]

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