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Articles: Basic Science/Genetics |
Prior Articles
Myocyte remodeling in response to hypertrophic stimuli requires nucleocytoplasmic shuttling of muscle LIM protein
Journal of Molecular and Cellular Cardiology, 09/08/09
S100A1 in cardiovascular health and disease: Closing the gap between basic science and clinical therapy
Journal of Molecular and Cellular Cardiology, 09/08/09 Hic-5 is required for fetal gene expression and cytoskeletal organization of neonatal cardiac myocytes
Journal of Molecular and Cellular Cardiology, 09/08/09 Kappa and delta opioid receptor signaling is augmented in the failing heart
Journal of Molecular and Cellular Cardiology, 09/08/09 Single nucleotide polymorphisms in homocysteine metabolism pathway genes: Association of CHDH A119C and MTHFR C677T with hyperhomocysteinemia
Circulation: Cardiovascular Genetics, 09/08/09 Association of AHSG Gene Polymorphisms with Fetuin-A Plasma Levels and Cardiovascular Diseases in the EPIC-Potsdam Study
Circulation: Cardiovascular Genetics, 09/08/09 Possible association of tumor necrosis factor receptor 2 gene polymorphism with severe hypertension using the extreme discordant phenotype design
Hypertension Research, 09/08/09 Determination of single-nucleotide polymorphism in the proximal promoter region of apolipoprotein M gene in coronary artery diseases
International Journal of General Medicine, 09/08/09
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A Human Atrial Natriuretic Peptide Gene Mutation Reveals a Novel Peptide With Enhanced Blood Pressure-Lowering, Renal-Enhancing, and Aldosterone-Suppressing Actions
JACC - Journal of the American College of Cardiology, 09/04/09 p300 Plays a Critical Role in Maintaining Cardiac Mitochondrial Function and Cell Survival in Postnatal Hearts
Circulation Research, 09/04/09 Association of the -757T>C polymorphism in the CRP gene with circulating C-reactive protein levels and carotid atherosclerosis
Thrombosis Research, 09/04/09 Association of V617F Jak2 mutation with the risk of thrombosis among patients with essential thrombocythaemia or idiopathic myelofibrosis: A systematic review
Thrombosis Research, 09/04/09 Osteopontin gene variation and cardio/cerebrovascular disease phenotypes
Atherosclerosis, 09/03/09 Conditional linkage and genome-wide association studies identify UGT1A1 as a major gene for anti-atherogenic serum bilirubin levels—The Framingham Heart Study
Atherosclerosis, 09/03/09 K201 improves aspects of the contractile performance of human failing myocardium via reduction in Ca2+ leak from the sarcoplasmic reticulum
Basic Research in Cardiology, 09/03/09 Association of Common Variants of UCP2 Gene With Low-Grade Inflammation in Swedish Children and Adolescents; The European Youth Heart Study
Pediatric Research, 09/03/09 Hyperhomocysteinemia, intima-media thickness and C677T MTHFR gene polymorphism: A correlation study in patients with cognitive impairment
Atherosclerosis, 09/02/09 Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test
Heart Rhythm, 09/02/09 Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia
Atherosclerosis, 09/02/09 The functional variant rs1048990 in PSMA6 is associated with susceptibility to myocardial infarction in a Chinese population
Atherosclerosis, 09/02/09
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Indexed Journals: American Heart Journal, American Journal of Cardiology, Circulationn, Heart
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250 Available Pages
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