Title | From Molecule to Men [electronic resource] : Molecular Basis of Congenital Cardiovascular Disorders / edited by M. Zehender, H. Just, G. Breithardt |
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Imprint | Heidelberg : Steinkopff : Imprint: Steinkopff, 2000 |
Connect to | http://dx.doi.org/10.1007/978-3-642-57724-6 |
Descript | X, 246 p. online resource |
Molecular Basis of Congenital Cardiovascular Disorders -- Genetics of dilated cardiomyopathy -- Registry of families with inherited dilated cardiomyopathy for molecular analyses -- Distinct phenotype patterns of Ca2+ handling proteins in end-stage failing human hearts -- Apoptosis in the overloaded myocardium: potential stimuli and modifying signals -- Analysis of inherited causes of hypertrophic cardiomyopathy as part of clinical practice -- Molecular genetics of arrhythmogenic right ventricular cardiomyopathy -- Cardiomyopathy: Genetics in muscular dystrophies -- Molecular impact of ion channel mutations for the pathogenesis of long-QT (LQT) syndromes -- Acquired abnormal QT prolongation and torsade de pointes โ clinical significance of genetic information from congenital long QT syndrome -- Molecular genetic approaches to human hypertension -- Renin-angiotensin system and coronary artery disease โ Interaction of angiotensin II with pro-inflammatory cytokines in human stable and unstable coronary plaques -- Genetics of Lipoprotein(a) -- The molecular mechanisms of inherited hypercholesterolemia -- Insulin resistance: A pathogenic link between cardiovascular risk factors and atherosclerosis -- Genetic control of hemostatic factors in relation to atherosclerosis -- Increased platelet aggregability associated with platelet GPIIIa PIA2 polymorphism: the Framingham Offspring Study -- Genetic aspects of chronobiologic rhythms in cardiovascular disease -- Is capillary sprouting enough? -- Angiogenesis and gene therapy -- Genetic engineering for human bypass vein grafts -- Molecular cardiology and physician