Locations

Langendorff-heart

Pipetting and spotting

Comparative genomic of left ventricular hypertrophy and dysfunction in hypertension

Functional genomics of cardiac end organ damage in hypertension

Functional genomics of vascular end organ damage in hypertension

Genome-wide assessment of siblings with myocardial infarction

Identification of genes for monogenic forms of myocardial infarction

Genetics of coronary morphology

Prevalence of Titin-mutations and identification of novel disease genes in patients with familial dilated cardiomyopathy

Zebra fish mutants as a model for human cardiomyopathies

Identification and characterization of molecular pathways in the pathogenesis of cardiomyopathies

Contribution of genetic variation in modifier genes to cardiomyopathy phenotypes

Identification of genetic modifiers of cardiomyopathies in mice

Genomic predictors of heart failure following anthracycline cancer therapy

Genomics of diastolic heart failure

Genetic epidemiology of heart failure

Inflammation and immune response in the pathogenesis of typ 2 diabetes and atherosclerosis: Testing the common soil hypothesis

Genetyp-phenotype association studies in clinically well characterized patients with inherited bleeding disorders

Von Willebrand Factor

Coordination office

Population genetics of cardiovascular diseases

Antisense oligonucleotide-mediated gene knock-down in Zebra fish embryo for the evaluation of novel cardiovascular genes

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Main Research

Hypertension and cardiovascular end organ damage

Coronary artery disease and myocardial infarction

Causes, pathways and modifiers of cardiomoypathies

Hemostaseology / Atherosclerosis

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Locations:

Berlin Frankfurt Göttingen Hamburg Heidelberg Lübeck Mainz München Regensburg Ulm