Search Results - "Esslinger, Ulrike B."
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Dysfunctional nitric oxide signalling increases risk of myocardial infarction
Published in Nature (London) (01-12-2013)“…Two private, heterozygous mutations in two functionally related genes, GUCY1A3 and CCT7 , are identified in an extended family with myocardial infarction;…”
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Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy
Published in PLoS genetics (21-10-2010)“…Dilated cardiomyopathy (DCM) is a structural heart disease with strong genetic background. Monogenic forms of DCM are observed in families with mutations…”
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Journal Article -
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Expression pattern in human macrophages dependent on 9p21.3 coronary artery disease risk locus
Published in Atherosclerosis (01-04-2013)“…Abstract Objective Genome-wide association studies identified a risk haplotype on chromosome 9p21.3 to be associated with coronary artery disease (CAD) and…”
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Genetic Association Study Identifies HSPB7 as a Risk Gene for Idiopathic Dilated Cardiomyopathy: e1001167
Published in PLoS genetics (01-10-2010)“…Dilated cardiomyopathy (DCM) is a structural heart disease with strong genetic background. Monogenic forms of DCM are observed in families with mutations…”
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Journal Article