PMID 15769782 2005 Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene.
PMID 11106718 2000 Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
PMID 12379228 2002 Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.
PMID 21846512 2012 Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy.
PMID 21127202 2011 Mutations in the sarcomere gene MYH7 in Ebstein anomaly.
rs121913642 in
MYH7 gene and
Cardiomyopathy, Dilated
PMID 16983074 2006 Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.
PMID 22949430 2012 Subtle abnormalities in contractile function are an early manifestation of sarcomere mutations in dilated cardiomyopathy.
PMID 11106718 2000 Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
PMID 17351073 2007 Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse alpha-cardiac myosin in the laser trap assay.
PMID 2753225 1989 Human growth hormone stimulates somatomedin C/insulin-like growth factor I production by the human lymphoid cell line, IM-9.
PMID 23313350 2013 Elevated rates of force development and MgATP binding in F764L and S532P myosin mutations causing dilated cardiomyopathy.
rs121913642 in
MYH7 gene and
Cardiomyopathy, Hypertrophic, Familial
PMID 27532257 2017 Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
PMID 17351073 2007 Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse alpha-cardiac myosin in the laser trap assay.
PMID 11106718 2000 Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
PMID 16983074 2006 Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.
PMID 23313350 2013 Elevated rates of force development and MgATP binding in F764L and S532P myosin mutations causing dilated cardiomyopathy.