×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.
7883988
1995
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
GeneticVariation
disease
CLINVAR
[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy].
17125710
2006
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.
20031619
2009
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
GeneticVariation
disease
CLINVAR
Prevalence and distribution of sarcomeric gene mutations in Japanese patients with familial hypertrophic cardiomyopathy.
22112859
2012
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Development and validation of a computational method for assessment of missense variants in hypertrophic cardiomyopathy.
21310275
2011
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
GeneticVariation
disease
CLINVAR
Good Intentions Gone Bad.
31112422
2019
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β.
20811150
2010
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience.
23349452
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
GeneticVariation
disease
CLINVAR
Echocardiographic strain imaging to assess early and late consequences of sarcomere mutations in hypertrophic cardiomyopathy.
20031602
2009
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Creatine kinase adenosine triphosphate and phosphocreatine energy supply in a single kindred of patients with hypertrophic cardiomyopathy.
23751935
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Microvascular function is selectively impaired in patients with hypertrophic cardiomyopathy and sarcomere myofilament gene mutations.
21835320
2011
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family.
9874056
1998
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
GeneticVariation
disease
CLINVAR
Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy.
21302287
2011
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
GeneticVariation
disease
CLINVAR
Gene-specific increase in the energetic cost of contraction in hypertrophic cardiomyopathy caused by thick filament mutations.
24835277
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Characterization of mutant myosins of Dictyostelium discoideum equivalent to human familial hypertrophic cardiomyopathy mutants. Molecular force level of mutant myosins may have a prognostic implication.
9062359
1997
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy.
18409188
2008
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
[Biochemical characterization of a high-molecular weight alkaline phosphatase in a patient with cholangiocarcinoma (alpha-1 alkaline phosphatase)].
2411171
1985
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Usefulness of Genetic Testing in Hypertrophic Cardiomyopathy: an Analysis Using Real-World Data.
28138913
2017
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
GeneticVariation
disease
CLINVAR
Penetrance of hypertrophic cardiomyopathy in children and adolescents: a 12-year follow-up study of clinical screening and predictive genetic testing.
23197161
2013
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
"Hypertrophic cardiomyopathy: two homozygous cases with ""typical"" hypertrophic cardiomyopathy and three new mutations in cases with progression to dilated cardiomyopathy."
12951062
2003
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
β-Myosin heavy chain variant Val606Met causes very mild hypertrophic cardiomyopathy in mice, but exacerbates HCM phenotypes in mice carrying other HCM mutations.
24829265
2014
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
GeneticVariation
disease
CLINVAR
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
11106718
2000
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
GeneticVariation
disease
CLINVAR
The in vitro motility activity of beta-cardiac myosin depends on the nature of the beta-myosin heavy chain gene mutation in hypertrophic cardiomyopathy.
9172070
1997
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
GeneticVariation
disease
CLINVAR
Development of a high resolution melting method for the detection of genetic variations in hypertrophic cardiomyopathy.
20800588
2010
×
Entrez Id:
4625
Gene Symbol:
MYH7
MYH7
0.500
CausalMutation
disease
CLINVAR
Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy.
8483915
1993