(Q37714017)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

review article

1 reference

title

Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

author name string

Qian Xu

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Shannamar Dewey

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

Susan Nguyen

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

publication date

16 March 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

Journal of Molecular and Cellular Cardiology

21 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

volume

48

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

page(s)

899-909

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

cites work

Familial cardiomegaly

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Left ventricular noncompaction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Hypertrophic cardiomyopathy: a systematic review

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Expression and functional assessment of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. Evidence for a dominant negative action

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Mutations in alpha-actinin-2 cause hypertrophic cardiomyopathy: a genome-wide analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Beyond the sarcomere: CSRP3 mutations cause hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Structural analysis of obscurin gene in hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Yield of genetic testing in hypertrophic cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Molecular epidemiology of hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Sudden death from cardiac causes in children and young adults

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Sudden cardiac death in the United States, 1989 to 1998.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Task Force on Sudden Cardiac Death of the European Society of Cardiology.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

The Genetic Basis for Cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Comparison of prevalence of apical hypertrophic cardiomyopathy in Japan and the United States

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Asymmetric apical hypertrophy: ten years experience

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Hypertrophic nonobstructive cardiomyopathy with giant negative T waves (apical hypertrophy): Ventriculographic and echocardiographic features in 30 patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Disappearance of giant negative T waves in patients with the Japanese form of apical hypertrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Hypertrophic cardiomyopathy with ventricular septal hypertrophy localized to the apical region of the left ventricle (apical hypertrophic cardiomyopathy)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Clinical and genetic issues in familial dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Familial dilated cardiomyopathy: a worse prognosis compared with sporadic forms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Clinical features of hypertrophic cardiomyopathy caused by a Lys183 deletion mutation in the cardiac troponin I gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Restrictive Cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Restrictive cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Mutations in human cardiac troponin I that are associated with restrictive cardiomyopathy affect basal ATPase activity and the calcium sensitivity of force development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Drastic Ca2+ sensitization of myofilament associated with a small structural change in troponin I in inherited restrictive cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Sarcomere mutations in cardiogenesis and ventricular noncompaction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Mutations in sarcomere protein genes in left ventricular noncompaction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Isolated left ventricular non-compaction, not hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Left ventricular noncompaction and cardiomyopathy: cause, contributor, or epiphenomenon?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Cardiomyopathy: a systematic review of disease-causing mutations in myosin heavy chain 7 and their phenotypic manifestations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Sudden death due to troponin T mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Hypertrophic cardiomyopathy. A study of the troponin-T gene in 127 Spanish families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Natural history of hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

A novel missense mutation in the myosin binding protein-C gene is responsible for hypertrophic cardiomyopathy with left ventricular dysfunction and dilation in elderly patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Abnormal contractile function in transgenic mice expressing a familial hypertrophic cardiomyopathy-linked troponin T (I79N) mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Ca2+ sensitization and potentiation of the maximum level of myofibrillar ATPase activity caused by mutations of troponin T found in familial hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Gene mutations in apical hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Mutations of the beta myosin heavy chain gene in hypertrophic cardiomyopathy: critical functional sites determine prognosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Rescue of cardiac alpha-actin-deficient mice by enteric smooth muscle gamma-actin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Functional aberration of myofibrils by cardiomyopathy-causing mutations in the coiled-coil region of the troponin-core domain.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Evaluation of the flanking nucleotide sequences of sarcomeric hypertrophic cardiomyopathy substitution mutations.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

SIFT: Predicting amino acid changes that affect protein function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

A mutation in the N-terminus of troponin I that is associated with hypertrophic cardiomyopathy affects the Ca(2+)-sensitivity, phosphorylation kinetics and proteolytic susceptibility of troponin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Sarcomeric proteins and inherited cardiomyopathies.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Sarcomeric proteins and familial hypertrophic cardiomyopathy: linking mutations in structural proteins to complex cardiovascular phenotypes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

The miscommunicative cardiac cell: when good proteins go bad.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Titin mutations as the molecular basis for dilated cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

A contemporary approach to hypertrophic cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Alterations of tension-dependent ATP utilization in a transgenic rat model of hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Increase in tension-dependent ATP consumption induced by cardiac troponin T mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Functional consequences of the human cardiac troponin I hypertrophic cardiomyopathy mutation R145G in transgenic mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

R-92L and R-92W mutations in cardiac troponin T lead to distinct energetic phenotypes in intact mouse hearts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Human homozygous R403W mutant cardiac myosin presents disproportionate enhancement of mechanical and enzymatic properties.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Shifts in the myosin heavy chain isozymes in the mouse heart result in increased energy efficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Disease-Modifying Mutations in Familial Hypertrophic Cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Molecular and phenotypic effects of heterozygous, homozygous, and compound heterozygote myosin heavy-chain mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

A child cohort study from southern Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

A mouse model of familial hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Severe Heart Failure and Early Mortality in a Double-Mutation Mouse Model of Familial Hypertrophic Cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Angiotensin II type 2 receptors and cardiac hypertrophy in women with hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

AT1 receptor A/C1166 polymorphism contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

A human polymorphism of protein phosphatase-1 inhibitor-1 is associated with attenuated contractile response of cardiomyocytes to beta-adrenergic stimulation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Genotype–phenotype correlations in familial hypertrophic cardiomyopathy A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

inferred from DOI database lookup

7 January 2021

based on heuristic

Novel insights into the clinical manifestations and treatment of hypertrophic cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FJ.YJMCC.2010.03.005

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/J.YJMCC.2010.03.005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20298698%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference