(Q41706960)

7 October 2017

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title

Molecular genetic basis of hypertrophic cardiomyopathy: genetic markers for sudden cardiac death (English)

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hypertrophic cardiomyopathy

7 October 2017

main subject

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Marian AJ

1

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7 October 2017

Roberts R

series ordinal

2

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7 October 2017

publication date

1 January 1998

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Journal of Cardiovascular Electrophysiology

7 October 2017

published in

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7 October 2017

volume

9

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7 October 2017

issue

1

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7 October 2017

page(s)

88-99

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Recent advances in the molecular genetics of hypertrophic cardiomyopathy.

7 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Molecular basis of familial cardiomyopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Population genetics of trinucleotide repeat polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Myocardial ultrastructure in idiopathic hypertrophic subaortic stenosis. A study of operatively excised left ventricular outflow tract muscle in 14 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Prognosis in hypertrophic cardiomyopathy observed in a large clinic population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Impact of patient selection biases on the perception of hypertrophic cardiomyopathy and its natural history.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Prognosis in hypertrophic cardiomyopathy: role of age and clinical, electrocardiographic and hemodynamic features

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Localization of gene for familial hypertrophic cardiomyopathy to chromosome 14q1 in a diverse US population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Single myosin molecule mechanics: piconewton forces and nanometre steps

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Molecular cloning and developmental expression of human cardiac troponin T.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Human cardiac troponin T: identification of fetal isoforms and assignment of the TNNT2 locus to chromosome 1q

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Human cardiac troponin T: cloning and expression of new isoforms in the normal and failing heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Molecular basis of human cardiac troponin T isoforms expressed in the developing, adult, and failing heart.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

A molecular map of the interactions between titin and myosin-binding protein C. Implications for sarcomeric assembly in familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Folding-unfolding transitions in single titin molecules characterized with laser tweezers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Skeletal muscle myosin light chains are essential for physiological speeds of shortening.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Transgenic remodeling of the regulatory myosin light chains in the mammalian heart

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Impairment of muscle function caused by mutations of phosphorylation sites in myosin regulatory light chain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

“Malignant” hypertrophic cardiomyopathy: Identification of a subgroup of families with unusually frequent premature death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Genotype-phenotype correlations in hypertrophic cardiomyopathy. Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Sudden death due to troponin T mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Expression of a mutation causing hypertrophic cardiomyopathy disrupts sarcomere assembly in adult feline cardiac myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Expression of a mutant (Arg92Gln) human cardiac troponin T, known to cause hypertrophic cardiomyopathy, impairs adult cardiac myocyte contractility

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Plasma levels of atrial natriuretic peptide in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Ventricular expression of brain natriuretic peptide in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Structural aspects of troponin-tropomyosin regulation of skeletal muscle contraction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

A De Novo Mutation in α-Tropomyosin That Causes Hypertrophic Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

Clinical Features of Hypertrophic Cardiomyopathy Caused by Mutation of a “Hot Spot” in the Alpha-Tropomyosin Gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1540-8167.1998.TB00871.X

10.1111/J.1540-8167.1998.TB00871.X

21 January 2018

Identifiers

DOI

1 reference

release_ynlp7jfrsbaitm2ob6dxplylba

7 October 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/ynlp7jfrsbaitm2ob6dxplylba

mapped directly with Wikidata item

24 November 2022

based on heuristic

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