Contractile protein mutations and heart disease (Q28288865)

Current Opinion in Cell Biology

Europe PubMed Central

title

Contractile protein mutations and heart disease (English)

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K L Vikstrom

1

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L A Leinwand

series ordinal

2

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language of work or name

English

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publication date

February 1996

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published in

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volume

8

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issue

1

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page(s)

97-105

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cites work

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A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene

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

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Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

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A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy

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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

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Functions of the myosin ATP and actin binding sites are required for C. elegans thick filament assembly

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Defects in the Drosophila myosin rod permit sarcomere assembly but cause flight muscle degeneration

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Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy

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Genetic heterogeneity of familial hypertrophic cardiomyopathy

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Sudden cardiac death in hypertrophic cardiomyopathy. Variability in phenotypic expression of beta-myosin heavy chain mutations

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Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations

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7 January 2021

Ifm(2)2 is a myosin heavy chain allele that disrupts myofibrillar assembly only in the indirect flight muscle of Drosophila melanogaster

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Genetic dissection of Drosophila myofibril formation: effects of actin and myosin heavy chain null alleles.

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Hypertrophic cardiomyopathy mutation is expressed in messenger RNA of skeletal as well as cardiac muscle

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Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes

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7 January 2021

Accumulation and assembly of myosin in hypertrophic cardiomyopathy with the 403 Arg to Gln beta-myosin heavy chain mutation

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7 January 2021

Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy

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7 January 2021

Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy.

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7 January 2021

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

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7 January 2021

Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy

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7 January 2021

Hypertrophic cardiomyopathy in pigs: quantitative pathologic features in 55 cases

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Identification of a mutation near a functional site of the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy.

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7 January 2021

The electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 gene

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7 January 2021

Left ventricular hypertrophy and morphology in familial hypertrophic cardiomyopathy associated with mutations of the beta-myosin heavy chain gene

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7 January 2021

Novel missense mutation in cardiac beta myosin heavy chain gene found in a Japanese patient with hypertrophic cardiomyopathy

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7 January 2021

Altered actin binding with myosin mutation in hypertrophic cardiomyopathy and sudden death.

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7 January 2021

Missense mutation of the beta-cardiac myosin heavy-chain gene in hypertrophic cardiomyopathy

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7 January 2021

A missense mutation of cardiac beta-myosin heavy chain gene linked to familial hypertrophic cardiomyopathy in affected Japanese families

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https://api.crossref.org/works/10.1016%2FS0955-0674%2896%2980053-6

7 January 2021

Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy

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https://api.crossref.org/works/10.1016%2FS0955-0674%2896%2980053-6

7 January 2021