Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy. (Q34399560)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11597833%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

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

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12 November 2019

1

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12 November 2019

author name string

J D Potter

series ordinal

2

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12 November 2019

publication date

1 July 2001

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Trends in Cardiovascular Medicine

12 November 2019

published in

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12 November 2019

volume

11

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12 November 2019

issue

5

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12 November 2019

page(s)

206-212

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Patients with familial hypertrophic cardiomyopathy caused by a Phe110Ile missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis

12 November 2019

cites work

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7 January 2021

A Mutant Tropomyosin That Causes Hypertrophic Cardiomyopathy Is Expressed In Vivo and Associated With an Increased Calcium Sensitivity

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Altered hemodynamics in transgenic mice harboring mutant tropomyosin linked to hypertrophic cardiomyopathy

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The troponin complex and regulation of muscle contraction.

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Transgenic rat hearts expressing a human cardiac troponin T deletion reveal diastolic dysfunction and ventricular arrhythmias

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7 January 2021

An online locus-specific mutation database for familial hypertrophic cardiomyopathy

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7 January 2021

Molecular switches in troponin.

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7 January 2021

Functional consequences of the deletion mutation deltaGlu160 in human cardiac troponin T

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7 January 2021

Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy

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7 January 2021

Transgenic modeling of a cardiac troponin I mutation linked to familial hypertrophic cardiomyopathy

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7 January 2021

Hypertrophic cardiomyopathy caused by a novel alpha-tropomyosin mutation (V95A) is associated with mild cardiac phenotype, abnormal calcium binding to troponin, abnormal myosin cycling, and poor prognosis

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7 January 2021

Inotropic stimulation induces cardiac dysfunction in transgenic mice expressing a troponin T (I79N) mutation linked to familial hypertrophic cardiomyopathy

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7 January 2021

Clinical manifestations of hypertrophic cardiomyopathy with mutations in the cardiac beta-myosin heavy chain gene or cardiac troponin T gene

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7 January 2021

Altered cardiac troponin T in vitro function in the presence of a mutation implicated in familial hypertrophic cardiomyopathy

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7 January 2021

Decreased left ventricular ejection fraction in transgenic mice expressing mutant cardiac troponin T-Q(92), responsible for human hypertrophic cardiomyopathy

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7 January 2021

Phenotypic variation of familial hypertrophic cardiomyopathy caused by the Phe(110)-->Ile mutation in cardiac troponin T

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7 January 2021

Regulatory properties of the NH2- and COOH-terminal domains of troponin T. ATPase activation and binding to troponin I and troponin C

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7 January 2021

Epidemiology of Hypertrophic Cardiomyopathy–Related Death

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7 January 2021

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

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7 January 2021

Sudden death due to troponin T mutations

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7 January 2021

Functional consequences of a carboxyl terminal missense mutation Arg278Cys in human cardiac troponin T

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7 January 2021

Ca2+-sensitizing effects of the mutations at Ile-79 and Arg-92 of troponin T in hypertrophic cardiomyopathy.

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7 January 2021

Altered regulatory function of two familial hypertrophic cardiomyopathy troponin T mutants.

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7 January 2021

Novel missense mutation in cardiac troponin T gene found in Japanese patient with hypertrophic cardiomyopathy

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7 January 2021

Functional changes in troponin T by a splice donor site mutation that causes hypertrophic cardiomyopathy

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7 January 2021

Effects of missense mutations Phe110Ile and Glu244Asp in human cardiac troponin T on force generation in skinned cardiac muscle fibers

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7 January 2021

Dominant-negative effect of a mutant cardiac troponin T on cardiac structure and function in transgenic mice

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7 January 2021

A direct regulatory role for troponin T and a dual role for troponin C in the Ca2+ regulation of muscle contraction

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7 January 2021

Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein

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7 January 2021

Identification of a contractile deficit in adult cardiac myocytes expressing hypertrophic cardiomyopathy-associated mutant troponin T proteins

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1050-1738%2801%2900115-3

7 January 2021

A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy

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7 January 2021

Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy

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7 January 2021

Functional consequences of troponin T mutations found in hypertrophic cardiomyopathy

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7 January 2021

A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy

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7 January 2021

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

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7 January 2021

Hypertrophic cardiomyopathy. Clinical spectrum and treatment.

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7 January 2021

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

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7 January 2021

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Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11597833%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

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