Cardiac myosin heavy chain isoform exchange alters the phenotype of cTnT-related cardiomyopathies in mouse hearts. - Wikidata - wikimedia - TriplyDB

Cardiac myosin heavy chain isoform exchange alters the phenotype of cTnT-related cardiomyopathies in mouse hearts.

Cardiac myosin heavy chain isoform exchange alters the phenotype of cTnT-related cardiomyopathies in mouse hearts.

http://www.wikidata.org/entity/Q34470455

about

Sexually dimorphic myofilament function and cardiac troponin I phosphospecies distribution in hypertrophic cardiomyopathy mice Unique transcriptional profile of sustained ligand-activated preconditioning in pre- and post-ischemic myocardium.Expression of slow skeletal TnI in adult mouse hearts confers metabolic protection to ischemia The functional effect of dilated cardiomyopathy mutation (R144W) in mouse cardiac troponin T is differently affected by α- and β-myosin heavy chain isoforms A Murine Hypertrophic Cardiomyopathy Model: The DBA/2J Strain Effects of R92 mutations in mouse cardiac troponin T are influenced by changes in myosin heavy chain isoform.The Importance of Biological Sex and Estrogen in Rodent Models of Cardiovascular Health and Disease Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca(2+)-sensitivity and suppress the modulation of Ca(2+)-sensitivity by troponin I phosphorylation.Sex dimorphisms of crossbridge cycling kinetics in transgenic hypertrophic cardiomyopathy mice Divergent effects of α- and β-myosin heavy chain isoforms on the N terminus of rat cardiac troponin T.Tri-modal regulation of cardiac muscle relaxation; intracellular calcium decline, thin filament deactivation, and cross-bridge cycling kinetics.β-myosin heavy chain is induced by pressure overload in a minor subpopulation of smaller mouse cardiac myocytes.Cardiomyopathy-related mutation (A30V) in mouse cardiac troponin T divergently alters the magnitude of stretch activation in α- and β-myosin heavy chain fibers.Preserved cross-bridge kinetics in human hypertrophic cardiomyopathy patients with MYBPC3 mutations.Novel large-particle FACS purification of adult ventricular myocytes reveals accumulation of myosin and actin disproportionate to cell size and proteome in normal post-weaning development.HIC2 regulates isoform switching during maturation of the cardiovascular system.The structural basis of alpha-tropomyosin linked (Asp230Asn) familial dilated cardiomyopathy.Intermittent cardiac overload results in adaptive hypertrophy and provides protection against left ventricular acute pressure overload insult.Hypertrophic cardiomyopathy mutations increase myofilament Ca2+ buffering, alter intracellular Ca2+ handling and stimulate Ca2+ dependent signalling.

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P2860

Cardiac myosin heavy chain isoform exchange alters the phenotype of cTnT-related cardiomyopathies in mouse hearts.

http://www.wikidata.org/entity/Q34470455

description

2009 nî lūn-bûn

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2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Cardiac myosin heavy chain iso ...... diomyopathies in mouse hearts.

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Cardiac myosin heavy chain iso ...... diomyopathies in mouse hearts.

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Cardiac myosin heavy chain iso ...... diomyopathies in mouse hearts.

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Cardiac myosin heavy chain iso ...... diomyopathies in mouse hearts.

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Cardiac myosin heavy chain iso ...... diomyopathies in mouse hearts.

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Cardiac myosin heavy chain iso ...... diomyopathies in mouse hearts.

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Cardiac myosin heavy chain iso ...... diomyopathies in mouse hearts.

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J.YJMCC.2009.11.018

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Journal of Molecular and Cellular Cardiology

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Cardiac myosin heavy chain iso ...... diomyopathies in mouse hearts.

@en

P2093

Candice Dowell-Martino

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Huamei He

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Jeffrey Robbins

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Jil C Tardiff

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Joanne S Ingwall

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Kirsten Hoyer

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Maike Krenz

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Pia Guinto

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Ron Rice

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P2860

Myosin heavy chain gene expression in human heart failure

Myosin heavy chain isoform expression in the failing and nonfailing human heart

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

Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy

Sudden death due to troponin T mutations

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

Impact of beta-myosin heavy chain isoform expression on cross-bridge cycling kinetics

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

Changes in the chemical and dynamic properties of cardiac troponin T cause discrete cardiomyopathies in transgenic mice.

Decreased energetics in murine hearts bearing the R92Q mutation in cardiac troponin T

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scholarly article

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10.1016/J.YJMCC.2009.11.018

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5

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48

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2009-12-31T00:00:00Z

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40682507

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20004663

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3016872

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