Mutations in the cardiac Troponin C gene are a cause of idiopathic dilated cardiomyopathy in childhood.
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Rare variant mutations identified in pediatric patients with dilated cardiomyopathyStructure and function of cardiac troponin C (TNNC1): Implications for heart failure, cardiomyopathies, and troponin modulating drugsA dilated cardiomyopathy troponin C mutation lowers contractile force by reducing strong myosin-actin bindingInvestigating the role of uncoupling of troponin I phosphorylation from changes in myofibrillar Ca(2+)-sensitivity in the pathogenesis of cardiomyopathy.Functional characterization of TNNC1 rare variants identified in dilated cardiomyopathy.Impaired relaxation is the main manifestation in transgenic mice expressing a restrictive cardiomyopathy mutation, R193H, in cardiac TnI.Biochemical characterisation of Troponin C mutations causing hypertrophic and dilated cardiomyopathies.Challenging current paradigms related to cardiomyopathies. Are changes in the Ca2+ sensitivity of myofilaments containing cardiac troponin C mutations (G159D and L29Q) good predictors of the phenotypic outcomes?Abnormal contractility in human heart myofibrils from patients with dilated cardiomyopathy due to mutations in TTN and contractile protein genes.
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P2860
Mutations in the cardiac Troponin C gene are a cause of idiopathic dilated cardiomyopathy in childhood.
description
2007 nî lūn-bûn
@nan
2007年の論文
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2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
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2007年论文
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2007年论文
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2007年论文
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name
Mutations in the cardiac Tropo ...... d cardiomyopathy in childhood.
@en
type
label
Mutations in the cardiac Tropo ...... d cardiomyopathy in childhood.
@en
prefLabel
Mutations in the cardiac Tropo ...... d cardiomyopathy in childhood.
@en
P2860
P1476
Mutations in the cardiac Tropo ...... ed cardiomyopathy in childhood
@en
P2093
Michael Burch
Perry M Elliott
P2860
P304
P356
10.1017/S1047951107001291
P50
P577
2007-11-01T00:00:00Z