Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
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Gene regulation, alternative splicing, and posttranslational modification of troponin subunits in cardiac development and adaptation: a focused reviewCardiomyopathy classification: ongoing debate in the genomics eraRare variant mutations identified in pediatric patients with dilated cardiomyopathyCoding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathyClinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathyThin filament mutations: developing an integrative approach to a complex disorderA novel arginine to tryptophan (R144W) mutation in troponin T (cTnT) gene in an indian multigenerational family with dilated cardiomyopathy (FDCM)Protective action of tetramethylpyrazine phosphate against dilated cardiomyopathy in cTnT(R141W) transgenic miceUsing large sequencing data sets to refine intragenic disease regions and prioritize clinical variant interpretation.Hypertrophic and dilated cardiomyopathy mutations differentially affect the molecular force generation of mouse alpha-cardiac myosin in the laser trap assay.Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy.Late onset sporadic dilated cardiomyopathy caused by a cardiac troponin T mutation.Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionalsThe functional effect of dilated cardiomyopathy mutation (R144W) in mouse cardiac troponin T is differently affected by α- and β-myosin heavy chain isoformsExpanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.Genetics of inherited cardiomyopathy.Gene-Targeted Mice with the Human Troponin T R141W Mutation Develop Dilated Cardiomyopathy with Calcium DesensitizationThe miscommunicative cardiac cell: when good proteins go bad.Myocardial regulatory proteins and heart failure.Genetics of dilated cardiomyopathy.Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy.Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology.Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it allDifferential interactions of thin filament proteins in two cardiac troponin T mouse models of hypertrophic and dilated cardiomyopathies.TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.Insights and Challenges of Multi-Scale Modeling of Sarcomere Mechanics in cTn and Tm DCM Mutants-Genotype to Cellular Phenotype.TNNT2 gene polymorphisms are associated with susceptibility to idiopathic dilated cardiomyopathy in the Han Chinese population.Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.Characterization of troponin T dilated cardiomyopathy mutations in the fetal troponin isoform.Multiple Species Comparison of Cardiac Troponin T and Dystrophin: Unravelling the DNA behind Dilated Cardiomyopathy.Cardioprotection by Hepc1 in cTnT(R141W) transgenic mice.Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene
P2860
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P2860
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
description
2001 nî lūn-bûn
@nan
2001 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
@ast
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
@en
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
@nl
type
label
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
@ast
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
@en
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
@nl
prefLabel
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
@ast
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
@en
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
@nl
P2093
P356
P1433
P1476
Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy
@en
P2093
G Z Czernuszewicz
J B Durand
J L Anderson
J M Gregoritch
L L Bachinski
M Quiñones
O Gonzalez
P304
P356
10.1161/HC4301.098285
P407
P577
2001-10-30T00:00:00Z