Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy
about
Cardiomyopathy classification: ongoing debate in the genomics eraGenetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathyTNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathyHomozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathyMany roads lead to a broken heart: the genetics of dilated cardiomyopathy.Targeted deletion of Dicer in the heart leads to dilated cardiomyopathy and heart failureCardiac Troponin and Tropomyosin: Structural and Cellular Perspectives to Unveil the Hypertrophic Cardiomyopathy PhenotypeMutational analysis of the beta- and delta-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathyCoding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathyCoding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathyFamilial dilated cardiomyopathy mutations uncouple troponin I phosphorylation from changes in myofibrillar Ca²⁺ sensitivitySodium channel mutations and susceptibility to heart failure and atrial fibrillationThin filament mutations: developing an integrative approach to a complex disorderDisruption of striated preferentially expressed gene locus leads to dilated cardiomyopathy in miceIntegrative structural modelling of the cardiac thin filament: energetics at the interface and conservation patterns reveal a spotlight on period 2 of tropomyosinImaging phenotype vs genotype in nonhypertrophic heritable cardiomyopathies: dilated cardiomyopathy and arrhythmogenic right ventricular cardiomyopathyExpression of TPM1κ, a Novel Sarcomeric Isoform of the TPM1 Gene, in Mouse Heart and Skeletal MuscleGenetic causes of human heart failure.Hereditary Dilated Cardiomyopathy: Recent Advances in Genetic Diagnostics.Omecamtiv Mecarbil, a Cardiac Myosin Activator, Increases Ca2+ Sensitivity in Myofilaments With a Dilated Cardiomyopathy Mutant Tropomyosin E54K.Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy.Dynamic regulation of sarcomeric actin filaments in striated muscleA Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy.Dominant mutations in KBTBD13, a member of the BTB/Kelch family, cause nemaline myopathy with cores.Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy.DCM-related tropomyosin mutants E40K/E54K over-inhibit the actomyosin interaction and lead to a decrease in the number of cycling cross-bridges.Structural and protein interaction effects of hypertrophic and dilated cardiomyopathic mutations in alpha-tropomyosin.Genes and their polymorphisms in mono- and multifactorial cardiomyopathies: towards pharmacogenomics in heart failure.Nemaline myopathy type 6: clinical and myopathological features.Molecular mechanisms of inherited cardiomyopathies.Update 2011: clinical and genetic issues in familial dilated cardiomyopathy.Molecular diagnosis of myocardial disease.Clinical and genetic issues in dilated cardiomyopathy: a review for genetics professionalsExpanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.Progression of familial and non-familial dilated cardiomyopathy: long term follow up.SERCA2 Haploinsufficiency in a Mouse Model of Darier Disease Causes a Selective Predisposition to Heart FailureMice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy.Genetics of inherited cardiomyopathies.Cardiac-specific deletion of the microtubule-binding protein CENP-F causes dilated cardiomyopathy
P2860
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P2860
Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy
description
2001 nî lūn-bûn
@nan
2001 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2001年の論文
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2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
name
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@ast
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@en
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@en-gb
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@nl
type
label
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@ast
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@en
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@en-gb
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@nl
prefLabel
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@ast
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@en
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@en-gb
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@nl
P2093
P3181
P356
P1476
Mutations that alter the surfa ...... ed with dilated cardiomyopathy
@en
P2093
F G Whitby
N Y Kishimoto
V V Michels
P304
P3181
P356
10.1006/JMCC.2000.1339
P407
P577
2001-04-01T00:00:00Z