The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms
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Gene regulation, alternative splicing, and posttranslational modification of troponin subunits in cardiac development and adaptation: a focused reviewConstitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathyIdiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutationsHuman actin mutations associated with hypertrophic and dilated cardiomyopathies demonstrate distinct thin filament regulatory properties in vitroProtein kinase cascades in the regulation of cardiac hypertrophyMutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromesMany roads lead to a broken heart: the genetics of dilated cardiomyopathy.Allele-specific silencing of mutant Myh6 transcripts in mice suppresses hypertrophic cardiomyopathyModulation of adverse cardiac remodeling by STARS, a mediator of MEF2 signaling and SRF activityABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gatingCardiac hypertrophy and histone deacetylase-dependent transcriptional repression mediated by the atypical homeodomain protein HopClinical utility of cardiovascular magnetic resonance in hypertrophic cardiomyopathyCell biology of sarcomeric protein engineering: disease modeling and therapeutic potentialCardiac MyBP-C regulates the rate and force of contraction in mammalian myocardiumImportance of genetic evaluation and testing in pediatric cardiomyopathyUnderstanding cardiac sarcomere assembly with zebrafish geneticsElevated expression of the integrin-associated protein PINCH suppresses the defects of Drosophila melanogaster muscle hypercontraction mutantsA Development of Nucleic Chromatin Measurements as a New Prognostic Marker for Severe Chronic Heart FailureChamber Specific Gene Expression Landscape of the Zebrafish HeartThe UNC-45 chaperone is critical for establishing myosin-based myofibrillar organization and cardiac contractility in the Drosophila heart modelSolution Structure of Human Cardiac Troponin C in Complex with the Green Tea Polyphenol, (-)-Epigallocatechin 3-GallateThe cell biology of disease: cellular mechanisms of cardiomyopathy.Cardiac Troponin and Tropomyosin: Structural and Cellular Perspectives to Unveil the Hypertrophic Cardiomyopathy PhenotypeRecent Advances in the Molecular Genetics of Familial Hypertrophic Cardiomyopathy in South Asian DescendantsThe critical role of Akt in cardiovascular functionASK1 associates with troponin T and induces troponin T phosphorylation and contractile dysfunction in cardiomyocytesImpaired cardiac contractility response to hemodynamic stress in S100A1-deficient miceCoding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathyShared genetic causes of cardiac hypertrophy in children and adultsAbnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cellsMutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humansTissue-specific GATA factors are transcriptional effectors of the small GTPase RhoACIP, a cardiac Isl1-interacting protein, represses cardiomyocyte hypertrophyA mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathyhnRNP U protein is required for normal pre-mRNA splicing and postnatal heart development and functionLoss of MicroRNA-155 protects the heart from pathological cardiac hypertrophyAberrant myofibril assembly in tropomodulin1 null mice leads to aborted heart development and embryonic lethalityProx1 maintains muscle structure and growth in the developing heartConditional mutation of the ErbB2 (HER2) receptor in cardiomyocytes leads to dilated cardiomyopathyCardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function.
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P2860
The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms
description
2001 nî lūn-bûn
@nan
2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի փետրվարին 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
The genetic basis for cardiomy ...... ation to mechanistic paradigms
@ast
The genetic basis for cardiomy ...... ation to mechanistic paradigms
@en
The genetic basis for cardiomy ...... ation to mechanistic paradigms
@nl
type
label
The genetic basis for cardiomy ...... ation to mechanistic paradigms
@ast
The genetic basis for cardiomy ...... ation to mechanistic paradigms
@en
The genetic basis for cardiomy ...... ation to mechanistic paradigms
@nl
prefLabel
The genetic basis for cardiomy ...... ation to mechanistic paradigms
@ast
The genetic basis for cardiomy ...... ation to mechanistic paradigms
@en
The genetic basis for cardiomy ...... ation to mechanistic paradigms
@nl
P1433
P1476
The genetic basis for cardiomy ...... ation to mechanistic paradigms
@en
P2093
J G Seidman
P304
P407
P577
2001-02-23T00:00:00Z