Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
about
The structure and regulation of human muscle α-actininFounder mutations in hypertrophic cardiomyopathy patients in the NetherlandsMutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humansThe actinin family of actin cross-linking proteins - a genetic perspective.Deletion of Drosophila muscle LIM protein decreases flight muscle stiffness and power generation.Z-band alternatively spliced PDZ motif protein (ZASP) is the major O-linked β-N-acetylglucosamine-substituted protein in human heart myofibrils"Z"eroing in on the role of Cypher in striated muscle function, signaling, and human disease.Selective deletion of long but not short Cypher isoforms leads to late-onset dilated cardiomyopathy.ZASP interacts with the mechanosensing protein Ankrd2 and p53 in the signalling network of striated muscle.Histologic characterization of hypertrophic cardiomyopathy with and without myofilament mutations.Investigation of Pathogenic Genes in Chinese sporadic Hypertrophic Cardiomyopathy Patients by Whole Exome SequencingEvolving molecular diagnostics for familial cardiomyopathies: at the heart of it allCardiac-specific ablation of Cypher leads to a severe form of dilated cardiomyopathy with premature death.Expression patterns of cardiac myofilament proteins: genomic and protein analysis of surgical myectomy tissue from patients with obstructive hypertrophic cardiomyopathy.Relationship between sex, shape, and substrate in hypertrophic cardiomyopathy.Role of the sarcomeric Z-disc in the pathogenesis of cardiomyopathy.Genetics in dilated cardiomyopathy.Animal Models of Congenital Cardiomyopathies Associated With Mutations in Z-Line Proteins.Coexistence of congenital left ventricular aneurysm and prominent left ventricular trabeculation in a patient with LDB3 mutation: a case report.Hypertrophic cardiomyopathy mutations in the calponin-homology domain of ACTN2 affect actin binding and cardiomyocyte Z-disc incorporation.Genetic basis of end-stage hypertrophic cardiomyopathy.A novel mutation in the PDZ-like motif of ZASP causes distal ZASP-related myofibrillar myopathy.Mechanical unfolding reveals stable 3-helix intermediates in talin and α-catenin.
P2860
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P2860
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
description
2006 nî lūn-bûn
@nan
2006 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
@ast
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
@en
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
@nl
type
label
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
@ast
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
@en
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
@nl
prefLabel
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
@ast
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
@en
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
@nl
P2093
P1476
Echocardiographic-determined septal morphology in Z-disc hypertrophic cardiomyopathy
@en
P2093
Bernard J Gersh
J Martijn Bos
Jeanne L Theis
Josepha Binder
Matteo Vatta
Melissa L Will
Michael J Ackerman
Steve R Ommen
Virginia B Bartleson
P304
P356
10.1016/J.BBRC.2006.10.119
P407
P577
2006-12-29T00:00:00Z