Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy - Wikidata - awgldk - TriplyDB

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

http://www.wikidata.org/entity/Q24642218

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Molecular genetic and functional characterization implicate muscle-restricted coiled-coil gene (MURC) as a causal gene for familial dilated cardiomyopathy Autoimmunoreactive IgGs from patients with postural orthostatic tachycardia syndrome Emerging directions in the genetics of atrial fibrillation Importance of genetic evaluation and testing in pediatric cardiomyopathy Chamber Specific Gene Expression Landscape of the Zebrafish Heart Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy Disrupted autophagy undermines skeletal muscle adaptation and integrity Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy Telethonin deficiency is associated with maladaptation to biomechanical stress in the mammalian heart Targeting the sarcomere to correct muscle function Shared genetic causes of cardiac hypertrophy in children and adults Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands A class III PDZ binding motif in the myotilin and FATZ families binds enigma family proteins: a common link for Z-disc myopathies Establishment of a prediction model of changing trends in cardiac hypertrophy disease based on microarray data screening.Rescue of familial cardiomyopathies by modifications at the level of sarcomere and Ca2+ fluxes.Post-translational regulation of calsarcin-1 during pressure overload-induced cardiac hypertrophy Hypertrophic cardiomyopathy: from genetics to treatment Experimental therapies in hypertrophic cardiomyopathy Genetics of hypertrophic cardiomyopathy.Cardiac Z-disc signaling network.Mutations in NEXN, a Z-disc gene, are associated with hypertrophic cardiomyopathy Sarcomere gene mutations in hypertrophy and heart failure.Research priorities in hypertrophic cardiomyopathy: report of a Working Group of the National Heart, Lung, and Blood Institute.Identifying sarcomere gene mutations in hypertrophic cardiomyopathy: a personal history Molecular biology of heart disease.Genetics and clinical destiny: improving care in hypertrophic cardiomyopathy Molecular cloning and characterization of different expression of MYOZ2 and MYOZ3 in Tianfu goat.Mechanotransduction in cardiac hypertrophy and failure.The sarcomeric Z-disc and Z-discopathies.Human molecular genetic and functional studies identify TRIM63, encoding Muscle RING Finger Protein 1, as a novel gene for human hypertrophic cardiomyopathy.Pathogenesis of hypertrophic cardiomyopathy caused by myozenin 2 mutations is independent of calcineurin activity Z-disc transcriptional coupling, sarcomeroptosis and mechanoptosis [corrected].Genetic determinants of cardiac hypertrophy.Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all Targeted next-generation sequencing helps to decipher the genetic and phenotypic heterogeneity of hypertrophic cardiomyopathy G9a inhibits MEF2C activity to control sarcomere assembly.Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.Role of the sarcomeric Z-disc in the pathogenesis of cardiomyopathy.Flexible expressed region analysis for RNA-seq with derfinder.Genetic anticipation in a special form of hypertrophic cardiomyopathy with sudden cardiac death in a family with 74 members across 5 generations.

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P2860

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

http://www.wikidata.org/entity/Q24642218

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2007 nî lūn-bûn

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2007 թուականի Մարտին հրատարակուած գիտական յօդուած

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2007 թվականի մարտին հրատարակված գիտական հոդված

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2007年の論文

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Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

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Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

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Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

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Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

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Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

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Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

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prefLabel

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

@ast

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

@en

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

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Circulation Research

P1476

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

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P2093

Adriana Osio

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Ali J Marian

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James T Willerson

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Lily Tan

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Robert Roberts

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Sanjay Shete

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Sherif F Nagueh

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Suet N Chen

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P2860

Calsarcins, a novel family of sarcomeric calcineurin-binding proteins

The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

Multiple sequence alignment with the Clustal series of programs

Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

Genetic causes of human heart failure.

Mice lacking calsarcin-1 are sensitized to calcineurin signaling and show accelerated cardiomyopathy in response to pathological biomechanical stress.

An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy.

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17347475

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2775141

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