Molecular genetics and pathogenesis of hypertrophic cardiomyopathy. - Test2 - elhamkhani - TriplyDB

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

http://www.wikidata.org/entity/Q34021080

about

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants.Molecular modeling of disease causing mutations in domain C1 of cMyBP-C Modifier genes for hypertrophic cardiomyopathy New insights into the pathology of inherited cardiomyopathy.Early results of sarcomeric gene screening from the Egyptian National BA-HCM Program.Reduction of left ventricular longitudinal global and segmental systolic functions in patients with hypertrophic cardiomyopathy: Study of two-dimensional tissue motion annular displacement.Survival and prognostic factors in hypertrophic cardiomyopathy: a meta-analysis.A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity Hypertrophic cardiomyopathy in daily practice: an introduction on diagnosis, prognosis and treatment.To screen or not is not the question--it is when and how to screen.Myosin Head Configurations in Resting and Contracting Murine Skeletal Muscle

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P2860

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

http://www.wikidata.org/entity/Q34021080

description

2001 nî lūn-bûn

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2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2001年の論文

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2001年学术文章

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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

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2001年學術文章

@yue

name

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

@ast

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

@en

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

@nl

type

label

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

@ast

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

@en

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

@nl

prefLabel

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

@ast

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

@en

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

@nl

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Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

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A J Marian

http://www.w3.org/2001/XMLSchema#string

L Salek

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S Lutucuta

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P2860

Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the alpha cardiac myosin heavy chain gene.

Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy

Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein

Hypertrophic cardiomyopathy caused by a novel alpha-tropomyosin mutation (V95A) is associated with mild cardiac phenotype, abnormal calcium binding to troponin, abnormal myosin cycling, and poor prognosis

Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle

Novel splice donor site mutation in the cardiac myosin-binding protein-C gene in familial hypertrophic cardiomyopathy. Characterization Of cardiac transcript and protein

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