Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.

Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.

Item
http://www.wikidata.org/entity/Q33909960
Cryo-EM structure of a human cytoplasmic actomyosin complex at near-atomic resolutionLong-term follow-up of R403WMYH7 and R92WTNNT2 HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progressionThe ubiquitin-proteasome system and nonsense-mediated mRNA decay in hypertrophic cardiomyopathyThe electrocardiogram is a more sensitive indicator than echocardiography of hypertrophic cardiomyopathy in families with a mutation in the MYH7 geneFamilial hypertrophic cardiomyopathy owing to double heterozygosity for a 403Arg--> Trp mutation in exon 13 of the MYH7 gene and a novel mutation, 453Arg--> His, in exon 14 of the MYH7 gene: A case report.The molecular genetic basis for hypertrophic cardiomyopathy.Biological, biochemical, and kinetic effects of mutations of the cardiomyopathy loop of Dictyostelium myosin II: importance of ALA400Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder eventsFunctional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy.Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathyModifier genes for hypertrophic cardiomyopathyMaternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene.Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations.Effects of ATP and actin-filament binding on the dynamics of the myosin II S1 domain.The cardiac myosin heavy chain Arg-403-->Gln mutation that causes hypertrophic cardiomyopathy does not affect the actin- or ATP-binding capacities of two size-limited recombinant myosin heavy chain fragments.Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy.
P2860

Familial hypertrophic cardiomyopathy. Microsatellite haplotyping and identification of a hot spot for mutations in the beta-myosin heavy chain gene.

Item
http://www.wikidata.org/entity/Q33909960
description
1993 nî lūn-bûn
@nan
1993 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Familial hypertrophic cardiomy ...... beta-myosin heavy chain gene.
@ast
Familial hypertrophic cardiomy ...... beta-myosin heavy chain gene.
@en
type
label
Familial hypertrophic cardiomy ...... beta-myosin heavy chain gene.
@ast
Familial hypertrophic cardiomy ...... beta-myosin heavy chain gene.
@en
prefLabel
Familial hypertrophic cardiomy ...... beta-myosin heavy chain gene.
@ast
Familial hypertrophic cardiomy ...... beta-myosin heavy chain gene.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921
P932
P356
P1433
P1476
Familial hypertrophic cardiomy ...... beta-myosin heavy chain gene.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921
P932