Hypertrophic cardiomyopathy: from gene defect to clinical disease.
about
Cardiomyopathy classification: ongoing debate in the genomics eraArray lessons from the heart: focus on the genome and transcriptome of cardiomyopathies.Approaching the facts between genetic mutation and clinical practice of hypertrophic cardiomyopathy: A case report with RAF1 770C>T mutant.Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy.Myosin binding protein C: structural abnormalities in familial hypertrophic cardiomyopathy.Focal exposure of limited lung volumes to high-dose irradiation down-regulated organ development-related functions and up-regulated the immune response in mouse pulmonary tissues.Genes, calcium and modifying factors in hypertrophic cardiomyopathy.Conformation and Dynamics of the Troponin I C-Terminal Domain: Combining Single-Molecule and Computational Approaches for a Disordered Protein Region.Left Ventricular Hypertrophy in Rhesus Macaques (Macaca mulatta) at the California National Primate Research Center (1992-2014)Alterations in Multi-Scale Cardiac Architecture in Association With Phosphorylation of Myosin Binding Protein-C.Anesthetic considerations in the patient with valvular heart disease undergoing noncardiac surgery.Advances in the prevention of sudden cardiac death in the young.Precision medicine approach to genetic cardiomyopathy.Order-Disorder Transitions in the Cardiac Troponin Complex.Fluid mechanics of blood flow in human fetal left ventricles based on patient-specific 4D ultrasound scans.Hypertrophic cardiomyopathy-linked mutation D145E drastically alters calcium binding by the C-domain of cardiac troponin C.Innate immunity and remodelling.Effect of hypertrophic cardiomyopathy-linked troponin C mutations on the response of reconstituted thin filaments to calcium upon troponin I phosphorylation.Absence of synemin in mice causes structural and functional abnormalities in heart.Mutation analysis of the natriuretic peptide precursor B (NPPB) gene in patients with hypertrophic cardiomyopathy.Connective tissue growth factor and bone morphogenetic protein 2 are induced following myocardial ischemia in mice and humans.Developmental cardiac hypertrophy in a mouse model of prolidase deficiency.A novel mouse model of X-linked cardiac hypertrophy.Ile90Met, a novel mutation in the cardiac troponin T gene for familial hypertrophic cardiomyopathy in a Chinese pedigree.
P2860
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P2860
Hypertrophic cardiomyopathy: from gene defect to clinical disease.
description
2003 nî lūn-bûn
@nan
2003 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Hypertrophic cardiomyopathy: from gene defect to clinical disease.
@ast
Hypertrophic cardiomyopathy: from gene defect to clinical disease.
@en
type
label
Hypertrophic cardiomyopathy: from gene defect to clinical disease.
@ast
Hypertrophic cardiomyopathy: from gene defect to clinical disease.
@en
prefLabel
Hypertrophic cardiomyopathy: from gene defect to clinical disease.
@ast
Hypertrophic cardiomyopathy: from gene defect to clinical disease.
@en
P2860
P356
P1433
P1476
Hypertrophic cardiomyopathy: from gene defect to clinical disease.
@en
P2093
Man-Wei Chung
Tatiana Tsoutsman
P2860
P2888
P356
10.1038/SJ.CR.7290146
P577
2003-02-01T00:00:00Z