A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy
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The cell biology of disease: cellular mechanisms of cardiomyopathy.The Role of Genetic Testing in the Identification of Young Athletes with Inherited Primitive Cardiac Disorders at Risk of Exercise Sudden DeathCombinatorial effects of double cardiomyopathy mutant alleles in rodent myocytes: a predictive cellular model of myofilament dysregulation in diseaseDiastolic dysfunction and thin filament dysregulation resulting from excitation-contraction uncoupling in a mouse model of restrictive cardiomyopathy.The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model.Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromesHypertrophic cardiomyopathy: from gene defect to clinical disease.Renin-angiotensin-aldosterone genotype influences ventricular remodeling in infants with single ventricle.Prolonged Cre expression driven by the α-myosin heavy chain promoter can be cardiotoxic.Molecular genetics in hypertrophic cardiomyopathy: towards individualized management of the disease.Genes, calcium and modifying factors in hypertrophic cardiomyopathy.Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy.Genetic basis of hypertrophic cardiomyopathy.Allele and species dependent contractile defects by restrictive and hypertrophic cardiomyopathy-linked troponin I mutantsGenetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy.Left Ventricular Hypertrophy in Rhesus Macaques (Macaca mulatta) at the California National Primate Research Center (1992-2014)Sex modifies exercise and cardiac adaptation in miceThe genetic landscape of cardiomyopathy and its role in heart failure.Myofilament mechanical performance is enhanced by R403Q myosin in mouse myocardium independent of sex.Genetic variation in angiotensin II type 2 receptor gene influences extent of left ventricular hypertrophy in hypertrophic cardiomyopathy independent of blood pressure
P2860
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P2860
A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy
description
2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2001
@ast
im November 2001 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2001/11/01)
@sk
vědecký článek publikovaný v roce 2001
@cs
wetenschappelijk artikel (gepubliceerd op 2001/11/01)
@nl
наукова стаття, опублікована в листопаді 2001
@uk
مقالة علمية (نشرت في نوفمبر 2001)
@ar
name
A polymorphic modifier gene al ...... al hypertrophic cardiomyopathy
@ast
A polymorphic modifier gene al ...... al hypertrophic cardiomyopathy
@en
A polymorphic modifier gene al ...... al hypertrophic cardiomyopathy
@nl
type
label
A polymorphic modifier gene al ...... al hypertrophic cardiomyopathy
@ast
A polymorphic modifier gene al ...... al hypertrophic cardiomyopathy
@en
A polymorphic modifier gene al ...... al hypertrophic cardiomyopathy
@nl
prefLabel
A polymorphic modifier gene al ...... al hypertrophic cardiomyopathy
@ast
A polymorphic modifier gene al ...... al hypertrophic cardiomyopathy
@en
A polymorphic modifier gene al ...... al hypertrophic cardiomyopathy
@nl
P2093
P3181
P356
P1476
A polymorphic modifier gene al ...... al hypertrophic cardiomyopathy
@en
P2093
C. E. Seidman
C. Semsarian
J. G. Seidman
M. J. Healey
P304
P3181
P356
10.1006/JMCC.2001.1466
P577
2001-11-01T00:00:00Z