About: A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy

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About: A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy Goto Sponge NotDistinct Permalink

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scientific journal article

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rdf:type	Item
description	artículu científicu espublizáu en 2001 (ast) vědecký článek publikovaný v roce 2001 (cs) 2001 թվականի նոյեմբերին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в листопаді 2001 (uk) 2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած (hyw) مقالة علمية (نشرت في نوفمبر 2001) (ar) vedecký článok (publikovaný 2001/11/01) (sk) wetenschappelijk artikel (gepubliceerd op 2001/11/01) (nl) im November 2001 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28586375-D3026BB4-5739-416F-9655-7B04F5F0E1BE
publication date	2001-11-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q28586375-1736D687-944C-4903-866F-BB66E773F8FD wds:Q28586375-5AD3771C-32AC-4221-A4F7-C185A2832B83 wds:Q28586375-729E335E-75AD-45C1-9643-FAB771BFA4B0 wds:Q28586375-BEE96457-24F8-425D-92CD-C25290A729D9 wds:Q28586375-CCC4A31F-11F6-45A9-9005-9FB20FAFB9C9 wds:Q28586375-D9FF4DC7-ED05-4841-934C-BF71B30F707E
OpenCitations bibliographic resource ID	wds:Q28586375-CFBBDC27-75CA-4233-98F2-378EBD886079
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/3858860
author name string	C. E. Seidman D. Fatkin C. Duffy C. Semsarian M. J. Healey M. Giewat
OpenCitations bibliographic resource ID	3858860
rdfs:label	A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy (en) A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy (nl) A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy (ast)
skos:prefLabel	A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy (en) A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy (nl) A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy (ast)
name	A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy (en) A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy (nl) A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy (ast)
author	wds:Q28586375-61584AC3-5C80-41D4-985C-5BC847D2C22E
author	Jonathan G Seidman
title	wds:Q28586375-E3CD0AC9-D25C-4679-9320-1724FE67F0C5
title	A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy (en)
page(s)	wds:Q28586375-64314129-CB48-4E5E-B727-FEE5E73AC8C6
page(s)	2055–2060
instance of	wds:Q28586375-138660C7-B062-4B0F-B66B-84D0A7CE1A0E
instance of	scholarly article
main subject	wds:Q28586375-6A79FEE9-8456-4263-9344-25C4F74D8E46 wds:Q28586375-832F6167-74F2-4C61-A25D-CC16434B3291 wds:Q28586375-833E65E6-3A7C-4D93-9CC2-8434A28CDCF0 wds:Q28586375-DED07188-D6CF-4858-9674-C9B0718B7E39
main subject	hypertrophic cardiomyopathy familial hypertrophic cardiomyopathy murine model Myosin, heavy polypeptide 6, cardiac muscle, alpha
PubMed ID	wds:Q28586375-A6F863E6-5111-458A-B18D-ECA44E728E8D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11708849
PubMed ID	11708849
published in	wds:Q28586375-2AE1BDED-9849-4A69-B40D-190347F60AB4
published in	Journal of Molecular and Cellular Cardiology
issue	wds:Q28586375-58E78989-28FD-49A8-A1EB-E0FCEDD5FCE4
volume	wds:Q28586375-0A551577-ACAA-4655-B86C-753B31086D4D
issue	11
volume	33
DOI	wds:Q28586375-BBF087AD-7ADB-45F6-B2B5-7B1C837E5ADC
DOI	http://dx.doi.org/10.1006/JMCC.2001.1466
DOI	10.1006/JMCC.2001.1466
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28586375
is cites work of	Allele and species dependent contractile defects by restrictive and hypertrophic cardiomyopathy-linked troponin I mutants The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model Prolonged Cre expression driven by the α-myosin heavy chain promoter can be cardiotoxic Cardiac phenotype of mitochondrial creatine kinase knockout mice is modified on a pure C57BL/6 genetic background Sex modifies exercise and cardiac adaptation in mice The cell biology of disease: cellular mechanisms of cardiomyopathy. Modifier genes and protective alleles in humans and mice Genetic basis of hypertrophic cardiomyopathy. Genes, calcium and modifying factors in hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy associated with cardiac beta-myosin heavy chain and troponin I mutations. Renin-angiotensin-aldosterone genotype influences ventricular remodeling in infants with single ventricle Hypertrophic cardiomyopathy: from gene defect to clinical disease Myofilament mechanical performance is enhanced by R403Q myosin in mouse myocardium independent of sex. Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy Genetic variation in angiotensin II type 2 receptor gene influences extent of left ventricular hypertrophy in hypertrophic cardiomyopathy independent of blood pressure Sex hormone receptor gene variation associated with phenotype in male hypertrophic cardiomyopathy patients Left Ventricular Hypertrophy in Rhesus Macaques (Macaca mulatta) at the California National Primate Research Center (1992-2014) Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy Diastolic dysfunction and thin filament dysregulation resulting from excitation-contraction uncoupling in a mouse model of restrictive cardiomyopathy. The genetic landscape of cardiomyopathy and its role in heart failure. Molecular genetics and pathogenesis of cardiomyopathy Molecular genetics in hypertrophic cardiomyopathy: towards individualized management of the disease The Role of Genetic Testing in the Identification of Young Athletes with Inherited Primitive Cardiac Disorders at Risk of Exercise Sudden Death Combinatorial effects of double cardiomyopathy mutant alleles in rodent myocytes: a predictive cellular model of myofilament dysregulation in disease Role of animal models in HCM research
is cites work of	wds:Q36021728-290D63AB-26CB-4A24-8191-3592349505AA wds:Q28472836-2AD8FB90-5CA8-477E-8D00-A1353BF02E44 wds:Q35109802-A8D472FB-6CE3-4CE0-BAB6-02B96F2A4B2E wds:Q34790975-95CCE05E-98EC-453A-9803-61A1768A29EE wds:Q36781777-29ABDF0F-7A06-4793-AD20-F466DA313C0A wds:Q37766184-F8469489-70A5-4DB5-AB83-F8745E5D08B3 wds:Q36773270-D0B14381-E8A6-4693-9DD8-93EBA4B0AA3C wds:Q36625673-D350720D-955A-4C88-9DD2-92B10556A3F9

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