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Volumn 277, Issue 14, 2002, Pages 11670-11678
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Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy
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Author keywords
[No Author keywords available]
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Indexed keywords
BIOASSAY;
CALCIUM;
DISEASES;
GENES;
MUSCLE;
POSITIVE IONS;
DIASTOLIC DYSFUNCTION;
BIOCHEMISTRY;
ACTIN;
CALCIUM;
MYOSIN ADENOSINE TRIPHOSPHATASE;
TROPOMYOSIN;
TROPONIN C;
TROPONIN I;
ANIMAL TISSUE;
ARTICLE;
CIRCULAR DICHROISM;
COMPUTER MODEL;
CONTROLLED STUDY;
ENZYME ACTIVITY;
FAMILIAL DISEASE;
GENE MUTATION;
HEART MUSCLE CELL;
HEART MUSCLE CONTRACTILITY;
HEART VENTRICLE HYPERTROPHY;
HYPERTROPHIC CARDIOMYOPATHY;
MISSENSE MUTATION;
MUSCLE TWITCH;
NONHUMAN;
PRIORITY JOURNAL;
ADENOSINE TRIPHOSPHATASES;
AMINO ACID SEQUENCE;
ANIMALS;
ARGININE;
BINDING SITES;
CALCIUM;
CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL;
CIRCULAR DICHROISM;
DOSE-RESPONSE RELATIONSHIP, DRUG;
HUMANS;
MODELS, THEORETICAL;
MOLECULAR SEQUENCE DATA;
MUSCLE CONTRACTION;
MUSCLE FIBERS;
MUTATION;
MUTATION, MISSENSE;
MYOCARDIUM;
MYOSINS;
STRESS, MECHANICAL;
SWINE;
TEMPERATURE;
TIME FACTORS;
TROPONIN;
TROPONIN I;
ANIMALIA;
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EID: 0037023758
PISSN: 00219258
EISSN: None
Source Type: Journal
DOI: 10.1074/jbc.M108912200 Document Type: Article |
Times cited : (77)
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References (46)
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