scholarly article | Q13442814 |
P2093 | author name string | Danuta Szczesna-Cordary | |
Katarzyna Kazmierczak | |||
Michelle Jones | |||
Hsin-Yueh Liang | |||
Theodore P Abraham | |||
Gary D Lopaschuk | |||
Cory S Wagg | |||
Aurelio C Pinheiro | |||
P2860 | cites work | Binding of monovalent and divalent myosin fragments onto sites on actin | Q40925828 |
Activation of striated muscle: nearest-neighbor regulatory-unit and cross-bridge influence on myofilament kinetics | Q44169829 | ||
Beneficial effects of trimetazidine in ex vivo working ischemic hearts are due to a stimulation of glucose oxidation secondary to inhibition of long-chain 3-ketoacyl coenzyme a thiolase | Q44517385 | ||
Familial Hypertrophic Cardiomyopathy-linked Alterations in Ca2+ Binding of Human Cardiac Myosin Regulatory Light Chain Affect Cardiac Muscle Contraction | Q44640488 | ||
One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region. | Q50579042 | ||
Echocardiographic measurement of left ventricular mass and volume in normotensive and hypertensive rats. Necropsy validation | Q68576295 | ||
The purification of cardiac myofibrils with Triton X-100 | Q68635492 | ||
Prolonged Ca2+ and force transients in myosin RLC transgenic mouse fibers expressing malignant and benign FHC mutations | Q79890549 | ||
Myosin regulatory light chain E22K mutation results in decreased cardiac intracellular calcium and force transients | Q80557981 | ||
Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylation | Q24290577 | ||
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle | Q24324826 | ||
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations | Q24680552 | ||
Identification of the genotypes causing hypertrophic cardiomyopathy in northern Sweden | Q28180906 | ||
Calcium and cardiac rhythms: physiological and pathophysiological | Q28184852 | ||
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy | Q28198707 | ||
The overall pattern of cardiac contraction depends on a spatial gradient of myosin regulatory light chain phosphorylation | Q28208615 | ||
Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy | Q28211536 | ||
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy | Q28267002 | ||
Altered intracellular Ca2+ handling in heart failure | Q33683757 | ||
Hypertrophic cardiomyopathy: a systematic review | Q34117625 | ||
Regulatory light chains of striated muscle myosin. Structure, function and malfunction | Q35137462 | ||
Sarcomeric proteins and familial hypertrophic cardiomyopathy: linking mutations in structural proteins to complex cardiovascular phenotypes | Q36369925 | ||
Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics | Q36960609 | ||
Malignant familial hypertrophic cardiomyopathy D166V mutation in the ventricular myosin regulatory light chain causes profound effects in skinned and intact papillary muscle fibers from transgenic mice | Q37123961 | ||
Regulatory light chain mutations associated with cardiomyopathy affect myosin mechanics and kinetics | Q37175862 | ||
Molecular genetic studies of familial hypertrophic cardiomyopathy | Q40829741 | ||
Noninvasive doppler echocardiographic evaluation of left ventricular filling pressures in patients with cardiomyopathies: a simultaneous Doppler echocardiographic and cardiac catheterization study | Q40922919 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | diastole | Q492905 |
hypertrophic cardiomyopathy | Q1364270 | ||
familial hypertrophic cardiomyopathy | Q56014654 | ||
Diastolic function | Q30314111 | ||
P304 | page(s) | 84-92 | |
P577 | publication date | 2009-04-01 | |
P1433 | published in | Cardiovascular Research | Q4642329 |
P1476 | title | Diastolic dysfunction in familial hypertrophic cardiomyopathy transgenic model mice | |
P478 | volume | 82 |
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