Diastolic dysfunction in familial hypertrophic cardiomyopathy transgenic model mice

scientific article

Diastolic dysfunction in familial hypertrophic cardiomyopathy transgenic model mice is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1093/CVR/CVP016
P8608Fatcat IDrelease_y24jyljmhvdmzjfme6gza3inbe
P3181OpenCitations bibliographic resource ID695266
P932PMC publication ID2721639
P698PubMed publication ID19150977
P5875ResearchGate publication ID23798073

P2093author name stringDanuta Szczesna-Cordary
Katarzyna Kazmierczak
Michelle Jones
Hsin-Yueh Liang
Theodore P Abraham
Gary D Lopaschuk
Cory S Wagg
Aurelio C Pinheiro
P2860cites workBinding of monovalent and divalent myosin fragments onto sites on actinQ40925828
Activation of striated muscle: nearest-neighbor regulatory-unit and cross-bridge influence on myofilament kineticsQ44169829
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 thiolaseQ44517385
Familial Hypertrophic Cardiomyopathy-linked Alterations in Ca2+ Binding of Human Cardiac Myosin Regulatory Light Chain Affect Cardiac Muscle ContractionQ44640488
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 validationQ68576295
The purification of cardiac myofibrils with Triton X-100Q68635492
Prolonged Ca2+ and force transients in myosin RLC transgenic mouse fibers expressing malignant and benign FHC mutationsQ79890549
Myosin regulatory light chain E22K mutation results in decreased cardiac intracellular calcium and force transientsQ80557981
Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylationQ24290577
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscleQ24324826
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populationsQ24680552
Identification of the genotypes causing hypertrophic cardiomyopathy in northern SwedenQ28180906
Calcium and cardiac rhythms: physiological and pathophysiologicalQ28184852
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategyQ28198707
The overall pattern of cardiac contraction depends on a spatial gradient of myosin regulatory light chain phosphorylationQ28208615
Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathyQ28211536
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyQ28267002
Altered intracellular Ca2+ handling in heart failureQ33683757
Hypertrophic cardiomyopathy: a systematic reviewQ34117625
Regulatory light chains of striated muscle myosin. Structure, function and malfunctionQ35137462
Sarcomeric proteins and familial hypertrophic cardiomyopathy: linking mutations in structural proteins to complex cardiovascular phenotypesQ36369925
Genetic basis of hypertrophic cardiomyopathy: from bench to the clinicsQ36960609
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 miceQ37123961
Regulatory light chain mutations associated with cardiomyopathy affect myosin mechanics and kineticsQ37175862
Molecular genetic studies of familial hypertrophic cardiomyopathyQ40829741
Noninvasive doppler echocardiographic evaluation of left ventricular filling pressures in patients with cardiomyopathies: a simultaneous Doppler echocardiographic and cardiac catheterization studyQ40922919
P433issue1
P407language of work or nameEnglishQ1860
P921main subjectdiastoleQ492905
hypertrophic cardiomyopathyQ1364270
familial hypertrophic cardiomyopathyQ56014654
Diastolic functionQ30314111
P304page(s)84-92
P577publication date2009-04-01
P1433published inCardiovascular ResearchQ4642329
P1476titleDiastolic dysfunction in familial hypertrophic cardiomyopathy transgenic model mice
P478volume82

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