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BMC Medical Genetics|March 30, 2006
Arrhythmogenic right ventricular cardiomyopathy type 6 (ARVC6): support for the locus assignment, narrowing of the critical region and mutation screening of three candidate genesLuzuko O Matolweni, Soraya Bardien, George Rebello, et al.The Journal of Biological Chemistry|June 1, 2005
Dilated cardiomyopathy mutations in three thin filament regulatory proteins result in a common functional phenotypeMahmooda Mirza, Steven Marston, Ruth Willott, et al.Cardiovascular Research|April 22, 2024
Mechanisms of ischaemia-induced arrhythmias in hypertrophic cardiomyopathy: a large-scale computational studyJames A Coleman, Ruben Doste, Zakariye Ashkir, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2017
"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes ProjectElizabeth Ormondroyd, Michael P Mackley, Edward Blair, et al.BMC Developmental Biology|June 24, 2010
Changes in creatine transporter function during cardiac maturation in the ratAlexandra Fischer, Michiel Ten Hove, Liam Sebag-Montefiore, et al.Journal of Molecular and Cellular Cardiology|February 9, 2005
Mechanisms of creatine depletion in chronically failing rat heartMichiel Ten Hove, Sharon Chan, Craig Lygate, et al.Journal of the American College of Cardiology|June 15, 2019
Genetic Risk Score for Coronary Disease Identifies Predispositions to Cardiovascular and Noncardiovascular DiseasesIoanna Ntalla, Stavroula Kanoni, Lingyao Zeng, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|November 27, 2018
Electrocardiogram phenotypes in hypertrophic cardiomyopathy caused by distinct mechanisms: apico-basal repolarization gradients vs. Purkinje-myocardial coupling abnormalitiesAurore Lyon, Alfonso Bueno-Orovio, Ernesto Zacur, et al.Journal of the American College of Cardiology|July 29, 2026
Cross-Ancestry Proteogenomic Analyses Identified New Therapeutic Insights for Ischemic Heart DiseaseMohsen Mazidi, Neil Wright, Alfred Pozarickij, et al.Pflugers Archiv : European Journal of Physiology|October 6, 2006
Functional effects of the DCM mutant Gly159Asp troponin C in skinned muscle fibresLaura C Preston, Simon Lipscomb, Paul Robinson, et al.Pageof 43