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Genome Biology|September 15, 2017
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathyMatthias Heinig, Michiel E Adriaens, Sebastian Schafer, et al.The New England Journal of Medicine|February 17, 2012
Truncations of titin causing dilated cardiomyopathyDaniel S Herman, Lien Lam, Matthew R G Taylor, et al.Plos One|March 16, 2017
Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathyUlrike Esslinger, Sophie Garnier, Agathe Korniat, et al.Plos One|February 15, 2020
Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathyUlrike Esslinger, Sophie Garnier, Agathe Korniat, et al.Journal of the American College of Cardiology|September 10, 2021
Phenotypic Expression and Outcomes in Individuals With Rare Genetic Variants of Hypertrophic CardiomyopathyAntonio de Marvao, Kathryn A McGurk, Sean L Zheng, et al.Nature|October 8, 2011
Endonuclease G is a novel determinant of cardiac hypertrophy and mitochondrial functionChris McDermott-Roe, Junmei Ye, Rizwan Ahmed, et al.Nature Medicine|August 2, 2024
The traditional Chinese medicine Qiliqiangxin in heart failure with reduced ejection fraction: a randomized, double-blind, placebo-controlled trialIokfai Cheang, Wenming Yao, Yanli Zhou, et al.Science Translational Medicine|April 17, 2024
Placental senescence pathophysiology is shared between peripartum cardiomyopathy and preeclampsia in mouse and humanJason D Roh, Claire Castro, Andy Yu, et al.American Journal of Human Genetics|May 22, 2021
Non-coding region variants upstream of MEF2C cause severe developmental disorder through three distinct loss-of-function mechanismsCaroline F Wright, Nicholas M Quaife, Laura Ramos-Hernández, et al.Journal of the American College of Cardiology|June 2, 2022
Precision Phenotyping of Dilated Cardiomyopathy Using Multidimensional DataUpasana Tayal, Job A J Verdonschot, Mark R Hazebroek, et al.Pageof 34