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Pharmacogenetics and Genomics|May 3, 2005
A mutation in the drug transporter gene ABCC2 associated with impaired methotrexate eliminationJean-Sébastien Hulot, Eric Villard, Ange Maguy, et al.
Lancet (London, England)|December 26, 2008
Cytochrome P450 2C19 polymorphism in young patients treated with clopidogrel after myocardial infarction: a cohort studyJean-Philippe Collet, Jean-Sébastien Hulot, Anna Pena, et al.
Plos One|October 3, 2013
Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient heartsAlexia Vite, Estelle Gandjbakhch, Catherine Prost, et al.
Applied Optics|May 2, 2008
In-flight performance and calibration of SPICAV SOIR onboard Venus ExpressArnaud Mahieux, Sophie Berkenbosch, Roland Clairquin, et al.
Archives of Medical Science : AMS|May 18, 2016
Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathiesAndreas Perrot, Pavol Tomasov, Eric Villard, et al.
European Journal of Heart Failure|November 16, 2012
A novel genetic variant in the transcription factor Islet-1 exerts gain of function on myocyte enhancer factor 2C promoter activityFelix W Friedrich, Gilles Dilanian, Patricia Khattar, et al.
Genetics in Medicine Open|January 16, 2026
Methodology of DNA extraction and sequencing from living cardiomyocytes collected by catheter in humansFlavie Ader, Céline Guilbeau-Frugier, Emeline Lhuillier, et al.
Human Molecular Genetics|May 6, 2025
Rare DCM associated variants in pre-miR-208a disrupt miRNA maturation and functionYolan J Reckman, Jan Haas, Ingeborg van der Made, et al.
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