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Stem Cells International|April 9, 2016
Mutation-Specific Phenotypes in hiPSC-Derived Cardiomyocytes Carrying Either Myosin-Binding Protein C Or α-Tropomyosin Mutation for Hypertrophic CardiomyopathyMarisa Ojala, Chandra Prajapati, Risto-Pekka Pölönen, et al.Cells|May 13, 2020
hiPSC-Derived Cardiomyocyte Model of LQT2 Syndrome Derived from Asymptomatic and Symptomatic Mutation Carriers Reproduces Clinical Differences in Aggregates but Not in Single CellsDisheet Shah, Chandra Prajapati, Kirsi Penttinen, et al.Biomedicines|June 28, 2023
The Junctophilin-2 Mutation p.(Thr161Lys) Is Associated with Hypertrophic Cardiomyopathy Using Patient-Specific iPS Cardiomyocytes and Demonstrates Prolonged Action Potential and Increased ArrhythmogenicityJoona Valtonen, Chandra Prajapati, Reeja Maria Cherian, et al.Cells|June 19, 2019
Modeling of LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem CellsDisheet Shah, Laura Virtanen, Chandra Prajapati, et al.Pageof 2