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Journal of Molecular and Cellular Cardiology|July 4, 2014
Hypertrophic cardiomyopathy associated Lys104Glu mutation in the myosin regulatory light chain causes diastolic disturbance in miceWenrui Huang, Jingsheng Liang, Katarzyna Kazmierczak, et al.The Journal of Clinical Investigation|October 22, 2024
Distinct mechanisms drive divergent phenotypes in hypertrophic and dilated cardiomyopathy-associated TPM1 variantsSaiti S Halder, Michael J Rynkiewicz, Lynne Kim, et al.Journal of Precision Medicine (Amsterdam, Netherlands)|June 4, 2026
Evaluating Pathogenicity of TPM1 Variants of Unknown Significance Using In-silico and In-vitro ModelsSaiti S Halder, Jenette G Bellitto, Michael J Rynkiewicz, et al.Journal of Molecular Biology|April 25, 2016
A Restrictive Cardiomyopathy Mutation in an Invariant Proline at the Myosin Head/Rod Junction Enhances Head Flexibility and Function, Yielding Muscle Defects in DrosophilaMadhulika Achal, Adriana S Trujillo, Girish C Melkani, et al.Proceedings of the National Academy of Sciences of the United States of America|October 5, 2017
Cell volume change through water efflux impacts cell stiffness and stem cell fateMing Guo, Adrian F Pegoraro, Angelo Mao, et al.Pageof 6