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1Academic Journal
المؤلفون: Carmen Suay-Corredera (10904886), Maria Rosaria Pricolo (10904889), Diana Velázquez-Carreras (10904892), Divya Pathak (79579), Neha Nandwani (10904895), Carolina Pimenta-Lopes (10904898), David Sánchez-Ortiz (10904901), Iñigo Urrutia-Irazabal (10904904), Silvia Vilches (442014), Fernando Dominguez (5650558), Giulia Frisso (5222282), Lorenzo Monserrat (2622139), Pablo García-Pavía (10904907), David de Sancho (9455422), James A. Spudich (10904910), Kathleen M. Ruppel (10904913), Elías Herrero-Galán (2005204), Jorge Alegre-Cebollada (1611883)
مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Cell Biology, Genetics, Molecular Biology, Physiology, Developmental Biology, Cancer, Computational Biology, Biological Sciences not elsewhere classified, Physical Sciences not elsewhere classified, cMyBP-C mutations, results show, nanomechanical phenotypes, 40 pN, Cause Hypertrophic Cardiomyopathy H., mutations cause, mutation R 495W, motor myosin, Cardiac Myosin-Binding Protein C Mu., actomyosin filaments, R 502Q, HCM mutations, protein structure, RNA, myosin-binding protein C, mutations perturb, nonpathogenic variants, cMyBP-C domains
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2
المؤلفون: Carmen Suay-Corredera (10904886), Maria Rosaria Pricolo (10904889), Diana Velázquez-Carreras (10904892), Divya Pathak (79579), Neha Nandwani (10904895), Carolina Pimenta-Lopes (10904898), David Sánchez-Ortiz (10904901), Iñigo Urrutia-Irazabal (10904904), Silvia Vilches (442014), Fernando Dominguez (5650558), Giulia Frisso (5222282), Lorenzo Monserrat (2622139), Pablo García-Pavía (10904907), David de Sancho (9455422), James A. Spudich (10904910), Kathleen M. Ruppel (10904913), Elías Herrero-Galán (2005204), Jorge Alegre-Cebollada (1611883)
مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Cell Biology, Genetics, Molecular Biology, Physiology, Developmental Biology, Cancer, Computational Biology, Biological Sciences not elsewhere classified, Physical Sciences not elsewhere classified, cMyBP-C mutations, results show, nanomechanical phenotypes, 40 pN, Cause Hypertrophic Cardiomyopathy H., mutations cause, mutation R 495W, motor myosin, Cardiac Myosin-Binding Protein C Mu., actomyosin filaments, R 502Q, HCM mutations, protein structure, RNA, myosin-binding protein C, mutations perturb, nonpathogenic variants, cMyBP-C domains
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3
المؤلفون: Carmen Suay-Corredera (10904886), Maria Rosaria Pricolo (10904889), Diana Velázquez-Carreras (10904892), Divya Pathak (79579), Neha Nandwani (10904895), Carolina Pimenta-Lopes (10904898), David Sánchez-Ortiz (10904901), Iñigo Urrutia-Irazabal (10904904), Silvia Vilches (442014), Fernando Dominguez (5650558), Giulia Frisso (5222282), Lorenzo Monserrat (2622139), Pablo García-Pavía (10904907), David de Sancho (9455422), James A. Spudich (10904910), Kathleen M. Ruppel (10904913), Elías Herrero-Galán (2005204), Jorge Alegre-Cebollada (1611883)
مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Cell Biology, Genetics, Molecular Biology, Physiology, Developmental Biology, Cancer, Computational Biology, Biological Sciences not elsewhere classified, Physical Sciences not elsewhere classified, cMyBP-C mutations, results show, nanomechanical phenotypes, 40 pN, Cause Hypertrophic Cardiomyopathy H., mutations cause, mutation R 495W, motor myosin, Cardiac Myosin-Binding Protein C Mu., actomyosin filaments, R 502Q, HCM mutations, protein structure, RNA, myosin-binding protein C, mutations perturb, nonpathogenic variants, cMyBP-C domains