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Myosin post-translational modifications and function in the presence of myopathy-linked truncating MYH2 mutations.
Sonne, Alexander; Peverelli, Lorenzo; Hernandez-Lain, Aurelio; Domínguez-González, Cristina; Andersen, Jesper L; Milone, Margherita; Beggs, Alan H; Ochala, Julien.
Afiliação
  • Sonne A; Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Peverelli L; Neuromuscular and Rare Diseases Unit, Department of Neuroscience, Fondazione, IRCCS Ca' Granda Ospedale Maggiore, Policlinico, Milan, Italy.
  • Hernandez-Lain A; Neuropathology Unit, Department of Pathology, 12 de Octubre University Hospital, Madrid, Spain.
  • Domínguez-González C; imas12 Research Institute, Rare Diseases Network Biomedical Research Center (CIBERER), 12 de Octubre University Hospital, Madrid, Spain.
  • Andersen JL; imas12 Research Institute, Rare Diseases Network Biomedical Research Center (CIBERER), 12 de Octubre University Hospital, Madrid, Spain.
  • Milone M; Neuromuscular Unit, Department of Neurology, 12 de Octubre University Hospital, Madrid, Spain.
  • Beggs AH; Department of Orthopaedic Surgery, Institute of Sports Medicine Copenhagen, University Copenhagen Hospital-Bispebjerg and Frederiksberg, Copenhagen, Denmark.
  • Ochala J; Center for Healthy Aging, Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Am J Physiol Cell Physiol ; 324(3): C769-C776, 2023 03 01.
Article em En | MEDLINE | ID: mdl-36745529

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Actomiosina / Doenças Musculares Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Actomiosina / Doenças Musculares Limite: Adult / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article