Your browser doesn't support javascript.
loading
Distinct pathological signatures in human cellular models of myotonic dystrophy subtypes.
Kim, Ellis Y; Barefield, David Y; Vo, Andy H; Gacita, Anthony M; Schuster, Emma J; Wyatt, Eugene J; Davis, Janel L; Dong, Biqin; Sun, Cheng; Page, Patrick; Dellefave-Castillo, Lisa; Demonbreun, Alexis; Zhang, Hao F; McNally, Elizabeth M.
Afiliação
  • Kim EY; Molecular Pathogenesis and Molecular Medicine, The University of Chicago, Chicago, Illinois, USA.
  • Barefield DY; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Vo AH; Committee on Development, Regeneration, and Stem Cell Biology, The University of Chicago, Chicago, Illinois, USA.
  • Gacita AM; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Schuster EJ; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Wyatt EJ; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Davis JL; Department of Biomedical Engineering and.
  • Dong B; Department of Biomedical Engineering and.
  • Sun C; Department of Mechanical Engineering, Northwestern University, Evanston, Illinois, USA.
  • Page P; Department of Mechanical Engineering, Northwestern University, Evanston, Illinois, USA.
  • Dellefave-Castillo L; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Demonbreun A; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Zhang HF; Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • McNally EM; Department of Biomedical Engineering and.
JCI Insight ; 4(6)2019 03 21.
Article em En | MEDLINE | ID: mdl-30730308
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína MyoD / Predisposição Genética para Doença / Distrofia Miotônica Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína MyoD / Predisposição Genética para Doença / Distrofia Miotônica Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article