Lysosomes and the pathogenesis of merosin-deficient congenital muscular dystrophy.

Smith, Sarah J; Fabian, Lacramioara; Sheikh, Adeel; Noche, Ramil; Cui, Xiucheng; Moore, Steven A; Dowling, James J

Smith, Sarah J; Fabian, Lacramioara; Sheikh, Adeel; Noche, Ramil; Cui, Xiucheng; Moore, Steven A; Dowling, James J.

Afiliação

Smith SJ; Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada.
Fabian L; Program for Genetics & Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Sheikh A; Department of Family Medicine, University of Calgary, Calgary T2R 0X7, Alberta.
Noche R; Program for Genetics & Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Cui X; Program for Genetics & Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Moore SA; Schulich School of Medicine and Dentistry, Western University, London, ON N6A 5C1, Canada.
Dowling JJ; Program for Genetics & Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.

Hum Mol Genet ; 31(5): 733-747, 2022 03 03.

Article em En | MEDLINE | ID: mdl-34568901

Assuntos

Distrofias Musculares; Peixe-Zebra; Animais; Humanos; Laminina/genética; Lisossomos/genética; Lisossomos/patologia; Músculo Esquelético/patologia; Distrofias Musculares/patologia; Fatores de Transcrição; Peixe-Zebra/genética

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peixe-Zebra / Distrofias Musculares Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Canadá

Texto completo

Imprimir

XML

PubMed Links

Buscar no Google