Cargando…
γ-Sarcoglycan Deficiency Leads to Muscle Membrane Defects and Apoptosis Independent of Dystrophin
γ-Sarcoglycan is a transmembrane, dystrophin-associated protein expressed in skeletal and cardiac muscle. The murine γ-sarcoglycan gene was disrupted using homologous recombination. Mice lacking γ-sarcoglycan showed pronounced dystrophic muscle changes in early life. By 20 wk of age, these mice deve...
Autores principales: | Hack, Andrew A., Ly, Chantal T., Jiang, Fang, Clendenin, Cynthia J., Sigrist, Kirsten S., Wollmann, Robert L., McNally, Elizabeth M. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1998
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2149352/ https://www.ncbi.nlm.nih.gov/pubmed/9732288 |
Ejemplares similares
-
Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex
por: Lancioni, Alessio, et al.
Publicado: (2011) -
Filamin 2 (Fln2): A Muscle-Specific Sarcoglycan Interacting Protein
por: Thompson, Terri G., et al.
Publicado: (2000) -
Myoclonus dystonia and muscular dystrophy: ɛ‐sarcoglycan is part of the dystrophin‐associated protein complex in brain
por: Waite, Adrian J., et al.
Publicado: (2016) -
Novel γ-sarcoglycan interactors in murine muscle membranes
por: Smith, Tara C., et al.
Publicado: (2022) -
In Vitro Glycosylation
of the Membrane Protein γ-Sarcoglycan
in Nanodiscs
por: Harris, Michael S., et al.
Publicado: (2023)