Cargando…
Muscle Chloride Channel Dysfunction in Two Mouse Models of Myotonic Dystrophy
Muscle degeneration and myotonia are clinical hallmarks of myotonic dystrophy type 1 (DM1), a multisystemic disorder caused by a CTG repeat expansion in the 3′ untranslated region of the myotonic dystrophy protein kinase (DMPK) gene. Transgenic mice engineered to express mRNA with expanded (CUG)(250...
Autores principales: | Lueck, John D., Mankodi, Ami, Swanson, Maurice S., Thornton, Charles A., Dirksen, Robert T. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2151606/ https://www.ncbi.nlm.nih.gov/pubmed/17158949 http://dx.doi.org/10.1085/jgp.200609635 |
Ejemplares similares
-
Combinatorial chloride and calcium channelopathy in myotonic dystrophy
por: Cisco, Lily A., et al.
Publicado: (2023) -
Sarcolemmal-restricted localization of functional ClC-1 channels in mouse skeletal muscle
por: Lueck, John D., et al.
Publicado: (2010) -
Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy
por: Sznajder, Łukasz J., et al.
Publicado: (2019) -
Benefits of aerobic exercise in myotonic dystrophy type 1
por: Mackenzie, Samuel J., et al.
Publicado: (2022) -
Downregulation of the Glial GLT1 Glutamate Transporter and Purkinje Cell Dysfunction in a Mouse Model of Myotonic Dystrophy
por: Sicot, Géraldine, et al.
Publicado: (2017)