Cargando…
Potassium dependent rescue of a myopathy with core-like structures in mouse
Myopathies decrease muscle functionality. Mutations in ryanodine receptor 1 (RyR1) are often associated with myopathies with microscopic core-like structures in the muscle fiber. In this study, we identify a mouse RyR1 model in which heterozygous animals display clinical and pathological hallmarks o...
Autores principales: | Hanson, M Gartz, Wilde, Jonathan J, Moreno, Rosa L, Minic, Angela D, Niswander, Lee |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309926/ https://www.ncbi.nlm.nih.gov/pubmed/25564733 http://dx.doi.org/10.7554/eLife.02923 |
Ejemplares similares
-
Nrf1 to the rescue
por: Ye, Jin
Publicado: (2014) -
BIN1 modulation in vivo rescues dynamin-related myopathy
por: Lionello, Valentina Maria, et al.
Publicado: (2022) -
TMEM132A, a Novel Wnt Signaling Pathway Regulator Through Wntless (WLS) Interaction
por: Li, Binbin, et al.
Publicado: (2020) -
Modulation of Potassium Channels Inhibits Bunyavirus Infection
por: Hover, Samantha, et al.
Publicado: (2016) -
Myopathy Associated With Dermatan Sulfate-Deficient Decorin and Myostatin in Musculocontractural Ehlers-Danlos Syndrome: A Mouse Model Investigation
por: Nitahara-Kasahara, Yuko, et al.
Publicado: (2021)