Cargando…
Calpain 3 deficiency affects SERCA expression and function in the skeletal muscle
Limb-girdle muscular dystrophy type 2A (LGMD2A) is a form of muscular dystrophy caused by mutations in calpain 3 (CAPN3). Several studies have implicated Ca(2+) dysregulation as an underlying event in several muscular dystrophies, including LGMD2A. In this study we used mouse and human myotube cultu...
Autores principales: | Toral-Ojeda, Ivan, Aldanondo, Garazi, Lasa-Elgarresta, Jaione, Lasa-Fernández, Haizpea, Fernández-Torrón, Roberto, López de Munain, Adolfo, Vallejo-Illarramendi, Ainara |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836212/ https://www.ncbi.nlm.nih.gov/pubmed/27055500 http://dx.doi.org/10.1017/erm.2016.9 |
Ejemplares similares
-
A genotyping method combining primer competition PCR with HRM analysis to identify point mutations in Duchenne animal models
por: Lasa-Fernandez, Haizpea, et al.
Publicado: (2020) -
Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations
por: Lasa-Elgarresta, Jaione, et al.
Publicado: (2019) -
Targeting the Ubiquitin-Proteasome System in Limb-Girdle Muscular Dystrophy With CAPN3 Mutations
por: Lasa-Elgarresta, Jaione, et al.
Publicado: (2022) -
Bacterial calpains and the evolution of the calpain (C2) family of peptidases
por: Rawlings, Neil D.
Publicado: (2015) -
Contractile force assessment methods for in vitro skeletal muscle tissues
por: Vesga-Castro, Camila, et al.
Publicado: (2022)