Cargando…
A human skeletal muscle interactome centered on proteins involved in muscular dystrophies: LGMD interactome
BACKGROUND: The complexity of the skeletal muscle and the identification of numerous human disease-causing mutations in its constitutive proteins make it an interesting tissue for proteomic studies aimed at understanding functional relationships of interacting proteins in both health and diseases. M...
Autores principales: | Blandin, Gaëlle, Marchand, Sylvie, Charton, Karine, Danièle, Nathalie, Gicquel, Evelyne, Boucheteil, Jean-Baptiste, Bentaib, Azéddine, Barrault, Laetitia, Stockholm, Daniel, Bartoli, Marc, Richard, Isabelle |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3610214/ https://www.ncbi.nlm.nih.gov/pubmed/23414517 http://dx.doi.org/10.1186/2044-5040-3-3 |
Ejemplares similares
-
Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T)
por: Oestergaard, S.T., et al.
Publicado: (2016) -
Defining Clinical Endpoints in Limb Girdle Muscular Dystrophy: A GRASP-LGMD study
por: Doody, Amy, et al.
Publicado: (2023) -
Dlk1-Dio3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in Duchenne muscular dystrophy
por: Vu Hong, Ai, et al.
Publicado: (2022) -
Schizophrenia interactome: fully-labeled interactome network
por: Ganapathiraju, Madhavi, et al.
Publicado: (2016) -
Duchenne muscular dystrophy–like phenotype in an LGMD2I patient with novel FKRP gene variants
por: Okazaki, Tetsuya, et al.
Publicado: (2020)