Cargando…
Transcriptomic analysis of dystrophin RNAi knockdown reveals a central role for dystrophin in muscle differentiation and contractile apparatus organization
BACKGROUND: Duchenne muscular dystrophy (DMD) is a fatal muscle wasting disorder caused by mutations in the dystrophin gene. DMD has a complex and as yet incompletely defined molecular pathophysiology hindering development of effective ameliorative approaches. Transcriptomic studies so far conducted...
Autores principales: | Ghahramani Seno, Mohammad M, Trollet, Capucine, Athanasopoulos, Takis, Graham, Ian R, Hu, Pingzhao, Dickson, George |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2890566/ https://www.ncbi.nlm.nih.gov/pubmed/20515474 http://dx.doi.org/10.1186/1471-2164-11-345 |
Ejemplares similares
-
The importance of dystrophin and the dystrophin associated proteins in vascular smooth muscle
por: Kaplan, Katherine M., et al.
Publicado: (2022) -
Dystrophins and dystrobrevins
por: Roberts, Roland G
Publicado: (2001) -
Effects of Mini-Dystrophin on Dystrophin-Deficient, Human Skeletal Muscle-Derived Cells
por: Meng, Jinhong, et al.
Publicado: (2020) -
piggyBac transposons expressing full-length human dystrophin enable genetic correction of dystrophic mesoangioblasts
por: Loperfido, Mariana, et al.
Publicado: (2016) -
Morpholino Oligomer-Induced Dystrophin Isoforms to Map the Functional Domains in the Dystrophin Protein
por: Li, Dunhui, et al.
Publicado: (2020)