Cargando…
α1-Syntrophin–deficient skeletal muscle exhibits hypertrophy and aberrant formation of neuromuscular junctions during regeneration
α1-Syntrophin is a member of the family of dystrophin-associated proteins; it has been shown to recruit neuronal nitric oxide synthase and the water channel aquaporin-4 to the sarcolemma by its PSD-95/SAP-90, Discs-large, ZO-1 homologous domain. To examine the role of α1-syntrophin in muscle regener...
Autores principales: | Hosaka, Yukio, Yokota, Toshifumi, Miyagoe-Suzuki, Yuko, Yuasa, Katsutoshi, Imamura, Michihiro, Matsuda, Ryoichi, Ikemoto, Takaaki, Kameya, Shuhei, Takeda, Shin'ichi |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2002
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173222/ https://www.ncbi.nlm.nih.gov/pubmed/12221071 http://dx.doi.org/10.1083/jcb.200204076 |
Ejemplares similares
-
Absence of α-Syntrophin Leads to Structurally Aberrant Neuromuscular Synapses Deficient in Utrophin
por: Adams, Marvin E., et al.
Publicado: (2000) -
Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains
por: Nichols, Bailey, et al.
Publicado: (2015) -
Syntrophin binds to an alternatively spliced exon of dystrophin
Publicado: (1995) -
Differential Association of Syntrophin Pairs with the Dystrophin Complex
por: Peters, Matthew F., et al.
Publicado: (1997) -
α-Syntrophin regulates ARMS localization at the neuromuscular junction and enhances EphA4 signaling in an ARMS-dependent manner
por: Luo, Shuo, et al.
Publicado: (2005)