Cargando…
Alterations of autophagy in the peripheral neuropathy Charcot-Marie-Tooth type 2B
Charcot-Marie-Tooth type 2B (CMT2B) disease is a dominant axonal peripheral neuropathy caused by 5 mutations in the RAB7A gene, a ubiquitously expressed GTPase controlling late endocytic trafficking. In neurons, RAB7A also controls neuronal-specific processes such as NTF (neurotrophin) trafficking a...
Autores principales: | Colecchia, David, Stasi, Mariangela, Leonardi, Margherita, Manganelli, Fiore, Nolano, Maria, Veneziani, Bianca Maria, Santoro, Lucio, Eskelinen, Eeva-Liisa, Chiariello, Mario, Bucci, Cecilia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103410/ https://www.ncbi.nlm.nih.gov/pubmed/29130394 http://dx.doi.org/10.1080/15548627.2017.1388475 |
Ejemplares similares
-
Alteration of the late endocytic pathway in Charcot–Marie–Tooth type 2B disease
por: Romano, Roberta, et al.
Publicado: (2020) -
Mitochondria dysfunction in Charcot Marie Tooth 2B Peripheral Sensory Neuropathy
por: Gu, Yingli, et al.
Publicado: (2022) -
The impact of symptoms on daily life as perceived by patients with Charcot-Marie-Tooth type 1A disease
por: Tozza, Stefano, et al.
Publicado: (2021) -
Emerging Therapies for Charcot-Marie-Tooth Inherited Neuropathies
por: Stavrou, Marina, et al.
Publicado: (2021) -
Frequency, entity and determinants of fatigue in Charcot–Marie–Tooth disease
por: Bellofatto, Marta, et al.
Publicado: (2022)