Cargando…
Charcot–Marie–Tooth disease and intracellular traffic
Mutations of genes whose primary function is the regulation of membrane traffic are increasingly being identified as the underlying causes of various important human disorders. Intriguingly, mutations in ubiquitously expressed membrane traffic genes often lead to cell type- or organ-specific disorde...
Autores principales: | Bucci, Cecilia, Bakke, Oddmund, Progida, Cinzia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pergamon Press
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514635/ https://www.ncbi.nlm.nih.gov/pubmed/22465036 http://dx.doi.org/10.1016/j.pneurobio.2012.03.003 |
Ejemplares similares
-
Charcot–Marie–Tooth type 2B disease-causing RAB7A mutant proteins show altered interaction with the neuronal intermediate filament peripherin
por: Cogli, Laura, et al.
Publicado: (2012) -
Held Up in Traffic—Defects in the Trafficking Machinery in Charcot-Marie-Tooth Disease
por: Markworth, Ronja, et al.
Publicado: (2021) -
Diagnosis of Charcot-Marie-Tooth Disease
por: Banchs, Isabel, et al.
Publicado: (2009) -
Characterization of the role of RILP in cell migration
por: Margiotta, Azzurra, et al.
Publicado: (2017) -
Rab7b at the intersection of intracellular trafficking and cell migration
por: Distefano, Marita Borg, et al.
Publicado: (2015)