Cargando…
Rab7 Mutants Associated with Charcot-Marie-Tooth Disease Exhibit Enhanced NGF-Stimulated Signaling
Missense mutants in the late endosomal Rab7 GTPase cause the autosomal dominant peripheral neuropathy Charcot-Marie-Tooth disease type 2B (CMT2B). As yet, the pathological mechanisms connecting mutant Rab7 protein expression to altered neuronal function are undefined. Here, we analyze the effects Ra...
Autores principales: | BasuRay, Soumik, Mukherjee, Sanchita, Romero, Elsa, Wilson, Michael C., Wandinger-Ness, Angela |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3000344/ https://www.ncbi.nlm.nih.gov/pubmed/21151572 http://dx.doi.org/10.1371/journal.pone.0015351 |
Ejemplares similares
-
Charcot Marie Tooth 2B Peripheral Sensory Neuropathy: How Rab7 Mutations Impact NGF Signaling?
por: Liu, Harry, et al.
Publicado: (2017) -
Rab GTPases as regulators of endocytosis, targets of disease and therapeutic opportunities
por: Agola, JO, et al.
Publicado: (2011) -
Diagnosis of Charcot-Marie-Tooth Disease
por: Banchs, Isabel, et al.
Publicado: (2009) -
Balance and muscle power of children with
Charcot-Marie-Tooth
por: Silva, Tais R., et al.
Publicado: (2014) -
Charcot–Marie–Tooth disease and intracellular traffic
por: Bucci, Cecilia, et al.
Publicado: (2012)