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Mitigating Motor Neuronal Loss in C. elegans Model of ALS8

ALS8 is a late-onset familial autosomal dominant form of Amyotrophic Lateral Sclerosis (ALS) caused by a point mutation (P56S) in the VAPB gene (VAMP associated protein isoform B). Here, we generated two C. elegans models of the disease: a transgenic model where human VAPB wild-type (WT) or P56S mut...

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Detalles Bibliográficos
Autores principales: Zhang, Wendy, Colavita, Antonio, Ngsee, Johnny K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599522/
https://www.ncbi.nlm.nih.gov/pubmed/28912432
http://dx.doi.org/10.1038/s41598-017-11798-6

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