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Motor neuron apoptosis and neuromuscular junction perturbation are prominent features in a Drosophila model of Fus-mediated ALS

BACKGOUND: Amyotrophic lateral sclerosis (ALS) is progressive neurodegenerative disease characterized by the loss of motor function. Several ALS genes have been identified as their mutations can lead to familial ALS, including the recently reported RNA-binding protein fused in sarcoma (Fus). However...

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Detalhes bibliográficos
Main Authors: Xia, Ruohan, Liu, Yajuan, Yang, Liuqing, Gal, Jozsef, Zhu, Haining, Jia, Jianhang
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3325858/
https://ncbi.nlm.nih.gov/pubmed/22443542
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1326-7-10
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