BMP- and neuropilin 1-mediated motor axon navigation relies on spastin alternative translation

Functional analyses of genes responsible for neurodegenerative disorders have unveiled crucial links between neurodegenerative processes and key developmental signalling pathways. Mutations in SPG4-encoding spastin cause hereditary spastic paraplegia (HSP). Spastin is involved in diverse cellular pr...

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Detalhes bibliográficos
Publicado no:Development
Main Authors: Jardin, Nicolas, Giudicelli, François, Ten Martín, Daniel, Vitrac, Anaïs, De Gois, Stéphanie, Allison, Rachel, Houart, Corinne, Reid, Evan, Hazan, Jamilé, Fassier, Coralie
Formato: Artigo
Idioma:Inglês
Publicado em: The Company of Biologists Ltd 2018
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6141775/
https://ncbi.nlm.nih.gov/pubmed/30082270
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dev.162701
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