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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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Bibliografiske detaljer
Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: The Company of Biologists Ltd 2018
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Online adgang: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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