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SCYL pseudokinases in neuronal function and survival

The generation of mice lacking SCYL1 or SCYL2 and the identification of Scyl1 as the causative gene in the motor neuron disease mouse model muscle deficient (Scyl1(mdf/mdf)) demonstrated the importance of the SCY1-like family of protein pseudokinases in neuronal function and survival. Several essent...

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Detalhes bibliográficos
Publicado no:Neural Regen Res
Autor principal: Pelletier, Stephane
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4774220/
https://ncbi.nlm.nih.gov/pubmed/26981075
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1673-5374.175040
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