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The C9orf72-interacting protein Smcr8 is a negative regulator of autoimmunity and lysosomal exocytosis
While a mutation in C9ORF72 is the most common genetic contributor to amyotrophic lateral sclerosis (ALS), much remains to be learned concerning the function of the protein normally encoded at this locus. To elaborate further on functions for C9ORF72, we used quantitative mass spectrometry-based pro...
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| Vydáno v: | Genes Dev |
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| Hlavní autoři: | , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Cold Spring Harbor Laboratory Press
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6075033/ https://ncbi.nlm.nih.gov/pubmed/29950492 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gad.313932.118 |
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