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Huntingtin-mediated axonal transport requires arginine methylation by PRMT6
The huntingtin (HTT) protein transports various organelles, including vesicles containing neurotrophic factors, from embryonic development throughout life. To better understand how HTT mediates axonal transport and why this function is disrupted in Huntington’s disease (HD), we study vesicle-associa...
שמור ב:
| הוצא לאור ב: | Cell Rep |
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| Main Authors: | , , , , , , , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2021
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8132453/ https://ncbi.nlm.nih.gov/pubmed/33852844 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.celrep.2021.108980 |
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