טוען...
Expression of mutant CHMP2B linked to neurodegeneration in humans disrupts circadian rhythms in Drosophila
Mutations in CHMP2B, an ESCRT‐III (endosomal sorting complexes required for transport) component, are associated with frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). Neurodegenerative disorders including FTD are also associated with a disruption in circadian rhythms, but the m...
שמור ב:
| הוצא לאור ב: | FASEB Bioadv |
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| Main Authors: | , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
John Wiley and Sons Inc.
2019
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6996329/ https://ncbi.nlm.nih.gov/pubmed/32123847 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fba.2019-00042 |
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