Loading...
Chetomin rescues pathogenic phenotype of LRRK2 mutation in drosophila
Leucine-rich repeat kinase 2 (LRRK2) is a complex protein kinase involved in a diverse set of functions. Mutations in LRRK2 are a common cause of autosomal dominant familial Parkinson’s disease. Peroxiredoxin 2 (PRDX2) belongs to a family of anti-oxidants that protect cells from oxidative stress. Im...
Na minha lista:
| Udgivet i: | Aging (Albany NY) |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Impact Journals
2020
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7585092/ https://ncbi.nlm.nih.gov/pubmed/32990658 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/aging.103843 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|