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Examining the relationship between astrocyte dysfunction and neurodegeneration in ALS using hiPSCs
Amyotrophic lateral sclerosis (ALS) is a complex and fatal neurodegenerative disease for which the causes of disease onset and progression remain unclear. Recent advances in human induced pluripotent stem cell (hiPSC)-based models permit the study of the genetic factors associated with ALS in patien...
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| Pubblicato in: | Neurobiol Dis |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6834907/ https://ncbi.nlm.nih.gov/pubmed/31381978 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2019.104562 |
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