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...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2019-12-01
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Series: | Neurobiology of Disease |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S096999611930230X |