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Chunk #32 — Use of iPSCs to model neurodegenerative diseases — iPSCs and amyotrophic lateral sclerosis

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Modeling Human Neurological and Neurodegenerative Diseases: From Induced Pluripotent Stem Cells to Neuronal Differentiation and Its Applications in Neurotrauma.
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the C9ORF72 mutation which is also involved in frontotemporal dementia and these have also uncovered some characteristic phenotypes in ALS (Donnelly et al., 2013; Sareen et al., 2013; Hedges et al., 2016). All this further supports the notion of iPSCs' culture studies as models unraveling a lot that needs to be known about neurodegenerative disease such as ALS that we know about the very little.