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Divergent and Convergent TMEM106B Pathology in Murine Models of Neurodegeneration and Human Disease

2024-10-18

Abstract excerpt

TMEM106B is a lysosomal/late endosome protein that is a potent genetic modifier of multiple neurodegenerative diseases as well as general aging. Recently, TMEM106B was shown to form insoluble aggregates in postmortem human brain tissue, drawing attention to TMEM106B pathology and the potential role of TMEM106B aggregation in disease. In the context of neurodegenerative diseases, TMEM106B has been studied in vivo...

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Literature Corpus work
b67d64b3-8b79-5397-af50-a8463a33f9b9
DOI
10.1101/2024.10.16.618765
Open publication

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Divergent and Convergent TMEM106B Pathology in Murine Models of Neurodegeneration and Human DiseaseDOI 10.1101/2024.10.16.618765
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