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Prion-like spreading of protein misfolding is characteristic for neurodegenerative diseases, but the exact mechanisms of intercellular protein aggregate dissemination remain unresolved. Evidence accumulates that endogenous retroviruses, remnants of viral germline infections that are normally epigene...
ORGANISM(S): Mus musculus (Mouse) 
2023-10-18 | PXD043201 | Pride
Both gain of toxicity and loss of normal function of the RNA-binding protein TDP-43 contribute to neurodegeneration in ALS and FTD, but their mechanistic connection remains unclear. Increasing evidence suggests that TDP-43 aggregates act as self-templating seeds, propagating pathology through the ce...
ORGANISM(S): Homo sapiens 
2025-02-20 | GSE285224 | GEO
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