QuickView for PRND;jsessionid=E4D84032C414C88CC107B7DB380EF937 (gene)

1. Decoding the Cellular Trafficking of Prion-like Proteins in Neurodegenerative Diseases.
2. Characterizing Prion-Like Protein Aggregation: Emerging Nanopore-Based Approaches.
3. Ataxia with cerebellar lesions in mice expressing chimeric PrP-Dpl protein.
4. Prion-Like Proteins in Phase Separation and Their Link to Disease.
5. Prion-like proteins as epigenetic devices of stress adaptation.

There were no clinical trials for PRND;jsessionid=E4D84032C414C88CC107B7DB380EF937