Early-Onset Spastic Ataxia in a Patient With the Prion (PRNP) p.Val180Ile Variant. [PDF]
Lee S, Yoo D, Park KS, Ahn TB.
europepmc +1 more source
Parkinsonism in Gerstmann-Sträussler-Scheinker disease: A case report. [PDF]
Poveda S +4 more
europepmc +1 more source
Search for a genetic cause of variably protease-sensitive prionopathy. [PDF]
Lian Y +7 more
europepmc +1 more source
A comprehensive phylogeny of mammalian PRNP gene reveals no influence of prion misfolding propensity on the evolution of this gene. [PDF]
Sampedro-Torres-Quevedo C +18 more
europepmc +1 more source
Genetic Variation and Strain Dynamics in Chronic Wasting Disease. [PDF]
Zemlyankina I +5 more
europepmc +1 more source
GPI-anchorless prion disease is sensitive to oxidative stress and shows potential for treatment with edaravone, based on iPS-derived neuron study. [PDF]
Matsuzono K +7 more
europepmc +1 more source
Soluble N-terminal region of prion protein causes rapid neurodegeneration in prion disease. [PDF]
Yan R +13 more
europepmc +1 more source
Machine learning-based transcriptomic analysis identifies NAMPT and SAT1 as potential biomarkers and therapeutic targets in ferroptosis-associated rheumatoid arthritis. [PDF]
Soorya Narayana Sasikumar D +1 more
europepmc +1 more source
Cerebrospinal Fluid Biomarkers in Creutzfeldt-Jakob Disease: Diagnostic Value, Limitations, and Future Multi-Omics Strategies. [PDF]
Xu R, Chen C, Shi Q, Dong XP.
europepmc +1 more source
Partial Deletion of the Carboxyl-Terminal Signal Sequence of the Cellular Prion Protein Alters Protein Expression via Endoplasmic Reticulum-Associated Degradation. [PDF]
Yoo M +12 more
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