Results 91 to 100 of about 7,097 (179)

The octapeptide repeats of prion protein play critical roles in the pathogenesis of prion diseases. [PDF]

Acta Neuropathol Commun
Zhang X, Zhang J, Zhang Y, Wang D, Liu G, Wang M, Li C, Shi Q, Dong X, Yuan C, Li W, Ma J.   +11 more
europepmc   +1 more source

CpG oligodeoxynucleotide reduces PrP^Sc accumulation and prolongs survival in prion-infected mice. [PDF]

Mol Cells
Mostafa MN, Jang B, Kim MJ, Choi MJ, Lee Y, Kim YS, Kwon HJ, Choi EK.   +7 more
europepmc   +1 more source

A model-based prion vaccine protects a transgenic mouse line carrying a Gerstmann-Sträussler-Scheinker disease mutation. [PDF]

Acta Neuropathol
Fang A, Tang X, Fleming M, Tancowny B, Wang X, Wang Y, Daude N, Dorosh L, Fleck SC, Rathod V, Coustou V, Cervantes SA, Velásquez CD, Westaway D, Aiken J, McKenzie D, Telling G, Stepanova M, Saupe SJ, Siemer AB, Wille H.   +20 more
europepmc   +1 more source

Mutant knock-in mice display enhanced susceptibility to pure prion protein fibrils. [PDF]

J Gen Virol
Walsh DJ, Standke H, Kraus A, Watts JC, Supattapone S.   +4 more
europepmc   +1 more source

Consequences of prion strain mixtures: Indifference, competition, or collusion. [PDF]

PLoS Pathog
Woerman AL, Bartz JC.
europepmc   +1 more source

PrP^C-facilitated cell signaling activates phospholipase Cɣ1 and triggers an Arc/Arg3.1 response in mouse and iPSC-derived human neurons. [PDF]

Stem Cell Reports
Ojeda-Juarez D, Funk G, McClatchy DB, Richards E, Rajic AJ, Soldau K, Geschwind MD, Chen X, Yates JR, Gonias SL, Sigurdson CJ.   +10 more
europepmc   +1 more source

Comparison of acetone and sodium phosphotungstic acid precipitation for sample enrichment prior to RT-QuIC for the detection of prion disease. [PDF]

BMC Res Notes
Nicholson EM, Veneziano SE.
europepmc   +1 more source

Preclinical serum alterations and tissue changes in protein and gene expression of early cerebrospinal fluid-validated biomarkers in scrapie. [PDF]

Vet Res
Pérez-Lázaro S, Barrio T, Sevilla E, Bolea R, Badiola JJ.   +4 more
europepmc   +1 more source

Prion Diseases-When Proteins Turn Lethal: Creutzfeldt-Jakob Disease (CJD) and the Quest for Classification, Diagnosis, Therapeutic Approaches, and Emerging Research. [PDF]

Molecules
Ramesh TS, Bartusik-Aebisher D, Dynarowicz K, Aebisher D.   +3 more
europepmc   +1 more source

Genetic Creutzfeldt-Jakob disease linked to the E200K mutation: a large cohort study. [PDF]

Acta Neuropathol
Appleby BS, Manca M, Piazza MS, Kerr TD, Cornacchia A, Bizzi A, Kraus A, Cohen ML, Cali I.   +8 more
europepmc   +1 more source