Results 131 to 140 of about 4,898,785 (204)

Refined Transgenic Mouse Models Which Recapitulate the Natural Features of Chronic Wasting Disease With Rapid Prion Disease Onsets. [PDF]

J Infect Dis
DeFranco JP, Kim S, Atkinson ZN, Crowell J, Lei S, Bian J, Telling GC.   +6 more
europepmc   +1 more source

Knockout of P2Y12 receptor facilitates neuronal envelopment by reactive microglia and accelerates prion disease. [PDF]

J Neuroinflammation
Makarava N, Safadi T, Bocharova O, Mychko O, Pandit NP, Molesworth K, Eyo UB, Baskakov IV.   +7 more
europepmc   +1 more source

Soluble N-terminal region of prion protein causes rapid neurodegeneration in prion disease. [PDF]

Sci Adv
Yan R, Zhang Y, Zhang J, Zhang X, Han Y, Wang M, Wang D, Huang S, Liu W, Shi Q, Dong X, Zou WQ, Li Z, Ma J.   +13 more
europepmc   +1 more source

Dysregulated microRNAs in blood correlate with central nervous system neuropathology of prion disease. [PDF]

Vet Res
Pérez-Lázaro S, Martín-Burriel I, Cozzuto L, Ponomarenko J, Badiola JJ, Bolea R, Toivonen JM.   +6 more
europepmc   +1 more source

Internal consistency, construct validity, and responsiveness of the MRC Prion Disease Rating Scale. [PDF]

J Patient Rep Outcomes
Leidy L, Yarlas A, Pulido RS, Ludwig J, Glisic K, Appleby BS.   +5 more
europepmc   +1 more source

Development of a user guide to support administration of the MRC Prion Disease Rating Scale in research and clinical settings for prion diseases. [PDF]

Prion
Pulido RS, Marshall C, Smith AV, Edge H, Yarlas A, Appleby B, Brandel JP, Collins S, Omer N, Zerr I, Mead S.   +10 more
europepmc   +1 more source

FDG-PET patterns associate with survival in patients with prion disease. [PDF]

Ann Clin Transl Neurol
Corriveau-Lecavalier N, Piura YD, Appleby BS, Shir D, Barnard LR, Gogineni V, Jones DT, Day GS.   +7 more
europepmc   +1 more source

Overexpression of bank vole PrP(I109) in mice induces a spontaneous atypical prion disease with sex-dependent onset, early NfL elevation, and universal prion strain permissiveness. [PDF]

Acta Neuropathol Commun
Eraña H, Vidal E, Fernández-Borges N, Charco JM, Díaz-Domínguez CM, Sampedro-Torres-Quevedo C, San-Juan-Ansoleaga M, Fernández-Muñoz E, Galarza-Ahumada J, Pérez-Castro MÁ, Gonçalves-Anjo N, Piñeiro P, Pirisinu L, Di Bari MA, Giler S, Raimondi I, Espinosa JC, Vanni I, D'Agostino C, Rodríguez-Cuesta J, Pasetto L, Bonetto V, González-Martín N, Teijeira S, Zou WQ, Geijo M, Torres JM, Chiesa R, Sánchez-Martín MA, Nonno R, Requena JR, Castilla J.   +31 more
europepmc   +1 more source

Limbic system synaptic dysfunctions associated with prion disease onset. [PDF]

Acta Neuropathol Commun
Foliaki ST, Groveman BR, Dews EA, Williams K, El Soufi H, Schwarz B, Leung JM, Schneider CA, Schwartz CL, Bohrnsen E, Kimzey CD, Race B, Haigh CL.   +12 more
europepmc   +1 more source

Inherited prion disease caused by a novel frameshift mutation of <i>PRNP</i> resulting in protein truncation at codon 157. [PDF]

J Alzheimers Dis
Holm-Mercer L, Mok TH, Sequeira D, Coysh T, Rudge P, Ramadan H, Darwent L, Campbell T, Murphy T, Smith C, Ritchie D, Brandner S, Jaunmuktane Z, Collinge J, Mead S.   +14 more
europepmc   +1 more source