Results 161 to 170 of about 75,114 (212)

White-Tailed Deer Prion Protein Gene Variability Suggests Selection Against Chronic Wasting Disease in Canada's Prairies. [PDF]

Viruses
Pilot W, Arifin MI, Staskevicius A, Haley NJ, Mitchell G, Guan J.   +5 more
europepmc   +1 more source

Circular bioeconomy: animal by-products from livestock carcass processing. [PDF]

Anim Front
Lee MRF, Ledgard S, Cypriano L, Woodgate S, Becquet P.   +4 more
europepmc   +1 more source

"Polyradiculoneuritis" as an Atypical Clinical Presentation of Creutzfeldt-Jakob Disease: A Case Report and Review of Literature. [PDF]

Life (Basel)
Colaizzo E, Ladogana A, Tiple D, Vaianella L, Bufano G, Moda F, Merlo D, Longo E, Perna A.   +8 more
europepmc   +1 more source

Cellular prion protein and its derived peptides: multifaceted roles in neurodegenerative diseases and potential as biomarkers. [PDF]

Cell Biosci
Mari E, Aventaggiato M, Paldino E, Ceccarelli S, Mucci N, Bellomo G, Mantuano E, Dugheri S, Martellucci S, Mattei V.   +9 more
europepmc   +1 more source

Endogenous Ecotropic Murine Leukemia Virus Promotes Prion Pathogenesis in Senescence-accelerated Mice. [PDF]

Exp Neurobiol
Choi MW, Mostafa MN, Kim MJ, Jang B, Choi MJ, Kim JI, Kim YS, Choi EK.   +7 more
europepmc   +1 more source

Strain-Dependent Susceptibility to Prion Infection Encoded by Arg171 and Lys176 Sheep Prion Protein Polymorphic Variants. [PDF]

J Infect Dis
Espinosa JC, Fernández-Borges N, Marín-Moreno A, Canoyra S, Aguilar-Calvo P, Pintado B, Pericuesta E, Benestad SL, Nonno R, Andréoletti O, Torres JM.   +10 more
europepmc   +1 more source

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THE TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES

Annual Review of Medicine, 1995
▪ Abstract  The human transmissible spongiform encephalopathies (TSEs), or prion diseases, are a group of rapidly progressive disorders characterized by a spectrum of clinical abnormalities that include cognitive impairment, ataxia, myoclonus, and visual, pyramidal, and extrapyramidal signs. They share a spongiform (vacuolar) degeneration and variable
L G, Goldfarb, P, Brown
openaire   +2 more sources

Transmissible spongiform encephalopathies

The Lancet, 2004
Nosologically, transmissible spongiform encephalopathies (TSE or prion diseases) should be grouped with other neurodegenerative disorders such as Alzheimer's and Parkinson's diseases, which are all caused by toxic gain of function of an aberrant form of a constitutively expressed protein.
Steven J, Collins, Victoria A, Lawson, Colin L, Masters   +2 more
openaire   +2 more sources

Transmissible Spongiform Encephalopathies

Biochemical and Biophysical Research Communications, 1998
Scrapie, bovine spongiform encephalopathy (BSE), and the Creutzfeldt-Jakob disease (CJD) belong to a group of lethal neurodegenerative disorders in mammals. Prion diseases or transmissible spongiform encephalopathies (TSEs) are characterized by the accumulation of an abnormal isoform (PrPSc) of the host-encoded cellular prion protein (PrPC) in the ...
S, Liemann, R, Glockshuber
openaire   +2 more sources

Transmissible Spongiform Encephalopathies

2007
Protein folding and misfolding, relevance to disease and function / Massimi Stefani -- Alzheimer's disease / Charlotte E. Teunissen and Tischa M. van der Cammen -- Improving Cholinergic Transmission -- Cholinergic transmission and acetylcholine release enhancers / Pierre Francotte, Pascal de Tullio and Bernard Pirotte -- AChE and its inhibition / Jure ...
Geschwind, M. D., Legname, G.
openaire   +3 more sources