Results 211 to 220 of about 8,574 (264)

Scalable assay to identify inhibitors of prion-like propagation of protein misfolding as potential therapeutics for neurodegeneration. [PDF]

Protein Sci
Narayan A, Neupane K, Woodside MT.
europepmc   +1 more source

Prions and protein aggregates as pathogens, self-propagating structures, biomarkers, and therapeutic targets. [PDF]

Microbiol Mol Biol Rev
Caughey B, Artikis E, Shoup D, Orrú CD, Alam P, Parveen S, King S, Soukup J, Hughson AG, Priola SA.   +9 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

A self-complementary recombinant adeno-associated virus vector coding for an anchorless prion protein carrying the G127V mutation extends survival in a rodent prion disease model. [PDF]

PLoS Pathog
Zerbes T, Verkuyl C, Zhang C, Grunnesjoe S, Eid S, Arshad H, Zhao W, Nasser Z, O'Shea T, Bel A, Lamoureux L, Frost KL, Myskiw J, Li LY, Stuart E, Wille H, Booth S, Watts JC, Schmitt-Ulms G.   +18 more
europepmc   +1 more source

The impact of formic acid treatment on brain tissues for prion inactivation. [PDF]

Acta Histochem
Shaaban D, Seerley A, Crew L, Kaylor C, McElroy S, Guter E, Pounder J, Panter AG.   +7 more
europepmc   +1 more source

A dividing cell model for stable propagation and curing of bona fide human sporadic Creutzfeldt-Jakob Disease prions

Nihat A, Arora P, Schmidt C, Rayner ML, Linehan J, Brandner S, Mead S, Collinge J, Jat PS.   +8 more
europepmc   +1 more source

Germinal centre innervation of bovine and human tonsils related to prion diseases.

, 2009
Defaweux, Valérie, Dorban, Gauthier, Antoine, Nadine, Toppets, Vinciane, Heinen, Ernst   +4 more
openaire   +1 more source

Control of Prion Uptake by Bone Morphogenetic Protein Signaling

De Cecco E, Mariutti G, Eraña H, Oueslati Morales CO, Caredio D, Appleton C, Bouris V, Sellitto S, Hornemann S, Scialò C, Yin J, Vidal E, Polymenidou M, Castilla J, Aguzzi A.   +14 more
europepmc   +1 more source

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Metallothioneins in Prion- and Amyloid-Related Diseases

Journal of Alzheimer's Disease, 2016
Prion and other amyloid-forming diseases represent a group of neurodegenerative disorders that affect both animals and humans. The role of metal ions, especially copper and zinc is studied intensively in connection with these diseases. Their involvement in protein misfolding and aggregation and their role in creation of reactive oxygen species have ...
Pavlína, Adam, Soňa, Křížková, Zbyněk, Heger, Petr, Babula, Vladimír, Pekařík, Markéta, Vaculovičoá, Cláudio M, Gomes, René, Kizek, Vojtěch, Adam   +8 more
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Molecular and chemical basis of prion-related diseases

Chemical Society Reviews, 1997
Prion-related diseases include scrapie in sheep, bovine spongiform encephalopathy in cattle and Creutzfeldt-Jakob disease in humans. The infectious agent for these diseases surprisingly contains no nucleic acid, but is a protein(PrP) which exists in two conformations, PrPC and PrPSc.
Sheila B. L. Ng, Andrew J. Doig
openaire   +1 more source