Results 151 to 160 of about 4,898,785 (204)

Inherited Prion Disease with a 5-octapeptide Repeat Insertion in the PRNP Gene Presenting with Familial Juvenile Dementia. [PDF]

Intern Med
Nishikawa M, Takeda A, Miyazawa N, Hara N, Ishii K, Ikeuchi T, Itoh Y.   +6 more
europepmc   +1 more source

In situ assessment of neuroinflammatory cytokines in different stages of ovine natural prion disease. [PDF]

Front Vet Sci
Guijarro IM, Garcés M, Badiola JJ, Monzón M.   +3 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]

Cell Mol Life Sci
Matsuzono K, Honda H, Mashiko T, Koide R, Sakashita E, Endo H, Kitamoto T, Fujimoto S.   +7 more
europepmc   +1 more source

Retraction: Fatal Prion Disease in a Mouse Model of Genetic E200K Creutzfeldt-Jakob Disease. [PDF]

PLoS Pathog
PLOS Pathogens Editors.
europepmc   +1 more source

Retraction: PrPST, a Soluble, Protease Resistant and Truncated PrP Form Features in the Pathogenesis of a Genetic Prion Disease. [PDF]

PLoS One
PLOS ONE Editors.
europepmc   +1 more source

Single-cell transcriptomics unveils molecular signatures of neuronal vulnerability in a mouse model of prion disease that overlap with Alzheimer's disease. [PDF]

Nat Commun
Slota JA, Lamoureux L, Frost KL, Sajesh BV, Booth SA.   +4 more
europepmc   +1 more source

Neurofilament Light Chain Levels in Serum and Cerebrospinal Fluid Do Not Correlate with Survival Times in Patients with Prion Disease. [PDF]

Biomolecules
Shimamura M, Weijie K, Nonaka T, Kosami K, Ae R, Fujita K, Matsubayashi T, Tsukamoto T, Sanjo N, Satoh K.   +9 more
europepmc   +1 more source

Update on human prion disease [PDF]

Biochimica Et Biophysica Acta - Molecular Basis of Disease, 2007
The recognition that variant Creutzfeldt–Jakob disease (vCJD) is caused by the same prion strain as bovine spongiform encephalopathy in cattle has dramatically highlighted the need for a precise understanding of the molecular biology of human prion ...
Jonathan Wadsworth, John Collinge
exaly   +2 more sources

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Prion diseases

Neurologic Clinics, 2018
The human prion diseases comprise Creutzfeldt-Jakob disease, variably protease-sensitive prionopathy, Gerstmann-Sträussler-Scheinker disease, fatal familial insomnia, and kuru. Each is a uniformly fatal rare neurodegenerative disease in which conformational changes in the prion protein are thought to be the central pathophysiologic event.
James W, Ironside, Diane L, Ritchie, Mark W, Head   +2 more
openaire   +4 more sources