Results 121 to 130 of about 4,885 (171)

Modelling human proteostasis and organelle homeostasis disorders in yeast and its application in drug discovery. [PDF]

FEMS Yeast Res
Do AV, Zahra M, Munn AL.
europepmc   +1 more source

Chronic wasting disease as a model for human prion therapy. [PDF]

Prion
Bordonaro M.
europepmc   +1 more source

Human Prion Disease: Pathogenesis, Diagnosis and Public Health. [PDF]

Viruses
Bellini P, Ruggiero F, Benedetti A, Cereda CW, Gobbi C, Bianco G, Bongiovanni M.   +6 more
europepmc   +1 more source

Breaking the Mould: How the First Structure of a Deer Prion Suggests the Framework for Interspecies Strain Diversity and Transmission Barriers. [PDF]

J Neurochem
Manka SW.
europepmc   +1 more source

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

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

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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

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
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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
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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