Corrigendum: The Role of the Gut Microbiota in the Pathogenesis of Parkinson's Disease
Frontiers in Neurology, 2020 Dongming Yang +12 more
doaj +1 more source
PLoS ONE, 2015 Bovine spongiform encephalopathy (BSE) is a zoonotic transmissible spongiform encephalopathy (TSE) thought to be caused by the same prion strain as variant Creutzfeldt-Jakob disease (vCJD).
Dongseob Tark +8 more
doaj +1 more source
NEUROPATHOLOGY OF ITALIAN CATS IN FELINE SPONGIFORM ENCEPHALOPATHY SURVEILLANCE
, 2008 Feline spongiform encephalopathy (FSE) is a transmissible spongiform encephalopathy associated with the Consumption of feedstuffs contaminated with tissue from bovine spongiform encephalopathy-affected cattle and characterized by the accumulation in the ...
MANDARA MT +12 more
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Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy
, 2002 We analyzed the prion protein gene (PRNP) region in patients with transmissible spongiform encephalopathy associated with the PRNP D178N mutation.
Lee, Hee Suk +8 more
core +1 more source
The 37kDa/67kDa laminin receptor as a therapeutic target in prion diseases: potency of antisense LRP RNA, siRNAs specific for LRP mRNA and a LRP decoy mutant [PDF]
, 2006 Prion diseases are a group of rare, fatal neurodegenerative diseases, also known as transmissible spongiform encephalopathies (TSEs), that affect both animals and humans and include bovine spongiform encephalopathy (BSE) in cattle, scrapie in sheep ...
Vana, Karen
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Human transmissible spongiform encephalopathy: Case report
Iatreia, 2014 We report the case of a 64 year-old woman with motor and cognitive deterioration that progressed rapidly during eight months. She was unsuccessfully treated with quinacrine, and died in a terminal status, by septic shock secondary to bronchopneumonia by ...
Duque Velásquez, Camilo +6 more
doaj
Prion protein PrP nucleic acid binding and mobilization implicates retroelements as the replicative component of transmissible spongiform encephalopathy. [PDF]
Arch Virol, 2020 Lathe R, Darlix JL.
europepmc +1 more source
Transmissible spongiform encephalopathies [PDF]
Journal of Medical Microbiology, 1995 openaire +2 more sources
Characterization of the prion protein in relation to normal cellular function and in disease [PDF]
, 2012 Transmissible spongiform encephalopathies (TSEs), also known as prion diseases, are a group of rare and fatal neurodegenerative disorders that can affect both human and animals.
Wik, Lotta
core
Transmissible spongiform encephalopathy in the gray tremor mutant mouse.
, 1985 Gray tremor (gt) is an autosomal recessive mutation in the mouse linked to caracul (Ca) on chromosome 15. The complex mutant phenotype includes pigmentation defects, tremor, seizures, hypo- and dysmyelination in central and peripheral nervous systems,
Sidman, R L, Kinney, H C, Sweet, H O
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