Results 261 to 270 of about 8,300 (285)
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Localization of disease-related PrP in Danish patients with different subtypes of prion disease.

Clinical neuropathology, 2009
The transmissible spongiform encephalopathies are characterized by vacuolization, neuronal loss, gliosis and deposition of a misfolded and Proteinase K resistant isoform of the prion protein (PrP(Sc)) in the central nervous system. METHODS MATERIALS AND PATIENTS: Paraffin-embedded tissue blot (PET-blot), immunohistochemistry (IHC) and Western blotting (
Bergstrom, A.L.   +4 more
openaire   +1 more source

New Structural Approaches to Understand the Disease Related Forms of the Prion Protein

2005
Abstract : Expression constructs have been prepared in order to generate the 89-143 fragment of the prion protein with isotopic labels using either in vitro translation or expression in E.coli cells. Initial testing of expression has been done.
openaire   +1 more source

Prion‐related diseases and Creutzfeldt–Jakob disease (subacute spongiform encephalopathy)

European Journal of Neurology, 1996
F. Boiler   +4 more
openaire   +1 more source

Prions, prionoids and protein misfolding disorders

Nature Reviews Genetics, 2018
Claudia Scheckel   +2 more
exaly  

Neurodegenerative Diseases and Prions

New England Journal of Medicine, 2001
Stanley B Prusiner, Prusiner Stanley B
exaly  

Prions are a common mechanism for phenotypic inheritance in wild yeasts

Nature, 2012
Randal Halfmann   +2 more
exaly  

Future counselling of donors and recipients of blood products concerning prion‐related diseases

Vox Sanguinis, 2003
Reesink, H. W.   +22 more
openaire   +3 more sources

Prions and their lethal journey to the brain

Nature Reviews Microbiology, 2006
Neil A Mabbott   +2 more
exaly  

Prions and Neurodegenerative Diseases

New England Journal of Medicine, 1987
Franklin H Epstein   +2 more
exaly  

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