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, 2009The 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
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New Structural Approaches to Understand the Disease Related Forms of the Prion Protein
2005Abstract : 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.
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Prion‐related diseases and Creutzfeldt–Jakob disease (subacute spongiform encephalopathy)
European Journal of Neurology, 1996F. Boiler +4 more
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Prions, prionoids and protein misfolding disorders
Nature Reviews Genetics, 2018Claudia Scheckel +2 more
exaly
Mammalian prions and their wider relevance in neurodegenerative diseases
Nature, 2016John Collinge, Collinge John
exaly
Neurodegenerative Diseases and Prions
New England Journal of Medicine, 2001Stanley B Prusiner, Prusiner Stanley B
exaly
Prions are a common mechanism for phenotypic inheritance in wild yeasts
Nature, 2012Randal Halfmann +2 more
exaly
Future counselling of donors and recipients of blood products concerning prion‐related diseases
Vox Sanguinis, 2003Reesink, H. W. +22 more
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Prions and their lethal journey to the brain
Nature Reviews Microbiology, 2006Neil A Mabbott +2 more
exaly
Prions and Neurodegenerative Diseases
New England Journal of Medicine, 1987Franklin H Epstein +2 more
exaly

