Pathogenic human prion protein rescues PrP null phenotype in transgenic mice
- 9 April 2004
- journal article
- research article
- Published by Elsevier in Neuroscience Letters
- Vol. 360 (1-2) , 33-36
- https://doi.org/10.1016/j.neulet.2004.01.049
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion proteinThe EMBO Journal, 2002
- Prion Diseases of Humans and Animals: Their Causes and Molecular BasisAnnual Review of Neuroscience, 2001
- Evidence of Presynaptic Location and Function of the Prion ProteinJournal of Neuroscience, 1999
- Hippocampal slices from prion protein null mice: disrupted Ca2+-activated K+ currentsNeuroscience Letters, 1996
- Prion protein is necessary for normal synaptic functionNature, 1994
- Mice devoid of PrP are resistant to scrapieCell, 1993
- Normal development and behaviour of mice lacking the neuronal cell-surface PrP proteinNature, 1992
- Genetic predisposition to iatrogenic Creutzfeldt-Jakob diseaseThe Lancet, 1991
- Aminoacid polymorphism in human prion protein and age at death in inherited prion diseaseThe Lancet, 1991
- Creutzfeldt-Jakob Disease: Focus among Libyan Jews in IsraelScience, 1974