Prion Protein Gene-Deficient Cell Lines: Powerful Tools for Prion Biology
Author:
Affiliation:
1. Department of Virology, Research Institute for Microbial Diseases; Osaka University; Suita Osaka 565-0871 Japan
2. Department of Molecular Immunology, School of Agricultural and Life Sciences; University of Tokyo; Bunkyo-ku Tokyo 113-8657 Japan
Publisher
Wiley
Subject
Virology,Immunology,Microbiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1348-0421.2007.tb03877.x/fullpdf
Reference84 articles.
1. Poliovirus type 1 infection of murine PRNP-knockout neuronal cells;Baj;J. Neurovirol.,2005
2. Changing a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers;Barron;EMBO J.,2001
3. Cell culture models of transmissible spongiform encephalopathies;Beranger;Biochem. Biophys. Res. Commun.,2001
4. Cultured cell sublines highly susceptible to prion infection;Bosque;J. Virol.,2000
5. Normal host prion protein necessary for scrapie-induced neurotoxicity;Brandner;Nature,1996
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1. The function of the cellular prion protein in health and disease;Acta Neuropathologica;2017-11-18
2. Modifiers of prion protein biogenesis and recycling identified by a highly parallel endocytosis kinetics assay;Journal of Biological Chemistry;2017-05
3. Dual role of cellular prion protein in normal host and Alzheimer’s disease;Proceedings of the Japan Academy, Series B;2017
4. Neurodegeneration and Unfolded-Protein Response in Mice Expressing a Membrane-Tethered Flexible Tail of PrP;PLOS ONE;2015-02-06
5. Prion protein (PrP) gene-knockout cell lines: insight into functions of the PrP;Frontiers in Cell and Developmental Biology;2015-01-15
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