Comparative ultrastructural neuropathology of naturally occurring bovine spongiform encephalopathy and experimentally induced scrapie and Creutzfeldt-Jakob disease-Reference-Cited by-同舟云学术

Comparative ultrastructural neuropathology of naturally occurring bovine spongiform encephalopathy and experimentally induced scrapie and Creutzfeldt-Jakob disease

Published:1992-05 Issue:4 Volume:106 Page:361-381
ISSN:0021-9975
Container-title:Journal of Comparative Pathology
language:en
Short-container-title:Journal of Comparative Pathology

Author:

Liberski P.P.,Yanagihara R.,Wells G.A.H.,Gibbs C.J.,Gajdusek D.C.

Publisher

Elsevier BV

Subject

General Veterinary,Pathology and Forensic Medicine

Reference103 articles.

1. Further observations on the neuropathology of experimental scrapie in mouse and hamsters;Baringer,1979

2. Dietary transmission of bovine spongiform encephalopathy to mice;Barlow;Veterinary Record,1990

3. Predicted secondary structure and membrane topology of the scrapie prion protein;Bazan;Protein Engineering,1987

4. Neuropathology of transmissible spongiform encephalopathy;Beck,1988

5. The ultrastructure of status spongiosus and neuronal vacuolation in Jakob-Creutzfeldt disease and other transmissible spongiform encephalopathies;Bignami,1974

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Diminished Neuronal ESCRT-0 Function Exacerbates AMPA Receptor Derangement and Accelerates Prion-Induced Neurodegeneration;The Journal of Neuroscience;2023-04-05

2. Ultrastructural changes in the progress of natural Scrapie regardless fixation protocol;Histochemistry and Cell Biology;2015-02-28

3. Sporadic Creutzfeldt-Jakob Disease;Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders;2011-09-21

4. Tubulovesicular structures are a consistent (and unexplained) finding in the brains of humans with prion diseases;Virus Research;2008-03

5. Prion Protein Disease and Neuropathology of Prion Disease;Neuroimaging Clinics of North America;2008-02