Non-amyloid and amyloid prion protein deposits in prion-infected mice differ in blockage of interstitial brain fluid-Reference-Cited by-同舟云学术

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Non-amyloid and amyloid prion protein deposits in prion-infected mice differ in blockage of interstitial brain fluid

Published:2013-03-11 Issue:3 Volume:39 Page:217-230
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:

Author:

Rangel A.¹,Race B.¹,Striebel J.¹,Chesebro B.¹

Affiliation:

1. Laboratory of Persistent Viral Diseases; Rocky Mountain Laboratories; National Institute of Allergy and Infectious Diseases; Hamilton; MT; USA

Publisher

Wiley

Subject

Physiology (medical),Clinical Neurology,Neurology,Histology,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2990.2012.01303.x/fullpdf

Reference31 articles.

1. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects;Parchi;Ann Neurol,1999

2. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases);Budka;Brain Pathol,1995

3. Effects of agent strain and host genotype on PrP accumulation in the brain of sheep naturally and experimentally affected with scrapie;Gonzalez;J Comp Pathol,2002

4. In vivo toxicity of prion protein in murine scrapie: ultrastructural and immunogold studies;Jeffrey;Neuropathol Appl Neurobiol,1997

5. Prion protein amyloidosis;Ghetti;Brain Pathol,1996

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1. Oscillations in Neuronal Activity: A Neuron-Centered Spatiotemporal Model of the Unfolded Protein Response in Prion Diseases;Bulletin of Mathematical Biology;2024-06-05

2. Noninvasive Antemortem Detection of Retinal Prions by a Fluorescent Tracer;Journal of Alzheimer's Disease;2022-08-02

3. PrP P102L and Nearby Lysine Mutations Promote Spontaneous In Vitro Formation of Transmissible Prions;Journal of Virology;2017-11

4. Subcellular and Molecular Changes Associated with Abnormal PrP Accumulation in Brain and Viscera of Classical and Atypical Prion Diseases;Neuromethods;2017

5. Prion Strain Differences in Accumulation of PrPSc on Neurons and Glia Are Associated with Similar Expression Profiles of Neuroinflammatory Genes: Comparison of Three Prion Strains;PLOS Pathogens;2016-04-05

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