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Literature DB >> 14003830

Further observations on the experimental transmission of scrapie from sheep and goats to laboratory mice.

I ZLOTNIK, J C RENNIE.

Abstract

Entities: Species

Keywords: BRAIN; SHEEP DISEASES

Mesh：

Year: 1963 PMID： 14003830 DOI： 10.1016/s0368-1742(63)80018-1

Source DB: PubMed Journal: J Comp Pathol ISSN： 0021-9975 Impact factor: 1.311

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19 in total

Review 1. Developing Therapeutics for PrP Prion Diseases.

Authors: Kurt Giles; Steven H Olson; Stanley B Prusiner
Journal: Cold Spring Harb Perspect Med Date: 2017-04-03 Impact factor: 6.915

2. [A scrapie-like epizootic disease in white mice induced by the inoculation of spinal fluid from a patient].

Authors: R Henn; W Müller; G Schaltenbrand
Journal: Dtsch Z Nervenheilkd Date: 1970

3. A single amino acid (Asp159) from the dog prion protein suppresses the toxicity of the mouse prion protein in Drosophila.

Authors: J Sanchez-Garcia; K Jensen; Y Zhang; D E Rincon-Limas; P Fernandez-Funez
Journal: Neurobiol Dis Date: 2016-07-28 Impact factor: 5.996

4. The occurrence of vacuolated neurons in the brains of hamsters affected with subacute sclerosing encephalitis following measles or Langat virus infection.

Authors: I Zlotnik; D P Grant
Journal: Br J Exp Pathol Date: 1975-02

5. Different 2-Aminothiazole Therapeutics Produce Distinct Patterns of Scrapie Prion Neuropathology in Mouse Brains.

Authors: Kurt Giles; David B Berry; Carlo Condello; Ronald C Hawley; Alejandra Gallardo-Godoy; Clifford Bryant; Abby Oehler; Manuel Elepano; Sumita Bhardwaj; Smita Patel; B Michael Silber; Shenheng Guan; Stephen J DeArmond; Adam R Renslo; Stanley B Prusiner
Journal: J Pharmacol Exp Ther Date: 2015-07-29 Impact factor: 4.030

10. Strain specific resistance to murine scrapie associated with a naturally occurring human prion protein polymorphism at residue 171.

Authors: James F Striebel; Brent Race; Kimberly D Meade-White; Rachel LaCasse; Bruce Chesebro
Journal: PLoS Pathog Date: 2011-09-29 Impact factor: 6.823

Further observations on the experimental transmission of scrapie from sheep and goats to laboratory mice.

Review 1. Developing Therapeutics for PrP Prion Diseases.

2. [A scrapie-like epizootic disease in white mice induced by the inoculation of spinal fluid from a patient].

3. A single amino acid (Asp159) from the dog prion protein suppresses the toxicity of the mouse prion protein in Drosophila.

4. The occurrence of vacuolated neurons in the brains of hamsters affected with subacute sclerosing encephalitis following measles or Langat virus infection.

5. Different 2-Aminothiazole Therapeutics Produce Distinct Patterns of Scrapie Prion Neuropathology in Mouse Brains.

6. PrPSc-Specific Antibody Reveals C-Terminal Conformational Differences between Prion Strains.

7. Investigation of mcp1 as a quantitative trait gene for prion disease incubation time in mouse.

8. D159 and S167 are protective residues in the prion protein from dog and horse, two prion-resistant animals.

9. Transmissibility of caprine scrapie in ovine transgenic mice.

10. Strain specific resistance to murine scrapie associated with a naturally occurring human prion protein polymorphism at residue 171.