Variations in prion protein and glial fibrillary acidic protein mRNAs in the brain of scrapie-infected newborn mouse

References

1. Alonso S., Minty A., Booklet Y., Buckingham M. L. 1986; Comparison of three actin-coding sequences in the mouse; evolutionary relationships between the actin genes of warm-blooded vertebrates. Journal of Molecular Evolution 23:11–22
   [Google Scholar]
2. Basler K., Oesch B., Scott M., Westaway D., Wälchli M., Groth D. F., McKinley M. P., Prusiner S. B., Weissmann C. 1986; Scrapie and cellular Prp isoforms are encoded by the same chromosomal gene. Cell 46:417–428
   [Google Scholar]
3. Billette de Villemeur T., Beauvais P., Gourmelen M., Richardet J. M. 1991; Creutzfeldt-Jakob disease in children treated with growth hormone. Lancet 337:864–865
   [Google Scholar]
4. Bolton D. C., Bendheim P. E. 1988; A modified host protein model of scrapie. In Novel Infectious Agents and the Central Nervous System, Ciba Foundation Symposium vol 135 pp 164–181 New York: John Wiley Interscience;
   [Google Scholar]
5. Brown P. 1990; Transmissible spongiform encephalopathies in humans: Kuru, Creutzfeldt-Jakob disease and Gerstmann-Straussler-Scheinker disease. Canadian Journal of Veterinary Research 54:38–41
   [Google Scholar]
6. Chesebro B., Race R., Wehrly K. 1985; Identification of scrapie prion protein-specific mRNA in scrapie-infected and uninfected brain. Nature, London 315:331–333
   [Google Scholar]
7. Chomczynski P., Sacchi W. 1987; Single-step method of RNA isolation by acid guanidinium thiocyanatephenolchloroform extraction. Analytical Biochemistry 162:156–159
   [Google Scholar]
8. Collee J. L. 1990; Foodbome illness, bovine spongiform encephalopathy. Lancet 336:1300–1304
   [Google Scholar]
9. Diedrich J. F., Bendheim P. E., Kim Y. S., Carp R. S., Haase A. T. 1991; Scrapie-associated prion protein accumulates in astrocytes during scrapie infection. Proceedings of the National Academy of Sciences, U.S.A. 88:375–379
   [Google Scholar]
10. Dormont D., Delpech A., Delpech M. N., Courcel J., Viret J., Markovits P., Court L. 1981; Hyperproduction de proteine gliofibrillaire acide (GFAP) au cours de 1’evolution de la tremblante experimentale de la souris. Comptes Rendus de l’Académie des Sciences, Paris 293:53–56
    [Google Scholar]
11. Fort P., Marty L., Piechaczyk M., Sabrouty S. E., Dani C., Jeanteur P., Blanchard J. M. 1985; Various rat tissues express only one major mRNA species from the glyceraldehyde-3-phosphate dehydrogenase multigenic family. Nucleic Acids Research 13:1431–1442
    [Google Scholar]
12. Hotchin J., Buckley R. 1977; Latent form of scrapie virus: a new factor in slow virus disease. Science 196:668–671
    [Google Scholar]
13. Kimberlin R. H. 1982 Scrapie agent: prions or virinos? Nature, London 297:107–108
    [Google Scholar]
14. Lampert P. W., Gajdusek D. C., Gibbs C. Jr 1972; Subacute spongiform virus encephalopathies, scrapie, Kuru, and Creutzfeldt-Jakob disease: a review. American Journal of Pathology 68:626–646
    [Google Scholar]
15. Lazarini F., Deslys J. P., Dormont D. 1991; Regulation of the glial fibrillary acidic protein, β actin and prion protein mRNAs during brain development in mouse. Molecular Brain Research 10:343–346
    [Google Scholar]
16. Lewis S. A., Balcarek J. M., Krek V., Shelanski M., Cowan N. J. 1984; Sequence of a cDNA clone encoding mouse glial fibrillary acidic protein: structural conservation of intermediate filaments. Proceedings of the National Academy of Sciences, U.S.A. 81:2743–2746
    [Google Scholar]
17. Lieberburg I. 1987; Developmental expression and regional distribution of the scrapie-associated protein mRNA in the rat central nervous system. Brain Research 417:363–366
    [Google Scholar]
18. Malloch G. D. A., Clark J. B., Burnet F. R. 1987; Glial fibrillary acidic protein in the cytoskeletal and soluble protein fraction of the developing rat brain. Journal of Neurochemistry 48:299–306
    [Google Scholar]
19. Manuelidis L., Tesin D. M., Sklaviadis T., Manuelidis E. E. 1987; Astrocyte gene expression in Creutzfeldt-Jakob disease. Proceedings of the National Academy of Sciences, U.S.A. 84:5937–5941
    [Google Scholar]
20. Mobley W. C., Neve R. L., Prusiner S. B., McKinley M. P. 1988; Nerve growth factor increases mRNA levels for the prion protein and the β-amyloid protein precursor in developing hamster brain. Proceedings of the National Academy of Sciences, U.S.A. 85:9811–9815
    [Google Scholar]
21. Murdoch G. H., Sklaviadis T., Manuelidis E. E., Manuelidis L. 1990; Potential retroviral RNAs in Creutzfeldt-Jakob disease. Journal of Virology 64:1477–1486
    [Google Scholar]
22. Prusiner S. B. 1991; Molecular biology of prion diseases. Science 252:1515–1522
    [Google Scholar]
23. Stahl N., Borchelt D. R., Hsiao K., Prusiner S. B. 1987; Scrapie prion protein contains a phosphatidylinositol glycolipid. Cell 51:229–240
    [Google Scholar]
24. Tardy M., Fages C., Riol H., Leprince G., Rataboul P., Charriere-Bertrand C., Nunez J. 1989; Developmental expression of the glial fibrillary acidic protein mRNA in the central nervous system and in cultured astrocytes. Journal of Neurochemistry 52:162–167
    [Google Scholar]
25. Weissmann C. 1991; The prion’s progress. Nature, London 349569–571
    [Google Scholar]