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Chiesa, R., Drisaldi, B., Quaglio, E., Migheli, A., Piccardo, P., Ghetti, B., Harris, D. A. (2000) Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation. Proceedings of the National Academy of Sciences, 97 (10) 5574-5579 doi:10.1073/pnas.97.10.5574

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Reference TypeJournal (article/letter/editorial)
TitleAccumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation
JournalProceedings of the National Academy of Sciences
AuthorsChiesa, R.Author
Drisaldi, B.Author
Quaglio, E.Author
Migheli, A.Author
Piccardo, P.Author
Ghetti, B.Author
Harris, D. A.Author
Year2000 (May 9)Volume97
Issue10
PublisherProceedings of the National Academy of Sciences
DOIdoi:10.1073/pnas.97.10.5574Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1640120Long-form Identifiermindat:1:5:1640120:4
GUID0
Full ReferenceChiesa, R., Drisaldi, B., Quaglio, E., Migheli, A., Piccardo, P., Ghetti, B., Harris, D. A. (2000) Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation. Proceedings of the National Academy of Sciences, 97 (10) 5574-5579 doi:10.1073/pnas.97.10.5574
Plain TextChiesa, R., Drisaldi, B., Quaglio, E., Migheli, A., Piccardo, P., Ghetti, B., Harris, D. A. (2000) Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation. Proceedings of the National Academy of Sciences, 97 (10) 5574-5579 doi:10.1073/pnas.97.10.5574
In(2000, May) Proceedings of the National Academy of Sciences Vol. 97 (10) Proceedings of the National Academy of Sciences

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Chiesa, R., Piccardo, P., Dossena, S., Nowoslawski, L., Roth, K. A., Ghetti, B., Harris, D. A. (2005) Bax deletion prevents neuronal loss but not neurological symptoms in a transgenic model of inherited prion disease. Proceedings of the National Academy of Sciences, 102 (1) 238-243 doi:10.1073/pnas.0406173102
Prusiner, S. B., Groth, D., Serban, A., Koehler, R., Foster, D., Torchia, M., Burton, D., Yang, S. L., DeArmond, S. J. (1993) Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies. Proceedings of the National Academy of Sciences, 90 (22) 10608-10612 doi:10.1073/pnas.90.22.10608
Piccardo, P., Manson, J. C., King, D., Ghetti, B., Barron, R. M. (2007) Accumulation of prion protein in the brain that is not associated with transmissible disease. Proceedings of the National Academy of Sciences, 104 (11) 4712-4717 doi:10.1073/pnas.0609241104
Raeber, A. J., Sailer, A., Hegyi, I., Klein, M. A., Rulicke, T., Fischer, M., Brandner, S., Aguzzi, A., Weissmann, C. (1999) Ectopic expression of prion protein (PrP) in T lymphocytes or hepatocytes of PrP knockout mice is insufficient to sustain prion replication. Proceedings of the National Academy of Sciences, 96 (7) 3987-3992 doi:10.1073/pnas.96.7.3987
Lemaire-Vieille, C., Schulze, T., Podevin-Dimster, V., Follet, J., Bailly, Y., Blanquet-Grossard, F., Decavel, J.-P., Heinen, E., Cesbron, J.-Y. (2000) Epithelial and endothelial expression of the green fluorescent protein reporter gene under the control of bovine prion protein (PrP) gene regulatory sequences in transgenic mice. Proceedings of the National Academy of Sciences, 97 (10) 5422-5427 doi:10.1073/pnas.080081197
Kaneko, K., Peretz, D., Pan, K. M., Blochberger, T. C., Wille, H., Gabizon, R., Griffith, O. H., Cohen, F. E., Baldwin, M. A., Prusiner, S. B. (1995) Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform. Proceedings of the National Academy of Sciences, 92 (24) 11160-11164 doi:10.1073/pnas.92.24.11160
Xia, D., Samols, D. (1997) Transgenic mice expressing rabbit C-reactive protein are resistant to endotoxemia. Proceedings of the National Academy of Sciences, 94 (6) 2575-2580 doi:10.1073/pnas.94.6.2575
Hornemann, S., Glockshuber, R. (1998) A scrapie-like unfolding intermediate of the prion protein domain PrP(121-231) induced by acidic pH. Proceedings of the National Academy of Sciences, 95 (11) 6010-6014 doi:10.1073/pnas.95.11.6010
Hansson, O., Petersen, A., Leist, M., Nicotera, P., Castilho, R. F., Brundin, P. (1999) Transgenic mice expressing a Huntington's disease mutation are resistant to quinolinic acid-induced striatal excitotoxicity. Proceedings of the National Academy of Sciences, 96 (15) 8727-8732 doi:10.1073/pnas.96.15.8727
Viswanath, V., Wu, Z., Fonck, C., Wei, Q., Boonplueang, R., Andersen, J. K. (2000) Transgenic mice neuronally expressing baculoviral p35 are resistant to diverse types of induced apoptosis, including seizure-associated neurodegeneration. Proceedings of the National Academy of Sciences, 97 (5) 2270-2275 doi:10.1073/pnas.030365297
Krulewski, T. F., Neumann, P. E., Gordon, J. W. (1989) Insertional mutation in a transgenic mouse allelic with Purkinje cell degeneration. Proceedings of the National Academy of Sciences, 86 (10) 3709-3712 doi:10.1073/pnas.86.10.3709
 
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