Doppel-induced cerebellar degeneration in transgenic mice-Reference-Cited by-同舟云学术

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Doppel-induced cerebellar degeneration in transgenic mice

Published:2001-12-04 Issue:26 Volume:98 Page:15288-15293
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Moore R. C.,Mastrangelo P.,Bouzamondo E.,Heinrich C.,Legname G.,Prusiner S. B.,Hood L.,Westaway D.,DeArmond S. J.,Tremblay P.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference33 articles.

1. Antibodies to a scrapie prion protein

2. Identification of prion amyloid filaments in scrapie-infected brain

3. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein

4. 129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal

5. Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene

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1. Impairment of cerebellar long-term depression and GABAergic transmission in prion protein deficient mice ectopically expressing PrPLP/Dpl;Scientific Reports;2020-09-28

2. The vascular endothelial cell-expressed prion protein Prnd/Doppel promotes angiogenesis and blood-brain barrier development;Development;2020-01-01

3. Prion diseases;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

4. Prion Proteins and Neuronal Death in the Cerebellum;Prions - Some Physiological and Pathophysiological Aspects;2019-01-30

5. The function of the cellular prion protein in health and disease;Acta Neuropathologica;2017-11-18

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