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

Détails

ID Serval
serval:BIB_1A06DA63C104
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein.
Périodique
Nature
Auteur⸱e⸱s
Büeler H., Fischer M., Lang Y., Bluethmann H., Lipp H.P., DeArmond S.J., Prusiner S.B., Aguet M., Weissmann C.
ISSN
0028-0836 (Print)
ISSN-L
0028-0836
Statut éditorial
Publié
Date de publication
1992
Volume
356
Numéro
6370
Pages
577-582
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
Publication Status: ppublish
Résumé
PrPC is a host protein anchored to the outer surface of neurons and to a lesser extent of lymphocytes and other cells. The transmissible agent (prion) responsible for scrapie is believed to be a modified form of PrPC. Mice homozygous for disrupted PrP genes have been generated. Surprisingly, they develop and behave normally for at least seven months, and no immunological defects are apparent. It is now feasible to determine whether mice devoid of PrPC can propagate prions and are susceptible to scrapie pathogenesis.
Mots-clé
Aging, Animals, Base Sequence, Blastocyst/physiology, Blotting, Northern, Blotting, Western, Brain/growth & development, Brain/physiology, Cell Membrane/physiology, Crosses, Genetic, Female, Heterozygote Detection, Male, Membrane Proteins/genetics, Mice, Molecular Sequence Data, Neurons/physiology, Oligodeoxyribonucleotides, Polymerase Chain Reaction, PrPSc Proteins, Pregnancy, Prions/genetics, RNA/genetics, RNA/isolation & purification, Recombination, Genetic, Restriction Mapping, Scrapie/genetics, Stem Cells/physiology
Pubmed
Web of science
Création de la notice
28/01/2008 12:37
Dernière modification de la notice
20/08/2019 13:51
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