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PMID: 7807578 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Neurological mouse mutants and the genes of myelin.

Journal of neuroscience research ·Vol. 38 ·No. 6 ·1994-08-15 ·Pages 607-12

Nave KA

Abstract

The prospect to create mouse mutants of virtually any cloned gene has renewed interest in the genetic analysis of mammalian brain development. A diverse group of spontaneous and engineered mouse mutants, characterized by a defect of myelin formation, has been intensively studied from the morphological to the molecular level. In this system, genetics has been successfully applied to analyze a corresponding set of membrane proteins which help to elaborate a defined structural entity, compact myelin. Shiverer, jimpy, Trembler, and protein zero (P0)-deficient mice demonstrate the overall function of myelination and have become models for human neurological diseases. They also illustrate some of the problems encountered in defining protein functions from complex mutant phenotypes.

MeSH Terms
Animals Genes Mice Mice, Neurologic Mutants/genetics Myelin Proteins/physiology Myelin Sheath/physiology
Chemicals
Myelin Proteins
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Nave K A
Zentrum für Molekulare Biologie, Universität Heidelberg, Germany.
Article Info
Journal
Journal of neuroscience research
Abbr.
J Neurosci Res
ISSN
0360-4012
Published
1994-08-15
Pages
607-12
Language
English
Region
United States
NLM ID
7600111
Subset
IM
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