Neuron
Volume 13, Issue 2, August 1994, Pages 427-442
ArticleGlial cell degeneration and hypomyelination caused by overexpression of myelin proteolipid protein gene
References (72)
- et al.
Isolation and sequence determination of cDNA encoding PMP-22 (PAS-IIISR131 GAS-3) of human peripheral myelin
Biochem. Biophys. Res. Commun.
(1992) - et al.
A proteolipid protein gene family: expression in sharks and rays and possible evolution from an ancestral gene encoding a pore-forming polypeptide
Neuron
(1993) - et al.
A defect in the cell cycle of neuroglia in the myelin deficient jimpy mouse
Dev. Brain Res.
(1987) - et al.
An AG-GG transition at a splice site in the myelin proteolipid protein gene in jimpy mice results in the removal of an exon
FEBS Lett.
(1987) - et al.
Nucleotide sequences of two mRNAs for rat brain myelin proteolipid protein
Cell
(1985) - et al.
The fifth exon of the myelin proteolipid protein-coding gene is not utilized in the brain of jimpy mutant mice
Gene
(1987) - et al.
The oligodendrocyte and its many cellular processes
Trends Cell Biol.
(1993) - et al.
Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage
Neuron
(1994) - et al.
Genes specifically expressed at growth arrest of mammalian cells
Cell
(1988) - et al.
Developmental profile and differential localization of mRNAs of myelin proteins (MBP and PLP) in oligodendrocytes in the brain and in culture
Dev. Brain Res.
(1989)
Monoclonal antibodies (01 to 04) to oligodendrocyte cell surfaces: an immunocytological study in the central nervous system
Dev. Biol.
(1981)
Molecular cloning of M6: identification of a PLP/DM20 gene family
Neuron
(1993)
Glial conditioned medium enables jimpy oligodendrocytes to express properties of normal oligodendrocytes; production of myelin antigens and membranes
Glia
(1988)
Myelin-deficient rat; a point mutation in exon 111, (A-C, Thr75-Pro) of the myelin proteolipid protein causes dysmyelination and oligodendrocyte death
EMBO J.
(1989)
A de novo Tyr206CyS mutation in the proteolipid protein gene causes Pelizaeus-Merzbacher disease
Am. J. Hum. Genet.
(1991)
Cellular and molecular aspects of myelin protein gene expression
Mol. Neurobiol.
(1988)
DM20 mRNA splice product of the myelin proteolipid protein gene is expressed in the murine heart
J. Neurosci. Res.
(1992)
Calcium movements mediated by proteolipid protein and nucleotides in liposomes prepared with the endogenous lipids from brain white matter
J. Neurochem.
(1990)
Molecular diagnostics for myelin proteolipid gene mutations in Pelizaeus-Merzbacher disease
Am. J. Hum. Genet.
(1992)
Conservative amino acid substitution in the myelin proteolipid protein of jimpymsd mice
J. Neurosci.
(1990)
Pelizaeus-Merzbacher disease; an X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid protein
Am. J. Hum. Genet.
(1989)
Expression of galactoce rebroside in developing normal and jimpy oligodendrocytes in situ
J. Neurocytol.
(1988)
Expression of myelin protein genes in Schwann cells
J. Neurocytol.
(1989)
Brain proteolipids
Eur. J. Biochem.
(1983)
Manipulating the Mouse Embryo
(1986)
Animal models of genetic disorders of myelin
Mutation of the proteolipid protein gene PLP in a human X chromosome-linked myelin disorder
Selective expression of DM-20, an alternatively spliced myelin proteolipid protein gene product, in developing nervous system and in nonglial cells
J. Neurochem.
(1992)
The glioarchitectonics of the chicken brain. IV. Electron microscopic study
Okajimas Folia Anat. Jpn.
(1986)
A missense mutation in the proteolipid protein gene responsible for Pelizaeus-Merzbacher disease in a Japanese family
Hum. Mol. Genet.
(1993)
Fate of jimpy-type oligodendrocytes in jimpy heterozygote
J. Neurochem.
(1994)
Oligodendroglial cell death in jimpy mice: an explanation for the myelin deficit
J. Neurosci.
(1986)
Oligodendrocytes of the jimpy phenotype can be partially restored by environmental factors in vivo
J. Neurosci. Res.
(1991)
Proteins of myelin
Demyelination in a transgenic mouse: a model for multiple sclerosis
J. Neurosci. Res.
(1993)
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A
Nature Genet.
(1992)
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Present address: Department of Physiology, School of Medicine, Keio University, Shinjuku-ku, Tokyo 160, Jpn.
Copyright © 1994