Axon-glial signaling and the glial support of axon function

KA Nave, BD Trapp - Annu. Rev. Neurosci., 2008 - annualreviews.org
Oligodendrocytes and Schwann cells are highly specialized glial cells that wrap axons with
a multilayered myelin membrane for rapid impulse conduction. Investigators have recently …

Cholesterol in myelin biogenesis and hypomyelinating disorders

G Saher, SK Stumpf - Biochimica Et Biophysica Acta (BBA)-Molecular and …, 2015 - Elsevier
The largest pool of free cholesterol in mammals resides in myelin membranes. Myelin
facilitates rapid saltatory impulse propagation by electrical insulation of axons. This function …

Transcriptional profiling reveals evidence for signaling and oligodendroglial abnormalities in the temporal cortex from patients with major depressive disorder

C Aston, L Jiang, BP Sokolov - Molecular psychiatry, 2005 - nature.com
Major depressive disorder is one of the most common and devastating psychiatric disorders.
To identify candidate mechanisms for major depressive disorder, we compared gene …

[HTML][HTML] Assembly of CNS myelin in the absence of proteolipid protein

M Klugmann, MH Schwab, A Pühlhofer, A Schneider… - Neuron, 1997 - cell.com
Two proteolipid proteins, PLP and DM20, are the major membrane components of central
nervous system (CNS) myelin. Mutations of the X-linked PLP/DM20 gene cause …

Influenza Virus-Susceptible Mice Carry Mx Genes with a Large Deletion or a Nonsense Mutation

P Staeheli, R Grob, E Meier, JG Sutcliffe… - Molecular and cellular …, 1988 - Taylor & Francis
The interferon-regulated mouse Mx gene encodes the 72-kilodalton nuclear Mx protein that
selectively inhibits influenza virus replication. Mice carrying Mx+ alleles synthesize Mx …

PLP1-related inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2

K Inoue - Neurogenetics, 2005 - Springer
Pelizaeus-Merzbacher disease (PMD) and its allelic disorder, spastic paraplegia type 2
(SPG2), are among the best-characterized dysmyelinating leukodystrophies of the central …

Mice deficient for the glycoprotein show subtle abnormalities in myelin

D Montag, KP Giese, U Bartsch, R Martini, Y Lang… - Neuron, 1994 - cell.com
Using homologous recombination in embryonic stem cells, we have generated mice with a
null mutation in the gene encoding the myelin-associated glycoprotein (MAG), a recognition …

Splice site selection in the proteolipid protein (PLP) gene transcript and primary structure of the DM-20 protein of central nervous system myelin.

KA Nave, C Lai, FE Bloom, RJ Milner - Proceedings of the National …, 1987 - pnas.org
Proteolipid protein (PLP) is the major myelin membrane protein of the central nervous
system. We have isolated a copy of an alternatively spliced PLP gene transcript from a …

Premature arrest of myelin formation in transgenic mice with increased proteolipid protein gene dosage

C Readhead, A Schneider, I Griffiths, KA Nave - Neuron, 1994 - Elsevier
Proteolipid protein (PLP) is an integral membrane protein of CNS myelin. Mutations of the X
chromosome-linked PLP gene cause glial cell death and myelin deficiency in jimpy mice …

The dysmyelinating mouse mutations shiverer (shi) and myelin deficient (shi mld )

C Readhead, L Hood - Behavior genetics, 1990 - Springer
Shiverer (shi/shi) is an autosomal recessive mouse mutation that produces a shivering
phenotype in affected mice. A shivering gait can be seen from a few weeks after birth until …