Disruption of the compacted myelin sheath of axons of the central nervous system in proteolipid protein-deficient mice.
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Oligodendroglial membrane dynamics in relation to myelin biogenesisExploring myelin dysfunction in multiple system atrophyActin-independent behavior and membrane deformation exhibited by the four-transmembrane protein M6aPelizaeus-Merzbacher disease and spastic paraplegia type 2: two faces of myelin loss from mutations in the same geneOpalin, a transmembrane sialylglycoprotein located in the central nervous system myelin paranodal loop membraneOligodendrocytes expressing exclusively the DM20 isoform of the proteolipid protein gene: myelination and developmentInduction of axon growth arrest without growth cone collapse through the N-terminal region of four-transmembrane glycoprotein M6aStathmin-deficient mice develop an age-dependent axonopathy of the central and peripheral nervous systemsMyelin-specific proteins: a structurally diverse group of membrane-interacting molecules.A common mechanism of PLP/DM20 misfolding causes cysteine-mediated endoplasmic reticulum retention in oligodendrocytes and Pelizaeus-Merzbacher disease.Clinical and pathological features of alcohol-related brain damage.Disease-associated mutations cause premature oligomerization of myelin proteolipid protein in the endoplasmic reticulum.Inhibitory RNA in epilepsy: research tools and therapeutic perspectivesAxon-glial interaction in the CNS: what we have learned from mouse models of Pelizaeus-Merzbacher disease.Divalent cation-mediated interaction between cerebroside sulfate and cerebrosides: an investigation of the effect of structural variations of lipids by electrospray ionization mass spectrometry.Membrane traffic in myelinating oligodendrocytes.Molecular pathways of oligodendrocyte apoptosis revealed by mutations in the proteolipid protein gene.CNS myelination and PLP gene dosage.Ethanol down regulates the expression of myelin proteolipid protein in the rat hippocampus.Using temporal genetic switches to synchronize the unfolded protein response in cell populations in vivo.The myelin mutants as models to study myelin repair in the leukodystrophies.Insertion of proteolipid protein into oligodendrocyte mitochondria regulates extracellular pH and adenosine triphosphateWhite matter abnormalities and animal models examining a putative role of altered white matter in schizophrenia.Disrupted proteolipid protein trafficking results in oligodendrocyte apoptosis in an animal model of Pelizaeus-Merzbacher disease.Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia.Survival of, and competition between, oligodendrocytes expressing different alleles of the Plp gene.Myelin-associated oligodendrocytic basic protein: a family of abundant CNS myelin proteins in search of a function.Functional breakdown of the lipid bilayer of the myelin membrane in central and peripheral nervous system by disrupted galactocerebroside synthesis.The molecular and cellular defects underlying Pelizaeus-Merzbacher disease.Differences in endoplasmic-reticulum quality control determine the cellular response to disease-associated mutants of proteolipid protein.Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1.Expression of proteolipid protein gene in spinal cord stem cells and early oligodendrocyte progenitor cells is dispensable for normal cell migration and myelination.Phylogeny of proteolipid proteins: divergence, constraints, and the evolution of novel functions in myelination and neuroprotection.Axonal transport defects in neurodegenerative diseases.Neuroprotection and repair in multiple sclerosis.Developmental window of sensorineural deafness in biotinidase-deficient mice.Progressive segregation of unmyelinated axons in peripheral nerves, myelin alterations in the CNS, and cyst formation in the kidneys of myelin and lymphocyte protein-overexpressing mice.Distinct modes of migration position oligodendrocyte precursors for localized cell division in the developing spinal cord.The proteolipid protein gene.Expression of molecular chaperones and vesicle transport proteins in differentiating oligodendrocytes.
P2860
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P2860
Disruption of the compacted myelin sheath of axons of the central nervous system in proteolipid protein-deficient mice.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Disruption of the compacted my ...... olipid protein-deficient mice.
@ast
Disruption of the compacted my ...... olipid protein-deficient mice.
@en
type
label
Disruption of the compacted my ...... olipid protein-deficient mice.
@ast
Disruption of the compacted my ...... olipid protein-deficient mice.
@en
prefLabel
Disruption of the compacted my ...... olipid protein-deficient mice.
@ast
Disruption of the compacted my ...... olipid protein-deficient mice.
@en
P2860
P356
P1476
Disruption of the compacted my ...... olipid protein-deficient mice.
@en
P2093
P2860
P304
11709-11713
P356
10.1073/PNAS.91.24.11709
P407
P577
1994-11-01T00:00:00Z