Absence of oligodendroglial glucosylceramide synthesis does not result in CNS myelin abnormalities or alter the dysmyelinating phenotype of CGT-deficient mice.
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Oligodendroglial membrane dynamics in relation to myelin biogenesisSialic acids in the brain: gangliosides and polysialic acid in nervous system development, stability, disease, and regenerationEffects of different tissue microenvironments on gene expression in breast cancer cellsNeurons and oligodendrocytes recycle sphingosine 1-phosphate to ceramide: significance for apoptosis and multiple sclerosisMyelination in the absence of UDP-galactose:ceramide galactosyl-transferase and fatty acid 2 -hydroxylase.Multi-system disorders of glycosphingolipid and ganglioside metabolismLipid metabolism in myelinating glial cells: lessons from human inherited disorders and mouse models.Simplifying complexity: genetically resculpting glycosphingolipid synthesis pathways in mice to reveal function.Substrate compositional variation with tissue/region and Gba1 mutations in mouse models--implications for Gaucher diseaseGanglioside biochemistryThe lipid sulfatide is a novel myelin-associated inhibitor of CNS axon outgrowth.Inhibition of GM3 synthase attenuates neuropathology of Niemann-Pick disease Type C. by affecting sphingolipid metabolism.Cholesterol: a novel regulatory role in myelin formation.A world of sphingolipids and glycolipids in the brain--novel functions of simple lipids modified with glucose.Quantitative metabolic profiling of lipid mediators.The consequences of genetic and pharmacologic reduction in sphingolipid synthesis.The Role of 3-O-Sulfogalactosylceramide, Sulfatide, in the Lateral Organization of Myelin Membrane.Short-term cuprizone feeding verifies N-acetylaspartate quantification as a marker of neurodegeneration.Genetic inactivation of PERK signaling in mouse oligodendrocytes: normal developmental myelination with increased susceptibility to inflammatory demyelination.Abnormal gangliosides are localized in lipid rafts in Sanfilippo (MPS3a) mouse brain.
P2860
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P2860
Absence of oligodendroglial glucosylceramide synthesis does not result in CNS myelin abnormalities or alter the dysmyelinating phenotype of CGT-deficient mice.
description
2010 nî lūn-bûn
@nan
2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
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2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Absence of oligodendroglial gl ...... enotype of CGT-deficient mice.
@ast
Absence of oligodendroglial gl ...... enotype of CGT-deficient mice.
@en
type
label
Absence of oligodendroglial gl ...... enotype of CGT-deficient mice.
@ast
Absence of oligodendroglial gl ...... enotype of CGT-deficient mice.
@en
prefLabel
Absence of oligodendroglial gl ...... enotype of CGT-deficient mice.
@ast
Absence of oligodendroglial gl ...... enotype of CGT-deficient mice.
@en
P2093
P2860
P356
P1433
P1476
Absence of oligodendroglial gl ...... enotype of CGT-deficient mice.
@en
P2093
Glyn Dawson
Jeffrey L Dupree
John Kilkus
Laleh Saadat
Maria Traka
Xianlin Han
P2860
P304
P356
10.1002/GLIA.20930
P577
2010-03-01T00:00:00Z