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UnknownOPALIN is an LGI1 receptor promoting oligodendrocyte differentiation.
Not available
S-EPMC11317624 | biostudies-literature
UnknownMammalian-Specific Central Myelin Protein Opalin Is Redundant for Normal Myelination: Structural and Behavioral Assessments.
Not available
S-EPMC5113975 | biostudies-literature
UnknownOpalin, a transmembrane sialylglycoprotein located in the central nervous system myelin paranodal loop membrane.
Not available
S-EPMC3258930 | biostudies-literature
TranscriptomicsIdentification of Tmem10/Opalin as a novel marker for oligodendrocytes using gene expression profiling
Background During the development of the central nervous system, oligodendrocytes generate large amounts of myelin, a multilayered insulating membrane that ensheathes axons, thereby allowing the fast conduction of the action potential and maintaining axonal integrity. Differentiation of oligodendroc...
ORGANISM(S): Mus musculus 
2008-05-07 | GSE10291 | GEO
TranscriptomicsTranscription profiling of human oligodendrocytes identifies o Tmem10/Opalin as a novel marker
Background; During the development of the central nervous system, oligodendrocytes generate large amounts of myelin, a multilayered insulating membrane that ensheathes axons, thereby allowing the fast conduction of the action potential and maintaining axonal integrity. Differentiation of oligodendro...
ORGANISM(S): Mus musculus 
2008-06-20 | E-GEOD-10291 | biostudies-arrayexpress
ProteomicsAltered turnover of the CNS myelin protein Opalin in a mouse model of hereditary spastic paraplegia 35
Fatty acid 2-hydroxylase (FA2H) is responsible for the synthesis of 2-hydroxylated fatty acids, which are a building block of sphingolipids. This 2-hydroxylated sphingolipids can be found in various tissues such as brain, spinal cord, skin, testis, ovary, kidney, stomach, or intestine with a notably...
ORGANISM(S): Mus musculus (Mouse) 
2021-01-04 | PXD021021 | Pride
Cns Mice Hereditary spastic paraplegia 35 Sphingolipids Neurodegeneration Disease model Fa2h Tmt Time course Myelin Fatty acid hydroxylation Isobaric labeling Fatty acid 2-hydroxylase Opalin 
GenomicsMus musculus
Identification of Tmem10/Opalin as a novel marker for oligodendrocytes using gene expression profiling
PRJNA108503 | ENA
UnknownTRPV2: A Key Player in Myelination Disorders of the Central Nervous System.
Not available
S-EPMC8999035 | biostudies-literature
UnknownSpontaneous mutation in 2310061I04Rik results in reduced expression of mitochondrial genes and impaired brain myelination.
Not available
S-EPMC11617004 | biostudies-literature
UnknownAltered hippocampal gene expression, glial cell population, and neuronal excitability in aminopeptidase P1 deficiency.
Not available
S-EPMC7806765 | biostudies-literature
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