(Q46558374)

English

Oligodendrocyte-specific ceramide galactosyltransferase (CGT) expression phenotypically rescues CGT-deficient mice and demonstrates that CGT activity does not limit brain galactosylceramide level

scientific article published in November 2005

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scholarly article

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

Oligodendrocyte-specific ceramide galactosyltransferase (CGT) expression phenotypically rescues CGT-deficient mice and demonstrates that CGT activity does not limit brain galactosylceramide level (English)

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

oligodendrocyte

1 reference

based on heuristic

inferred from title

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author name string

Inge Zöller

1

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

Heinrich Büssow

2

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

Volkmar Gieselmann

3

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

Matthias Eckhardt

4

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

publication date

1 November 2005

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

52

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

3

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

190-198

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

A mammalian fatty acid hydroxylase responsible for the formation of alpha-hydroxylated galactosylceramide in myelin

1 reference

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Accumulation of sulfatide in neuronal and glial cells of arylsulfatase A deficient mice

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The human FA2H gene encodes a fatty acid 2-hydroxylase

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Genetic background determines phenotypic severity of the Plp rumpshaker mutation.

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Biology of oligodendrocyte and myelin in the mammalian central nervous system

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7 January 2021

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Functional breakdown of the lipid bilayer of the myelin membrane in central and peripheral nervous system by disrupted galactocerebroside synthesis

1 reference

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7 January 2021

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Galactosphingolipids and axono-glial interaction in myelin of the central nervous system

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Composition and biophysical properties of myelin lipid define the neurological defects in galactocerebroside- and sulfatide-deficient mice

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Schwann cell myelin ensheathing C.N.S. axons in the nerve fibre layer of the cat retina

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Myelination in the absence of galactocerebroside and sulfatide: normal structure with abnormal function and regional instability.

1 reference

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7 January 2021

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Demyelination and altered expression of myelin-associated glycoprotein isoforms in the central nervous system of galactolipid-deficient mice.

1 reference

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7 January 2021

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Myelin abnormalities in mice deficient in galactocerebroside and sulfatide.

1 reference

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7 January 2021

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Axo-glial interactions regulate the localization of axonal paranodal proteins

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Binding of Clostridium botulinum C2 toxin to asparagine-linked complex and hybrid carbohydrates

1 reference

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7 January 2021

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Biochemistry and neuropathology of mice doubly deficient in synthesis and degradation of galactosylceramide.

1 reference

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rMAL is a glycosphingolipid-associated protein of myelin and apical membranes of epithelial cells in kidney and stomach

1 reference

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Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy

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Sulfatide is a negative regulator of oligodendrocyte differentiation: development in sulfatide-null mice

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20230

7 January 2021

based on heuristic

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Paranodal junction formation and spermatogenesis require sulfoglycolipids

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20230

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A myelin galactolipid, sulfatide, is essential for maintenance of ion channels on myelinated axon but not essential for initial cluster formation.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20230

7 January 2021

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Motor function analysis of myelin mutant mice using a rotarod

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7 January 2021

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Proteolipid promoter activity distinguishes two populations of NG2-positive cells throughout neonatal cortical development.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20230

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Expression of the myelin and oligodendrocyte progenitor marker sulfatide in neurons and astrocytes of adult rat brain

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20230

7 January 2021

based on heuristic

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Thin-layer chromatography of glycosphingolipids

1 reference

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7 January 2021

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UDP-galactose:ceramide galactosyltransferase is a class I integral membrane protein of the endoplasmic reticulum.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20230

7 January 2021

based on heuristic

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Delay of myelin formation in arylsulphatase A-deficient mice

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20230

7 January 2021

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Microanalysis of complex tissue lipids by high-performance thin-layer chromatography.

1 reference

https://api.crossref.org/works/10.1002%2FGLIA.20230

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GLIA.20230

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

1 reference

Europe PubMed Central

23 December 2017

http://europepmc.org/abstract/MED/15968630

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