(Q80866231)

English

Increasing sulfatide synthesis in myelin-forming cells of arylsulfatase A-deficient mice causes demyelination and neurological symptoms reminiscent of human metachromatic leukodystrophy

scientific article published on 01 August 2007

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scholarly article

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4 January 2020

Increasing sulfatide synthesis in myelin-forming cells of arylsulfatase A-deficient mice causes demyelination and neurological symptoms reminiscent of human metachromatic leukodystrophy (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728461%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

metachromatic leukodystrophy

1 reference

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inferred from title

Hariharasubramanian Ramakrishnan

1

1 reference

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4 January 2020

author name string

Kerstin Khalaj Hedayati

2

1 reference

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4 January 2020

Renate Lüllmann-Rauch

3

1 reference

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4 January 2020

Carsten Wessig

4

1 reference

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4 January 2020

Simon Ngamli Fewou

5

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4 January 2020

Helena Maier

6

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4 January 2020

Hans-Hilmar Goebel

7

1 reference

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4 January 2020

Volkmar Gieselmann

8

1 reference

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4 January 2020

Matthias Eckhardt

9

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4 January 2020

publication date

1 August 2007

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4 January 2020

Journal of Neuroscience

1 reference

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4 January 2020

27

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4 January 2020

35

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4 January 2020

9482-9490

1 reference

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4 January 2020

Negative regulation of oligodendrocyte differentiation by galactosphingolipids.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Axonal pathology in myelin disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperactivity, neuromotor defects, and impaired learning and memory in a mouse model for metachromatic leukodystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Normal CNS myelination in transgenic mice overexpressing MHC class I H-2L(d) in oligodendrocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An adult case of metachromatic leukodystrophy. Light, polarization and electron microscopic study

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late onset neurological phenotype of the X-ALD gene inactivation in mice: a mouse model for adrenomyeloneuropathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paranodal junction formation and spermatogenesis require sulfoglycolipids

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-glycosylation is required for full enzymic activity of the murine galactosylceramide sulphotransferase

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metachromatic Leukodystrophy: Recent Research Developments

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lysosomal sulfatide storage in the brain of arylsulfatase A-deficient mice: cellular alterations and topographic distribution

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biological roles of sulfoglycolipids and pathophysiology of their deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Delay of myelin formation in arylsulphatase A-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Laminin-sulfatide binding initiates basement membrane assembly and enables receptor signaling in Schwann cells and fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reversal of non-hydroxy:alpha-hydroxy galactosylceramide ratio and unstable myelin in transgenic mice overexpressing UDP-galactose:ceramide galactosyltransferase

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sulfatide is essential for the maintenance of CNS myelin and axon structure

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A morphometric study on sural nerves in metachromatic leucodystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metachromatic leukodystrophy without arylsulfatase A deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myelination in rat brain: method of myelin isolation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synthesis and turnover of cerebroside sulfate of myelin in adult and developing rat brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The lipid composition of purified bovine brain myelin

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse models of Tay-Sachs and Sandhoff diseases differ in neurologic phenotype and ganglioside metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional abnormalities in P0-deficient mice resemble human hereditary neuropathies linked to P0 gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Motor function analysis of myelin mutant mice using a rotarod

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

alpha-Galactosidase A deficient mice: a model of Fabry disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycosphingolipid degradation and animal models of GM2-gangliosidoses

1 reference

https://pubmed.ncbi.nlm.nih.gov/17728461

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.2287-07.2007

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728461%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728461%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17728461%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

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