(Q33544235)

27 July 2017

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title

The neurobiology of X-linked adrenoleukodystrophy, a demyelinating peroxisomal disorder (English)

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X-linked adrenoleukodystrophy

27 July 2017

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Dubois-Dalcq M

1

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27 July 2017

Feigenbaum V

series ordinal

2

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27 July 2017

Aubourg P

series ordinal

3

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27 July 2017

language of work or name

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1 January 1999

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27 July 2017

published in

Trends in Neurosciences

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27 July 2017

volume

22

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27 July 2017

issue

1

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27 July 2017

page(s)

4-12

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Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy

27 July 2017

cites work

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7 January 2021

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

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7 January 2021

Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement

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7 January 2021

Peroxisomal beta-oxidation: enzymology and molecular biology

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Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene

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7 January 2021

Identification of PAHX, a Refsum disease gene

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7 January 2021

Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders

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7 January 2021

Identification and characterization of the putative human peroxisomal C-terminal targeting signal import receptor

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7 January 2021

Peroxisomal disorders: genotype, phenotype, major neuropathologic lesions, and pathogenesis.

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7 January 2021

Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor

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7 January 2021

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

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7 January 2021

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor

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7 January 2021

The ABC of channel regulation

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7 January 2021

A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern

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7 January 2021

cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter.

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Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome

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7 January 2021

Primary structure of human PMP69, a putative peroxisomal ABC-transporter

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7 January 2021

Identification of a fourth half ABC transporter in the human peroxisomal membrane

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7 January 2021

Expression of the adrenoleukodystrophy protein in the human and mouse central nervous system

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7 January 2021

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7 January 2021

A Saccharomyces cerevisiae homolog of the human adrenoleukodystrophy transporter is a heterodimer of two half ATP-binding cassette transporters

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7 January 2021

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7 January 2021

Transport of activated fatty acids by the peroxisomal ATP-binding-cassette transporter Pxa2 in a semi-intact yeast cell system

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7 January 2021

Topography of very-long-chain-fatty-acid-activating activity in peroxisomes from rat liver

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7 January 2021

Topographical localization of peroxisomal acyl-CoA ligases: differential localization of palmitoyl-CoA and lignoceroyl-CoA ligases

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7 January 2021

Localization of mRNAs for adrenoleukodystrophy and the 70 kDa peroxisomal (PMP70) proteins in the rat brain during post-natal development

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7 January 2021

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7 January 2021

Suppression of peroxisomal membrane protein defects by peroxisomal ATP binding cassette (ABC) proteins

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7 January 2021

Identification of a new frameshift mutation (1801delAG) in the ALD gene

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7 January 2021

Abnormal messenger RNA expression and a missense mutation in patients with X-linked adrenoleukodystrophy

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7 January 2021

Topology of ATP-binding domain of adrenoleukodystrophy gene product in peroxisomes

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7 January 2021

Mutational analysis of patients with X-linked adrenoleukodystrophy

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7 January 2021

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy

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7 January 2021

Adrenoleukodystrophy. A clinical and pathological study of 17 cases

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7 January 2021

The inflammatory myelinopathy of adreno-leukodystrophy: cells, effector molecules, and pathogenetic implications

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7 January 2021

Phospholipids in X-linked adrenoleukodystrophy white matter: fatty acid abnormalities before the onset of demyelination

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7 January 2021

A mouse model for X-linked adrenoleukodystrophy

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7 January 2021

Histochemical characteristics of the striated inclusions of adrenoleukodystrophy

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7 January 2021

Interactions of a very long chain fatty acid with model membranes and serum albumin. Implications for the pathogenesis of adrenoleukodystrophy

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7 January 2021

Cytokine-induced accumulation of very long-chain fatty acids in rat C6 glial cells: implication for X-adrenoleukodystrophy.

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7 January 2021

Fatty acids from degenerating myelin lipids are conserved and reutilized for myelin synthesis during regeneration in peripheral nerve

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7 January 2021

Bone marrow derived elements and resident microglia in brain inflammation

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7 January 2021

Macrophages and inflammation in the central nervous system

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7 January 2021

Hematopoietic cells differentiate into both microglia and macroglia in the brains of adult mice

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7 January 2021

Reversal of early neurologic and neuroradiologic manifestations of X-linked adrenoleukodystrophy by bone marrow transplantation

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7 January 2021

In vitro evidence for a dual role of tumor necrosis factor‐α in human immunodeficiency virus type 1 encephalopathy

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7 January 2021

Excessive production of tumour necrosis factor alpha by peripheral blood mononuclear cells in X-linked adrenoleukodystrophy

1 reference

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7 January 2021

Lovastatin and sodium phenylacetate normalize the levels of very long chain fatty acids in skin fibroblasts of X- adrenoleukodystrophy

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https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901319-8

7 January 2021

Cholesterol metabolism and embryogenesis

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7 January 2021

Adrenoleukodystrophy protein-deficient mice represent abnormality of very long chain fatty acid metabolism

1 reference

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7 January 2021

Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901319-8

7 January 2021

Retroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901319-8

7 January 2021

Retroviral transfer and long-term expression of the adrenoleukodystrophy gene in human CD34+ cells

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901319-8

7 January 2021

Regeneration of oligodendrocytes and myelin

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901319-8

7 January 2021

Lovastatin for X-linked adrenoleukodystrophy

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https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901319-8

7 January 2021

Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901319-8

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0166-2236%2898%2901319-8

7 January 2021

10.1016/S0166-2236(98)01319-8

Identifiers

DOI

1 reference

release_g6eyrnivcrdi5cftihpi2hgede

27 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/g6eyrnivcrdi5cftihpi2hgede

24 November 2022

mapped directly with Wikidata item

1 reference