(Q37576855)

21 August 2017

1 reference

title

Peroxisomes, myelination, and axonal integrity in the CNS. (English)

1 reference

21 August 2017

1 reference

Myriam Baes

1

1 reference

PubMed ID

19666893

21 August 2017

Patrick Aubourg

series ordinal

2

1 reference

21 August 2017

1 August 2009

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21 August 2017

1 reference

21 August 2017

15

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21 August 2017

4

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21 August 2017

367-379

1 reference

Differential expression of peroxisomal matrix and membrane proteins during postnatal development of mouse brain.

21 August 2017

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

The neuronal migration defect in mice with Zellweger syndrome (Pex5 knockout) is not caused by the inactivity of peroxisomal beta-oxidation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Generalised and conditional inactivation of Pex genes in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

MRI of the brain and cervical spinal cord in rhizomelic chondrodysplasia punctata

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Neuroimaging of peroxisome biogenesis disorders (Zellweger spectrum) with prolonged survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Functions and biosynthesis of plasmalogens in health and disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in ALS Mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Metabolism of prostaglandin F2 alpha in Zellweger syndrome. Peroxisomal beta-oxidation is a major importance for in vivo degradation of prostaglandins in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Metabolism and functions of glutathione in brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Molecular pathogenesis of megalencephalic leukoencephalopathy with subcortical cysts: mutations in MLC1 cause folding defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Is microglial apoptosis an early pathogenic change in cerebral X-linked adrenoleukodystrophy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Clinical and biochemical spectrum of D-bifunctional protein deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of leukotrienes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Ataxia with loss of Purkinje cells in a mouse model for Refsum disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Early oxidative damage underlying neurodegeneration in X-adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

A key role for the peroxisomal ABCD2 transporter in fatty acid homeostasis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

The ether lipid-deficient mouse: tracking down plasmalogen functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Axonal swellings and degeneration in mice lacking the major proteolipid of myelin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Distribution and cellular localization of adrenoleukodystrophy protein in human tissues: implications for X-linked adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Absence of functional peroxisomes from mouse CNS causes dysmyelination and axon degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Peroxisomal multifunctional protein-2: the enzyme, the patients and the knockout mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Peroxisomal multifunctional protein-2 deficiency causes motor deficits and glial lesions in the adult central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Potential environmental and host participants in the early white matter lesion of adreno-leukodystrophy: morphologic evidence for CD8 cytotoxic T cells, cytolysis of oligodendrocytes, and CD1-mediated lipid antigen presentation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

20-hydroxyeicosatetraenoic acid (20-HETE) metabolism in coronary endothelial cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Axonal loss and neuroinflammation caused by peroxisome-deficient oligodendrocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Evidence that plasmalogen is protective against oxidative stress in the rat brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Focal transplantation-based astrocyte replacement is neuroprotective in a model of motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Impaired degradation of leukotrienes in patients with peroxisome deficiency disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Adrenomyeloneuropathy: a neuropathologic review featuring its noninflammatory myelopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Targeting gene-modified hematopoietic cells to the central nervous system: use of green fluorescent protein uncovers microglial engraftment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Childhood ataxia with CNS hypomyelination/vanishing white matter disease--a common leukodystrophy caused by abnormal control of protein synthesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Mammalian peroxisomes and reactive oxygen species

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Silencing of Abcd1 and Abcd2 genes sensitizes astrocytes for inflammation: implication for X-adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Peroxisome biogenesis disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Murine model of Alexander disease: analysis of GFAP aggregate formation and its pathological significance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Multiple sclerosis: an immune or neurodegenerative disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl-CoA esters

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Peroxisomal disorders: the single peroxisomal enzyme deficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Biochemistry of mammalian peroxisomes revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Cerebral MRI as a valuable diagnostic tool in Zellweger spectrum patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

Absence of 2-hydroxylated sphingolipids is compatible with normal neural development but causes late-onset axon and myelin sheath degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F1073858409336297

21 January 2018

Identifiers

DOI

10.1177/1073858409336297

1 reference

21 August 2017

1 reference

PubMed ID

19666893