Distribution and cellular localization of adrenoleukodystrophy protein in human tissues: implications for X-linked adrenoleukodystrophy (Q24338719)

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4 January 2020

title

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

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ATP binding cassette subfamily D member 1

4 January 2020

main subject

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X-linked adrenoleukodystrophy

GOA release 2020-03-11

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9

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Johannes Berger

10

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author name string

Romana Höftberger

1

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Markus Kunze

2

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4 January 2020

Isabelle Weinhofer

3

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4 January 2020

Fahmy Aboul-Enein

4

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4 January 2020

Till Voigtländer

5

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4 January 2020

Iris Oezen

6

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Gabriele Amann

7

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Hanno Bernheimer

8

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language of work or name

English

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publication date

29 August 2007

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4 January 2020

published in

Neurobiology of Disease

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volume

28

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issue

2

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page(s)

165-174

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Adrenoleukodystrophy: Elevated C26 fatty acid in cultured skin fibroblasts

4 January 2020

cites work

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Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies

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Opioid precursor gene expression in the human hypothalamus

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Genomic organization of the adrenoleukodystrophy gene

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

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Brain, liver, and adipose tissue erucic and very long chain fatty acid levels in adrenoleukodystrophy patients treated with glyceryl trierucate and trioleate oils (Lorenzo's oil).

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7 January 2021

Lignoceroyl-CoASH ligase: enzyme defect in fatty acid beta-oxidation system in X-linked childhood adrenoleukodystrophy

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

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Hemorrhage activates proopiomelanocortin neurons in the rat hypothalamus

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alpha-Melanocyte-stimulating hormone is neuroprotective in rat global cerebral ischemia

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Mirror expression of adrenoleukodystrophy and adrenoleukodystrophy related genes in mouse tissues and human cell lines

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7 January 2021

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

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The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expression.

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Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells

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Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy

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7 January 2021

Peroxisomal lignoceroyl-CoA ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy

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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

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

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7 January 2021

The dorsal root ganglia in adrenomyeloneuropathy: neuronal atrophy and abnormal mitochondria.

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7 January 2021

Endoplasmic reticulum stress features are prominent in Alzheimer disease but not in prion diseases in vivo

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Pro-opiomelanocortin colocalizes with corticotropin- releasing factor in axon terminals of the noradrenergic nucleus locus coeruleus.

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Role of ALDP (ABCD1) and mitochondria in X-linked adrenoleukodystrophy

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7 January 2021

Regional variations in ABC transporter expression along the mouse intestinal tract

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Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids

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7 January 2021

Real-time reverse transcription-PCR expression profiling of the complete human ATP-binding cassette transporter superfamily in various tissues.

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Testicular dysfunction in adrenomyeloneuropathy

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Variability of endocrinological dysfunction in 55 patients with X-linked adrenoleucodystrophy: clinical, laboratory and genetic findings.

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7 January 2021

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Identifiers

DOI

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4 January 2020

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