A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern (Q24567552)

4

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Stephane Savary

object named as

S Savary

2

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author name string

G Lombard-Platet

1

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C O Sarde

3

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G Chimini

Proceedings of the National Academy of Sciences of the United States of America

5

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language of work or name

English

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publication date

6 February 1996

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published in

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volume

93

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issue

3

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page(s)

1265-9

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cites work

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Spectrum of mutations in the gene encoding the adrenoleukodystrophy protein

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

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

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A human gene responsible for Zellweger syndrome that affects peroxisome assembly

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Structure, localization and transcriptional properties of two classes of retinoic acid receptor alpha fusion proteins in acute promyelocytic leukemia (APL): structural similarities with a new family of oncoproteins

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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Cloning of two novel ABC transporters mapping on human chromosome 9

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The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein

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Genomic organization of the adrenoleukodystrophy gene

24 March 2017

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Mutational analysis of patients with X-linked adrenoleukodystrophy

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The 70-kDa peroxisomal membrane protein is a member of the Mdr (P-glycoprotein)-related ATP-binding protein superfamily

24 March 2017

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The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

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Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping

27 September 2017

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The yeast YKL741 gene situated on the left arm of chromosome XI codes for a homologue of the human ALD protein.

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

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PXA1, a possible Saccharomyces cerevisiae ortholog of the human adrenoleukodystrophy gene

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YAC-assisted cloning of a putative G-protein mapping to the MHC class I region

27 September 2017

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27 September 2017

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cDNA sequence of Aldgh, the mouse homolog of the X-linked adrenoleukodystrophy gene.

30 May 2018

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Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.

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Penetrating the peroxisome

28 November 2018

1 reference

12 December 2020

Localization of Refsum disease with increased pipecolic acidaemia to chromosome 10p by homozygosity mapping and carrier testing in a single nuclear family

1 reference

12 December 2020

X-linked adrenoleukodystrophy: identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts

1 reference

12 December 2020

Adrenoleukodystrophy: impaired oxidation of fatty acids due to peroxisomal lignoceroyl-CoA ligase deficiency

1 reference

12 December 2020

Transport of fatty acids into human and rat peroxisomes. Differential transport of palmitic and lignoceric acids and its implication to X-adrenoleukodystrophy

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.93.3.1265

1 reference

3289087

ADS bibcode

1996PNAS...93.1265L

0 references

3289087

1 reference

1 reference

1 reference