(Q24321939)

ATPase-coupled transmembrane transporter activity

GOA release 2020-03-11

1 reference

X-linked adrenoleukodystrophy

GOA release 2020-03-11

1 reference

8

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Robert Feil

object named as

R Feil

5

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P Kioschis

4

object named as

P Kioschis

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author name string

J Mosser

1

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A M Douar

2

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C O Sarde

3

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H Moser

6

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A M Poustka

7

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P Aubourg

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

9

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language of work or name

English

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publication date

25 February 1993

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published in

Nature

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volume

361

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issue

6414

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page(s)

726-30

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cites work

1 reference

7 January 2021

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

1 reference

7 January 2021

Peroxisomal lignoceroyl-CoA ligase deficiency in childhood adrenoleukodystrophy and adrenomyeloneuropathy

1 reference

7 January 2021

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

7 January 2021

Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach

1 reference

7 January 2021

Identification of a chromosome 18q gene that is altered in colorectal cancers

1 reference

7 January 2021

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

1 reference

7 January 2021

First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe

1 reference

7 January 2021

Linkage of adrenoleukodystrophy to a polymorphic DNA probe

1 reference

7 January 2021

Molecular genetics of human color vision: the genes encoding blue, green, and red pigments

1 reference

7 January 2021

Nucleotide sequence of the human 70 kDa peroxisomal membrane protein: a member of ATP-binding cassette transporters

1 reference

7 January 2021

Cloning, expression, and transcriptional properties of the human enhancer factor TEF-1

1 reference

7 January 2021

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1 reference

7 January 2021

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

1 reference

7 January 2021

1 reference

7 January 2021

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

1 reference

7 January 2021

Sequences encoded in the class II region of the MHC related to the 'ABC' superfamily of transporters

1 reference

7 January 2021

Two putative subunits of a peptide pump encoded in the human major histocompatibility complex class II region

1 reference

7 January 2021

A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein

1 reference

7 January 2021

Binding protein-dependent transport systems

1 reference

7 January 2021

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

1 reference

7 January 2021

PAS1, a yeast gene required for peroxisome biogenesis, encodes a member of a novel family of putative ATPases

1 reference

7 January 2021

PAS3, a Saccharomyces cerevisiae gene encoding a peroxisomal integral membrane protein essential for peroxisome biogenesis

1 reference

7 January 2021

Translocation of acyl-CoA oxidase into peroxisomes requires ATP hydrolysis but not a membrane potential

1 reference

7 January 2021

Rapid and sensitive protein similarity searches

1 reference

7 January 2021

Sequence of the malK gene in E.coli K12

1 reference

7 January 2021

Adrenoleukodystrophy: phenotypic variability and implications for therapy

1 reference

7 January 2021