(Q33948568)

30 July 2017

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title

Disorders related to peroxisomal membranes (English)

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30 July 2017

Gärtner J

1

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30 July 2017

publication date

1 May 2000

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Journal of Inherited Metabolic Disease

30 July 2017

published in

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30 July 2017

volume

23

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30 July 2017

issue

3

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30 July 2017

page(s)

264-272

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https://scigraph.springernature.com/pub.10.1023/a:1005636113499

30 July 2017

exact match

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cites work

Peroxisomal ABC transporters

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical and genetic aspects of X-linked adrenoleukodystrophy

1 reference

12 December 2020

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

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12 December 2020

The sorting sequence of the peroxisomal integral membrane protein PMP47 is contained within a short hydrophilic loop

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12 December 2020

Peroxisome assembly factor-2, a putative ATPase cloned by functional complementation on a peroxisome-deficient mammalian cell mutant

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12 December 2020

The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor

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12 December 2020

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

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12 December 2020

Identification of a common PEX1 mutation in Zellweger syndrome

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12 December 2020

Biogenesis of peroxisomes

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12 December 2020

A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase

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12 December 2020

Targeting of proteins into the peroxisomal matrix

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12 December 2020

Peroxisomes in the methylotrophic yeast Hansenula polymorpha do not necessarily derive from pre-existing organelles

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12 December 2020

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

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12 December 2020

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

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12 December 2020

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

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12 December 2020

A conserved tripeptide sorts proteins to peroxisomes

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12 December 2020

Peroxisomes (microbodies and related particles)

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12 December 2020

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

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12 December 2020

Identification and characterization of the human peroxin PEX3

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12 December 2020

Cloning and characterization of the gene encoding the human peroxisomal assembly protein Pex3p

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12 December 2020

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

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12 December 2020

PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders

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12 December 2020

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

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12 December 2020

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

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12 December 2020

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

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12 December 2020

Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

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12 December 2020

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy

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12 December 2020

Peroxisome synthesis in the absence of preexisting peroxisomes

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12 December 2020

Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype

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12 December 2020

Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapy

1 reference

12 December 2020

PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p

1 reference

12 December 2020

Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy

1 reference

12 December 2020

Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders

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12 December 2020

Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders

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12 December 2020

Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders

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12 December 2020

Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly

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12 December 2020

Identifiers

DOI

10.1023/A:1005636113499

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Dimensions Publication ID

30 July 2017

1045211351

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