(Q22003909)

ATP binding cassette subfamily D member 3

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

peroxisome organization

1 reference

GOA release 2020-03-11

1 reference

J Gärtner

1

J

Gärtner

1 reference

7 February 2023

U Brosius

2

U

Brosius

1 reference

7 February 2023

C Obie

3

C

Obie

1 reference

7 February 2023

P A Watkins

4

P A

Watkins

1 reference

7 February 2023

D Valle

5

D

Valle

1 reference

European Journal of Cell Biology

7 February 2023

language of work or name

English

0 references

publication date

August 1998

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published in

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volume

76

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issue

4

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page(s)

237-45

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cites work

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

High-efficiency transformation of mammalian cells by plasmid DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Mating signals control expression of mutations resulting from insertion of a transposable repetitive element adjacent to diverse yeast genes

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Identification and characterization of the putative human peroxisomal C-terminal targeting signal import receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Isolation of intracellular membranes by means of sodium carbonate treatment: application to endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor protein

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Restoration of peroxisome biogenesis in a peroxisome-deficient mammalian cell line by expression of either the 35 kDa or the 70 kDa peroxisomal membrane proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

A conserved tripeptide sorts proteins to peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Synthetic enhancement in gene interaction: a genetic tool come of age.

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

The ABC of channel regulation

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Primary structure of human PMP69, a putative peroxisomal ABC-transporter

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter.

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Identification and preliminary characterization of a protein motif related to the zinc finger

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

A mouse model for X-linked adrenoleukodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

An internal region of the peroxisomal membrane protein PMP47 is essential for sorting to peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

A rapid selection for animal cell mutants with defective peroxisomes.

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Absence of mutations raises doubts about the role of the 70-kD peroxisomal membrane protein in Zellweger syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Peroxisomal lipid metabolism.

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Roles for calreticulin and a novel glycoprotein, tapasin, in the interaction of MHC class I molecules with TAP

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Does this have a familiar RING?

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

A Saccharomyces cerevisiae homolog of the human adrenoleukodystrophy transporter is a heterodimer of two half ATP-binding cassette transporters

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Identification of a fourth half ABC transporter in the human peroxisomal membrane

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

The transporters associated with antigen presentation

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Penetrating the peroxisome

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly

1 reference

https://api.crossref.org/works/10.1016%2FS0171-9335%2898%2980001-0

7 January 2021

10.1016/S0171-9335(98)80001-0

Identifiers

DOI

0 references

Fatcat ID

release_rpf3lxfigfdf7ji2hfl7d7pspe

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rpf3lxfigfdf7ji2hfl7d7pspe

24 November 2022

mapped directly with Wikidata item