Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene (Q24293282)

protein import into peroxisome matrix

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

10

Ronald J A Wanders

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author name string

Nobuyuki Shimozawa

1

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Toshiro Tsukamoto

2

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Tomoko Nagase

3

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Yasuhiko Takemoto

4

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Naoki Koyama

5

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Yasuyuki Suzuki

6

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Masayuki Komori

7

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Takashi Osumi

8

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Gootjes Jeannette

9

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Naomi Kondo

High-efficiency transformation of mammalian cells by plasmid DNA

11

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language of work or name

English

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publication date

June 2004

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published in

Human Mutation

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volume

23

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issue

6

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page(s)

552-8

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cites work

1 reference

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Identification and characterization of the human orthologue of yeast Pex14p

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20032

Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways

21 January 2018

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7 January 2021

Peroxisome biogenesis and selective degradation converge at Pex14p

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https://api.crossref.org/works/10.1002%2FHUMU.20032

7 January 2021

Identification of a human PTS1 receptor docking protein directly required for peroxisomal protein import

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7 January 2021

Involvement of Pex13p in Pex14p localization and peroxisomal targeting signal 2-dependent protein import into peroxisomes

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https://api.crossref.org/works/10.1002%2FHUMU.20032

7 January 2021

Peroxisomes are formed from complex membrane structures in PEX6-deficient CHO cells upon genetic complementation.

1 reference

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7 January 2021

Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders

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7 January 2021

Insertion of the 70-kDa peroxisomal membrane protein into peroxisomal membranes in vivo and in vitro

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https://api.crossref.org/works/10.1002%2FHUMU.20032

7 January 2021

The Hansenula polymorpha PEX14 gene encodes a novel peroxisomal membrane protein essential for peroxisome biogenesis

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https://api.crossref.org/works/10.1002%2FHUMU.20032

7 January 2021

The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes

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7 January 2021

Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation

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7 January 2021

Mammalian Pex14p: membrane topology and characterisation of the Pex14p-Pex14p interaction

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7 January 2021

The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p.PTS2 protein complex into peroxisomes via its initial docking site, Pex14p

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20032

7 January 2021

The ScPex13p SH3 domain exposes two distinct binding sites for Pex5p and Pex14p

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7 January 2021

The peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis

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7 January 2021

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

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7 January 2021

Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts

1 reference

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7 January 2021

Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients

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7 January 2021

Different intracellular localization of peroxisomal proteins in fibroblasts from patients with aberrant peroxisome assembly

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7 January 2021

D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder

1 reference

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7 January 2021

Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disorders

1 reference

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7 January 2021

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

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7 January 2021

Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells

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7 January 2021