(Q24293136)

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Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex

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scholarly article

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Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex (English)

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Peroxisomal biogenesis factor 26

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GOA release 2020-03-11

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GOA release 2020-03-11

author name string

Satomi Furuki

1

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Shigehiko Tamura

2

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Naomi Matsumoto

3

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Non Miyata

4

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Ann Moser

5

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Hugo W Moser

6

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Yukio Fujiki

7

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language of work or name

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publication date

20 January 2006

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Journal of Biological Chemistry

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281

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3

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1317-23

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describes a project that uses

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Peroxisome biogenesis and peroxisome biogenesis disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

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/10.1074%2FJBC.M510044200

21 January 2018

Shuttling mechanism of peroxisome targeting signal type 1 receptor Pex5: ATP-independent import and ATP-dependent export

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

Functional role of the AAA peroxins in dislocation of the cycling PTS1 receptor back to the cytosol

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction

2 references

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

https://api.crossref.org/works/10.1074%2FJBC.M510044200

7 January 2021

based on heuristic

inferred from DOI database lookup

Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

PEX1 mutations in the Zellweger spectrum of the peroxisome biogenesis disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M510044200

21 January 2018

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/10.1074%2FJBC.M510044200

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1074/JBC.M510044200

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