(Q41011005)

English

Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals.

scientific article published on September 1998

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scholarly article

1 reference

Europe PubMed Central

25 September 2017

Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals. (English)

1 reference

Europe PubMed Central

25 September 2017

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author name string

Kinoshita N

1

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Europe PubMed Central

25 September 2017

Ghaedi K

2

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Europe PubMed Central

25 September 2017

Shimozawa N

3

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Europe PubMed Central

25 September 2017

Wanders RJ

4

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Europe PubMed Central

25 September 2017

Matsuzono Y

5

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Europe PubMed Central

25 September 2017

Imanaka T

6

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Europe PubMed Central

25 September 2017

Okumoto K

7

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Europe PubMed Central

25 September 2017

Suzuki Y

8

1 reference

Europe PubMed Central

25 September 2017

Kondo N

9

1 reference

Europe PubMed Central

25 September 2017

Fujiki Y

10

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Europe PubMed Central

25 September 2017

language of work or name

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publication date

1 September 1998

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Europe PubMed Central

25 September 2017

Journal of Biological Chemistry

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Europe PubMed Central

25 September 2017

273

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Europe PubMed Central

25 September 2017

24122-24130

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Europe PubMed Central

25 September 2017

37

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Europe PubMed Central

25 September 2017

describes a project that uses

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A unified nomenclature for peroxisome biogenesis factors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Molecular defects in genetic diseases of peroxisomes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Peroxisomes: Organelles at the crossroads

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

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.273.37.24122

21 January 2018

Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

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.273.37.24122

21 January 2018

Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

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.273.37.24122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

A rapid selection for animal cell mutants with defective peroxisomes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Peroxisome assembly mutations in humans: structural heterogeneity in Zellweger syndrome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

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.273.37.24122

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.273.37.24122

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.273.37.24122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

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/10.1074%2FJBC.273.37.24122

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.273.37.24122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

PEX12 encodes an integral membrane protein of peroxisomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

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

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Isolation of a new peroxisome-deficient CHO cell mutant defective in peroxisome targeting signal-1 receptor.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

FACS-optimized mutants of the green fluorescent protein (GFP)

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Polypeptide and phospholipid composition of the membrane of rat liver peroxisomes: comparison with endoplasmic reticulum and mitochondrial membranes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Multiple proteolytic systems, including the proteasome, contribute to CFTR processing.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Four distinct secretory pathways serve protein secretion, cell surface growth, and peroxisome biogenesis in the yeast Yarrowia lipolytica

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Overexpression of Pex15p, a phosphorylated peroxisomal integral membrane protein required for peroxisome assembly in S.cerevisiae, causes proliferation of the endoplasmic reticulum membrane

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Peroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

The Hansenula polymorpha PER9 gene encodes a peroxisomal membrane protein essential for peroxisome assembly and integrity.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Isolation and characterization of Pas2p, a peroxisomal membrane protein essential for peroxisome biogenesis in the methylotrophic yeast Pichia pastoris.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Biochemical and morphologic aspects of peroxisomes in the human rectal mucosa: diagnosis of Zellweger syndrome simplified by rectal biopsy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Peroxisome biogenesis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

PEX genes on the rise

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.37.24122

21 January 2018

Identifiers

10.1074/JBC.273.37.24122

1 reference

Europe PubMed Central

25 September 2017

1 reference

Europe PubMed Central

25 September 2017

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