The peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis (Q28142062)

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scientific article (publication date: 30 April 1999)

Language	Label	Description	Also known as
English	The peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis	scientific article (publication date: 30 April 1999)

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scholarly article

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

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author name string

N Shimizu

1

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R Itoh

2

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Y Hirono

3

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H Otera

4

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K Ghaedi

5

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K Tateishi

6

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S Tamura

7

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K Okumoto

8

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T Harano

9

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S Mukai

10

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Y Fujiki

11

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language of work or name

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publication date

30 April 1999

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Journal of Biological Chemistry

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274

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12593-604

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18

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Molecular defects in genetic diseases of peroxisomes

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https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

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.274.18.12593

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.274.18.12593

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

A unified nomenclature for peroxisome biogenesis factors

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https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

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

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https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

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

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https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

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

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https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

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.274.18.12593

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

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https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

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

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https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

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

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https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

PEX12 encodes an integral membrane protein of peroxisomes

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https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

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.274.18.12593

21 January 2018

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

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.274.18.12593

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

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.274.18.12593

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.274.18.12593

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

Pex14p is a member of the protein linkage map of Pex5p

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

A rapid selection for animal cell mutants with defective peroxisomes.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

Acyl-Coa oxidase and hydratase-dehydrogenase, two enzymes of the peroxisomal beta-oxidation system, are synthesized on free polysomes of clofibrate-treated rat liver

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

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.274.18.12593

21 January 2018

Synthesis of a major integral membrane polypeptide of rat liver peroxisomes on free polysomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

An isoform of pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

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.274.18.12593

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.274.18.12593

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.274.18.12593

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.274.18.12593

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.274.18.12593

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.274.18.12593

21 January 2018

Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

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.274.18.12593

21 January 2018

Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

NATURE OF THE HEPATOMEGALIC EFFECT PRODUCED BY ETHYL-CHLOROPHENOXY-ISOBUTYRATE IN THE RAT

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.18.12593

21 January 2018

Identifiers

10.1074/JBC.274.18.12593

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