Peroxisome biogenesis and peroxisome biogenesis disorders (Q33957100)

30 July 2017

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title

Peroxisome biogenesis and peroxisome biogenesis disorders (English)

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30 July 2017

Fujiki Y

1

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30 July 2017

language of work or name

English

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publication date

1 June 2000

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30 July 2017

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30 July 2017

volume

476

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30 July 2017

issue

1-2

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30 July 2017

page(s)

42-46

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Biogenesis of peroxisomes

30 July 2017

cites work

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Molecular defects in genetic diseases of peroxisomes

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21 January 2018

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21 January 2018

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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

21 January 2018

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Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein

21 January 2018

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Common principles of protein translocation across membranes

21 January 2018

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

21 January 2018

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

21 January 2018

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A rapid selection for animal cell mutants with defective peroxisomes.

21 January 2018

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

21 January 2018

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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

21 January 2018

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Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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The peroxin pex3p initiates membrane assembly in peroxisome biogenesis

21 January 2018

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

21 January 2018

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

21 January 2018

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PEX12 encodes an integral membrane protein of peroxisomes

21 January 2018

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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

21 January 2018

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

21 January 2018

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Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly

21 January 2018

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A human gene responsible for Zellweger syndrome that affects peroxisome assembly

21 January 2018

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Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Peroxisome synthesis in the absence of preexisting peroxisomes

21 January 2018

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A conserved tripeptide sorts proteins to peroxisomes

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Identification and characterization of the human orthologue of yeast Pex14p

21 January 2018

1 reference

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

21 January 2018

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Cloning and characterization of the gene encoding the human peroxisomal assembly protein Pex3p

21 January 2018

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Identification and characterization of the human peroxin PEX3

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

Pex19p, a farnesylated protein essential for peroxisome biogenesis

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

Pex19p interacts with Pex3p and Pex10p and is essential for peroxisome biogenesis in Pichia pastoris

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

Saccharomyces cerevisiae pex3p and pex19p are required for proper localization and stability of peroxisomal membrane proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

The endoplasmic reticulum plays an essential role in peroxisome biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

A mouse model for Zellweger syndrome

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement

21 January 2018

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https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901667-7

10.1016/S0014-5793(00)01667-7

7 January 2021

Identifiers

DOI

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30 July 2017

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