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Peroxisome biogenesis disorders: genetics and cell biology
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Peroxisome biogenesis disorders: genetics and cell biology
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
main subject
cell biology
1 reference
based on heuristic
inferred from title
author name string
Gould SJ
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
Valle D
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
publication date
1 August 2000
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
published in
Trends in Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
volume
16
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
page(s)
340-345
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
issue
8
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
cites work
Lipid metabolism in peroxisomes in relation to human disease
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisomes in human fibroblasts have a basic pH
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Biogenesis of peroxisomes
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Protein import into peroxisomes and biogenesis of the organelle
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisome biogenesis: from yeast to man.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisome synthesis in the absence of preexisting peroxisomes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inhibitors of COPI and COPII do not block PEX3-mediated peroxisome synthesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A human gene responsible for Zellweger syndrome that affects peroxisome assembly
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The endoplasmic reticulum plays an essential role in peroxisome biogenesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fusion of small peroxisomal vesicles in vitro reconstructs an early step in the in vivo multistep peroxisome assembly pathway of Yarrowia lipolytica
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
PAS7 encodes a novel yeast member of the WD-40 protein family essential for import of 3-oxoacyl-CoA thiolase, a PTS2-containing protein, into peroxisomes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
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7 January 2021
based on heuristic
inferred from DOI database lookup
The pas8 mutant of Pichia pastoris exhibits the peroxisomal protein import deficiencies of Zellweger syndrome cells--the PAS8 protein binds to the COOH-terminal tripeptide peroxisomal targeting signal, and is a member of the TPR protein family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: evidence that PTS1 protein import is mediated by a cycling receptor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisomes: simple in function but complex in maintenance.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disorders of peroxisome biogenesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a human PTS1 receptor docking protein directly required for peroxisomal protein import
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Hansenula polymorpha PER3 gene is essential for the import of PTS1 proteins into the peroxisomal matrix.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The SH3 domain of the Saccharomyces cerevisiae peroxisomal membrane protein Pex13p functions as a docking site for Pex5p, a mobile receptor for the import PTS1-containing proteins.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The import receptor for the peroxisomal targeting signal 2 (PTS2) in Saccharomyces cerevisiae is encoded by the PAS7 gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of Pex13p a peroxisomal membrane receptor for the PTS1 recognition factor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Formation of the peroxisome lumen is abolished by loss of Pichia pastoris Pas7p, a zinc-binding integral membrane protein of the peroxisome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two AAA family peroxins, PpPex1p and PpPex6p, interact with each other in an ATP-dependent manner and are associated with different subcellular membranous structures distinct from peroxisomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PAS1, a yeast gene required for peroxisome biogenesis, encodes a member of a novel family of putative ATPases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutants of the yeast Yarrowia lipolytica defective in protein exit from the endoplasmic reticulum are also defective in peroxisome biogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hansenula polymorpha Pex1p and Pex6p are peroxisome-associated AAA proteins that functionally and physically interact.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Saccharomyces cerevisiae pex3p and pex19p are required for proper localization and stability of peroxisomal membrane proteins
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of PEX11beta mediates peroxisome proliferation in the absence of extracellular stimuli
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Peroxisome biogenesis: involvement of ARF and coatomer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Giant peroxisomes in oleic acid-induced Saccharomyces cerevisiae lacking the peroxisomal membrane protein Pmp27p
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pmp27 promotes peroxisomal proliferation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pay32p of the yeast Yarrowia lipolytica is an intraperoxisomal component of the matrix protein translocation machinery
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Enlarged peroxisomes are present in oleic acid-grown Yarrowia lipolytica overexpressing the PEX16 gene encoding an intraperoxisomal peripheral membrane peroxin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0168-9525%2800%2902056-4
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0168-9525(00)02056-4
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
PubMed ID
10904262
1 reference
stated in
Europe PubMed Central
PubMed ID
10904262
retrieved
30 July 2017
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