(Q33607758)

English

Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireview

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scholarly article

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Europe PubMed Central

PubMed publication ID

28 July 2017

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Europe PubMed Central

Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireview (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

rhizomelic chondrodysplasia punctata

1 reference

based on heuristic

inferred from title

peroxisomal biogenesis disorder

1 reference

based on heuristic

inferred from title

Marek Skoneczny

2

object named as

Skoneczny M

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Europe PubMed Central

PubMed publication ID

28 July 2017

author name string

Purdue PE

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Yang X

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Zhang JW

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Lazarow PB

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

publication date

1 April 1999

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Neurochemical Research

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Europe PubMed Central

PubMed publication ID

28 July 2017

24

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

581-586

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

https://scigraph.springernature.com/pub.10.1023/a:1023957110171

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sterol carrier protein X (SCPx) is a peroxisomal branched-chain beta-ketothiolase specifically reacting with 3-oxo-pristanoyl-CoA: a new, unique role for SCPx in branched-chain fatty acid metabolism in peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nucleotide sequence of human alkyl-dihydroxyacetonephosphate synthase cDNA reveals the presence of a peroxisomal targeting signal 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The peroxisomal targeting signal of 3-oxoacyl-CoA thiolase from Saccharomyces cerevisiae

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of PAHX, a Refsum disease gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peb1p (Pas7p) is an intraperoxisomal receptor for the NH2-terminal, type 2, peroxisomal targeting sequence of thiolase: Peb1p itself is targeted to peroxisomes by an NH2-terminal peptide.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ether lipid biosynthesis: isolation and molecular characterization of human dihydroxyacetonephosphate acyltransferase

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PEB1 (PAS7) in Saccharomyces cerevisiae encodes a hydrophilic, intra-peroxisomal protein that is a member of the WD repeat family and is essential for the import of thiolase into peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cholesterol biosynthesis, peroxisomes and peroxisomal disorders: mevalonate kinase is not only deficient in Zellweger syndrome but also in rhizomelic chondrodysplasia punctata

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Pichia pastoris peroxisomal protein PAS8p is the receptor for the C-terminal tripeptide peroxisomal targeting signal

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human alkyldihydroxyacetonephosphate synthase deficiency: a new peroxisomal disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of peroxisomal membrane ghosts with an epitope-tagged integral membrane protein in yeast mutants lacking peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pay32p of the yeast Yarrowia lipolytica is an intraperoxisomal component of the matrix protein translocation machinery

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mobile PTS2 receptor for peroxisomal protein import in Pichia pastoris.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhizomelic chondrodysplasia punctata: another peroxisomal disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Hansenula polymorpha PER3 gene is essential for the import of PTS1 proteins into the peroxisomal matrix

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID 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

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomes: Organelles at the crossroads

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential protein import deficiencies in human peroxisome assembly disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PEX genes on the rise

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of rhizomelic chondrodysplasia punctata type I: high frequency of the Leu-292 stop mutation in 38 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal biogenesis: multiple pathways of protein import

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phytanoyl-CoA hydroxylase is not only deficient in classical Refsum disease but also in rhizomelic chondrodysplasia punctata

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutagenesis of the amino targeting signal of Saccharomyces cerevisiae 3-ketoacyl-CoA thiolase reveals conserved amino acids required for import into peroxisomes in vivo

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PAS10 is a tetratricopeptide-repeat protein that is essential for the import of most matrix proteins into peroxisomes of Saccharomyces cerevisiae

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID 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

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Refsum disease is caused by mutations in the phytanoyl-CoA hydroxylase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal integral membrane proteins in control and Zellweger fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal disorders: a newly recognised group of genetic diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme

1 reference

https://pubmed.ncbi.nlm.nih.gov/10227689

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1023957110171

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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