(Q73614032)

English

Genetic heterogeneity in patients with a disorder of peroxisomal beta-oxidation: a complementation study based on pristanic acid beta-oxidation suggesting different enzyme defects

scientific article published on 01 July 1997

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9266375%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Genetic heterogeneity in patients with a disorder of peroxisomal beta-oxidation: a complementation study based on pristanic acid beta-oxidation suggesting different enzyme defects (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9266375%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference

based on heuristic

inferred from title

author name string

E G van Grunsven

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9266375%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

R J Wanders

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9266375%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

publication date

1 July 1997

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9266375%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9266375%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

20

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9266375%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9266375%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

437-440

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9266375%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

https://scigraph.springernature.com/pub.10.1023/a:1005323221660

0 references

Purification and properties of acyl-CoA oxidase from rat liver

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal bifunctional enzyme deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidney

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sterol carrier protein X is peroxisomal 3-oxoacyl coenzyme A thiolase with intrinsic sterol carrier and lipid transfer activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Postnatal diagnosis of peroxisomal disorders: a biochemical approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal beta-oxidation. Purification of four novel 3-hydroxyacyl-CoA dehydrogenases from rat liver peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID 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

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal disorders: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The presence of a new 3-oxoacyl-CoA thiolase in rat liver peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9266375

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/9266375

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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