(Q24313725)

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Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

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Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency (English)

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hydroxysteroid 17-beta dehydrogenase 4

1 reference

GOA release 2020-03-11

very long-chain fatty-acyl-CoA metabolic process

1 reference

GOA release 2020-03-11

protein deficiency

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based on heuristic

inferred from title

author name string

E G van Grunsven

1

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E van Berkel

2

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L Ijlst

3

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P Vreken

4

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J B de Klerk

5

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J Adamski

6

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H Lemonde

7

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P T Clayton

8

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D A Cuebas

9

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R J Wanders

10

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language of work or name

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publication date

3 March 1998

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Proceedings of the National Academy of Sciences of the United States of America

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95

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5

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2128-33

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Molecular cloning of a novel widely expressed human 80 kDa 17 beta-hydroxysteroid dehydrogenase IV

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

19 March 2017

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

19 March 2017

Bile acid profiles in peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

19 March 2017

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

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

19 March 2017

https://api.crossref.org/works/10.1073/PNAS.95.5.2128

22 April 2017

Physiological role of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

19 March 2017

Purification and properties of human D-3-hydroxyacyl-CoA dehydratase: medium-chain enoyl-CoA hydratase is D-3-hydroxyacyl-CoA dehydratase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

19 March 2017

The reactions catalyzed by the inducible bifunctional enzyme of rat liver peroxisomes cannot lead to the formation of bile acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

19 March 2017

Structure of human estrogenic 17β-hydroxysteroid dehydrogenase at 2.20 å resolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

19 March 2017

Purification and properties of acyl-CoA oxidase from rat liver

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

19 March 2017

Peroxisomal multifunctional beta-oxidation protein of Saccharomyces cerevisiae. Molecular analysis of the fox2 gene and gene product

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

19 March 2017

Complementation analysis of fibroblasts from peroxisomal fatty acid oxidation deficient patients shows high frequency of bifunctional enzyme deficiency plus intragenic complementation: unequivocal evidence for differential defects in the same enzyme

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

beta-oxidation of fatty acids in mitochondria, peroxisomes, and bacteria: a century of continued progress

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

Porcine 80-kDa protein reveals intrinsic 17 beta-hydroxysteroid dehydrogenase, fatty acyl-CoA-hydratase/dehydrogenase, and sterol transfer activities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

Molecular cloning and amino acid sequence of the porcine 17 beta-estradiol dehydrogenase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

Postnatal diagnosis of peroxisomal disorders: a biochemical approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

Peroxisomal disorders: a review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

Peroxisomal bifunctional enzyme deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

Biochemistry of peroxisomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

27 September 2017

Peroxisomal multifunctional enzyme of beta-oxidation metabolizing D-3-hydroxyacyl-CoA esters in rat liver: molecular cloning, expression and characterization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

30 May 2018

Studies on the three-dimensional structure of estrogenic 17 beta-hydroxysteroid dehydrogenase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

30 May 2018

Complementation analysis of patients with intact peroxisomes and impaired peroxisomal beta-oxidation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

30 May 2018

An efficient positive selection procedure for the isolation of peroxisomal import and peroxisome assembly mutants of Saccharomyces cerevisiae.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

30 May 2018

Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

30 May 2018

Peroxisomal disorders: complementation analysis using beta-oxidation of very long chain fatty acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

30 May 2018

Peroxisomal lipid metabolism.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.5.2128

21 January 2018

Evidence for gene duplication forming similar binding folds for NAD(P)H and FAD in pyridine nucleotide-dependent flavoenzymes.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.5.2128

21 January 2018

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.5.2128

21 January 2018

Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the alpha-subunit of the mitochondrial trifunctional protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19272

29 November 2018

Simple diagnosis of the Zellweger syndrome by gas-liquid chromatography of dimethylacetals

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482850

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The sequence of porcine 80 kDa 17 beta-estradiol dehydrogenase reveals similarities to the short chain alcohol dehydrogenase family, to actin binding motifs and to sterol carrier protein 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482850

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/9482850

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further characterization of the peroxisomal 3-hydroxyacyl-CoA dehydrogenases from rat liver. Relationship between the different dehydrogenases and evidence that fatty acids and the C27 bile acids di- and tri-hydroxycoprostanic acids are metabolized

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482850

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metabolic aspects of peroxisomal disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/9482850

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.5.2128

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1073/PNAS.95.5.2128

0 references

1998PNAS...95.2128V

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release_7joiam3h6vg4rh74dime6wzapa

1 reference

https://api.fatcat.wiki/v0/release/7joiam3h6vg4rh74dime6wzapa

24 November 2022

based on heuristic

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