(Q35888833)

English

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

scientific article published in January 1994

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

peroxisomal acyl-CoA oxidase deficiency

0 references

author name string

Suzuki Y

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Shimozawa N

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Yajima S

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Tomatsu S

4

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Kondo N

5

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Nakada Y

6

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Akaboshi S

7

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Lai M

8

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Tanabe Y

9

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Hashimoto T

10

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

language of work or name

0 references

publication date

1 January 1994

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

54

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

36-43

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

Defective peroxisomal cleavage of the C27-steroid side chain in the cerebro-hepato-renal syndrome of Zellweger

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

A method for enrichment of hybrid somatic cells: complementation studies in certain lysosomal enzymopathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

A possible role for plasmalogens in protecting animal cells against photosensitized killing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

Inherited peroxisomal disorders involving the nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

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=1918057

11 July 2018

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=1918057

11 July 2018

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=1918057

11 July 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=1918057

11 July 2018

Peroxisomal bifunctional protein from rat liver is a trifunctional enzyme possessing 2-enoyl-CoA hydratase, 3-hydroxyacyl-CoA dehydrogenase, and delta 3, delta 2-enoyl-CoA isomerase activities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 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=1918057

11 July 2018

Effects of sodium 2-[5-(4-chlorophenyl)pentyl]-oxirane-2-carboxylate (POCA) on fatty acid oxidation in fibroblasts from patients with peroxisomal diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

Photosensitized killing of cultured fibroblasts from patients with peroxisomal disorders due to pyrene fatty acid-mediated ultraviolet damage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

Substrate specificities of rat liver peroxisomal acyl-CoA oxidases: palmitoyl-CoA oxidase (inducible acyl-CoA oxidase), pristanoyl-CoA oxidase (non-inducible acyl-CoA oxidase), and trihydroxycoprostanoyl-CoA oxidase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

A fatty acyl-CoA oxidizing system in rat liver peroxisomes; enhancement by clofibrate, a hypolipidemic drug

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

11 July 2018

Deficiency of acyl-CoA: dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

24 September 2018

Deficient activities and proteins of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918057

24 September 2018

Minor physical anomalies in alcoholic and schizophrenic adults and hyperactive and autistic children

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320540108

21 January 2018

The incidence of minor physical anomalies in adult male schizophrenics.

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320540108

21 January 2018

The genetics of schizophrenia: a current, genetic-epidemiologic perspective

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320540108

21 January 2018

National Institute of Mental Health Diagnostic Interview Schedule. Its history, characteristics, and validity.

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320540108

21 January 2018

SCAN. Schedules for Clinical Assessment in Neuropsychiatry

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320540108

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Properties of mitochondria and peroxisomal enoyl-CoA hydratases from rat liver

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormality of long-chain fatty acids in erythrocyte membrane sphingomyelin from patients with adrenoleukodystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inhibition of 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoic acid oxidation and of bile acid secretion in rat liver by fatty acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive course

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First prenatal diagnosis of acyl-CoA oxidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A bifunctional protein with deficient enzymic activity: identification of a new peroxisomal disorder using novel methods to measure the peroxisomal beta-oxidation enzyme activities

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonspecific lipid transfer protein (sterol carrier protein-2) defective in patients with deficient peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification and purification of a peroxisomal branched chain fatty acyl-CoA oxidase

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of pristanoyl-CoA oxidase as a distinct, clofibrate non-inducible enzyme in rat liver peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Zellweger-like phenotype in two siblings: a defect in peroxisomal beta-oxidation with elevated very long-chain fatty acids but normal bile acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acyl-CoA oxidase of rat liver: a new enzyme for fatty acid oxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8279468

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/AJMG.1320540108

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

reason for deprecated rank

incorrect identifier value

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