(Q73117547)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

Measurement of dihydroxyacetone-phosphate acyltransferase (DHAPAT) in chorionic villous samples, blood cells and cultured cells (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

author name string

R J Wanders

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

R Ofman

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

G J Romeijn

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

R B Schutgens

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

P A Mooijer

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

C Dekker

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

H van den Bosch

7

1 reference

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1 November 2019

publication date

1 January 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

1 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

18 Suppl 1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

page(s)

90-100

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9053559%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00711432

1 November 2019

exact match

0 references

cites work

Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation

1 reference

12 December 2020

Properties of guinea pig liver peroxisomal dihydroxyacetone phosphate acyltransferase.

1 reference

12 December 2020

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

12 December 2020

First prenatal diagnosis of acyl-CoA oxidase deficiency

1 reference

12 December 2020

Peroxisomal bifunctional enzyme deficiency

1 reference

12 December 2020

Prenatal and perinatal diagnosis of peroxisomal disorders

1 reference

12 December 2020

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

1 reference

12 December 2020

Stereochemical specificity of the biosynthesis of the alkyl ether bond in alkyl ether lipids

1 reference

12 December 2020

Deficiency of acyl-CoA:dihydroxyacetone phosphate acyltransferase in thrombocytes of Zellweger patients: a simple postnatal diagnostic test

1 reference

12 December 2020

Glycerolipid biosynthesis in peroxisomes via the acyl dihydroxyacetone phosphate pathway

1 reference

12 December 2020

Biochemistry of peroxisomes

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Long term survival of a patient with the cerebro-hepato-renal (Zellweger) syndrome

1 reference

12 December 2020

Rhizomelic chondrodysplasia punctata: another peroxisomal disorder.

1 reference

12 December 2020

Rat liver dihydroxyacetone-phosphate acyltransferase: enzyme characteristics and localization studies.

1 reference

12 December 2020

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

1 reference

12 December 2020

Rat liver dihydroxyacetone-phosphate acyltransferases and their contribution to glycerolipid synthesis.

1 reference

12 December 2020

Purification of dihydroxyacetone phosphate acyltransferase from guinea pig liver peroxisomes

1 reference

12 December 2020

Purification of peroxisomal acyl-CoA: dihydroxyacetonephosphate acyltransferase from human placenta

1 reference

12 December 2020

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

1 reference

12 December 2020

Postnatal diagnosis of peroxisomal disorders: a biochemical approach

1 reference

12 December 2020

Isolated defect of peroxisomal beta-oxidation in a 16-year-old patient.

1 reference

12 December 2020

A sibship with a mild variant of Zellweger syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders

1 reference

12 December 2020

Peroxisomal disorders in neurology

1 reference

12 December 2020

Pseudo-Zellweger syndrome: deficiencies in several peroxisomal oxidative activities

1 reference

12 December 2020

Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.

1 reference

12 December 2020

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

12 December 2020

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

12 December 2020

Acyl-CoA:dihydroxyacetone phosphate acyltransferase in human skin fibroblasts: study of its properties using a new assay method.

1 reference

12 December 2020

Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency

1 reference

12 December 2020

Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes

1 reference

12 December 2020

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

1 reference

12 December 2020

Platelet-activating factor in inflammation and pulmonary disorders

1 reference

12 December 2020

Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Peroxisomal localization of the immunoreactive beta-oxidation enzymes in a neonate with a beta-oxidation defect. Pathological observations in liver, adrenal cortex and kidney.

1 reference

12 December 2020

Isolated dihydroxyacetonephosphate acyltransferase deficiency presenting with developmental delay.

1 reference

12 December 2020