Measurement of very long-chain fatty acids, phytanic and pristanic acid in plasma and cultured fibroblasts by gas chromatography

scientific article published in January 1995

Measurement of very long-chain fatty acids, phytanic and pristanic acid in plasma and cultured fibroblasts by gas chromatography is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1031600598
P356DOI10.1007/BF00711430
P698PubMed publication ID9053557

P2093author name stringG Vincent
G Dacremont
G Cocquyt
P2860cites workThe 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 kidneyQ28613019
Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophyQ36265198
Postnatal diagnosis of peroxisomal disorders: a biochemical approachQ40487387
Pristanic acid and phytanic acid in plasma from patients with peroxisomal disorders: stable isotope dilution analysis with electron capture negative ion mass fragmentographyQ67895674
Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same familyQ68461928
Improved determination of very-long-chain fatty acids in plasma and cultured skin fibroblasts: applications to the diagnosis of peroxisomal disordersQ69114680
Direct transesterification of all classes of lipids in a one-step reactionQ70032561
Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctataQ72885965
P304page(s)76-83
P577publication date1995-01-01
P1433published inJournal of Inherited Metabolic DiseaseQ6295359
P1476titleMeasurement of very long-chain fatty acids, phytanic and pristanic acid in plasma and cultured fibroblasts by gas chromatography
P478volume18 Suppl 1

Reverse relations

cites work (P2860)
Q33729632A Pex7 hypomorphic mouse model for plasmalogen deficiency affecting the lens and skeleton
Q55053133A mutation in PEX19 causes a severe clinical phenotype in a patient with peroxisomal biogenesis disorder
Q35975137Abnormality in catalase import into peroxisomes leads to severe neurological disorder
Q36976826Ataxia with loss of Purkinje cells in a mouse model for Refsum disease
Q60961904Case report of dysregulation of primary bile acid synthesis in a family with X-linked adrenoleukodystrophy
Q38363640Dissection of transient oxidative stress response in Saccharomyces cerevisiae by using DNA microarrays
Q44597106Effect of dehydroepiandrosterone supplementation on fatty acid and hormone levels in patients with X‐linked adrenoleucodystrophy
Q36133280Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6
Q36894737Infantile Refsum Disease: Influence of Dietary Treatment on Plasma Phytanic Acid Levels.
Q42542201Lovastatin and sodium phenylacetate normalize the levels of very long chain fatty acids in skin fibroblasts of X- adrenoleukodystrophy
Q41881694Lymphoblastoid cell lines for diagnosis of peroxisome biogenesis disorders
Q90731853Mitochondrial fission factor (MFF) is a critical regulator of peroxisome maturation
Q55670954Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype
Q33586155Plasma and erythrocyte fatty acid patterns in patients with recurrent depression: a matched case-control study
Q34488327Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls
Q54656357Rhizomelic chondrodysplasia punctata and cardiac pathology.
Q46892757Rotenone-like action of the branched-chain phytanic acid induces oxidative stress in mitochondria
Q43546708Significantly reduced docosahexaenoic and docosapentaenoic acid concentrations in erythrocyte membranes from schizophrenic patients compared with a carefully matched control group
Q34207819Statistical methodological issues in handling of fatty acid data: percentage or concentration, imputation and indices
Q37037646The important role of biochemical and functional studies in the diagnostics of peroxisomal disorders
Q34493856The neurology of rhizomelic chondrodysplasia punctata
Q36264711X-linked adreno leukodistrophy: Profiles of very long chain fatty acids in plasma and fibroblasts in eigth Serbian patients
Q30393521Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthood

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