Literature DB >> 9053557

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

G Dacremont1, G Cocquyt, G Vincent.   

Abstract

Two methods are described, both currently used in our laboratory, for the quantitative analysis of very long-chain fatty acids, phytanic acid and pristanic acid in plasma and cultured fibroblasts by gas-liquid chromatography. The first method is based on the procedure developed by Moser and Moser (1991) and the second is based on the method of Onkenhout and colleagues (1989), which is an application of the original method of Lepage and Roy for plasma and fibroblasts. A survey is given of the concentrations of very long-chain fatty acids, pristanic and phytanic acid in plasma and fibroblasts from control subjects and all patients investigated so far in our laboratory.

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Year:  1995        PMID： 9053557     DOI： 10.1007/bf00711430

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


  8 in total

1.  Improved determination of very-long-chain fatty acids in plasma and cultured skin fibroblasts: applications to the diagnosis of peroxisomal disorders.

Authors:  W Onkenhout; P F van der Poel; M P van den Heuvel
Journal:  J Chromatogr       Date:  1989-09-29

2.  Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same family.

Authors:  P J Willems; L Vits; R J Wanders; P J Coucke; B J Van der Auwera; A F Van Elsen; P Raeymaekers; C Van Broeckhoven; R B Schutgens; G Dacremont
Journal:  Arch Neurol       Date:  1990-06

Review 3.  Postnatal diagnosis of peroxisomal disorders: a biochemical approach.

Authors:  R J Wanders; R B Schutgens; P G Barth; J M Tager; H van den Bosch
Journal:  Biochimie       Date:  1993       Impact factor: 4.079

4.  Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctata.

Authors:  R B Schutgens; I W Bouman; A A Nijenhuis; R J Wanders; M E Frumau
Journal:  Clin Chem       Date:  1993-08       Impact factor: 8.327

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

Authors:  I Singh; A E Moser; S Goldfischer; H W Moser
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

6.  Pristanic acid and phytanic acid in plasma from patients with peroxisomal disorders: stable isotope dilution analysis with electron capture negative ion mass fragmentography.

Authors:  H J ten Brink; F Stellaard; C M van den Heuvel; R M Kok; D S Schor; R J Wanders; C Jakobs
Journal:  J Lipid Res       Date:  1992-01       Impact factor: 5.922

7.  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.

Authors:  G F Vanhove; P P Van Veldhoven; M Fransen; S Denis; H J Eyssen; R J Wanders; G P Mannaerts
Journal:  J Biol Chem       Date:  1993-05-15       Impact factor: 5.157

8.  Direct transesterification of all classes of lipids in a one-step reaction.

Authors:  G Lepage; C C Roy
Journal:  J Lipid Res       Date:  1986-01       Impact factor: 5.922
  8 in total
  16 in total

1.  Lymphoblastoid cell lines for diagnosis of peroxisome biogenesis disorders.

Authors:  Sabine Grønborg; Ralph Krätzner; Hendrik Rosewich; Jutta Gärtner
Journal:  JIMD Rep       Date:  2011-06-22

2.  Abnormality in catalase import into peroxisomes leads to severe neurological disorder.

Authors:  F G Sheikh; K Pahan; M Khan; E Barbosa; I Singh
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-17       Impact factor: 11.205

3.  Plasma and erythrocyte fatty acid patterns in patients with recurrent depression: a matched case-control study.

Authors:  Johanna Assies; François Pouwer; Anja Lok; Roel J T Mocking; Claudi L H Bockting; Ieke Visser; Nico G G M Abeling; Marinus Duran; Aart H Schene
Journal:  PLoS One       Date:  2010-05-14       Impact factor: 3.240

4.  Infantile Refsum Disease: Influence of Dietary Treatment on Plasma Phytanic Acid Levels.

Authors:  Maria João Nabais Sá; Júlio C Rocha; Manuela F Almeida; Carla Carmona; Esmeralda Martins; Vasco Miranda; Miguel Coutinho; Rita Ferreira; Sara Pacheco; Francisco Laranjeira; Isaura Ribeiro; Ana Maria Fortuna; Lúcia Lacerda
Journal:  JIMD Rep       Date:  2015-08-25

5.  X-linked adreno leukodistrophy: Profiles of very long chain fatty acids in plasma and fibroblasts in eigth Serbian patients.

Authors:  Sanja Grkovic; Rajko Nikolic; Maja Djordjevic; Ljubomir Stojanov; Snezana Zivancevic-Simonovic; Gordana Djordjevic-Denic; Bozica Kecman
Journal:  Indian J Clin Biochem       Date:  2007-09

6.  A Pex7 hypomorphic mouse model for plasmalogen deficiency affecting the lens and skeleton.

Authors:  Nancy Braverman; Rui Zhang; Li Chen; Graeme Nimmo; Sarah Scheper; Tammy Tran; Rupsa Chaudhury; Ann Moser; Steven Steinberg
Journal:  Mol Genet Metab       Date:  2009-12-11       Impact factor: 4.797

7.  Dissection of transient oxidative stress response in Saccharomyces cerevisiae by using DNA microarrays.

Authors:  Marian Groot Koerkamp; Martijn Rep; Harmen J Bussemaker; Guy P M A Hardy; Adri Mul; Kasia Piekarska; Cristina Al-Khalili Szigyarto; Joost M Teixeira De Mattos; Henk F Tabak
Journal:  Mol Biol Cell       Date:  2002-08       Impact factor: 4.138

8.  Ataxia with loss of Purkinje cells in a mouse model for Refsum disease.

Authors:  Sacha Ferdinandusse; Anna W M Zomer; Jasper C Komen; Christina E van den Brink; Melissa Thanos; Frank P T Hamers; Ronald J A Wanders; Paul T van der Saag; Bwee Tien Poll-The; Pedro Brites
Journal:  Proc Natl Acad Sci U S A       Date:  2008-11-11       Impact factor: 11.205

9.  Statistical methodological issues in handling of fatty acid data: percentage or concentration, imputation and indices.

Authors:  Roel J T Mocking; Johanna Assies; Anja Lok; Henricus G Ruhé; Maarten W J Koeter; Ieke Visser; Claudi L H Bockting; Aart H Schene
Journal:  Lipids       Date:  2012-03-25       Impact factor: 1.880

10.  Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6.

Authors:  Ilham Ratbi; Kim D Falkenberg; Manou Sommen; Nada Al-Sheqaih; Soukaina Guaoua; Geert Vandeweyer; Jill E Urquhart; Kate E Chandler; Simon G Williams; Neil A Roberts; Mustapha El Alloussi; Graeme C Black; Sacha Ferdinandusse; Hind Ramdi; Audrey Heimler; Alan Fryer; Sally-Ann Lynch; Nicola Cooper; Kai Ren Ong; Claire E L Smith; Christopher F Inglehearn; Alan J Mighell; Claire Elcock; James A Poulter; Marc Tischkowitz; Sally J Davies; Abdelaziz Sefiani; Aleksandr A Mironov; William G Newman; Hans R Waterham; Guy Van Camp
Journal:  Am J Hum Genet       Date:  2015-09-17       Impact factor: 11.025
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