scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1031600598 |
P356 | DOI | 10.1007/BF00711430 |
P698 | PubMed publication ID | 9053557 |
P2093 | author name string | G Vincent | |
G Dacremont | |||
G Cocquyt | |||
P2860 | cites work | 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 | Q28613019 |
Lignoceric acid is oxidized in the peroxisome: implications for the Zellweger cerebro-hepato-renal syndrome and adrenoleukodystrophy | Q36265198 | ||
Postnatal diagnosis of peroxisomal disorders: a biochemical approach | Q40487387 | ||
Pristanic acid and phytanic acid in plasma from patients with peroxisomal disorders: stable isotope dilution analysis with electron capture negative ion mass fragmentography | Q67895674 | ||
Linkage of DNA markers at Xq28 to adrenoleukodystrophy and adrenomyeloneuropathy present within the same family | Q68461928 | ||
Improved determination of very-long-chain fatty acids in plasma and cultured skin fibroblasts: applications to the diagnosis of peroxisomal disorders | Q69114680 | ||
Direct transesterification of all classes of lipids in a one-step reaction | Q70032561 | ||
Profiles of very-long-chain fatty acids in plasma, fibroblasts, and blood cells in Zellweger syndrome, X-linked adrenoleukodystrophy, and rhizomelic chondrodysplasia punctata | Q72885965 | ||
P304 | page(s) | 76-83 | |
P577 | publication date | 1995-01-01 | |
P1433 | published in | Journal of Inherited Metabolic Disease | Q6295359 |
P1476 | title | Measurement of very long-chain fatty acids, phytanic and pristanic acid in plasma and cultured fibroblasts by gas chromatography | |
P478 | volume | 18 Suppl 1 |
Q33729632 | A Pex7 hypomorphic mouse model for plasmalogen deficiency affecting the lens and skeleton |
Q55053133 | A mutation in PEX19 causes a severe clinical phenotype in a patient with peroxisomal biogenesis disorder |
Q35975137 | Abnormality in catalase import into peroxisomes leads to severe neurological disorder |
Q36976826 | Ataxia with loss of Purkinje cells in a mouse model for Refsum disease |
Q60961904 | Case report of dysregulation of primary bile acid synthesis in a family with X-linked adrenoleukodystrophy |
Q38363640 | Dissection of transient oxidative stress response in Saccharomyces cerevisiae by using DNA microarrays |
Q44597106 | Effect of dehydroepiandrosterone supplementation on fatty acid and hormone levels in patients with X‐linked adrenoleucodystrophy |
Q36133280 | Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6 |
Q36894737 | Infantile Refsum Disease: Influence of Dietary Treatment on Plasma Phytanic Acid Levels. |
Q42542201 | Lovastatin and sodium phenylacetate normalize the levels of very long chain fatty acids in skin fibroblasts of X- adrenoleukodystrophy |
Q41881694 | Lymphoblastoid cell lines for diagnosis of peroxisome biogenesis disorders |
Q90731853 | Mitochondrial fission factor (MFF) is a critical regulator of peroxisome maturation |
Q55670954 | Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype |
Q33586155 | Plasma and erythrocyte fatty acid patterns in patients with recurrent depression: a matched case-control study |
Q34488327 | Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls |
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Q46892757 | Rotenone-like action of the branched-chain phytanic acid induces oxidative stress in mitochondria |
Q43546708 | Significantly reduced docosahexaenoic and docosapentaenoic acid concentrations in erythrocyte membranes from schizophrenic patients compared with a carefully matched control group |
Q34207819 | Statistical methodological issues in handling of fatty acid data: percentage or concentration, imputation and indices |
Q37037646 | The important role of biochemical and functional studies in the diagnostics of peroxisomal disorders |
Q34493856 | The neurology of rhizomelic chondrodysplasia punctata |
Q36264711 | X-linked adreno leukodistrophy: Profiles of very long chain fatty acids in plasma and fibroblasts in eigth Serbian patients |
Q30393521 | Zellweger spectrum disorders: clinical manifestations in patients surviving into adulthood |
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