van den Brink DM et al. |
Identification of fatty aldehyde dehydrogenase in the breakdown of phytol to phytanic acid. |
2004 |
Mol. Genet. Metab. |
pmid:15110319
|
Peduto A et al. |
Hyperpipecolic acidaemia: a diagnostic tool for peroxisomal disorders. |
2004 |
Mol. Genet. Metab. |
pmid:15234336
|
Roe DS et al. |
Differentiation of long-chain fatty acid oxidation disorders using alternative precursors and acylcarnitine profiling in fibroblasts. |
2006 |
Mol. Genet. Metab. |
pmid:16297647
|
Werner LB et al. |
Effect of dairy fat on plasma phytanic acid in healthy volunteers - a randomized controlled study. |
2011 |
Lipids Health Dis |
pmid:21663648
|
Terre'Blanche G et al. |
Treatment of an adrenomyeloneuropathy patient with Lorenzo's oil and supplementation with docosahexaenoic acid--a case report. |
2011 |
Lipids Health Dis |
pmid:21871076
|
Busanello EN et al. |
Disruption of oxidative phosphorylation and synaptic Na(+), K(+)-ATPase activity by pristanic acid in cerebellum of young rats. |
2014 |
Life Sci. |
pmid:24211616
|
Mamedov IS et al. |
[The diagnostic of peroxisomic diseases in children]. |
2012 |
Klin. Lab. Diagn. |
pmid:22712285
|
Busanello EN et al. |
Experimental evidence that pristanic acid disrupts mitochondrial homeostasis in brain of young rats. |
2012 |
J. Neurosci. Res. |
pmid:22183871
|
McLean BN et al. |
A new defect of peroxisomal function involving pristanic acid: a case report. |
2002 |
J. Neurol. Neurosurg. Psychiatr. |
pmid:11861706
|
Thompson SA et al. |
Relapsing encephalopathy in a patient with alpha-methylacyl-CoA racemase deficiency. |
2008 |
J. Neurol. Neurosurg. Psychiatr. |
pmid:18032455
|
Ferdinandusse S et al. |
Plasma analysis of di- and trihydroxycholestanoic acid diastereoisomers in peroxisomal alpha-methylacyl-CoA racemase deficiency. |
2001 |
J. Lipid Res. |
pmid:11160375
|
Atshaves BP et al. |
Sexually dimorphic metabolism of branched-chain lipids in C57BL/6J mice. |
2004 |
J. Lipid Res. |
pmid:14993239
|
Gloerich J et al. |
A phytol-enriched diet induces changes in fatty acid metabolism in mice both via PPARalpha-dependent and -independent pathways. |
2005 |
J. Lipid Res. |
pmid:15654129
|
Ferdinandusse S et al. |
Stereochemistry of the peroxisomal branched-chain fatty acid alpha- and beta-oxidation systems in patients suffering from different peroxisomal disorders. |
2002 |
J. Lipid Res. |
pmid:11893780
|
ten Brink HJ et al. |
Pristanic acid and phytanic acid in plasma from patients with peroxisomal disorders: stable isotope dilution analysis with electron capture negative ion mass fragmentography. |
1992 |
J. Lipid Res. |
pmid:1372637
|
Gloerich J et al. |
Metabolism of phytol to phytanic acid in the mouse, and the role of PPARalpha in its regulation. |
2007 |
J. Lipid Res. |
pmid:17015885
|
Verhoeven NM et al. |
Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblasts. |
1998 |
J. Lipid Res. |
pmid:9469587
|
Verhoeven NM et al. |
Phytanic acid alpha-oxidation: decarboxylation of 2-hydroxyphytanoyl-CoA to pristanic acid in human liver. |
1997 |
J. Lipid Res. |
pmid:9374128
|
Van Veldhoven PP |
Biochemistry and genetics of inherited disorders of peroxisomal fatty acid metabolism. |
2010 |
J. Lipid Res. |
pmid:20558530
|
Al-Dirbashi OY et al. |
Rapid UPLC-MS/MS method for routine analysis of plasma pristanic, phytanic, and very long chain fatty acid markers of peroxisomal disorders. |
2008 |
J. Lipid Res. |
pmid:18441019
|