Leipnitz G et al. |
Pristanic acid promotes oxidative stress in brain cortex of young rats: a possible pathophysiological mechanism for brain damage in peroxisomal disorders. |
2011 |
Brain Res. |
pmid:21241675
|
Mobley JA et al. |
Branched fatty acids in dairy and beef products markedly enhance alpha-methylacyl-CoA racemase expression in prostate cancer cells in vitro. |
2003 |
Cancer Epidemiol. Biomarkers Prev. |
pmid:12917210
|
Wright ME et al. |
Serum phytanic and pristanic acid levels and prostate cancer risk in Finnish smokers. |
2014 |
Cancer Med |
pmid:25132681
|
Harris HM et al. |
Phytanic acid, pristanic acid, and very-long-chain fatty acid methyl esters measured simultaneously by capillary gas chromatography. |
1989 |
Clin. Chem. |
pmid:2702761
|
ten Brink HJ et al. |
Diagnosis of peroxisomal disorders by analysis of phytanic and pristanic acids in stored blood spots collected at neonatal screening. |
1993 |
Clin. Chem. |
pmid:8375069
|
Poulos A et al. |
Defective oxidation of pristanic acid by fibroblasts from patients with disorders in propionic acid metabolism. |
1990 |
Clin. Genet. |
pmid:2311265
|
Rizzo WB |
The role of fatty aldehyde dehydrogenase in epidermal structure and function. |
2011 |
Dermatoendocrinol |
pmid:21695018
|
Huyghe S et al. |
Peroxisomal multifunctional protein 2 is essential for lipid homeostasis in Sertoli cells and male fertility in mice. |
2006 |
Endocrinology |
pmid:16484321
|
Dahlgren J et al. |
Cluster of systemic lupus erythematosus (SLE) associated with an oil field waste site: a cross sectional study. |
2007 |
Environ Health |
pmid:17316448
|
Van Veldhoven PP et al. |
Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency. |
2001 |
Eur. J. Clin. Invest. |
pmid:11473573
|
Krause C et al. |
Rational diagnostic strategy for Zellweger syndrome spectrum patients. |
2009 |
Eur. J. Hum. Genet. |
pmid:19142205
|
Poulos A et al. |
Accumulation of pristanic acid (2, 6, 10, 14 tetramethylpentadecanoic acid) in the plasma of patients with generalised peroxisomal dysfunction. |
1988 |
Eur. J. Pediatr. |
pmid:2452737
|
Wanders RJ et al. |
Clinical and biochemical characteristics of peroxisomal disorders: an update. |
1994 |
Eur. J. Pediatr. |
pmid:7957386
|
Schluter A et al. |
Phytanic acid, but not pristanic acid, mediates the positive effects of phytol derivatives on brown adipocyte differentiation. |
2002 |
FEBS Lett. |
pmid:12062414
|
Singh H and Poulos A |
Substrate specificity of rat liver mitochondrial carnitine palmitoyl transferase I: evidence against alpha-oxidation of phytanic acid in rat liver mitochondria. |
1995 |
FEBS Lett. |
pmid:7867794
|
Verhoeven NM et al. |
Involvement of microsomal fatty aldehyde dehydrogenase in the alpha-oxidation of phytanic acid. |
1998 |
FEBS Lett. |
pmid:9662422
|
Setchell KD et al. |
Liver disease caused by failure to racemize trihydroxycholestanoic acid: gene mutation and effect of bile acid therapy. |
2003 |
Gastroenterology |
pmid:12512044
|
Schrader M and Fahimi HD |
The peroxisome: still a mysterious organelle. |
2008 |
Histochem. Cell Biol. |
pmid:18274771
|
Mota CR et al. |
Rhizomelic chondrodysplasia punctata-like phenotype in a newborn male with normal peroxisomal function. |
1997 |
J Pediatr Orthop B |
pmid:9039662
|
GarcÃa-Rojas P et al. |
Induction of peroxisomal proliferator-activated receptor gamma and peroxisomal proliferator-activated receptor gamma coactivator 1 by unsaturated fatty acids, retinoic acid, and carotenoids in preadipocytes obtained from bovine white adipose tissue1,2. |
2010 |
J. Anim. Sci. |
pmid:20154154
|
Steinberg D |
Chance and serendipity in science: two examples from my own career. |
2011 |
J. Biol. Chem. |
pmid:21908608
|
Westin MA et al. |
Molecular cloning and characterization of two mouse peroxisome proliferator-activated receptor alpha (PPARalpha)-regulated peroxisomal acyl-CoA thioesterases. |
2004 |
J. Biol. Chem. |
pmid:15007068
|
Idel S et al. |
Branched chain fatty acids induce nitric oxide-dependent apoptosis in vascular smooth muscle cells. |
2002 |
J. Biol. Chem. |
pmid:12368296
|
Hunt MC et al. |
Characterization of an acyl-coA thioesterase that functions as a major regulator of peroxisomal lipid metabolism. |
2002 |
J. Biol. Chem. |
pmid:11673457
|
Singh H et al. |
Peroxisomal beta-oxidation of branched chain fatty acids in rat liver. Evidence that carnitine palmitoyltransferase I prevents transport of branched chain fatty acids into mitochondria. |
1994 |
J. Biol. Chem. |
pmid:8144536
|
Westin MA et al. |
Peroxisomes contain a specific phytanoyl-CoA/pristanoyl-CoA thioesterase acting as a novel auxiliary enzyme in alpha- and beta-oxidation of methyl-branched fatty acids in mouse. |
2007 |
J. Biol. Chem. |
pmid:17613526
|
Johnson DW et al. |
Measurement of plasma pristanic, phytanic and very long chain fatty acids by liquid chromatography-electrospray tandem mass spectrometry for the diagnosis of peroxisomal disorders. |
2003 |
J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. |
pmid:14630371
|
Vreken P et al. |
Rapid stable isotope dilution analysis of very-long-chain fatty acids, pristanic acid and phytanic acid using gas chromatography-electron impact mass spectrometry. |
1998 |
J. Chromatogr. B Biomed. Sci. Appl. |
pmid:9746242
|
Paton BC et al. |
Oxidation of pristanic acid in fibroblasts and its application to the diagnosis of peroxisomal beta-oxidation defects. |
1996 |
J. Clin. Invest. |
pmid:8609223
|
Zheng BS et al. |
Arabidopsis sterol carrier protein-2 is required for normal development of seeds and seedlings. |
2008 |
J. Exp. Bot. |
pmid:18687588
|
Wanders RJ et al. |
The enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results. |
2010 |
J. Inherit. Metab. Dis. |
pmid:20490924
|
ten Brink HJ et al. |
Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: evidence for a distinct peroxisomal pristanyl-CoA oxidase. |
1991 |
J. Inherit. Metab. Dis. |
pmid:1779614
|
ten Brink HJ et al. |
Pristanic acid and phytanic acid in plasma from patients with a single peroxisomal enzyme deficiency. |
1991 |
J. Inherit. Metab. Dis. |
pmid:1722861
|
Jakobs BS and Wanders RJ |
Impaired peroxisomal fatty acid oxidation in human skin fibroblasts with a mitochondrial acylcarnitine/carnitine translocase deficiency. |
1996 |
J. Inherit. Metab. Dis. |
pmid:8739961
|
Clayton PT et al. |
Ataxia associated with increased plasma concentrations of pristanic acid, phytanic acid and C27 bile acids but normal fibroblast branched-chain fatty acid oxidation. |
1996 |
J. Inherit. Metab. Dis. |
pmid:8982949
|
Wanders RJ et al. |
Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblasts. |
1995 |
J. Inherit. Metab. Dis. |
pmid:9053546
|
Verhoeven NM et al. |
Pre- and postnatal diagnosis of peroxisomal disorders using stable-isotope dilution gas chromatography--mass spectrometry. |
1995 |
J. Inherit. Metab. Dis. |
pmid:9053555
|
Dacremont G et al. |
Measurement of very long-chain fatty acids, phytanic and pristanic acid in plasma and cultured fibroblasts by gas chromatography. |
1995 |
J. Inherit. Metab. Dis. |
pmid:9053557
|
van Grunsven EG and Wanders RJ |
Genetic heterogeneity in patients with a disorder of peroxisomal beta-oxidation: a complementation study based on pristanic acid beta-oxidation suggesting different enzyme defects. |
1997 |
J. Inherit. Metab. Dis. |
pmid:9266375
|
Verhoeven NM et al. |
Formation of 2,3-pristenic acid and 3-hydroxypristanic acid from pristanic acid in human liver. |
1997 |
J. Inherit. Metab. Dis. |
pmid:9266376
|
Wanders RJ et al. |
Identification of the newly discovered 58 kDa peroxisomal thiolase SCPx as the main thiolase involved in both pristanic acid and trihydroxycholestanoic acid oxidation: implications for peroxisomal beta-oxidation disorders. |
1998 |
J. Inherit. Metab. Dis. |
pmid:9686381
|
Sequeira JS et al. |
Niemann-Pick disease type C and defective peroxisomal beta-oxidation of branched-chain substrates. |
1998 |
J. Inherit. Metab. Dis. |
pmid:9584266
|
Verhoeven NM et al. |
The metabolism of phytanic acid and pristanic acid in man: a review. |
1998 |
J. Inherit. Metab. Dis. |
pmid:9819701
|
Verhoeven NM et al. |
Studies on the oxidation of phytanic acid and pristanic acid in human fibroblasts by acylcarnitine analysis. |
1998 |
J. Inherit. Metab. Dis. |
pmid:9819705
|
Smith EH et al. |
An adult onset case of alpha-methyl-acyl-CoA racemase deficiency. |
2010 |
J. Inherit. Metab. Dis. |
pmid:20821052
|
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
|
Singh H et al. |
Peroxisomal beta-oxidation of branched chain fatty acids in human skin fibroblasts. |
1992 |
J. Lipid Res. |
pmid:1464743
|
ten Brink HJ et al. |
Phytanic acid alpha-oxidation: accumulation of 2-hydroxyphytanic acid and absence of 2-oxophytanic acid in plasma from patients with peroxisomal disorders. |
1992 |
J. Lipid Res. |
pmid:1385561
|
Zomer AW et al. |
Pristanic acid and phytanic acid: naturally occurring ligands for the nuclear receptor peroxisome proliferator-activated receptor alpha. |
2000 |
J. Lipid Res. |
pmid:11060349
|
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
|