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Items: 1 to 20 of 92

1.

Role of thiamine pyrophosphate in oligomerisation, functioning and import of peroxisomal 2-hydroxyacyl-CoA lyase.

Fraccascia P, Casteels M, De Schryver E, Van Veldhoven PP.

Biochim Biophys Acta. 2011 Oct;1814(10):1226-33. doi: 10.1016/j.bbapap.2011.06.007. Epub 2011 Jun 25.

PMID:
21708296
2.

The role of 2-hydroxyacyl-CoA lyase, a thiamin pyrophosphate-dependent enzyme, in the peroxisomal metabolism of 3-methyl-branched fatty acids and 2-hydroxy straight-chain fatty acids.

Casteels M, Sniekers M, Fraccascia P, Mannaerts GP, Van Veldhoven PP.

Biochem Soc Trans. 2007 Nov;35(Pt 5):876-80. Review.

PMID:
17956236
3.

Presence of thiamine pyrophosphate in mammalian peroxisomes.

Fraccascia P, Sniekers M, Casteels M, Van Veldhoven PP.

BMC Biochem. 2007 Jun 27;8:10.

4.

Phytol-induced pathology in 2-hydroxyacyl-CoA lyase (HACL1) deficient mice. Evidence for a second non-HACL1-related lyase.

Mezzar S, De Schryver E, Asselberghs S, Meyhi E, Morvay PL, Baes M, Van Veldhoven PP.

Biochim Biophys Acta. 2017 Sep;1862(9):972-990. doi: 10.1016/j.bbalip.2017.06.004. Epub 2017 Jun 17.

PMID:
28629946
5.

Breakdown of 2-hydroxylated straight chain fatty acids via peroxisomal 2-hydroxyphytanoyl-CoA lyase: a revised pathway for the alpha-oxidation of straight chain fatty acids.

Foulon V, Sniekers M, Huysmans E, Asselberghs S, Mahieu V, Mannaerts GP, Van Veldhoven PP, Casteels M.

J Biol Chem. 2005 Mar 18;280(11):9802-12. Epub 2005 Jan 11.

6.
7.

RP-HPLC-fluorescence analysis of aliphatic aldehydes: application to aldehyde-generating enzymes HACL1 and SGPL1.

Mezzar S, de Schryver E, Van Veldhoven PP.

J Lipid Res. 2014 Mar;55(3):573-82. doi: 10.1194/jlr.D044230. Epub 2013 Dec 9.

8.

The activity of the glyoxylate cycle in peroxisomes of Candida albicans depends on a functional beta-oxidation pathway: evidence for reduced metabolite transport across the peroxisomal membrane.

Piekarska K, Hardy G, Mol E, van den Burg J, Strijbis K, van Roermund C, van den Berg M, Distel B.

Microbiology. 2008 Oct;154(Pt 10):3061-72. doi: 10.1099/mic.0.2008/020289-0.

PMID:
18832312
9.

Peroxisomal lipid degradation via beta- and alpha-oxidation in mammals.

Mannaerts GP, Van Veldhoven PP, Casteels M.

Cell Biochem Biophys. 2000;32 Spring:73-87. Review.

PMID:
11330072
11.

Thiamine and magnesium deficiencies: keys to disease.

Lonsdale D.

Med Hypotheses. 2015 Feb;84(2):129-34. doi: 10.1016/j.mehy.2014.12.004. Epub 2014 Dec 15.

PMID:
25542071
12.
14.

Peroxisomal degradation of trans-unsaturated fatty acids in the yeast Saccharomyces cerevisiae.

Gurvitz A, Hamilton B, Ruis H, Hartig A.

J Biol Chem. 2001 Jan 12;276(2):895-903.

15.

Hitchhiking of Cu/Zn superoxide dismutase to peroxisomes--evidence for a natural piggyback import mechanism in mammals.

Islinger M, Li KW, Seitz J, Völkl A, Lüers GH.

Traffic. 2009 Nov;10(11):1711-21. doi: 10.1111/j.1600-0854.2009.00966.x. Epub 2009 Jul 21.

17.

Regulation of peroxisome size and number by fatty acid beta -oxidation in the yeast yarrowia lipolytica.

Smith JJ, Brown TW, Eitzen GA, Rachubinski RA.

J Biol Chem. 2000 Jun 30;275(26):20168-78.

18.

Peroxisomes and beta-oxidation of long-chain unsaturated carboxylic acids.

Hiltunen JK.

Scand J Clin Lab Invest Suppl. 1991;204:33-46. Review.

PMID:
2042025
19.

[alpha-Oxidation of 3-methyl-branched fatty acids: unraveling of a pathway].

Casteels M.

Verh K Acad Geneeskd Belg. 2006;68(3):199-221; discussion 221-2. Dutch.

PMID:
16796018

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