Publications
Complete publication list (Pubmed search) :
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Representative publications :
1. Deglycation
Fortpied J, Gemayel R, Vertommen D, Van Schaftingen E.
Identification of protein-ribulosamine-5-phosphatase as human low-molecular-mass protein tyrosine phosphatase-A.
Biochem J. 2007 Aug 15;406(1):139-45.
Veiga da-Cunha M, Jacquemin P, Delpierre G, Godfraind C, Théate I, Vertommen D, Clotman F, Lemaigre F, Devuyst O, Van Schaftingen E.
Increased protein glycation in fructosamine 3-kinase-deficient mice.
Biochem J. 2006 Oct 15;399(2):257-64.
Fortpied J, Maliekal P, Vertommen D, Van Schaftingen E.
Magnesium-dependent phosphatase-1 is a protein-fructosamine-6-phosphatase potentially involved in glycation repair.
J Biol Chem. 2006 Jul 7;281(27):18378-85.
Wiame E, Lamosa P, Santos H, Van Schaftingen E.
Identification of glucoselysine-6-phosphate deglycase, an enzyme involved in the metabolism of the fructation product glucoselysine.
Biochem J. 2005 Dec 1;392(Pt 2):263-9.
Fortpied J, Gemayel R, Stroobant V, van Schaftingen E.
Plant ribulosamine/erythrulosamine 3-kinase, a putative protein-repair enzyme.
Biochem J. 2005 Jun 15;388(Pt 3):795-802.
Delplanque J, Delpierre G, Opperdoes FR, Van Schaftingen E.
Tissue distribution and evolution of fructosamine 3-kinase and fructosamine 3-kinase-related protein.
J Biol Chem. 2004 Nov 5;279(45):46606-13.
Collard F, Wiame E, Bergans N, Fortpied J, Vertommen D, Vanstapel F, Delpierre G, Van Schaftingen E.
Fructosamine 3-kinase-related protein and deglycation in human erythrocytes.
Biochem J. 2004 Aug 15;382(Pt 1):137-43.
2. Metabolic Disorders
Maliekal P, Sokolova T, Vertommen D, Veiga-da-Cunha M, Van Schaftingen E.
Molecular identification of mammalian phosphopentomutase and glucose-1,6-bisphosphate synthase, two members of the alpha-D-phosphohexomutase family.
J Biol Chem. 2007 Nov 2;282(44):31844-51.
Hart CE, Race V, Achouri Y, Wiame E, Sharrard M, Olpin SE, Watkinson J, Bonham JR, Jaeken J, Matthijs G, Van Schaftingen E.
Phosphoserine aminotransferase deficiency: a novel disorder of the serine biosynthesis pathway.
Am J Hum Genet. 2007 May;80(5):931-7.
Maliekal P, Vertommen D, Delpierre G, Van Schaftingen E.
Identification of the sequence encoding N-acetylneuraminate-9-phosphate phosphatase.
Glycobiology. 2006 Feb;16(2):165-72.
Struys EA, Salomons GS, Achouri Y, Van Schaftingen E, Grosso S, Craigen WJ, Verhoeven NM, Jakobs C.
Mutations in the D-2-hydroxyglutarate dehydrogenase gene cause D-2-hydroxyglutaric aciduria.
Am J Hum Genet. 2005 Feb;76(2):358-60.
Rzem R, Veiga-da-Cunha M, Noël G, Goffette S, Nassogne MC, Tabarki B, Schöller C, Marquardt T, Vikkula M, Van Schaftingen E.
A gene encoding a putative FAD-dependent L-2-hydroxyglutarate dehydrogenase is mutated in L-2-hydroxyglutaric aciduria.
Proc Natl Acad Sci U S A. 2004 Nov 30;101(48):16849-54.
