Zobrazeno 1 - 10
of 239
pro vyhledávání: '"G. P. Mannaerts"'
Autor:
G. P. Mannaerts, P. P. Van Veldhoven
Publikováno v:
ChemInform. 22
Autor:
Henk F. Tabak, Yukio Fujiki, Suresh Subramani, W. W. Just, Stephen Jay Gould, P. B. Lazarow, Marten Veenhuis, J. A. K. W. Kiel, Ralf Erdmann, I.J. van der Klei, Ben Distel, T. Tsukamoto, G. P. Mannaerts, P. P. Van Veldhoven, A. Roscher, Richard A. Rachubinski, H. W. Moser, Joel M. Goodman, J. M. Cregg, T. Osumi, W.-H. Kunau, G. Blobel, Gabriele Dodt, Denis I. Crane, D. Valle
Publikováno v:
The Journal of Cell Biology
Journal of Cell Biology, 135, 1-3. Rockefeller University Press
Journal of Cell Biology, 135, 1-3. Rockefeller University Press
Ben Distel,* Ralf Erdmann, ¢ Stephen J. Gould, ~ Gtinter Blobel,I Denis I. Crane, I James M. Cregg,** Gabriele Dodt,* Yukio Fujiki, *~ Joel M. Goodman, ~ Wilhelm W. Just, D Jan A.K.W. Kiel, 11 Wolf-Hubert Kunau,* Paul B. Lazarow,*** Guy P. Mannaerts
Publikováno v:
Combinatorial chemistryhigh throughput screening. 4(7)
Recently, we reported the successful use of the gVI-cDNA phage display technology to clone cDNAs coding for novel peroxisomal enzymes by affinity selection using immobilized antisera directed against peroxisomal subfractions (Fransen, M.; Van Veldhov
Publikováno v:
Biochimica et biophysica acta. 1533(1)
Based on the primary structure of the rat peroxisomal 2,4-dienoyl-CoA reductase (M. Fransen, P.P. Van Veldhoven, S. Subramani, Biochem. J. 340 (1999) 561-568), the cDNA of the human counterpart was cloned. It contained an open reading frame of 878 ba
Autor:
P P, Van Veldhoven, E, Meyhi, R H, Squires, M, Fransen, B, Fournier, V, Brys, M J, Bennett, G P, Mannaerts
Publikováno v:
European journal of clinical investigation. 31(8)
2-Methylacyl-CoA racemase interconverts the 2-methyl group of pristanoyl-CoA or the 25-methyl group of hydroxylated cholestanoyl-CoAs, allowing further peroxisomal desaturation of these compounds in man by the branched chain acyl-CoA oxidase, which r
Publikováno v:
Biochemical Society transactions. 29(Pt 2)
Mammalian peroxisomes degrade fatty carboxylates via two pathways, beta-oxidation and, as shown more recently, alpha-oxidation. The latter process consists of an activation step, followed by a hydroxylation at position 2 and cleavage of the 2-hydroxy
Publikováno v:
Cell biochemistry and biophysics.
Peroxisomal beta-oxidation is involved in the degradation of long chain and very long chain fatty acyl-(coenzyme A)CoAs, long chain dicarboxylyl-CoAs, the CoA esters of eicosanoids, 2-methyl-branched fatty acyl-CoAs (e.g. pristanoyl-CoA), and the CoA
Autor:
S, Huyghe, M, Casteels, A, Janssen, L, Meulders, G P, Mannaerts, P E, Declercq, P P, Van Veldhoven, M, Baes
Publikováno v:
The Biochemical journal. 353(Pt 3)
The ontogeny of the following peroxisomal metabolic pathways was evaluated in mouse liver and brain: alpha-oxidation, beta-oxidation and ether phospholipid synthesis. In mouse embryos lacking functional peroxisomes (PEX5(-/-) knock-out), a deficiency
Publikováno v:
Biochimica et biophysica acta. 1487(2-3)
Sphingosine-1-phosphate lyase catalyzes the last step in sphingolipid breakdown, the cleavage of phosphorylated sphingoid bases such as sphingenine-1-phosphate. The latter lipid is not only a catabolite, but can influence as an inter- and/or intracel
Publikováno v:
Advances in experimental medicine and biology. 466
Synthetic 3-methyl-branched chain fatty acids were used to decipher the breakdown of phytanic acid. Based on results obtained in intact or permeabilized rat hepatocytes, rat liver homogenates or subcellular fractions, a revised alpha-oxidation pathwa