Risultati della ricerca - Lodewijk IJlst

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  1. 1
    Fatty acid metabolism in Saccharomyces cerevisiae

    Fatty acid metabolism in Saccharomyces cerevisiae di Carlo W.T. van Roermund, Hans R. Waterham, Lodewijk IJlst, Ronald J. A. Wanders

    Pubblicazione 2003
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  2. 2
    Subcellular localization and physiological role of α-methylacyl-CoA racemase

    Subcellular localization and physiological role of α-methylacyl-CoA racemase di Sacha Ferdinandusse, Simone Denis, Lodewijk IJlst, G. Dacremont, Hans R. Waterham, Ronald J. A. Wanders

    Pubblicazione 2000
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  3. 3
    Peroxisomal Metabolite and Cofactor Transport in Humans

    Peroxisomal Metabolite and Cofactor Transport in Humans di Serhii Chornyi, Lodewijk IJlst, Carlo W.T. van Roermund, Ronald J. A. Wanders, Hans R. Waterham

    Pubblicazione 2021
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  4. 4
    Metabolite transport across the peroxisomal membrane

    Metabolite transport across the peroxisomal membrane di Wouter F. Visser, Carlo W.T. van Roermund, Lodewijk IJlst, Hans R. Waterham, Ronald J. A. Wanders

    Pubblicazione 2006
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  5. 5
    Molecular basis of hepatic carnitine palmitoyltransferase I deficiency.

    Molecular basis of hepatic carnitine palmitoyltransferase I deficiency. di Lodewijk IJlst, Hanna Mandel, W. Oostheim, Jos P.N. Ruiter, Alisa Gutman, R. J. A. Wanders

    Pubblicazione 1998
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  6. 6
    The enzymology of mitochondrial fatty acid beta‐oxidation and its application to follow‐up analysis of positive neonatal screening results

    The enzymology of mitochondrial fatty acid beta‐oxidation and its application to follow‐up analysis of positive neonatal screening results di Ronald J. A. Wanders, Jos P.N. Ruiter, Lodewijk IJlst, Hans R. Waterham, Sander M. Houten

    Pubblicazione 2010
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  7. 7
    Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene.

    Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA an... di Lodewijk IJlst, Jos P.N. Ruiter, J.M.N. Hoovers, Marja E. Jakobs, Ronald J. A. Wanders

    Pubblicazione 1996
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  8. 8
    Alkyl-Dihydroxyacetonephosphate Synthase

    Alkyl-Dihydroxyacetonephosphate Synthase di Edwin C.J.M. de Vet, Lodewijk IJlst, W. Oostheim, Ronald J. A. Wanders, H. van den Bosch

    Pubblicazione 1998
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  9. 9
    The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives

    The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives di Annet M. Bosch, Kevin Stroek, N. G. G. M. Abeling, Hans R. Waterham, Lodewijk IJlst, Ronald J. A. Wanders

    Pubblicazione 2012
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  10. 10
    Peroxisomal Fatty Acid Uptake Mechanism in Saccharomyces cerevisiae

    Peroxisomal Fatty Acid Uptake Mechanism in Saccharomyces cerevisiae di Carlo W.T. van Roermund, Lodewijk IJlst, Wiktor Majczak, Hans R. Waterham, Hendrik Folkerts, Ronald J. A. Wanders, Klaas J. Hellingwerf

    Pubblicazione 2012
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  11. 11
    Disorders of mitochondrial fatty acyl‐CoA β‐oxidation

    Disorders of mitochondrial fatty acyl‐CoA β‐oxidation di Ronald J. A. Wanders, P. Vreken, M. E. J. den Boer, Frits A. Wijburg, A. H. van Gennip, Lodewijk IJlst

    Pubblicazione 1999
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  12. 12
    Human peroxisomal NAD+/NADH homeostasis is regulated by two independent NAD(H) shuttle systems

    Human peroxisomal NAD+/NADH homeostasis is regulated by two independent NAD(H) shuttle systems di Serhii Chornyi, Cláudio F. Costa, Lodewijk IJlst, Marc Fransen, Ronald J. A. Wanders, Carlo W.T. van Roermund, Hans R. Waterham

    Pubblicazione 2023
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  13. 13
    The peroxisomal lumen in Saccharomyces cerevisiae is alkaline

    The peroxisomal lumen in Saccharomyces cerevisiae is alkaline di Carlo W.T. van Roermund, Mark de Jong, Lodewijk IJlst, Jan van Marle, Tobias B. Dansen, Ronald J. A. Wanders, Hans R. Waterham

    Pubblicazione 2004
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  14. 14
    Genistein in Sanfilippo disease: A randomized controlled crossover trial

    Genistein in Sanfilippo disease: A randomized controlled crossover trial di Jessica de Ruijter, Marlies J. Valstar, Magdalena Narajczyk, Grzegorz Węgrzyn, Wim Kulik, Lodewijk IJlst, Tom Wagemans, Willem M. van der Wal, Frits A. Wijburg

    Pubblicazione 2011
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  15. 15
    Clinical, biochemical, and mutational spectrum of peroxisomal acyl–coenzyme A oxidase deficiency

    Clinical, biochemical, and mutational spectrum of peroxisomal acyl–coenzyme A oxidase deficiency di Sacha Ferdinandusse, Simone Denis, Eveline M. Hogenhout, Janet Koster, Carlo W.T. van Roermund, Lodewijk IJlst, Ann B. Moser, Ronald J. A. Wanders, Hans R. Waterham

    Pubblicazione 2007
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  16. 16
    Identification of a Peroxisomal ATP Carrier Required for Medium-Chain Fatty Acid β-Oxidation and Normal Peroxisome Proliferation in <i>Saccharomyces cerevisiae</i>

    Identification of a Peroxisomal ATP Carrier Required for Medium-Chain Fatty Acid β-Oxidation and Normal Peroxisome Proliferation in <i>Saccharomyces cerevisiae</i> di Carlo W.T. van Roermund, Roy Drissen, Marlene van den Berg, Lodewijk IJlst, Ewald H. Hettema, Henk F. Tabak, Hans R. Waterham, Ronald J. A. Wanders

    Pubblicazione 2001
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  17. 17
    Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosis

    Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosis di C. C. P. Aires, Lodewijk IJlst, Femke S. Stet, Carina Prip‐Buus, Isabel Tavares de Almeida, Marinus Durán, Ronald J. A. Wanders, M. F. B. Silva

    Pubblicazione 2009
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  18. 18
    Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

    Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle di Suzan J. G. Knottnerus, Jeannette C. Bleeker, Rob C. I. Wüst, Sacha Ferdinandusse, Lodewijk IJlst, Frits A. Wijburg, Ronald J. A. Wanders, Gepke Visser, Riekelt H. Houtkooper

    Pubblicazione 2018
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  19. 19
    <i>N</i> -lactoyl-amino acids are ubiquitous metabolites that originate from CNDP2-mediated reverse proteolysis of lactate and amino acids

    <i>N</i> -lactoyl-amino acids are ubiquitous metabolites that originate from CNDP2-mediated reverse proteolysis of lactate and amino acids di Robert S. Jansen, Ruben D. Addie, Remco Merkx, Alexander Fish, Sunny Mahakena, Onno B. Bleijerveld, Maarten Altelaar, Lodewijk IJlst, Ronald J. A. Wanders, Piet Borst, Koen van de Wetering

    Pubblicazione 2015
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  20. 20
    Peroxisomal <scp>d</scp> -hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

    Peroxisomal <scp>d</scp> -hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency di E.G. van Grunsven, E. van Berkel, Lodewijk IJlst, P. Vreken, Johannis B.C. de Klerk, Jerzy Adamski, Hugh Lemonde, Peter T. Clayton, D Cuebas, Ronald J. A. Wanders

    Pubblicazione 1998
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