खोज परिणाम - Lodewijk IJlst

परिणाम को परिष्कृत करें
  1. 1
    Fatty acid metabolism in Saccharomyces cerevisiae

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

    प्रकाशित 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 द्वारा Sacha Ferdinandusse, Simone Denis, Lodewijk IJlst, G. Dacremont, Hans R. Waterham, Ronald J. A. Wanders

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

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

    प्रकाशित 2021
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  4. 4
    Metabolite transport across the peroxisomal membrane

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

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

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

    प्रकाशित 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 द्वारा Ronald J. A. Wanders, Jos P.N. Ruiter, Lodewijk IJlst, Hans R. Waterham, Sander M. Houten

    प्रकाशित 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... द्वारा Lodewijk IJlst, Jos P.N. Ruiter, J.M.N. Hoovers, Marja E. Jakobs, Ronald J. A. Wanders

    प्रकाशित 1996
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  8. 8
    Alkyl-Dihydroxyacetonephosphate Synthase

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

    प्रकाशित 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 द्वारा Annet M. Bosch, Kevin Stroek, N. G. G. M. Abeling, Hans R. Waterham, Lodewijk IJlst, Ronald J. A. Wanders

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

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

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

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

    प्रकाशित 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 द्वारा Serhii Chornyi, Cláudio F. Costa, Lodewijk IJlst, Marc Fransen, Ronald J. A. Wanders, Carlo W.T. van Roermund, Hans R. Waterham

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

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

    प्रकाशित 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 द्वारा Jessica de Ruijter, Marlies J. Valstar, Magdalena Narajczyk, Grzegorz Węgrzyn, Wim Kulik, Lodewijk IJlst, Tom Wagemans, Willem M. van der Wal, Frits A. Wijburg

    प्रकाशित 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 द्वारा 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

    प्रकाशित 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> द्वारा 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

    प्रकाशित 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 द्वारा 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

    प्रकाशित 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 द्वारा 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

    प्रकाशित 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 द्वारा 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

    प्रकाशित 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 द्वारा 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

    प्रकाशित 1998
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