检索结果 - Lodewijk IJlst

Refine Results
  1. 1
    Fatty acid metabolism in Saccharomyces cerevisiae

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

    出版 2003
    获取全文
    Revisão
    加到收藏夹
    Saved in:
  2. 2
    Subcellular localization and physiological role of α-methylacyl-CoA racemase

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

    出版 2000
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  3. 3
    Peroxisomal Metabolite and Cofactor Transport in Humans

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

    出版 2021
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  4. 4
    Metabolite transport across the peroxisomal membrane

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

    出版 2006
    获取全文
    Revisão
    加到收藏夹
    Saved in:
  5. 5
    Molecular basis of hepatic carnitine palmitoyltransferase I deficiency.

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

    出版 1998
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  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 由 Ronald J. A. Wanders, Jos P.N. Ruiter, Lodewijk IJlst, Hans R. Waterham, Sander M. Houten

    出版 2010
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  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... 由 Lodewijk IJlst, Jos P.N. Ruiter, J.M.N. Hoovers, Marja E. Jakobs, Ronald J. A. Wanders

    出版 1996
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  8. 8
    Alkyl-Dihydroxyacetonephosphate Synthase

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

    出版 1998
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  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 由 Annet M. Bosch, Kevin Stroek, N. G. G. M. Abeling, Hans R. Waterham, Lodewijk IJlst, Ronald J. A. Wanders

    出版 2012
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  10. 10
    Peroxisomal Fatty Acid Uptake Mechanism in Saccharomyces cerevisiae

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

    出版 2012
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  11. 11
    Disorders of mitochondrial fatty acyl‐CoA β‐oxidation

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

    出版 1999
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  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 由 Serhii Chornyi, Cláudio F. Costa, Lodewijk IJlst, Marc Fransen, Ronald J. A. Wanders, Carlo W.T. van Roermund, Hans R. Waterham

    出版 2023
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  13. 13
    The peroxisomal lumen in Saccharomyces cerevisiae is alkaline

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

    出版 2004
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  14. 14
    Genistein in Sanfilippo disease: A randomized controlled crossover trial

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

    出版 2011
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  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 由 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

    出版 2007
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  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> 由 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

    出版 2001
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  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 由 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

    出版 2009
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  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 由 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

    出版 2018
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  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 由 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

    出版 2015
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  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 由 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

    出版 1998
    获取全文
    Artigo
    加到收藏夹
    Saved in:

检索工具: