Resultados de procura - Simone Denis

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  1. 1
    Bile acids: the role of peroxisomes

    Bile acids: the role of peroxisomes por Sacha Ferdinandusse, Simone Denis, Phyllis L. Faust, Ronald J. A. Wanders

    Publicado 2009
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  2. 2
    Identification of the peroxisomal β-oxidation enzymes involved in the degradation of long-chain dicarboxylic acids

    Identification of the peroxisomal β-oxidation enzymes involved in the degradation of long-chain dicarboxylic acids por Sacha Ferdinandusse, Simone Denis, Carlo W.T. van Roermund, Ronald J. A. Wanders, G. Dacremont

    Publicado 2004
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  3. 3
    Sterol Carrier Protein X (SCPx) Is a Peroxisomal Branched-Chain β-Ketothiolase Specifically Reacting with 3-Oxo-pristanoyl-CoA: A New, Unique Role for SCPx in Branched-Chain Fatty Acid Metabolism in Peroxisomes

    Sterol Carrier Protein X (SCPx) Is a Peroxisomal Branched-Chain β-Ketothiolase Specifically Reacting with 3-Oxo-pristanoyl-CoA: A New, Unique Role for SCPx in Branched-Chain Fatty... por R. J. A. Wanders, Simone Denis, Fred S. Wouters, K.W.A. Wirtz, Udo Seedorf

    Publicado 1997
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  4. 4
    Subcellular localization and physiological role of α-methylacyl-CoA racemase

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

    Publicado 2000
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  5. 5
    Peroxisomal L-bifunctional enzyme (Ehhadh) is essential for the production of medium-chain dicarboxylic acids

    Peroxisomal L-bifunctional enzyme (Ehhadh) is essential for the production of medium-chain dicarboxylic acids por Sander M. Houten, Simone Denis, Carmen Argmann, Yuzhi Jia, Sacha Ferdinandusse, Janardan K. Reddy, Ronald J. A. Wanders

    Publicado 2012
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  6. 6
    The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidney

    The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain a... por Geertrui F. Vanhove, Paul P. Van Veldhoven, Marc Fransen, Simone Denis, H. Eyssen, Ronald J. A. Wanders, G P Mannaerts

    Publicado 1993
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  7. 7
    Phytanoyl-CoA Hydroxylase Is Present in Human Liver, Located in Peroxisomes, and Deficient in Zellweger Syndrome: Direct, Unequivocal Evidence for the New, Revised Pathway of Phytanic Acid α-Oxidation in Humans

    Phytanoyl-CoA Hydroxylase Is Present in Human Liver, Located in Peroxisomes, and Deficient in Zellweger Syndrome: Direct, Unequivocal Evidence for the New, Revised Pathway of Phyta... por Gerbert A. Jansen, Stephanie J. Mihalik, Paul A. Watkins, H. W. Moser, C. Jakobs, Simone Denis, R. J. A. Wanders

    Publicado 1996
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  8. 8
    Identification of the peroxisomal β-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid

    Identification of the peroxisomal β-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid por Sacha Ferdinandusse, Simone Denis, Petra A.W. Mooijer, Zhongyi Zhang, Janardan K. Reddy, Arthur A. Spector, Ronald J. A. Wanders

    Publicado 2001
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  9. 9
    A novel case of ACOX2 deficiency leads to recognition of a third human peroxisomal acyl-CoA oxidase

    A novel case of ACOX2 deficiency leads to recognition of a third human peroxisomal acyl-CoA oxidase por Sacha Ferdinandusse, Simone Denis, Carlo W.T. van Roermund, Mary Anne Preece, Janet Koster, Merel S. Ebberink, Hans R. Waterham, Ronald J. A. Wanders

    Publicado 2017
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  10. 10
    Altered lipid metabolism in synovial fibroblasts of individuals at risk of developing rheumatoid arthritis

    Altered lipid metabolism in synovial fibroblasts of individuals at risk of developing rheumatoid arthritis por Tineke A. de Jong, Johanna F. Semmelink, Simone Denis, M. G. H. Van de Sande, Riekelt H. Houtkooper, Lisa G. M. van Baarsen

    Publicado 2022
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  11. 11
    Mutations in the Gene Encoding Peroxisomal Sterol Carrier Protein X (SCPx) Cause Leukencephalopathy with Dystonia and Motor Neuropathy

    Mutations in the Gene Encoding Peroxisomal Sterol Carrier Protein X (SCPx) Cause Leukencephalopathy with Dystonia and Motor Neuropathy por Sacha Ferdinandusse, Panagiotis Kostopoulos, Simone Denis, H. Rusch, Henk Overmars, Ulrich Dillmann, Wolfgang Reith, Dorothea Haas, Ronald J. A. Wanders, M. Durán, Martin Marziniak

    Publicado 2006
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  12. 12
    Cardiolipin-induced activation of pyruvate dehydrogenase links mitochondrial lipid biosynthesis to TCA cycle function

    Cardiolipin-induced activation of pyruvate dehydrogenase links mitochondrial lipid biosynthesis to TCA cycle function por Yiran Li, Wenjia Lou, Vaishnavi Raja, Simone Denis, Wenxi Yu, Michael W. Schmidtke, Christian A. Reynolds, Michael Schlame, Riekelt H. Houtkooper, Miriam L. Greenberg

    Publicado 2019
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  13. 13
    Clinical, biochemical, and mutational spectrum of peroxisomal acyl–coenzyme A oxidase deficiency

    Clinical, biochemical, and mutational spectrum of peroxisomal acyl–coenzyme A oxidase deficiency por 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

    Publicado 2007
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  14. 14
    A phytol-enriched diet induces changes in fatty acid metabolism in mice both via PPARα-dependent and -independent pathways

    A phytol-enriched diet induces changes in fatty acid metabolism in mice both via PPARα-dependent and -independent pathways por Jolein Gloerich, Naomi van Vlies, Gerbert A. Jansen, Simone Denis, Jos P.N. Ruiter, Michiel Adriaan van Werkhoven, M. Durán, Frédéric M. Vaz, Ronald J. A. Wanders, Sacha Ferdinandusse

    Publicado 2005
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  15. 15
    Barth syndrome cells display widespread remodeling of mitochondrial complexes without affecting metabolic flux distribution

    Barth syndrome cells display widespread remodeling of mitochondrial complexes without affecting metabolic flux distribution por Iliana A. Chatzispyrou, Sergio Guerrero‐Castillo, Ntsiki M. Held, Jos P.N. Ruiter, Simone Denis, Lodewijk IJlst, R. J. A. Wanders, Michel van Weeghel, Sacha Ferdinandusse, Frédéric M. Vaz, Ulrich Brandt, Riekelt H. Houtkooper

    Publicado 2018
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  16. 16
    Impaired amino acid metabolism contributes to fasting-induced hypoglycemia in fatty acid oxidation defects

    Impaired amino acid metabolism contributes to fasting-induced hypoglycemia in fatty acid oxidation defects por Sander M. Houten, Hilde Herrema, Heleen te Brinke, Simone Denis, Jos P.N. Ruiter, Theo H. van Dijk, Carmen Argmann, Roelof Ottenhoff, Michael Müller, Albert K. Groen, Folkert Kuipers, Dirk‐Jan Reijngoud, Ronald J. A. Wanders

    Publicado 2013
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  17. 17
    Pyruvate dehydrogenase complex plays a central role in brown adipocyte energy expenditure and fuel utilization during short-term beta-adrenergic activation

    Pyruvate dehydrogenase complex plays a central role in brown adipocyte energy expenditure and fuel utilization during short-term beta-adrenergic activation por Ntsiki M. Held, Eline N. Kuipers, Michel van Weeghel, Jan B. van Klinken, Simone Denis, Marc Lombès, Ronald J. A. Wanders, Frédéric M. Vaz, Patrick C.N. Rensen, Arthur J. Verhoeven, Mariëtte R. Boon, Riekelt H. Houtkooper

    Publicado 2018
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  18. 18
    Reduced nicotinamide mononucleotide is a new and potent NAD<sup>+</sup>precursor in mammalian cells and mice

    Reduced nicotinamide mononucleotide is a new and potent NAD<sup>+</sup>precursor in mammalian cells and mice por Rubén Zapata‐Pérez, Alessandra Tammaro, Bauke V. Schomakers, Angelique M. L. Scantlebery, Simone Denis, Hyung L. Elfrink, Judith Giroud‐Gerbetant, Carles Cantó, Carmen López‐Leonardo, Rebecca L. McIntyre, Michel van Weeghel, Álvaro Sánchez‐Ferrer, Riekelt H. Houtkooper

    Publicado 2021
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  19. 19
    Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia

    Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia por Sander M. Houten, Simone Denis, Heleen te Brinke, Aldo Jongejan, Antoine H. C. van Kampen, Edward J. Bradley, Frank Baas, Raoul C. M. Hennekam, David S. Millington, Sarah P. Young, Dianne M. Frazier, Müge Güçsavaş‐Çalıkoğlu, Ronald J. A. Wanders

    Publicado 2014
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  20. 20
    Genetic basis of hyperlysinemia

    Genetic basis of hyperlysinemia por Sander M. Houten, Heleen te Brinke, Simone Denis, Jos P.N. Ruiter, Alida C. Knegt, J. B. de Klerk, Persephone Augoustides‐Savvopoulou, Johannes Häberle, Matthias R. Baumgartner, Turgay Coşkun, Johannes Zschocke, Jörn Oliver Sass, Bwee Tien Poll‐The, Ronald J. A. Wanders, Marinus Durán

    Publicado 2013
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