Canlyniadau Chwilio - Simone Denis

Mireinio'r Canlyniadau
  1. 1
    Bile acids: the role of peroxisomes

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

    Cyhoeddwyd 2009
    Cael y testun llawn Cael y testun llawn
    Revisão
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan Sacha Ferdinandusse, Simone Denis, Carlo W.T. van Roermund, Ronald J. A. Wanders, G. Dacremont

    Cyhoeddwyd 2004
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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... gan R. J. A. Wanders, Simone Denis, Fred S. Wouters, K.W.A. Wirtz, Udo Seedorf

    Cyhoeddwyd 1997
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  4. 4
    Subcellular localization and physiological role of α-methylacyl-CoA racemase

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

    Cyhoeddwyd 2000
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan Sander M. Houten, Simone Denis, Carmen Argmann, Yuzhi Jia, Sacha Ferdinandusse, Janardan K. Reddy, Ronald J. A. Wanders

    Cyhoeddwyd 2012
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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... gan Geertrui F. Vanhove, Paul P. Van Veldhoven, Marc Fransen, Simone Denis, H. Eyssen, Ronald J. A. Wanders, G P Mannaerts

    Cyhoeddwyd 1993
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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... gan Gerbert A. Jansen, Stephanie J. Mihalik, Paul A. Watkins, H. W. Moser, C. Jakobs, Simone Denis, R. J. A. Wanders

    Cyhoeddwyd 1996
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan Sacha Ferdinandusse, Simone Denis, Petra A.W. Mooijer, Zhongyi Zhang, Janardan K. Reddy, Arthur A. Spector, Ronald J. A. Wanders

    Cyhoeddwyd 2001
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan Sacha Ferdinandusse, Simone Denis, Carlo W.T. van Roermund, Mary Anne Preece, Janet Koster, Merel S. Ebberink, Hans R. Waterham, Ronald J. A. Wanders

    Cyhoeddwyd 2017
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan Tineke A. de Jong, Johanna F. Semmelink, Simone Denis, M. G. H. Van de Sande, Riekelt H. Houtkooper, Lisa G. M. van Baarsen

    Cyhoeddwyd 2022
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan Sacha Ferdinandusse, Panagiotis Kostopoulos, Simone Denis, H. Rusch, Henk Overmars, Ulrich Dillmann, Wolfgang Reith, Dorothea Haas, Ronald J. A. Wanders, M. Durán, Martin Marziniak

    Cyhoeddwyd 2006
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan Yiran Li, Wenjia Lou, Vaishnavi Raja, Simone Denis, Wenxi Yu, Michael W. Schmidtke, Christian A. Reynolds, Michael Schlame, Riekelt H. Houtkooper, Miriam L. Greenberg

    Cyhoeddwyd 2019
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan 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

    Cyhoeddwyd 2007
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan 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

    Cyhoeddwyd 2005
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan 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

    Cyhoeddwyd 2018
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan 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

    Cyhoeddwyd 2013
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan 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

    Cyhoeddwyd 2018
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan 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

    Cyhoeddwyd 2021
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  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 gan 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

    Cyhoeddwyd 2014
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:
  20. 20
    Genetic basis of hyperlysinemia

    Genetic basis of hyperlysinemia gan 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

    Cyhoeddwyd 2013
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:

Offerynnau Chwilio: