Ngā hua rapu kaituhi :: APM

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

I whakaputaina 2009

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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2

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

I whakaputaina 2004

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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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... mā R. J. A. Wanders, Simone Denis, Fred S. Wouters, K.W.A. Wirtz, Udo Seedorf

I whakaputaina 1997

Whiwhi kuputuhi katoa
Artigo

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4

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

I whakaputaina 2000

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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5

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

I whakaputaina 2012

Whiwhi kuputuhi katoa
Artigo

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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 a... mā Geertrui F. Vanhove, Paul P. Van Veldhoven, Marc Fransen, Simone Denis, H. Eyssen, Ronald J. A. Wanders, G P Mannaerts

I whakaputaina 1993

Whiwhi kuputuhi katoa
Artigo

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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 Phyta... mā Gerbert A. Jansen, Stephanie J. Mihalik, Paul A. Watkins, H. W. Moser, C. Jakobs, Simone Denis, R. J. A. Wanders

I whakaputaina 1996

Whiwhi kuputuhi katoa
Artigo

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8

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

I whakaputaina 2001

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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9

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

I whakaputaina 2017

Whiwhi kuputuhi katoa
Artigo

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10

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

I whakaputaina 2022

Whiwhi kuputuhi katoa
Artigo

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11

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

I whakaputaina 2006

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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12

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

I whakaputaina 2019

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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13

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

I whakaputaina 2007

Whiwhi kuputuhi katoa
Artigo

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14

A phytol-enriched diet induces changes in fatty acid metabolism in mice both via PPARα-dependent and -independent pathways mā 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

I whakaputaina 2005

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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15

Barth syndrome cells display widespread remodeling of mitochondrial complexes without affecting metabolic flux distribution mā 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

I whakaputaina 2018

Whiwhi kuputuhi katoa
Artigo

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16

Impaired amino acid metabolism contributes to fasting-induced hypoglycemia in fatty acid oxidation defects mā 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

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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17

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

I whakaputaina 2018

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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18

Reduced nicotinamide mononucleotide is a new and potent NAD<sup>+</sup>precursor in mammalian cells and mice mā 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

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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19

Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia mā 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

I whakaputaina 2014

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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20

Genetic basis of hyperlysinemia mā 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

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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