Ngā hua rapu kaituhi

1

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

I whakaputaina 2003

Whiwhi kuputuhi katoa
Revisão

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2

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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3

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

I whakaputaina 2021

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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4

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

I whakaputaina 2006

Whiwhi kuputuhi katoa
Revisão

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5

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

I whakaputaina 1998

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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6

The enzymology of mitochondrial fatty acid beta‐oxidation and its application to follow‐up analysis of positive neonatal screening results mā Ronald J. A. Wanders, Jos P.N. Ruiter, Lodewijk IJlst, Hans R. Waterham, Sander M. Houten

I whakaputaina 2010

Whiwhi kuputuhi katoa
Artigo

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

I whakaputaina 1996

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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8

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

I whakaputaina 1998

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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9

The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives mā Annet M. Bosch, Kevin Stroek, N. G. G. M. Abeling, Hans R. Waterham, Lodewijk IJlst, Ronald J. A. Wanders

I whakaputaina 2012

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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10

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

I whakaputaina 2012

Whiwhi kuputuhi katoa
Artigo

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11

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

I whakaputaina 1999

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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12

Human peroxisomal NAD+/NADH homeostasis is regulated by two independent NAD(H) shuttle systems mā Serhii Chornyi, Cláudio F. Costa, Lodewijk IJlst, Marc Fransen, Ronald J. A. Wanders, Carlo W.T. van Roermund, Hans R. Waterham

I whakaputaina 2023

Whiwhi kuputuhi katoa
Artigo

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13

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

I whakaputaina 2004

Whiwhi kuputuhi katoa
Artigo

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14

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

I whakaputaina 2011

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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15

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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16

Identification of a Peroxisomal ATP Carrier Required for Medium-Chain Fatty Acid β-Oxidation and Normal Peroxisome Proliferation in <i>Saccharomyces cerevisiae</i> mā 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

I whakaputaina 2001

Whiwhi kuputuhi katoa
Artigo

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17

Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosis mā 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

I whakaputaina 2009

Whiwhi kuputuhi katoa
Artigo

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18

Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle mā 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

I whakaputaina 2018

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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19

<i>N</i> -lactoyl-amino acids are ubiquitous metabolites that originate from CNDP2-mediated reverse proteolysis of lactate and amino acids mā 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

I whakaputaina 2015

Whiwhi kuputuhi katoa
Artigo

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20

Peroxisomal <scp>d</scp> -hydroxyacyl-CoA dehydrogenase deficiency: Resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency mā 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

I whakaputaina 1998

Whiwhi kuputuhi katoa
Artigo

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Ngā hua rapu - Lodewijk IJlst

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

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

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

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

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

The enzymology of mitochondrial fatty acid beta‐oxidation and its application to follow‐up analysis of positive neonatal screening results mā Ronald J. A. Wanders, Jos P.N. Ruiter, Lodewijk IJlst, Hans R. Waterham, Sander M. Houten

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

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

The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives mā Annet M. Bosch, Kevin Stroek, N. G. G. M. Abeling, Hans R. Waterham, Lodewijk IJlst, Ronald J. A. Wanders

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

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

Human peroxisomal NAD+/NADH homeostasis is regulated by two independent NAD(H) shuttle systems mā Serhii Chornyi, Cláudio F. Costa, Lodewijk IJlst, Marc Fransen, Ronald J. A. Wanders, Carlo W.T. van Roermund, Hans R. Waterham

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

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

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

Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosis mā 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

Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle mā 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

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