general introduction to the biochemistry of mitochondrial fatty acid β-oxidation
Houten, Sander Michel, Wanders, Ronald J. A
Published in Journal of inherited metabolic disease (01.10.2010)
Published in Journal of inherited metabolic disease (01.10.2010)
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The Secret Life of NAD+: An Old Metabolite Controlling New Metabolic Signaling Pathways
Houtkooper, Riekelt H, Cantó, Carles, Wanders, Ronald J, Auwerx, Johan
Published in Endocrine reviews (01.04.2010)
Published in Endocrine reviews (01.04.2010)
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Journal Article
X-linked adrenoleukodystrophy (X-ALD): clinical presentation and guidelines for diagnosis, follow-up and management
Engelen, Marc, Kemp, Stephan, de Visser, Marianne, van Geel, Björn M, Wanders, Ronald J A, Aubourg, Patrick, Poll-The, Bwee Tien
Published in Orphanet journal of rare diseases (13.08.2012)
Published in Orphanet journal of rare diseases (13.08.2012)
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Journal Article
Malnutrition-associated liver steatosis and ATP depletion is caused by peroxisomal and mitochondrial dysfunction
van Zutphen, Tim, Ciapaite, Jolita, Bloks, Vincent W, Ackereley, Cameron, Gerding, Albert, Jurdzinski, Angelika, de Moraes, Roberta Allgayer, Zhang, Ling, Wolters, Justina C, Bischoff, Rainer, Wanders, Ronald J, Houten, Sander M, Bronte-Tinkew, Dana, Shatseva, Tatiana, Lewis, Gary F, Groen, Albert K, Reijngoud, Dirk-Jan, Bakker, Barbara M, Jonker, Johan W, Kim, Peter K, Bandsma, Robert H.J
Published in Journal of hepatology (01.12.2016)
Published in Journal of hepatology (01.12.2016)
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NAD+ homeostasis in human health and disease
Zapata‐Pérez, Rubén, Wanders, Ronald J A, van Karnebeek, Clara D M, Houtkooper, Riekelt H
Published in EMBO molecular medicine (07.07.2021)
Published in EMBO molecular medicine (07.07.2021)
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enzymology of mitochondrial fatty acid beta-oxidation and its application to follow-up analysis of positive neonatal screening results
Wanders, Ronald J. A, Ruiter, Jos P. N, IJlst, Lodewijk, Waterham, Hans R, Houten, Sander M
Published in Journal of inherited metabolic disease (01.10.2010)
Published in Journal of inherited metabolic disease (01.10.2010)
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Journal Article
X-linked adrenoleukodystrophy in women: a cross-sectional cohort study
ENGELEN, Marc, BARBIER, Mathieu, DE VISSER, Marianne, POLL-THE, Bwee T, KEMP, Stephan, DIJKSTRA, Inge M. E, SCHÜR, Remmelt, DE BIE, Rob M. A, VERHAMME, Camiel, DIJKGRAAF, Marcel G. W, AUBOURG, Patrick A, WANDERS, Ronald J. A, VAN GEEL, Bjorn M
Published in Brain (London, England : 1878) (01.03.2014)
Published in Brain (London, England : 1878) (01.03.2014)
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Abnormal activation of MAPKs pathways and inhibition of autophagy in a group of patients with Zellweger spectrum disorders and X-linked adrenoleukodystrophy
Gragnaniello, Vincenza, Gueraldi, Daniela, Puma, Andrea, Commone, Anna, Cazzorla, Chiara, Loro, Christian, Porcù, Elena, Stornaiuolo, Maria, Miglioranza, Paolo, Salviati, Leonardo, Wanders, Ronald J. A, Burlina, Alberto
Published in Orphanet journal of rare diseases (16.11.2023)
Published in Orphanet journal of rare diseases (16.11.2023)
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The Brown-Vialetto-Van Laere and Fazio Londe syndrome revisited: natural history, genetics, treatment and future perspectives
Bosch, Annet M, Stroek, Kevin, Abeling, Nico G, Waterham, Hans R, Ijlst, Lodewijk, Wanders, Ronald J A
Published in Orphanet journal of rare diseases (29.10.2012)
Published in Orphanet journal of rare diseases (29.10.2012)
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Journal Article
Intrinsic acyl-CoA thioesterase activity of a peroxisomal ATP binding cassette transporter is required for transport and metabolism of fatty acids
De Marcos Lousa, Carine, van Roermund, Carlo W. T., Postis, Vincent L. G., Dietrich, Daniela, Kerr, Ian D., Wanders, Ronald J. A., Baldwin, Stephen A., Baker, Alison, Theodoulou, Frederica L.
Published in Proceedings of the National Academy of Sciences - PNAS (22.01.2013)
Published in Proceedings of the National Academy of Sciences - PNAS (22.01.2013)
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N-lactoyl-amino acids are ubiquitous metabolites that originate from CNDP2-mediated reverse proteolysis of lactate and amino acids
Jansen, Robert S., Addie, Ruben, Merkx, Remco, Fish, Alexander, Mahakena, Sunny, Bleijerveld, Onno B., Altelaar, Maarten, IJlst, Lodewijk, Wanders, Ronald J., Borst, P., van de Wetering, Koen
Published in Proceedings of the National Academy of Sciences - PNAS (26.05.2015)
Published in Proceedings of the National Academy of Sciences - PNAS (26.05.2015)
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Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact
Shai, Nadav, Yifrach, Eden, van Roermund, Carlo W. T., Cohen, Nir, Bibi, Chen, IJlst, Lodewijk, Cavellini, Laetitia, Meurisse, Julie, Schuster, Ramona, Zada, Lior, Mari, Muriel C., Reggiori, Fulvio M., Hughes, Adam L., Escobar-Henriques, Mafalda, Cohen, Mickael M., Waterham, Hans R., Wanders, Ronald J. A., Schuldiner, Maya, Zalckvar, Einat
Published in Nature communications (02.05.2018)
Published in Nature communications (02.05.2018)
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Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle
Knottnerus, Suzan J. G., Bleeker, Jeannette C., Wüst, Rob C. I., Ferdinandusse, Sacha, IJlst, Lodewijk, Wijburg, Frits A., Wanders, Ronald J. A., Visser, Gepke, Houtkooper, Riekelt H.
Published in Reviews in endocrine & metabolic disorders (01.03.2018)
Published in Reviews in endocrine & metabolic disorders (01.03.2018)
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Journal Article
A Lethal Defect of Mitochondrial and Peroxisomal Fission
Waterham, Hans R, Koster, Janet, van Roermund, Carlo W.T, Mooyer, Petra A.W, Wanders, Ronald J.A, Leonard, James V
Published in The New England journal of medicine (26.04.2007)
Published in The New England journal of medicine (26.04.2007)
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