Human disorders of peroxisome metabolism and biogenesis von Waterham, Hans R., Ferdinandusse, Sacha, Wanders, Ronald J.A.

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Genetics and molecular basis of human peroxisome biogenesis disorders von Waterham, Hans R., Ebberink, Merel S.

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Compromised Protein Prenylation as Pathogenic Mechanism in Mevalonate Kinase Deficiency von Politiek, Frouwkje A. A., Waterham, Hans R. R.

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The physiological functions of human peroxisomes von Wanders, Ronald J A, Baes, Myriam, Ribeiro, Daniela, Ferdinandusse, Sacha, Waterham, Hans R

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Applying CRISPR-Cas9 Genome Editing to Study Genes Involved in Peroxisome Biogenesis or Peroxisomal Functions von Chornyi, Serhii, Koster, Janet, Waterham, Hans R.

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

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Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact von 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

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Biochemistry of mammalian peroxisomes revisited von Wanders, Ronald J A, Waterham, Hans R

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The origin of long-chain fatty acids required for de novo ether lipid/plasmalogen synthesis von Chornyi, Serhii, Ofman, Rob, Koster, Janet, Waterham, Hans R.

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Studying the topology of peroxisomal acyl-CoA synthetases using self-assembling split sfGFP von Chornyi, Serhii, Koster, Janet, IJlst, Lodewijk, Waterham, Hans R.

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Peroxisomes can oxidize medium‐ and long‐chain fatty acids through a pathway involving ABCD3 and HSD17B4 von Violante, Sara, Achetib, Nihad, Roermund, Carlo W. T., Hagen, Jacob, Dodatko, Tetyana, Vaz, Frédéric M., Waterham, Hans R., Chen, Hongjie, Baes, Myriam, Yu, Chunli, Argmann, Carmen A., Houten, Sander M.

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Metabolic Interplay between Peroxisomes and Other Subcellular Organelles Including Mitochondria and the Endoplasmic Reticulum von Wanders, Ronald J A, Waterham, Hans R, Ferdinandusse, Sacha

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Mevalonate kinase-deficient THP-1 cells show a disease-characteristic pro-inflammatory phenotype von Politiek, Frouwkje A, Turkenburg, Marjolein, Ofman, Rob, Waterham, Hans R

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Molecular and cellular consequences of mevalonate kinase deficiency von Politiek, Frouwkje A., Turkenburg, Marjolein, Henneman, Linda, Ofman, Rob, Waterham, Hans R.

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The proteome of human liver peroxisomes: identification of five new peroxisomal constituents by a label-free quantitative proteomics survey von Gronemeyer, Thomas, Wiese, Sebastian, Ofman, Rob, Bunse, Christian, Pawlas, Magdalena, Hayen, Heiko, Eisenacher, Martin, Stephan, Christian, Meyer, Helmut E, Waterham, Hans R, Erdmann, Ralf, Wanders, Ronald J, Warscheid, Bettina

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Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: Conjugated hypercholanemia without a clear clinical phenotype von Vaz, Frédéric M., Paulusma, Coen C., Huidekoper, Hidde, de Ru, Minke, Lim, Cynthia, Koster, Janet, Ho‐Mok, Kam, Bootsma, Albert H., Groen, Albert K., Schaap, Frank G., Oude Elferink, Ronald P. J., Waterham, Hans R., Wanders, Ronald J.A.

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Identification of FDA‐approved drugs that increase mevalonate kinase in hyper IgD syndrome von Politiek, Frouwkje A., Turkenburg, Marjolein, Koster, Janet, Ofman, Rob, Waterham, Hans R.

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Deciphering the potential involvement of PXMP2 and PEX11B in hydrogen peroxide permeation across the peroxisomal membrane reveals a role for PEX11B in protein sorting von Lismont, Celien, Koster, Janet, Provost, Sarah, Baes, Myriam, Van Veldhoven, Paul P., Waterham, Hans R., Fransen, Marc

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Alkyl-glycerol rescues plasmalogen levels and pathology of ether-phospholipid deficient mice von Brites, Pedro, Ferreira, Ana Sofia, da Silva, Tiago Ferreira, Sousa, Vera F, Malheiro, Ana R, Duran, Marinus, Waterham, Hans R, Baes, Myriam, Wanders, Ronald J A

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A novel bile acid biosynthesis defect due to a deficiency of peroxisomal ABCD3 von Ferdinandusse, Sacha, Jimenez-Sanchez, Gerardo, Koster, Janet, Denis, Simone, Van Roermund, Carlo W, Silva-Zolezzi, Irma, Moser, Ann B, Visser, Wouter F, Gulluoglu, Mine, Durmaz, Ozlem, Demirkol, Mubeccel, Waterham, Hans R, Gökcay, Gülden, Wanders, Ronald J A, Valle, David

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