Calcium Absorption Across Epithelia von Hoenderop, Joost G. J, Nilius, Bernd, Bindels, Rene J. M

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Magnesium in man: implications for health and disease von de Baaij, Jeroen H F, Hoenderop, Joost G J, Bindels, René J M

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Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia von Groenestege, Wouter M Tiel, Thébault, Stéphanie, van der Wijst, Jenny, van den Berg, Dennis, Janssen, Rob, Tejpar, Sabine, van den Heuvel, Lambertus P, van Cutsem, Eric, Hoenderop, Joost G, Knoers, Nine V, Bindels, René J

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Renal physiology: TRPC5 inhibition to treat progressive kidney disease von van der Wijst, Jenny, Bindels, René J M

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Molecular Determinants of Magnesium Homeostasis : Insights from Human Disease von ALEXANDER, R. Todd, HOENDEROP, Joost G, BINDELS, René J

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Fibroblast growth factor 23 modifies the pharmacological effects of angiotensin receptor blockade in experimental renal fibrosis von de Jong, Maarten A, Mirkovic, Katarina, Mencke, Rik, Hoenderop, Joost G, Bindels, René J, Vervloet, Marc G, Hillebrands, Jan-Luuk, van den Born, Jacob, Navis, Gerjan, de Borst, Martin H

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Learning Physiology From Inherited Kidney Disorders von van der Wijst, Jenny, Belge, Hendrica, Bindels, René J M, Devuyst, Olivier

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TRPC5 inhibition to treat progressive kidney disease von van der Wijst, Jenny, Bindels, René J. M.

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MAGE-D2 and the Regulation of Renal Salt Transporters von Knoers, Nine V.A.M, Bindels, René J

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Sensing of tubular flow and renal electrolyte transport von Verschuren, Eric H. J., Castenmiller, Charlotte, Peters, Dorien J. M., Arjona, Francisco J., Bindels, René J. M., Hoenderop, Joost G. J.

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Hypomagnesemia in Type 2 Diabetes: A Vicious Circle? von Gommers, Lisanne M M, Hoenderop, Joost G J, Bindels, René J M, de Baaij, Jeroen H F

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2009 Homer W. Smith Award: Minerals in Motion: From New Ion Transporters to New Concepts von BINDELS, René J. M

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The role of transient receptor potential channels in kidney disease von Hoenderop, Joost G. J, Woudenberg-Vrenken, Titia E, Bindels, René J. M

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De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy von Blanchard, Maxime G, Willemsen, Marjolein H, Walker, Jaclyn B, Dib-Hajj, Sulayman D, Waxman, Stephen G, Jongmans, Marjolijn CJ, Kleefstra, Tjitske, van de Warrenburg, Bart P, Praamstra, Peter, Nicolai, Joost, Yntema, Helger G, Bindels, René JM, Meisler, Miriam H, Kamsteeg, Erik-Jan

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Transcriptional and functional analyses of SLC12A3 mutations : New clues for the pathogenesis of gitelman syndrome von RIVEIRA-MUNOZ, Eva, QING CHANG, GODEFROID, Nathalie, HOENDEROP, Joost G, BINDELS, René J, DAHAN, Karin, DEVUYST, Olivier

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A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia von Glaudemans, Bob, van der Wijst, Jenny, Scola, Rosana H, Lorenzoni, Paulo J, Heister, Angelien, van der Kemp, Annemiete W, Knoers, Nine V, Hoenderop, Joost G, Bindels, René J

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Sodium-dependent transporters in health and disease—a special issue von Bindels, René J. M., Wagner, Carsten A.

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Calcium and phosphate homeostasis: Concerted interplay of new regulators von Renkema, Kirsten Y., Alexander, R. Todd, Bindels, René J., Hoenderop, Joost G.

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CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemia von Arjona, Francisco J, de Baaij, Jeroen H F, Schlingmann, Karl P, Lameris, Anke L L, van Wijk, Erwin, Flik, Gert, Regele, Sabrina, Korenke, G Christoph, Neophytou, Birgit, Rust, Stephan, Reintjes, Nadine, Konrad, Martin, Bindels, René J M, Hoenderop, Joost G J

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A primary culture of distal convoluted tubules expressing functional thiazide-sensitive NaCl transport von Markadieu, Nicolas, San-Cristobal, Pedro, Nair, Anil V, Verkaart, Sjoerd, Lenssen, Ellen, Tudpor, Kukiat, van Zeeland, Femke, Loffing, Johannes, Bindels, René J M, Hoenderop, Joost G J

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