CNNM2, Encoding a Basolateral Protein Required for Renal Mg2+ Handling, Is Mutated in Dominant Hypomagnesemia von STUIVER, Marchel, LAINEZ, Sergio, QUERFELD, Uwe, WILLNOW, Thomas E, NEMEC, Vladimir, WAGNER, Carsten A, HOENDEROP, Joost G, DEVUYST, Olivier, KNOERS, Nine V. A. M, BINDELS, René J, MEIJ, Iwan C, MÜLLER, Dominik, WILL, Constanze, TERRYN, Sara, GÜNZEL, Dorothee, DEBAIX, Huguette, SOMMER, Kerstin, KOPPLIN, Kathrin, THUMFART, Julia, KAMPIK, Nicole B

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Deletion of claudin-10 (Cldn10) in the thick ascending limb impairs paracellular sodium permeability and leads to hypermagnesemia and nephrocalcinosis von Breiderhoff, Tilman, Himmerkus, Nina, Stuiver, Marchel, Mutig, Kerim, Will, Constanze, Meij, Iwan C, Bachmann, Sebastian, Bleich, Markus, Willnow, Thomas E, Müller, Dominik

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Membrane Topology and Intracellular Processing of Cyclin M2 (CNNM2) von de Baaij, Jeroen H.F., Stuiver, Marchel, Meij, Iwan C., Lainez, Sergio, Kopplin, Kathrin, Venselaar, Hanka, Müller, Dominik, Bindels, René J.M., Hoenderop, Joost G.J.

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Disturbed function of the blood–cerebrospinal fluid barrier aggravates neuro-inflammation von Kooij, Gijs, Kopplin, Kathrin, Blasig, Rosel, Stuiver, Marchel, Koning, Nathalie, Goverse, Gera, van der Pol, Susanne M. A., van het Hof, Bert, Gollasch, Maik, Drexhage, Joost A. R., Reijerkerk, Arie, Meij, Iwan C., Mebius, Reina, Willnow, Thomas E., Müller, Dominik, Blasig, Ingolf E., de Vries, Helga E.

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L1 retrotransposition can occur early in human embryonic development von van den Hurk, José A.J.M., Meij, Iwan C., del Carmen Seleme, Maria, Kano, Hiroki, Nikopoulos, Konstantinos, Hoefsloot, Lies H., Sistermans, Erik A., de Wijs, Ilse J., Mukhopadhyay, Arijit, Plomp, Astrid S., de Jong, Paulus T.V.M., Kazazian, Haig H., Cremers, Frans P.M.

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Claudin-10 exists in six alternatively spliced isoforms that exhibit distinct localization and function von Günzel, Dorothee, Stuiver, Marchel, Kausalya, P. Jaya, Haisch, Lea, Krug, Susanne M, Rosenthal, Rita, Meij, Iwan C, Hunziker, Walter, Fromm, Michael, Müller, Dominik

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Unusual Clinical Presentation and Possible Rescue of a Novel Claudin-16 Mutation von Müller, Dominik, Kausalya, P. Jaya, Bockenhauer, Detlef, Thumfart, Julia, Meij, Iwan C., Dillon, Michael J., Hoff, William van’t, Hunziker, Walter

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Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca2+ and Mg2+ wasting von Will, Constanze, Breiderhoff, Tilman, Thumfart, Julia, Stuiver, Marchel, Kopplin, Kathrin, Sommer, Kerstin, Günzel, Dorothee, Querfeld, Uwe, Meij, Iwan C, Shan, Qixian, Bleich, Markus, Willnow, Thomas E, Müller, Dominik

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A Novel Claudin 16 Mutation Associated with Childhood Hypercalciuria Abolishes Binding to ZO-1 and Results in Lysosomal Mistargeting von Müller, Dominik, Kausalya, P. Jaya, Claverie-Martin, Felix, Meij, Iwan C., Eggert, Paul, Garcia-Nieto, Victor, Hunziker, Walter

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Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: blocking endocytosis restores surface expression of a novel Claudin-16 mutant that lacks the entire C-terminal cyt... von Müller, Dominik, Kausalya, P. Jaya, Meij, Iwan C., Hunziker, Walter

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Dominant isolated renal magnesium loss is caused by misrouting of the Na + ,K + -ATPase γ-subunit von Knoers, Nine V.A.M, van Bokhoven, Hans, Koenderink, Jan B, Tiel Groenestege, Wouter, de Pont, Jan Joep H.H.M, van den Heuvel, Lambert P.W.J, Meij, Iwan C, Monnens, Leo A.H, Assink, Karin F.H, Bindels, René J.M

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Dominant Isolated Renal Magnesium Loss Is Caused by Misrouting of the Na+,K+-ATPase γ-Subunit von MEIJ, IWAN C., KOENDERINK, JAN B., DE JONG, JOKE C., DE PONT, JAN JOEP H. H. M., MONNENS, LEO A. H., VAN DEN HEUVEL, LAMBERT P. W. J., KNOERS, NINE V. A. M.

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Exclusion of mutations in FXYD2, CLDN16 and SLC12A3 in two families with primary renal Mg2+ loss von Meij, Iwan C., van den Heuvel, Lambert P. W. J., Hemmes, Sies, van der Vliet, Walter A., Willems, Johannes L., Monnens, Leo A. H., Knoers, Nine V. A. M.

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Genetic disorders of magnesium homeostasis von Meij, Iwan C, van den Heuvel, Lambert P W J, Knoers, Nine V A M

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Genetic renal disorders with hypomagnesemia and hypocalciuria von Knoers, Nine V A M, de Jong, Joke C, Meij, Iwan C, Van Den Heuvel, Lambert P W J, Bindels, Rene J M

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Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca^sup 2+^ and Mg^sup 2+^ wasting von Will, Constanze, Breiderhoff, Tilman, Thumlart, Julia, Stuiver, Marchel, Kopplin, Kathrin, Sommer, Kerstin, Günzel, Dorothee, Querfeld, Uwe, Meij, Iwan C, Shan, Qixian, Bleich, Markus, Willnow, Thomas E, Müller, Dominik

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Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca 2+ and Mg 2+ wasting von Will, Constanze, Breiderhoff, Tilman, Thumfart, Julia, Stuiver, Marchel, Kopplin, Kathrin, Sommer, Kerstin, Günzel, Dorothee, Querfeld, Uwe, Meij, Iwan C., Shan, Qixian, Bleich, Markus, Willnow, Thomas E., Müller, Dominik

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Targeted deletion of murine Cldn16 identifies extra- and intrarenal compensatory mechanisms of Ca2+ and Mg2+ wasting von WILL, Constanze, BREIDERHOFF, Tilman, BLEICH, Markus, WILLNOW, Thomas E, MÜLLER, Dominik, THUMFART, Julia, STUIVER, Marchel, KOPPLIN, Kathrin, SOMMER, Kerstin, GÜNZEL, Dorothee, QUERFELD, Uwe, MEIJ, Iwan C, QIXIAN SHAN

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CNNM2, Encoding a Basolateral Protein Required for Renal Mg super(2+) Handling, Is Mutated in Dominant Hypomagnesemia von Stuiver, Marchel, Lainez, Sergio, Will, Constanze, Terryn, Sara, Guenzel, Dorothee, Debaix, Huguette, Sommer, Kerstin, Kopplin, Kathrin, Thumfart, Julia, Kampik, Nicole B, Querfeld, Uwe, Willnow, Thomas E, Nemec, Vladimir, Wagner, Carsten A, Hoenderop, Joost G, Devuyst, Olivier, Knoers, Nine VAM, Bindels, Rene J, Meij, Iwan C, Mueller, Dominik

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CNNM2, Encoding a Basolateral Protein Required for Renal Mg^sup 2+^ Handling, Is Mutated in Dominant Hypomagnesemia von Stuiver, Marchel, Lainez, Sergio, Will, Constanze, Terryn, Sara, Günzel, Dorothee, Debaix, Huguette, Sommer, Kerstin, Kopplin, Kathrin, Thumfart, Julia, Kampik, Nicole B, Querfeld, Uwe, Willnow, Thomas E, N-mec, Vladimír, Wagner, Carsten A, Hoenderop, Joost G, Devuyst, Olivier, Knoers, Nine VAM, Bindels, René J, Meij, Iwan C, Müller, Dominik

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