Claudin-4 forms paracellular chloride channel in the kidney and requires claudin-8 for tight junction localization von Hou, Jianghui, Renigunta, Aparna, Yang, Jing, Waldegger, Siegfried, Burg, Maurice B.

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Disease Recurrence-The Sword of Damocles in Kidney Transplantation for Primary Focal Segmental Glomerulosclerosis von Kienzl-Wagner, Katrin, Waldegger, Siegfried, Schneeberger, Stefan

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Twelve-month outcome in juvenile proliferative lupus nephritis: results of the German registry study von Suhlrie, Adriana, Hennies, Imke, Gellermann, Jutta, Büscher, Anja, Hoyer, Peter, Waldegger, Siegfried, Wygoda, Simone, Beetz, Rolf, Lange-Sperandio, Bärbel, Klaus, Günter, Konrad, Martin, Holder, Martin, Staude, Hagen, Rascher, Wolfgang, Oh, Jun, Pape, Lars, Tönshoff, Burkhard, Haffner, Dieter

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Claudin-16 and claudin-19 interaction is required for their assembly into tight junctions and for renal reabsorption of magnesium von Hou, Jianghui, Renigunta, Aparna, Gomes, Antonio S, Hou, Mingli, Paul, David L, Waldegger, Siegfried, Goodenough, Daniel A

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Claudin-16 and claudin-19 interact and form a cation-selective tight junction complex von Hou, Jianghui, Renigunta, Aparna, Konrad, Martin, Gomes, Antonio S, Schneeberger, Eveline E, Paul, David L, Waldegger, Siegfried, Goodenough, Daniel A

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TGF-β directs trafficking of the epithelial sodium channel ENaC which has implications for ion and fluid transport in acute lung injury von Peters, Dorothea M, Vadász, István, Wujak, Lukasz, Wygrecka, Malgorzata, Olschewski, Andrea, Becker, Christin, Herold, Susanne, Papp, Rita, Mayer, Konstantin, Rummel, Sebastian, Brandes, Ralph P, Günther, Andreas, Waldegger, Siegfried, Eickelberg, Oliver, Seeger, Werner, Morty, Rory E

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Disruption of TRPM6/TRPM7 Complex Formation by a Mutation in the TRPM6 Gene Causes Hypomagnesemia with Secondary Hypocalcemia von Chubanov, Vladimir, Waldegger, Siegfried, Michael Mederos y Schnitzler, Vitzthum, Helga, Sassen, Martin C., Seyberth, Hannsjörg W., Konrad, Martin, Gudermann, Thomas, Jan, Lily Y.

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Functional Significance of Cell Volume Regulatory Mechanisms von LANG, FLORIAN, BUSCH, GILLIAN L, RITTER, MARKUS, VOLKL, HARALD, WALDEGGER, SIEGFRIED, GULBINS, ERICH, HAUSSINGER, DIETER

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Colocalization of KCNQ1/KCNE channel subunits in the mouse gastrointestinal tract von Dedek, K, Waldegger, S

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Intracellular Anions as the Voltage Sensor of Prestin, the Outer Hair Cell Motor Protein von Oliver, Dominik, David Z. Z. He, Klöcker, Nikolaj, Ludwig, Jost, Schulte, Uwe, Waldegger, Siegfried, Ruppersberg, J. P., Dallos, Peter, Fakler, Bernd

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Hypomagnesemia with Secondary Hypocalcemia due to a Missense Mutation in the Putative Pore-forming Region of TRPM6 von Chubanov, Vladimir, Schlingmann, Karl P., Wäring, Janine, Heinzinger, Jolanta, Kaske, Silke, Waldegger, Siegfried, Schnitzler, Michael Mederos y, Gudermann, Thomas

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A constitutively open potassium channel formed by KCNQ1 and KCNE3 von Jentsch, Thomas J, Schroeder, Björn C, Waldegger, Siegfried, Fehr, Susanne, Bleich, Markus, Warth, Richard, Greger, Rainer

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Cloning and Characterization of a Putative Human Serine/Threonine Protein Kinase Transcriptionally Modified during Anisotonic and Isotonic Alterations of Cell Volume von Waldegger, Siegfried, Barth, Petra, Raber, Gertraud, Lang, Florian

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Successful management of recurrent focal segmental glomerulosclerosis von Kienzl-Wagner, Katrin, Rosales, Alejandra, Scheidl, Stefan, Giner, Thomas, Bösmüller, Claudia, Rudnicki, Michael, Oberhuber, Rupert, Margreiter, Christian, Soleiman, Afschin, Öfner, Dietmar, Waldegger, Siegfried, Schneeberger, Stefan

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A common sequence variation of the CLCNKB gene strongly activates ClC-Kb chloride channel activity von Jeck, Nikola, Waldegger, Petra, Doroszewicz, Jolanta, Seyberth, Hannsjörg, Waldegger, Siegfried

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Late-onset manifestation of antenatal bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl- co-transporter von PRESSLER, Carsten A, HEINZINGER, Jolanta, JECK, Nikola, WALDEGGER, Petra, PECHMANN, Ulla, REINALTER, Stephan, KONRAD, Martin, BEETZ, Rolf, SEYBERTH, Hannsjörg W, WALDEGGER, Siegfried

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Salt handling in the distal nephron: lessons learned from inherited human disorders von Jeck, Nikola, Schlingmann, Karl P, Reinalter, Stephan C, Komhoff, Martin, Peters, Melanie, Waldegger, Siegfried, Seyberth, Hannsjorg W

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Salt wasting and deafness resulting from mutations in two chloride channels von SCHLINGMANN, Karl P, KONRAD, Martin, JECK, Nikola, WALDEGGER, Petra, REINALTER, Stephan C, HOLDER, Martin, SEYBERTH, Hannsjörg W, WALDEGGER, Siegfried

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Activating Mutation of the Renal Epithelial Chloride Channel ClC-Kb Predisposing to Hypertension von Jeck, Nikola, Waldegger, Siegfried, Lampert, Angelika, Boehmer, Christoph, Waldegger, Petra, Lang, Philipp A, Wissinger, Bernd, Friedrich, Björn, Risler, Teut, Moehle, Robert, Lang, Undine E, Zill, Peter, Bondy, Brigitta, Schaeffeler, Elke, Asante-Poku, Stephen, Seyberth, Hannsjörg, Schwab, Matthias, Lang, Florian

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Functional and Structural Analysis of ClC-K Chloride Channels Involved in Renal Disease von Waldegger, Siegfried, Jentsch, Thomas J.

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