Cloning and characterization of a putative human serine/threonine protein kinase transcriptionally modified during anisotonic and isotonic alterations of cell volume

Por Waldegger, Siegfried, Barth, Petra, Raber, Gertraud, Lang, Florian
Publicado em 1997

Potent stimulation and inhibition of the CFTR Cl(−) current by phloxine B

Por Bachmann, Alexander, Russ, Ulrich, Waldegger, Siegfried, Quast, Ulrich
Publicado em 2000

Claudin-4 forms paracellular chloride channel in the kidney and requires claudin-8 for tight junction localization

Por Hou, Jianghui, Renigunta, Aparna, Yang, Jing, Waldegger, Siegfried
Publicado em 2010

Tamm-Horsfall Glycoprotein Interacts with Renal Outer Medullary Potassium Channel ROMK2 and Regulates Its Function

Por Renigunta, Aparna, Renigunta, Vijay, Saritas, Turgay, Decher, Niels, Mutig, Kerim, Waldegger, Siegfried
Publicado em 2011

Claudin-16 and claudin-19 interaction is required for their assembly into tight junctions and for renal reabsorption of magnesium

Por Hou, Jianghui, Renigunta, Aparna, Gomes, Antonio S., Hou, Mingli, Paul, David L., Waldegger, Siegfried, Goodenough, Daniel A.
Publicado em 2009

Claudin-16 and claudin-19 interact and form a cation-selective tight junction complex

Por Hou, Jianghui, Renigunta, Aparna, Konrad, Martin, Gomes, Antonio S., Schneeberger, Eveline E., Paul, David L., Waldegger, Siegfried, Goodenough, Daniel A.
Publicado em 2008

Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia

Por Chubanov, Vladimir, Waldegger, Siegfried, Schnitzler, Michael Mederos y, Vitzthum, Helga, Sassen, Martin C., Seyberth, Hannsjörg W., Konrad, Martin, Gudermann, Thomas
Publicado em 2004

TGF-β directs trafficking of the epithelial sodium channel ENaC which has implications for ion and fluid transport in acute lung injury

Por Peters, Dorothea M., Vadász, István, Wujak, Łukasz, Wygrecka, Małgorzata, 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.
Publicado em 2014

Deficiency of the sphingosine-1-phosphate lyase SGPL1 is associated with congenital nephrotic syndrome and congenital adrenal calcifications

Por Janecke, Andreas R, Xu, Ruijuan, Steichen-Gersdorf, Elisabeth, Waldegger, Siegfried, Entenmann, Andreas, Giner, Thomas, Krainer, Iris, Huber, Lukas A, Hess, Michael W, Frishberg, Yaacov, Barash, Hila, Tzur, Shay, Schreyer-Shafir, Nira, Sukenik–Halevy, Rivka, Zehavi, Tania, Raas-Rothschild, Annick, Mao, Cungui, Müller, Thomas
Publicado no Hum Mutat (2017)

Mutations in the Tight-Junction Gene Claudin 19 (CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement

Por Konrad, Martin, Schaller, André, Seelow, Dominik, Pandey, Amit V., Waldegger, Siegfried, Lesslauer, Annegret, Vitzthum, Helga, Suzuki, Yoshiro, Luk, John M., Becker, Christian, Schlingmann, Karl P., Schmid, Marcel, Rodriguez-Soriano, Juan, Ariceta, Gema, Cano, Francisco, Enriquez, Ricardo, Jüppner, Harald, Bakkaloglu, Sevcan A., Hediger, Matthias A., Gallati, Sabina, Neuhauss, Stephan C. F., Nürnberg, Peter, Weber, Stefanie
Publicado em 2006