Einträge von Jordan, Katrin auf dem Publikationsserver

Jordan, Katrin (2024) Pathophysiology of EHD1-related hearing impairment. Dissertation, Universität Regensburg.

Issler, Naomi, Afonso, Sara, Weissman, Irith, Jordan, Katrin, Cebrian-Serrano, Alberto, Meindl, Katrin, Dahlke, Eileen, Tziridis, Konstantin, Yan, Guanhua, Robles-López, José M., Tabernero, Lydia , Patel, Vaksha, Kesselheim, Anne, Klootwijk, Enriko D., Stanescu, Horia C., Dumitriu, Simona, Iancu, Daniela, Tekman, Mehmet, Mozere, Monika, Jaureguiberry, Graciana, Outtandy, Priya, Russell, Claire, Forst, Anna-Lena, Sterner, Christina, Heinl, Elena-Sofia, Othmen, Helga, Tegtmeier, Ines, Reichold, Markus, Schiessl, Ina Maria , Limm, Katharina, Oefner, Peter, Witzgall, Ralph, Fu, Lifei, Theilig, Franziska, Schilling, Achim, Shuster Biton, Efrat, Kalfon, Limor, Fedida, Ayalla, Arnon-Sheleg, Elite, Ben Izhak, Ofer, Magen, Daniella, Anikster, Yair, Schulze, Holger, Ziegler, Christine, Lowe, Martin, Davies, Benjamin, Böckenhauer, Detlef, Kleta, Robert, Falik Zaccai, Tzipora C. und Warth, Richard (2022) A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. Journal of the American Society of Nephrology 33 (4), S. 732-745.

Issler, Naomi, Afonso, Sara Cerqueira, Weissman, Irith, Jordan, Katrin, Cebrian-Serrano, Alberto, Meindl, Katrin, Dahlke, Eileen, Tziridis, Konstantin, Yan, Guanhua, Robles-López, José M., Tabernero, Lydia , Patel, Vaksha, Kesselheim, Anne, Klootwijk, Enriko D., Stanescu, Horia C., Dumitriu, Simona, Iancu, Daniela, Tekman, Mehmet, Mozere, Monika, Jaureguiberry, Graciana, Outtandy, Priya, Russell, Claire, Forst, Anna-Lena, Sterner, Christina, Heinl, Elena-Sofia, Othmen, Helga, Tegtmeier, Ines, Reichold, Markus, Schiessl, Ina Maria , Limm, Katharina, Oefner, Peter J., Witzgall, Ralph, Fu, Lifei, Theilig, Franziska, Schilling, Achim, Shuster Biton, Efrat, Kalfon, Limor, Fedida, Ayalla, Arnon-Sheleg, Elite, Ben Izhak, Ofer, Magen, Daniella, Anikster, Yair, Schulze, Holger, Ziegler, Christine, Lowe, Martin, Davies, Benjamin, Böckenhauer, Detlef, Kleta, Robert, Falik Zaccai, Tzipora C. und Warth, Richard (2022) A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. Nicht ausgewählt, Universität Regensburg. Volltext nicht vorhanden.

Drexler, Konstantin, Schmidt, Katharina M., Jordan, Katrin , Federlin, Marianne, Milenkovic, Vladimir M., Liebisch, Gerhard , Artati, Anna, Schmidl, Christian , Madej, Gregor , Tokarz, Janina , Cecil, Alexander, Jagla, Wolfgang, Haerteis, Silke, Aung, Thiha, Wagner, Christine, Kolodziejczyk, Maria, Heinke, Stefanie, Stanton, Evan H., Schwertner, Barbara, Riegel, Dania, Wetzel, Christian H. , Buchalla, Wolfgang, Proescholdt, Martin, Klein, Christoph A., Berneburg, Mark, Schlitt, Hans J., Brabletz, Thomas, Ziegler, Christine , Parkinson, Eric K., Gaumann, Andreas, Geissler, Edward K., Adamski, Jerzy , Haferkamp, Sebastian und Mycielska, Maria E. (2021) Cancer-associated cells release citrate to support tumour metastatic progression. Life Science Alliance 4 (6), e202000903.

Gürtler, Florian, Jordan, Katrin, Tegtmeier, Ines, Herold, Janina , Stindl, Julia, Warth, Richard und Bandulik, Sascha (2020) Cellular Pathophysiology of Mutant Voltage-Dependent Ca2+ Channel CACNA1H in Primary Aldosteronism. Endocrinology 161 (10). Volltext nicht vorhanden.