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Publications by Jordan, Katrin

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Jump to: 2022 | 2021 | 2020
Number of items: 4.

2022

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. and Warth, Richard (2022) A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. Journal of the American Society of Nephrology 33 (4), pp. 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. and Warth, Richard (2022) A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. Journal of the American Society of Nephrology 33. Fulltext not available.

2021

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 and Mycielska, Maria E. (2021) Cancer-associated cells release citrate to support tumour metastatic progression. Life Science Alliance 4 (6), e202000903.

2020

Gürtler, Florian, Jordan, Katrin, Tegtmeier, Ines, Herold, Janina , Stindl, Julia, Warth, Richard and Bandulik, Sascha (2020) Cellular Pathophysiology of Mutant Voltage-Dependent Ca2+ Channel CACNA1H in Primary Aldosteronism. Endocrinology 161 (10). Fulltext not available.

This list was generated on Wed Nov 29 13:10:31 2023 CET.
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