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Number of items at this level: 86.

2024

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

Plain, Allein , Knödl, Laura, Tegtmeier, Ines , Bandulik, Sascha and Warth, Richard (2024) The ex vivo perfused mouse adrenal gland—a new model to study aldosterone secretion. Pflügers Archiv - European Journal of Physiology 476, pp. 911-922.

Plain, Allein , Knödl, Laura and Warth, Richard (2024) The ex vivo perfused mouse adrenal gland - a new model to study aldosterone secretion. [Video]

Meindl, Katrin (2024) Die Rolle von EHD1 in der Spermatogenese - Untersuchungen zur Auswirkung der p.R398W-Mutation auf die männliche Fertilität. PhD, Universität Regensburg.

2023

Meindl, Katrin, Issler, Naomi, Afonso, Sara Cerqueira, Cebrian-Serrano, Alberto, Müller-Decker, Karin, Sterner, Christina, Othmen, Helga, Tegtmeier, Ines, Witzgall, Ralph, Klootwijk, Enriko D., Davies, Benjamin, Kleta, Robert and Warth, Richard (2023) A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility. Frontiers in Cell and Developmental Biology 11.

Stanzick, Kira J. , Stark, Klaus J., Gorski, Mathias , Schödel, Johannes, Krüger, René, Kronenberg, Florian, Warth, Richard , Heid, Iris M. and Winkler, Thomas W. (2023) KidneyGPS: a user-friendly web application to help prioritize kidney function genes and variants based on evidence from genome-wide association studies. BMC Bioinformatics 24 (1).

Lorenz, Sebastian (2023) Untersuchung der Migrations- und Adhäsionsfähigkeit von CLN7-knockout Zellen. PhD, Universität Regensburg.

2022

Gürtler, Florian (2022) Pathogenese des mutierten Ca2+-Kanals CACNA1H beim primären Hyperaldosteronismus und Rolle der zellulären pH-Homöostase für die Regulation der Aldosteronproduktion in Nebennierenzellen. PhD, 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. 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.

Lo, Jacky, Forst, Anna-Lena , Warth, Richard and Zdebik, Anselm A. (2022) EAST/SeSAME Syndrome and Beyond: The Spectrum of Kir4.1- and Kir5.1-Associated Channelopathies. Frontiers in Physiology 2022 (13), p. 852674.

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. UNSPECIFIED, Universität Regensburg. Fulltext not available.

Neubauer, Jacqueline , Forst, Anna-Lena, Warth, Richard , Both, Christian Peter, Haas, Cordula and Thomas, Jörg (2022) Genetic variants in eleven central and peripheral chemoreceptor genes in sudden infant death syndrome. Pediatric Research 92 (4), pp. 1026-1033. Fulltext not available.

2021

Schöller, Eva, Marks, James, Marchand, Virginie , Bruckmann, Astrid, Powell, Christopher A., Reichold, Markus, Mutti, Christian Daniel , Dettmer, Katja , Feederle, Regina , Hüttelmaier, Stefan, Helm, Mark, Oefner, Peter J., Minczuk, Michal , Motorin, Yuri , Hafner, Markus and Meister, Gunter (2021) Balancing of mitochondrial translation through METTL8-mediated m3C modification of mitochondrial tRNAs. Molecular Cell 81 (23), 4810-4825.e12. Fulltext not available.

Warth, Richard, Forst, Anna-Lena, Reichold, Markus and Kleta, Robert (2021) Distinct Mitochondrial Pathologies Caused by Mutations of the Proximal Tubular Enzymes EHHADH and GATM. Frontiers in Physiology 12 (715485), pp. 1-10. (Submitted)

Schlingmann, Karl P., Renigunta, Aparna, Hoorn, Ewout J., Forst, Anna-Lena, Renigunta, Vijay, Atanasov, Velko, Mahendran, Sinthura, Barakat, Tahsin Stefan , Gillion, Valentine, Godefroid, Nathalie, Brooks, Alice S., Lugtenberg, Dorien, Lake, Jennifer , Debaix, Huguette, Rudin, Christoph, Knebelmann, Bertrand, Tellier, Stephanie, Rousset-Rouvière, Caroline, Viering, Daan, de Baaij, Jeroen H. F. , Weber, Stefanie, Palygin, Oleg , Staruschenko, Alexander, Kleta, Robert, Houillier, Pascal, Bockenhauer, Detlef, Devuyst, Olivier, Vargas-Poussou, Rosa, Warth, Richard , Zdebik, Anselm A. and Konrad, Martin (2021) Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness. Journal of the American Society of Nephrology 32 (6), pp. 1498-1512. Fulltext not available.

2020

Döllerer, Hannes (2020) Bestimmung mitochondrialer und lysosomaler Parameter im Zuge der Untersuchung eines hereditären Fanconi-Syndroms. PhD, Universität Regensburg.

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.

Penton, David, Vohra, Twinkle, Banki, Eszter, Wengi, Agnieszka, Weigert, Maria, Forst, Anna-Lena, Bandulik, Sascha, Warth, Richard and Loffing, Johannes (2020) Collecting system–specific deletion of Kcnj10 predisposes for thiazide- and low-potassium diet–induced hypokalemia. Kidney International 97 (6), pp. 1208-1218. Fulltext not available.

Morin, Matias , Forst, Anna-Lena, Pérez-Torre, Paula, Jiménez-Escrig, Adriano, Barca-Tierno, Verónica, García-Galloway, Eva, Warth, Richard, Lopez-Sendón Moreno, Jose Luis and Moreno-Pelayo, Miguel Angel (2020) Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype. neurogenetics 21 (2), pp. 135-143. Fulltext not available.

2019

Afonso, Sara Cerqueira (2019) Role of EHD1 in Renal Proximal Tubular Endocytosis and Recycling. PhD, Universität Regensburg.

2018

Reichold, M., Klootwijk, E. D., Reinders, Jörg , Otto, E. A., Milani, M., Broeker, C., Laing, C., Wiesner, J., Devi, S., Zhou, W., Schmitt, R., Tegtmeier, I., Sterner, C., Doellerer, H., Renner, K., Oefner, Peter J. , Dettmer, Katja , Simbuerger, J., Witzgall, R., Stanescu, H. C., Dumitriu, S., Iancu, D., Patel, V., Mozere, M., Tekman, M., Jaureguiberry, G., Issler, N., Kesselheim, A., Walsh, S. B., Gale, D. P., Howie, A. J., Martins, J. R., Hall, A. M., Kasgharian, M., O'Brien, K., Ferreira, C. R., Atwal, P. S., Jain, M., Hammers, A., Charles-Edwards, G., Choe, C. U., Isbrandt, D., Cebrian-Serrano, A., Davies, B., Sandford, R. N., Pugh, C., Konecki, D. S., Povey, S., Bockenhauer, D., Lichter-Konecki, U., Gahl, W. A., Unwin, R. J., Warth, Richard and Kleta, R. (2018) Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure. J. Am. Soc. Nephrol. 29 (7), pp. 1849-1858. Fulltext not available.

Wiesner, Julia (2018) Mutationen des Fanconi-assoziierten Proteins 2 (FAP2) als Ursache einer erblichen renalen Tubulopathie. PhD, Universität Regensburg.

Quintanova, Catarina Isabel Rina (2018) The role of the inwardly rectifying potassium channel Kir5.1 in the distal convoluted tubule. PhD, Universität Regensburg.

Reichold, Markus, Klootwijk, Enriko D., Reinders, Joerg, Otto, Edgar A., Milani, Mario , Broeker, Carsten, Laing, Chris, Wiesner, Julia, Devi, Sulochana, Zhou, Weibin, Schmitt, Roland, Tegtmeier, Ines, Sterner, Christina, Doellerer, Hannes, Renner, Kathrin, Oefner, Peter J., Dettmer, Katja, Simbuerger, Johann M., Witzgall, Ralph, Stanescu, Horia C., Dumitriu, Simona, Iancu, Daniela, Patel, Vaksha, Mozere, Monika, Tekman, Mehmet , Jaureguiberry, Graciana, Issler, Naomi, Kesselheim, Anne, Walsh, Stephen B., Gale, Daniel P. , Howie, Alexander J., Martins, Joana R. , Hall, Andrew M., Kasgharian, Michael, O’Brien, Kevin, Ferreira, Carlos R., Atwal, Paldeep S., Jain, Mahim, Hammers, Alexander , Charles-Edwards, Geoffrey, Choe, Chi-Un, Isbrandt, Dirk, Cebrian-Serrano, Alberto, Davies, Ben, Sandford, Richard N., Pugh, Christopher, Konecki, David S., Povey, Sue, Bockenhauer, Detlef, Lichter-Konecki, Uta, Gahl, William A., Unwin, Robert J., Warth, Richard and Kleta, Robert (2018) Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure. Journal of the American Society of Nephrology 29 (7), pp. 1849-1858. Fulltext not available.

2017

Buehler, Philipp K., Bleiler, Doris, Tegtmeier, Ines, Heitzmann, Dirk, Both, Christian, Georgieff, Michael, Lesage, Florian , Warth, Richard and Thomas, Jörg (2017) Abnormal respiration under hyperoxia in TASK-1/3 potassium channel double knockout mice. Respiratory Physiology & Neurobiology 244, pp. 17-25. Fulltext not available.

Jungbauer, Stefan, Buehler, Philipp Karl , Neubauer, Jacqueline , Haas, Cordula , Heitzmann, Dirk, Tegtmeier, Ines, Sterner, Christina, Barhanin, Jacques, Georgieff, Michael, Warth, Richard and Thomas, Jörg (2017) Sex-dependent differences in the in vivo respiratory phenotype of the TASK-1 potassium channel knockout mouse. Respiratory Physiology & Neurobiology 245, pp. 13-28. Fulltext not available.

2016

Tondorf, Felizitas (2016) Pathophysiologie der p.A167V-Mutation von KCNJ10. PhD, Universität Regensburg.

Kattner, Anna-Sophia (2016) Untersuchungen zur Bedeutung von Kaliumkanälen für die geschlechtsspezifischen Unterschiede in der Aldosteronproduktion bei Task1-/- Mäusen. PhD, Universität Regensburg.

Assmann, Nadine, Dettmer, Katja , Simbürger, Johann, Broeker, Carsten, Nuernberger, Nadine, Renner, Kathrin, Courtneidge, H., Klootwijk, E. D., Duerkop, Axel , Hall, A., Kleta, R., Oefner, Peter J. , Reichold, Markus and Reinders, Jörg (2016) Renal Fanconi Syndrome Is Caused by a Mistargeting-Based Mitochondriopathy. Cell Reports (Cell Rep) 15 (7), pp. 1423-1429.

Broeker, Carsten (2016) Mitochondriopathien als Ursache des renalen Fanconi-Syndroms. PhD, Universität Regensburg.

Stindl, Julia (2016) Untersuchungen zur Entstehung des primären Hyperaldosteronismus: Einfluss von Mutationen der Na+/K+-ATPase auf adrenokortikale Zellen. PhD, Universität Regensburg.

Ripper, Maria (2016) Die Bedeutung des basolateralen Kalium-Kanals KCNJ10 für die Transportfunktion in der Niere. PhD, Universität Regensburg.

Heitzmann, Dirk, Buehler, Philipp , Schweda, Frank, Georgieff, Michael, Warth, Richard and Thomas, Joerg (2016) The in vivo respiratory phenotype of the adenosine A1 receptor knockout mouse. Respiratory Physiology & Neurobiology 222, pp. 16-28. Fulltext not available.

2015

Monticone, Silvia, Bandulik, Sascha, Stindl, Julia, Zilbermint, Mihail , Dedov, Ivan , Mulatero, Paolo, Allgaeuer, Michael , Lee, Chyi-Chia Richard, Stratakis, Constantine A., Williams, Tracy A. and Tiulpakov, Anatoly (2015) A Case of Severe Hyperaldosteronism Caused by a De Novo Mutation Affecting a Critical Salt Bridge Kir3.4 Residue. The Journal of Clinical Endocrinology & Metabolism 100 (1), E114-E118. Fulltext not available.

2014

Humberg, Evelyn (2014) Die physiologische und pathophysiologische Bedeutung von KCNJ16. PhD, Universität Regensburg.

Schmidt, Katharina Maria (2014) Renale Elektrolyt-Volumen-Homöostase und basolaterale Kaliumleitfähigkeit des distalen Konvoluts - ontogenetische und pathophysiologische Aspekte. PhD, Universität Regensburg.

Tauber, Philipp (2014) Untersuchungen zur Pathogenese von primärem Hyperaldosteronismus in neugeborenen Task3-/- Mäusen und adrenokortikalen Zellen mit KCNJ5-Mutation. PhD, Universität Regensburg.

Williams, Tracy Ann, Monticone, Silvia, Schack, Vivien R., Stindl, Julia, Burrello, Jacopo, Buffolo, Fabrizio, Annaratone, Laura , Castellano, Isabella , Beuschlein, Felix , Reincke, Martin, Lucatello, Barbara, Ronconi, Vanessa , Fallo, Francesco, Bernini, Giampaolo, Maccario, Mauro, Giacchetti, Gilberta, Veglio, Franco, Warth, Richard , Vilsen, Bente and Mulatero, Paolo (2014) Somatic ATP1A1 , ATP2B3 , and KCNJ5 Mutations in Aldosterone-Producing Adenomas. Hypertension 63 (1), pp. 188-195. Fulltext not available.

Kuppusamy, Maniselvan, Caroccia, Brasilina, Stindl, Julia, Bandulik, Sascha, Lenzini, Livia, Gioco, Francesca, Fishman, Veniamin , Zanotti, Giuseppe, Gomez-Sanchez, Celso, Bader, Michael , Warth, Richard and Rossi, Gian Paolo (2014) A Novel KCNJ5-insT149 Somatic Mutation Close to, but Outside, the Selectivity Filter Causes Resistant Hypertension by Loss of Selectivity for Potassium. The Journal of Clinical Endocrinology & Metabolism 99 (9), E1765-E1773. Fulltext not available.

Warth, R., Bandulik, S., Barhanin, J., Reincke, M., Beuschlein, F., Sterner, C., Tegtmeier, I., Humberg, E., Stindl, J., Penton, D. and Tauber, P. (2014) Pharmacology and Pathophysiology of Mutated KCNJ5 Found in Adrenal Aldosterone-Producing Adenomas. Endocrinology 155 (4), pp. 1353-1362. Fulltext not available.

2013

Burghardt, Tillmann, Kastner, Jürgen, Suleiman, Hani, Rivera-Milla, Eric, Stepanova, Natalya, Lottaz, Claudio, Kubitza, Marion, Böger, Carsten A., Schmidt, Sarah, Gorski, Mathias, de Vries, Uwe, Schmidt, Helga, Hertting, Irmgard, Kopp, Jeffrey , Rascle, Anne, Moser, Markus, Heid, Iris M., Warth, Richard , Spang, Rainer, Wegener, Joachim, Mierke, Claudia T. , Englert, Christoph and Witzgall, Ralph (2013) LMX1B is essential for the maintenance of differentiated podocytes in adult kidneys. Journal of the American Society of Nephrology : JASN 24 (11), pp. 1830-1848. Fulltext not available.

Monticone, Silvia, Hattangady, Namita G., Penton, David, Isales, Carlos M., Edwards, Michael A., Williams, Tracy A., Sterner, Christina, Warth, Richard , Mulatero, Paolo and Rainey, William E. (2013) A Novel Y152C KCNJ5 Mutation Responsible for Familial Hyperaldosteronism Type III. The Journal of Clinical Endocrinology & Metabolism 98 (11), E1861-E1865. Fulltext not available.

Schmidt, Katharina, Ripper, Maria, Tegtmeier, Ines, Humberg, Evelyn, Sterner, Christina, Reichold, Markus, Warth, Richard and Bandulik, Sascha (2013) Dynamics of Renal Electrolyte Excretion in Growing Mice. Nephron Physiology 124, pp. 7-13.

Warth, Richard, Barhanin, Jacques, Hartmann, Michaela, Lesage, Florian, Lalli, Enzo, Sterner, Christina, Tegtmeier, Ines , Schweda, Frank , Penton, David, Tauber, Philipp and Bandulik, Sascha (2013) Severe Hyperaldosteronism in Neonatal Task3 Potassium Channel Knockout Mice Is Associated With Activation of the Intraadrenal Renin-Angiotensin System. Endocrinology 154 (8), pp. 2712-2722. Fulltext not available.

Beuschlein, Felix , Boulkroun, Sheerazed , Osswald, Andrea, Wieland, Thomas, Nielsen, Hang N, Lichtenauer, Urs D, Penton, David, Schack, Vivien R, Amar, Laurence , Fischer, Evelyn, Walther, Anett, Tauber, Philipp, Schwarzmayr, Thomas, Diener, Susanne, Graf, Elisabeth, Allolio, Bruno, Samson-Couterie, Benoit, Benecke, Arndt, Quinkler, Marcus, Fallo, Francesco, Plouin, Pierre-Francois, Mantero, Franco, Meitinger, Thomas , Mulatero, Paolo, Jeunemaitre, Xavier, Warth, Richard , Vilsen, Bente , Zennaro, Maria-Christina , Strom, Tim M and Reincke, Martin (2013) Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension. Nature Genetics 45 (4), pp. 440-444. Fulltext not available.

2012

Peindl, Dominika Elisabeth (2012) Mitochondriales Maltargeting eines peroxisomalen Proteins als Ursache eines autosomal-dominant vererbten renalen Fanconi-Syndroms. PhD, UNSPECIFIED.

Utz, Doris (2012) Die Bedeutung des 2-P-Domänen-Kaliumkanals TASK3 für die Regulation der Atmung. PhD, Universität Regensburg.

Pentón Ribas, David (2012) The role of Task3 potassium channels in the regulation of aldosterone secretion in the adrenal gland. PhD, Universität Regensburg.

Mulatero, Paolo, Tauber, Philipp, Zennaro, Maria-Christina , Monticone, Silvia, Lang, Katharina, Beuschlein, Felix , Fischer, Evelyn, Tizzani, Davide, Pallauf, Anna, Viola, Andrea, Amar, Laurence , Williams, Tracy Ann, Strom, Tim M., Graf, Elisabeth, Bandulik, Sascha, Penton, David, Plouin, Pierre-François, Warth, Richard , Allolio, Bruno, Jeunemaitre, Xavier, Veglio, Franco and Reincke, Martin (2012) KCNJ5 Mutations in European Families With Nonglucocorticoid Remediable Familial Hyperaldosteronism. Hypertension 59 (2), pp. 235-240. Fulltext not available.

Williams, Tracy Ann, Monticone, Silvia, Crudo, Valentina, Warth, Richard , Veglio, Franco and Mulatero, Paolo (2012) Visinin-Like 1 Is Upregulated in Aldosterone-Producing Adenomas With KCNJ5 Mutations and Protects From Calcium-Induced Apoptosis. Hypertension 59 (4), pp. 833-839. Fulltext not available.

El Wakil, Abeer , Bandulik, Sascha, Guy, Nicolas, Bendahhou, Saïd, Zennaro, Maria-Christina , Niehrs, Christof, Mari, Bernard , Warth, Richard , Barhanin, Jacques and Lalli, Enzo (2012) Dkk3 is a component of the genetic circuitry regulating aldosterone biosynthesis in the adrenal cortex. Human Molecular Genetics 21 (22), pp. 4922-4929. Fulltext not available.

Chatelain, Franck C., Bichet, Delphine , Douguet, Dominique, Feliciangeli, Sylvain , Bendahhou, Saïd, Reichold, Markus, Warth, Richard , Barhanin, Jacques and Lesage, Florian (2012) TWIK1, a unique background channel with variable ion selectivity. Proceedings of the National Academy of Sciences 109 (14), pp. 5499-5504. Fulltext not available.

Barhanin, Jacques, Warth, Richard, Zennaro, Maria-Christina, Lalli, Enzo, Lesage, Florian, Budde, Thomas, El Wakil, Abeer, Cong, Lu Dang , Reichold, Markus, Tauber, Philipp , Haubs, Sophia , Schweda, Frank , Bandulik, Sascha and Penton, David (2012) Task3 Potassium Channel Gene Invalidation Causes Low Renin and Salt-Sensitive Arterial Hypertension. Endocrinology 153 (10), pp. 4740-4748. Fulltext not available.

2011

Dostert, Karin (2011) The role of PI3K p110gamma in chronic liver injury. PhD, Universität Regensburg.

Meier, Christine (2011) Das entwicklungsabhängige Expressionsmuster von Kaliumkanälen in der Niere. PhD, Universität Regensburg.

Thompson, Dorothy A. , Feather, Sally, Stanescu, Horia C., Freudenthal, Bernard , Zdebik, Anselm A., Warth, Richard , Ognjanovic, Milos, Hulton, Sally A., Wassmer, Evangeline, van't Hoff, William, Russell‐Eggitt, Isabelle, Dobbie, Angus, Sheridan, Eamonn, Kleta, Robert and Bockenhauer, Detlef (2011) Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome. The Journal of Physiology 589 (7), pp. 1681-1689. Fulltext not available.

Liu, Wen, Schreck, Carlos, Coleman, Richard A., Wade, James B., Hernandez, Yubelka, Zavilowitz, Beth, Warth, Richard , Kleyman, Thomas R. and Satlin, Lisa M. (2011) Role of NKCC in BK channel-mediated net K+secretion in the CCD. American Journal of Physiology-Renal Physiology 301 (5), F1088-F1097. Fulltext not available.

Bandulik, Sascha, Schmidt, Katharina, Bockenhauer, Detlef , Zdebik, Anselm A., Humberg, Evelyn, Kleta, Robert, Warth, Richard and Reichold, Markus (2011) The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel. Pflügers Archiv - European Journal of Physiology 461 (4), pp. 423-435. Fulltext not available.

2010

Singer, Katrin (2010) Die immunsuppressive Wirkung von Tumormetaboliten auf humane T-Zellen. PhD, Universität Regensburg.

Jungbauer, Stefan (2010) Untersuchungen an der Knockoutmaus zur Bedeutung des TASK1-Kaliumkanals für die Atmungs- und die Blutdruckregulation. PhD, Universität Regensburg.

Denzel, Andrea Johanna (2010) Bedeutung basophiler Granulozyten für das Zustandekommen einer humoralen Gedächtnisimmunantwort. PhD, Universität Regensburg.

Niedermeier, Marianne (2010) Die Abstammung von Fibrozyten und ihre Bedeutung bei der Entstehung einer Nierenfibrose. PhD, Universität Regensburg.

Bandulik, Sascha (2010) Untersuchungen zur Bedeutung der 2-P-Domänen-Kaliumkanäle TASK1 und TASK3 für die Funktion der Nebenniere. PhD, Universität Regensburg.

Preston, Patricia, Wartosch, Lena, Günzel, Dorothee, Fromm, Michael , Kongsuphol, Patthara, Ousingsawat, Jiraporn, Kunzelmann, Karl , Barhanin, Jacques, Warth, Richard and Jentsch, Thomas J. (2010) Disruption of the K+ Channel β-Subunit KCNE3 Reveals an Important Role in Intestinal and Tracheal Cl− Transport. Journal of Biological Chemistry 285 (10), pp. 7165-7175. Fulltext not available.

Schreiber, Rainer, Uliyakina, Inna , Kongsuphol, Patthara, Warth, Richard , Mirza, Myriam, Martins, Joana R. and Kunzelmann, Karl (2010) Expression and Function of Epithelial Anoctamins. Journal of Biological Chemistry 285 (10), pp. 7838-7845. Fulltext not available.

Reichold, Markus, Zdebik, Anselm A., Lieberer, Evelyn, Rapedius, Markus, Schmidt, Katharina, Bandulik, Sascha, Sterner, Christina, Tegtmeier, Ines, Penton, David, Baukrowitz, Thomas, Hulton, Sally-Anne, Witzgall, Ralph , Ben-Zeev, Bruria, Howie, Alexander J., Kleta, Robert, Bockenhauer, Detlef and Warth, Richard (2010) KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function. Proceedings of the National Academy of Sciences 107 (32), pp. 14490-14495. Fulltext not available.

Feliciangeli, Sylvain F. , Bendahhou, Said, Tardy, Magalie P., Sandoz, Guillaume, Chatelain, Franck C., Reichold, Markus, Warth, Richard , Barhanin, Jacques and Lesage, Florian (2010) Membrane Trafficking Controls K2P1/TWIK1 Channel Expression at the Cell Surface. Biophysical Journal 98 (3), 537a. Fulltext not available.

Feliciangeli, Sylvain , Tardy, Magalie P., Sandoz, Guillaume , Chatelain, Franck C., Warth, Richard , Barhanin, Jacques, Bendahhou, Saïd and Lesage, Florian (2010) Potassium Channel Silencing by Constitutive Endocytosis and Intracellular Sequestration. Journal of Biological Chemistry 285 (7), pp. 4798-4805. Fulltext not available.

Bandulik, S., Penton, D., Barhanin, J. and Warth, R. (2010) TASK1 and TASK3 Potassium Channels: Determinants of Aldosterone Secretion and Adrenocortical Zonation. Hormone and Metabolic Research 42 (06), pp. 450-457. Fulltext not available.

2009

Schütz, Christian (2009) Generierung von Killer-artifiziellen-antigenpräsentierenden Zellen (KaAPC) zur antigenspezifischen Eliminierung von humanen primären CD8+ zytotoxischen T-Lymphozyten in vitro. PhD, Universität Regensburg.

Koren, Viktoria (2009) Einfluss der Beta-Untereinheiten hKCNE1-3 auf die pH-Sensibilität und Pharmakologie des Kaliumkanals hKCNQ1. PhD, Universität Regensburg.

Röhrl, Johann (2009) Identifizierung und Charakterisierung von Beta-Defensin 14 der Maus. PhD, Universität Regensburg.

Lee, Wing-Kee , Reichold, Markus, Edemir, Bayram, Ciarimboli, Giuliano , Warth, Richard , Koepsell, Hermann and Thévenod, Frank (2009) Organic cation transporters OCT1, 2, and 3 mediate high-affinity transport of the mutagenic vital dye ethidium in the kidney proximal tubule. American Journal of Physiology-Renal Physiology 296 (6), F1504-F1513. Fulltext not available.

2008

Reichold, Markus (2008) Die physiologische Rolle des 2-P-Domänen Kaliumkanals TWIK1 in der Niere und im Pankreas. PhD, Universität Regensburg.

Heitzmann, Dirk, Derand, Renaud, Jungbauer, Stefan, Bandulik, Sascha, Sterner, Christina, Schweda, Frank, Wakil, Abeer El , Lalli, Enzo , Guy, Nicolas, Mengual, Raymond, Reichold, Markus, Tegtmeier, Ines, Bendahhou, Saïd, Gomez-Sanchez, Celso E, Isabel Aller, M , Wisden, William , Weber, Achim, Lesage, Florian , Warth, Richard and Barhanin, Jacques (2008) Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis. The EMBO Journal 27 (1), pp. 179-187. Fulltext not available.

Heitzmann, Dirk and Warth, Richard (2008) Physiology and Pathophysiology of Potassium Channels in Gastrointestinal Epithelia. Physiological Reviews 88 (3), pp. 1119-1182. Fulltext not available.

2007

Hofmann, Claudia (2007) Einfluss von Zell-Zell-Kontakten auf das Apoptoseverhalten primärer humaner Kolonepithelzellen. PhD, Universität Regensburg.

Feliciangeli, Sylvain , Bendahhou, Saïd, Sandoz, Guillaume , Gounon, Pierre, Reichold, Markus, Warth, Richard , Lazdunski, Michel, Barhanin, Jacques and Lesage, Florian (2007) Does Sumoylation Control K2P1/TWIK1 Background K+ Channels? Cell 130 (3), pp. 563-569. Fulltext not available.

Heitzmann, Dirk, Koren, Viktoria, Wagner, Michael , Sterner, Christina, Reichold, Markus, Tegtmeier, Ines, Volk, Tilmann and Warth, Richard (2007) KCNE Beta Subunits Determine pH Sensitivity of KCNQ1 Potassium Channels. Cellular Physiology and Biochemistry 19 (1-4), pp. 21-32. Fulltext not available.

Heitzmann, Dirk and Warth, Richard (2007) No Potassium, No Acid: K+Channels and Gastric Acid Secretion. Physiology 22 (5), pp. 335-341. Fulltext not available.

2006

Kritzenberger, M. and Wrobel, K.-H. (2006) Immunophenotyping and spatio-temporal distribution of aortic cell clusters in the bovine embryo. Anatomy and Embryology 211 (6), pp. 739-755. Fulltext not available.

2005

Ullrich, Susanne, Su, Jiping, Ranta, Felicia, Wittekindt, Oliver H., Ris, Frederic, Rösler, Martin, Gerlach, Uwe, Heitzmann, Dirk, Warth, Richard and Lang, Florian (2005) Effects of IKs channel inhibitors in insulin-secreting INS-1 cells. Pflügers Archiv - European Journal of Physiology 451 (3), pp. 428-436. Fulltext not available.

2004

Warth, Richard , Barrière, Hervé, Meneton, Pierre, Bloch, May, Thomas, Jörg, Tauc, Michel , Heitzmann, Dirk, Romeo, Elisa, Verrey, François, Mengual, Raymond, Guy, Nicolas, Bendahhou, Saïd, Lesage, Florian , Poujeol, Philippe and Barhanin, Jacques (2004) Proximal renal tubular acidosis in TASK2 K + channel-deficient mice reveals a mechanism for stabilizing bicarbonate transport. Proceedings of the National Academy of Sciences 101 (21), pp. 8215-8220. Fulltext not available.

Decressac, Sonia, Franco, Michel, Bendahhou, Said, Warth, Richard , Knauer, Sebastian, Barhanin, Jacques, Lazdunski, Michel and Lesage, Florian (2004) ARF6‐dependent interaction of the TWIK1 K+ channel with EFA6, a GDP/GTP exchange factor for ARF6. EMBO reports 5 (12), pp. 1171-1175. Fulltext not available.

Heitzmann, Dirk, Grahammer, Florian, von Hahn, Thomas, Schmitt‐Gräff, Annette, Romeo, Elisa, Nitschke, Roland , Gerlach, Uwe, Lang, Hans Jochen, Verrey, François , Barhanin, Jacques and Warth, Richard (2004) Heteromeric KCNE2/KCNQ1 potassium channels in the luminal membrane of gastric parietal cells. The Journal of Physiology 561 (2), pp. 547-557. Fulltext not available.

Kleta, Robert, Romeo, Elisa, Ristic, Zorica, Ohura, Toshihiro, Stuart, Caroline, Arcos-Burgos, Mauricio , Dave, Mital H, Wagner, Carsten A, Camargo, Simone R M , Inoue, Sumiko, Matsuura, Norio, Helip-Wooley, Amanda, Bockenhauer, Detlef , Warth, Richard , Bernardini, Isa, Visser, Gepke, Eggermann, Thomas, Lee, Philip, Chairoungdua, Arthit, Jutabha, Promsuk, Babu, Ellappan, Nilwarangkoon, Sirinun, Anzai, Naohiko, Kanai, Yoshikatsu, Verrey, Francois , Gahl, William A and Koizumi, Akio (2004) Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder. Nature Genetics 36 (9), pp. 999-1002. Fulltext not available.

This list was generated on Tue Jun 24 16:32:49 2025 CEST.
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