Anzahl der Einträge: 15.
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 und
Warth, Richard
(2023)
A missense mutation in Ehd1 associated with defective spermatogenesis and male infertility.
Frontiers in Cell and Developmental Biology 11.
Heinl, Elena-Sofia,
Lorenz, Sebastian,
Schmidt, Barbara ,
Laqtom, Nouf Nasser M.,
Mazzulli, Joseph R.,
Francelle, Laetitia ,
Yu, Timothy W.,
Greenberg, Benjamin ,
Storch, Stephan,
Tegtmeier, Ines,
Othmen, Helga,
Maurer, Katja,
Steinfurth, Malin,
Witzgall, Ralph,
Milenkovic, Vladimir M.,
Wetzel, Christian H. und
Reichold, Markus
(2022)
CLN7/MFSD8 may be an important factor for SARS-CoV-2 cell entry.
iScience 25 (10), S. 105082.
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.
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.
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 und
Kleta, Robert
(2018)
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.
Journal of the American Society of Nephrology 29 (7), S. 1849-1858.
Volltext nicht vorhanden.
Buehler, Philipp K.,
Bleiler, Doris,
Tegtmeier, Ines,
Heitzmann, Dirk,
Both, Christian,
Georgieff, Michael,
Lesage, Florian ,
Warth, Richard und
Thomas, Jörg
(2017)
Abnormal respiration under hyperoxia in TASK-1/3 potassium channel double knockout mice.
Respiratory Physiology & Neurobiology 244, S. 17-25.
Volltext nicht vorhanden.
Jungbauer, Stefan,
Buehler, Philipp Karl ,
Neubauer, Jacqueline ,
Haas, Cordula ,
Heitzmann, Dirk,
Tegtmeier, Ines,
Sterner, Christina,
Barhanin, Jacques,
Georgieff, Michael,
Warth, Richard und
Thomas, Jörg
(2017)
Sex-dependent differences in the in vivo respiratory phenotype of the TASK-1 potassium channel knockout mouse.
Respiratory Physiology & Neurobiology 245, S. 13-28.
Volltext nicht vorhanden.
Schmidt, Katharina,
Ripper, Maria,
Tegtmeier, Ines,
Humberg, Evelyn,
Sterner, Christina,
Reichold, Markus,
Warth, Richard und
Bandulik, Sascha
(2013)
Dynamics of Renal Electrolyte Excretion in Growing Mice.
Nephron Physiology 124, S. 7-13.
Warth, Richard,
Barhanin, Jacques,
Hartmann, Michaela,
Lesage, Florian,
Lalli, Enzo,
Sterner, Christina,
Tegtmeier, Ines ,
Schweda, Frank ,
Penton, David,
Tauber, Philipp und
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), S. 2712-2722.
Volltext nicht vorhanden.
Gestreau, Christian ,
Heitzmann, Dirk,
Thomas, Joerg,
Dubreuil, Véronique,
Bandulik, Sascha,
Reichold, Markus,
Bendahhou, Saïd,
Pierson, Patricia,
Sterner, Christina,
Peyronnet-Roux, Julie,
Benfriha, Chérif,
Tegtmeier, Ines,
Ehnes, Hannah,
Georgieff, Michael,
Lesage, Florian ,
Brunet, Jean-Francois,
Goridis, Christo,
Warth, Richard und
Barhanin, Jacques
(2010)
Task2 potassium channels set central respiratory CO 2 and O 2 sensitivity.
Proceedings of the National Academy of Sciences 107 (5), S. 2325-2330.
Volltext nicht vorhanden.
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 und
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), S. 14490-14495.
Volltext nicht vorhanden.
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 und
Barhanin, Jacques
(2008)
Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis.
The EMBO Journal 27 (1), S. 179-187.
Volltext nicht vorhanden.
Heitzmann, Dirk,
Koren, Viktoria,
Wagner, Michael ,
Sterner, Christina,
Reichold, Markus,
Tegtmeier, Ines,
Volk, Tilmann und
Warth, Richard
(2007)
KCNE Beta Subunits Determine pH Sensitivity of KCNQ1 Potassium Channels.
Cellular Physiology and Biochemistry 19 (1-4), S. 21-32.
Volltext nicht vorhanden.
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