Anzahl der Einträge in dieser Kategorie: 89.
2026
Forst, Anna-Lena 
,
Süß, Lena-Marie,
Süß, Anja,
Warth, Richard 
,
Broeker, Katharina A. E. 
,
Firmke, Bettina K. M. und
Tran, Linh Minh
(2026)
Data archive of Inhibition of (interstitial) P2Y<sub>6</sub> receptors attenuates fibrosis progression.
[Datensatz]
2025
2024
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 und
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. und
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).
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. 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.
Neubauer, Jacqueline 
,
Forst, Anna-Lena,
Warth, Richard 
,
Both, Christian Peter,
Haas, Cordula 
und
Thomas, Jörg 
(2022)
Genetic variants in eleven central and peripheral chemoreceptor genes in sudden infant death syndrome.
Pediatric Research 92 (4), S. 1026-1033.
Volltext nicht vorhanden.
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 und
Meister, Gunter
(2021)
Balancing of mitochondrial translation through METTL8-mediated m3C modification of mitochondrial tRNAs.
Molecular Cell 81 (23), 4810-4825.e12.
Volltext nicht vorhanden.
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. und
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), S. 1498-1512.
Volltext nicht vorhanden.
2020
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.
Penton, David,
Vohra, Twinkle,
Banki, Eszter,
Wengi, Agnieszka,
Weigert, Maria,
Forst, Anna-Lena,
Bandulik, Sascha,
Warth, Richard und
Loffing, Johannes 
(2020)
Collecting system–specific deletion of Kcnj10 predisposes for thiazide- and low-potassium diet–induced hypokalemia.
Kidney International 97 (6), S. 1208-1218.
Volltext nicht vorhanden.
Morin, Matias 
,
Forst, Anna-Lena,
Pérez-Torre, Paula,
Jiménez-Escrig, Adriano,
Barca-Tierno, Verónica,
García-Galloway, Eva,
Warth, Richard,
Lopez-Sendón Moreno, Jose Luis und
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), S. 135-143.
Volltext nicht vorhanden.
2019
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 
und
Kleta, R.
(2018)
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure.
J. Am. Soc. Nephrol. 29 (7), S. 1849-1858.
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.
2017
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.
2016
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 und
Reinders, Jörg
(2016)
Renal Fanconi Syndrome Is Caused by a Mistargeting-Based Mitochondriopathy.
Cell Reports (Cell Rep) 15 (7), S. 1423-1429.
Heitzmann, Dirk,
Buehler, Philipp 
,
Schweda, Frank,
Georgieff, Michael,
Warth, Richard 
und
Thomas, Joerg
(2016)
The in vivo respiratory phenotype of the adenosine A1 receptor knockout mouse.
Respiratory Physiology & Neurobiology 222, S. 16-28.
Volltext nicht vorhanden.
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. und
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.
Volltext nicht vorhanden.
2014
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 
und
Mulatero, Paolo
(2014)
Somatic ATP1A1 , ATP2B3 , and KCNJ5 Mutations in Aldosterone-Producing Adenomas.
Hypertension 63 (1), S. 188-195.
Volltext nicht vorhanden.
Kuppusamy, Maniselvan,
Caroccia, Brasilina,
Stindl, Julia,
Bandulik, Sascha,
Lenzini, Livia,
Gioco, Francesca,
Fishman, Veniamin 
,
Zanotti, Giuseppe,
Gomez-Sanchez, Celso,
Bader, Michael 
,
Warth, Richard 
und
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.
Volltext nicht vorhanden.
Warth, R.,
Bandulik, S.,
Barhanin, J.,
Reincke, M.,
Beuschlein, F.,
Sterner, C.,
Tegtmeier, I.,
Humberg, E.,
Stindl, J.,
Penton, D. und
Tauber, P. 
(2014)
Pharmacology and Pathophysiology of Mutated KCNJ5 Found in Adrenal Aldosterone-Producing Adenomas.
Endocrinology 155 (4), S. 1353-1362.
Volltext nicht vorhanden.
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 
und
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), S. 1830-1848.
Volltext nicht vorhanden.
Monticone, Silvia,
Hattangady, Namita G.,
Penton, David,
Isales, Carlos M.,
Edwards, Michael A.,
Williams, Tracy A.,
Sterner, Christina,
Warth, Richard 
,
Mulatero, Paolo und
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.
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.
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 und
Reincke, Martin
(2013)
Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension.
Nature Genetics 45 (4), S. 440-444.
Volltext nicht vorhanden.
2012
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 und
Reincke, Martin
(2012)
KCNJ5 Mutations in European Families With Nonglucocorticoid Remediable Familial Hyperaldosteronism.
Hypertension 59 (2), S. 235-240.
Volltext nicht vorhanden.
Williams, Tracy Ann,
Monticone, Silvia,
Crudo, Valentina,
Warth, Richard 
,
Veglio, Franco und
Mulatero, Paolo
(2012)
Visinin-Like 1 Is Upregulated in Aldosterone-Producing Adenomas With KCNJ5 Mutations and Protects From Calcium-Induced Apoptosis.
Hypertension 59 (4), S. 833-839.
Volltext nicht vorhanden.
El Wakil, Abeer 
,
Bandulik, Sascha,
Guy, Nicolas,
Bendahhou, Saïd,
Zennaro, Maria-Christina 
,
Niehrs, Christof,
Mari, Bernard 
,
Warth, Richard 
,
Barhanin, Jacques und
Lalli, Enzo 
(2012)
Dkk3 is a component of the genetic circuitry regulating aldosterone biosynthesis in the adrenal cortex.
Human Molecular Genetics 21 (22), S. 4922-4929.
Volltext nicht vorhanden.
Chatelain, Franck C.,
Bichet, Delphine 
,
Douguet, Dominique,
Feliciangeli, Sylvain 
,
Bendahhou, Saïd,
Reichold, Markus,
Warth, Richard 
,
Barhanin, Jacques und
Lesage, Florian 
(2012)
TWIK1, a unique background channel with variable ion selectivity.
Proceedings of the National Academy of Sciences 109 (14), S. 5499-5504.
Volltext nicht vorhanden.
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 
und
Penton, David
(2012)
Task3 Potassium Channel Gene Invalidation Causes Low Renin and Salt-Sensitive Arterial Hypertension.
Endocrinology 153 (10), S. 4740-4748.
Volltext nicht vorhanden.
2011
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 und
Bockenhauer, Detlef 
(2011)
Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome.
The Journal of Physiology 589 (7), S. 1681-1689.
Volltext nicht vorhanden.
Liu, Wen,
Schreck, Carlos,
Coleman, Richard A.,
Wade, James B.,
Hernandez, Yubelka,
Zavilowitz, Beth,
Warth, Richard 
,
Kleyman, Thomas R. und
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.
Volltext nicht vorhanden.
Bandulik, Sascha,
Schmidt, Katharina,
Bockenhauer, Detlef 
,
Zdebik, Anselm A.,
Humberg, Evelyn,
Kleta, Robert,
Warth, Richard 
und
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), S. 423-435.
Volltext nicht vorhanden.
2010
Preston, Patricia,
Wartosch, Lena,
Günzel, Dorothee,
Fromm, Michael 
,
Kongsuphol, Patthara,
Ousingsawat, Jiraporn,
Kunzelmann, Karl 
,
Barhanin, Jacques,
Warth, Richard 
und
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), S. 7165-7175.
Volltext nicht vorhanden.
Schreiber, Rainer,
Uliyakina, Inna 
,
Kongsuphol, Patthara,
Warth, Richard 
,
Mirza, Myriam,
Martins, Joana R. 
und
Kunzelmann, Karl 
(2010)
Expression and Function of Epithelial Anoctamins.
Journal of Biological Chemistry 285 (10), S. 7838-7845.
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.
Feliciangeli, Sylvain F. 
,
Bendahhou, Said,
Tardy, Magalie P.,
Sandoz, Guillaume,
Chatelain, Franck C.,
Reichold, Markus,
Warth, Richard 
,
Barhanin, Jacques und
Lesage, Florian 
(2010)
Membrane Trafficking Controls K2P1/TWIK1 Channel Expression at the Cell Surface.
Biophysical Journal 98 (3), 537a.
Volltext nicht vorhanden.
Feliciangeli, Sylvain 
,
Tardy, Magalie P.,
Sandoz, Guillaume 
,
Chatelain, Franck C.,
Warth, Richard 
,
Barhanin, Jacques,
Bendahhou, Saïd und
Lesage, Florian 
(2010)
Potassium Channel Silencing by Constitutive Endocytosis and Intracellular Sequestration.
Journal of Biological Chemistry 285 (7), S. 4798-4805.
Volltext nicht vorhanden.
2009
Lee, Wing-Kee 
,
Reichold, Markus,
Edemir, Bayram,
Ciarimboli, Giuliano 
,
Warth, Richard 
,
Koepsell, Hermann und
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.
Volltext nicht vorhanden.
2008
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.
2007
Feliciangeli, Sylvain 
,
Bendahhou, Saïd,
Sandoz, Guillaume 
,
Gounon, Pierre,
Reichold, Markus,
Warth, Richard 
,
Lazdunski, Michel,
Barhanin, Jacques und
Lesage, Florian 
(2007)
Does Sumoylation Control K2P1/TWIK1 Background K+ Channels?
Cell 130 (3), S. 563-569.
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.
2006
2005
Ullrich, Susanne,
Su, Jiping,
Ranta, Felicia,
Wittekindt, Oliver H.,
Ris, Frederic,
Rösler, Martin,
Gerlach, Uwe,
Heitzmann, Dirk,
Warth, Richard 
und
Lang, Florian
(2005)
Effects of IKs channel inhibitors in insulin-secreting INS-1 cells.
Pflügers Archiv - European Journal of Physiology 451 (3), S. 428-436.
Volltext nicht vorhanden.
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 und
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), S. 8215-8220.
Volltext nicht vorhanden.
Decressac, Sonia,
Franco, Michel,
Bendahhou, Said,
Warth, Richard 
,
Knauer, Sebastian,
Barhanin, Jacques,
Lazdunski, Michel und
Lesage, Florian 
(2004)
ARF6‐dependent interaction of the TWIK1 K+ channel with EFA6, a GDP/GTP exchange factor for ARF6.
EMBO reports 5 (12), S. 1171-1175.
Volltext nicht vorhanden.
Heitzmann, Dirk,
Grahammer, Florian,
von Hahn, Thomas,
Schmitt‐Gräff, Annette,
Romeo, Elisa,
Nitschke, Roland 
,
Gerlach, Uwe,
Lang, Hans Jochen,
Verrey, François 
,
Barhanin, Jacques und
Warth, Richard 
(2004)
Heteromeric KCNE2/KCNQ1 potassium channels in the luminal membrane of gastric parietal cells.
The Journal of Physiology 561 (2), S. 547-557.
Volltext nicht vorhanden.
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 und
Koizumi, Akio
(2004)
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.
Nature Genetics 36 (9), S. 999-1002.
Volltext nicht vorhanden.
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