Number of items at this level: 86.
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 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).
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.
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.
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
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
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.
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
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.
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
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
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
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
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.
2009
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
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.
2007
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.
2006
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.