Einträge von Reichold, Markus auf dem Publikationsserver

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.

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.

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

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.

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.

Klootwijk, Enriko D., Reichold, Markus, Helip-Wooley, Amanda, Tolaymat, Asad, Broeker, Carsten, Robinette, Steven, Reinders, Jörg, Peindl, Dominika Elisabeth, Renner, Kathrin, Eberhart, Karin, Aßmann, Nadine, Oefner, Peter J., Dettmer, Katja, Sterner, Christina, Schroeder, Josef, Zorger, Niels, Witzgall, Ralph, Reinhold, Stephan W., Stanescu, Horia C., Bockenhauer, Detlef, Jaureguiberry, Gracian, Courtneidge, Holly, Hall, Andrew M., Wijeyesekera, Anisha, Holmes, Elaine, Nicholson, Jeremy K., O'Brien, Kevin, Bernardini, Isa, Krasnewich, Donna M., Arcos-Burgos, Mauricio, Izumi, Yuichiro, Nonoguchi, Hiroshi, Jia, Yuzhi, Reddy, Janardan K., Ilya, Mohammad, Unwin, Robert J., Gahl, William A., Warth, Richard und Kleta, Robert (2014) Mistargeting of Peroxisomal EHHADH and Inherited Renal Fanconi's Syndrome. The New England Journal of Medicine 370, S. 129-138. 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.

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.

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.

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.

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.

Bockenhauer, Detlef , Feather, Sally, Stanescu, Horia C., Bandulik, Sascha, Zdebik, Anselm A., Reichold, Markus, Tobin, Jonathan, Lieberer, Evelyn, Sterner, Christina, Landoure, Guida, Arora, Ruchi, Sirimanna, Tony, Thompson, Dorothy , Cross, J. Helen, van't Hoff, William, Al Masri, Omar, Tullus, Kjell, Yeung, Stella, Anikster, Yair, Klootwijk, Enriko, Hubank, Mike , Dillon, Michael J., Heitzmann, Dirk, Arcos-Burgos, Mauricio , Knepper, Mark A., Dobbie, Angus, Gahl, William A., Warth, Richard , Sheridan, Eamonn und Kleta, Robert (2009) Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, andKCNJ10Mutations. New England Journal of Medicine 360 (19), S. 1960-1970. Volltext nicht vorhanden.

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.

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

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.