Resultats de la cerca - Markus Reichold

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  1. 1
    Renal Fanconi syndrome: taking a proximal look at the nephron

    Renal Fanconi syndrome: taking a proximal look at the nephron per Enriko Klootwijk, Markus Reichold, Robert J. Unwin, Robert Kleta, Richard Warth, Detlef Böckenhauer

    Publicat 2014
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  2. 2
    Does Sumoylation Control K2P1/TWIK1 Background K+ Channels?

    Does Sumoylation Control K2P1/TWIK1 Background K+ Channels? per Sylvain Féliciangéli, Saı̈d Bendahhou, Guillaume Sandoz, Pierre Gounon, Markus Reichold, Richard Warth, Michel Lazdunski, Jacques Barhanin, Florian Lesage

    Publicat 2007
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  3. 3
    TWIK1, a unique background channel with variable ion selectivity

    TWIK1, a unique background channel with variable ion selectivity per Franck C. Chatelain, Delphine Bichet, Dominique Douguet, Sylvain Féliciangéli, Saı̈d Bendahhou, Markus Reichold, Richard Warth, Jacques Barhanin, Florian Lesage

    Publicat 2012
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  4. 4
    Task3 Potassium Channel Gene Invalidation Causes Low Renin and Salt-Sensitive Arterial Hypertension

    Task3 Potassium Channel Gene Invalidation Causes Low Renin and Salt-Sensitive Arterial Hypertension per David Pentón, Sascha Bandulik, Frank Schweda, Sophia Haubs, Philipp Tauber, Markus Reichold, Lu Dang Cong, Abeer El Wakil, Thomas Budde, Florian Lesage, Enzo Lalli, Maria‐Christina Zennaro, Richard Warth, Jacques Barhanin

    Publicat 2012
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  5. 5
    Balancing of mitochondrial translation through METTL8-mediated m3C modification of mitochondrial tRNAs

    Balancing of mitochondrial translation through METTL8-mediated m3C modification of mitochondrial tRNAs per Eva Schöller, James Marks, Virginie Marchand, Astrid Bruckmann, Christopher A. Powell, Markus Reichold, Christian D. Mutti, Katja Dettmer, Regina Feederle, Stefan Hüttelmaier, Mark Helm, Peter J. Oefner, Michal Minczuk, Yuri Motorin, Markus Hafner, Gunter Meister

    Publicat 2021
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  6. 6
    KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function

    KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function per Markus Reichold, Anselm A. Zdebik, Evelyn Lieberer, Markus Rapedius, Katharina Schmidt, Sascha Bandulik, Christina Sterner, Ines Tegtmeier, David Pentón, Thomas Baukrowitz, Sally‐Anne Hulton, Ralph Witzgall, Bruria Ben‐Zeev, Alexander J. Howie, Robert Kleta, Detlef Böckenhauer, Richard Warth

    Publicat 2010
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  7. 7
    Task2 potassium channels set central respiratory CO <sub>2</sub> and O <sub>2</sub> sensitivity

    Task2 potassium channels set central respiratory CO <sub>2</sub> and O <sub>2</sub> sensitivity per Christian Gestreau, Dirk Heitzmann, Joerg Thomas, Véronique Dubreuil, Sascha Bandulik, Markus Reichold, Saı̈d Bendahhou, Patricia Pierson, Christina Sterner, Julie Peyronnet, Chérif Benfriha, Ines Tegtmeier, Hannah Ehnes, Michael Georgieff, Florian Lesage, Jean‐François Brunet, Christo Goridis, Richard Warth, Jacques Barhanin

    Publicat 2010
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  8. 8
    Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis

    Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis per Dirk Heitzmann, Renaud Dérand, Stefan Jungbauer, Sascha Bandulik, Christina Sterner, Frank Schweda, Abeer El Wakil, Enzo Lalli, Nicolas Guy, Raymond Mengual, Markus Reichold, Ines Tegtmeier, Saı̈d Bendahhou, Celso E. Gómez-Sánchez, M. Isabel Aller, William Wisden, Achim Weber, Florian Lesage, Richard Warth, Jacques Barhanin

    Publicat 2007
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  9. 9
    Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and<i>KCNJ10</i>Mutations

    Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and<i>KCNJ10</i>Mutations per Detlef Böckenhauer, Sally Feather, Horia Stanescu, Sascha Bandulik, Anselm A. Zdebik, Markus Reichold, Jonathan L. Tobin, Evelyn Lieberer, Christina Sterner, Guida Landouré, Ruchi Arora, Tony Sirimanna, Dorothy Thompson, J. Helen Cross, William van’t Hoff, Omar Masri, Kjell Tullus, Stella Yeung, Yair Anikster, Enriko Klootwijk, Michael Hubank, Michael J. Dillon, Dirk Heitzmann, Mauricio Arcos‐Burgos, Mark A. Knepper, Angus Dobbie, William A. Gahl, Richard Warth, Eamonn Sheridan, Robert Kleta

    Publicat 2009
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  10. 10
    Mistargeting of Peroxisomal EHHADH and Inherited Renal Fanconi's Syndrome

    Mistargeting of Peroxisomal EHHADH and Inherited Renal Fanconi's Syndrome per Enriko Klootwijk, Markus Reichold, Amanda Helip‐Wooley, Asad Tolaymat, Carsten Broeker, Steven L. Robinette, Jörg Reinders, Dominika Elisabeth Peindl, Kathrin Renner, Karin Eberhart, Nadine Aßmann, Peter J. Oefner, Katja Dettmer, Christina Sterner, Josef Schroeder, Niels Zorger, Ralph Witzgall, Stephan W. Reinhold, Horia Stanescu, Detlef Böckenhauer, Graciana Jaureguiberry, Holly Courtneidge, Andrew M. Hall, Anisha Wijeyesekera, Elaine Holmes, Jeremy K. Nicholson, Kevin O’Brien, Isa Bernardini, Donna M. Krasnewich, Mauricio Arcos‐Burgos, Yuichiro Izumi, Hiroshi Nonoguchi, Yuzhi Jia, Janardan K. Reddy, Mohammad Ilyas, Robert J. Unwin, William A. Gahl, Richard Warth, Robert Kleta

    Publicat 2014
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  11. 11
    Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure

    Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure per Markus Reichold, Enriko Klootwijk, Jörg Reinders, Edgar A. Otto, Mario Milani, Carsten Broeker, Chris Laing, J. Wiesner, Sulochana Devi, Weibin Zhou, Roland Schmitt, Ines Tegtmeier, Christina Sterner, Hannes Doellerer, Kathrin Renner, Peter J. Oefner, Katja Dettmer, Johann M.B. Simbuerger, Ralph Witzgall, Horia Stanescu, Simona Dumitriu, Daniela Iancu, Vaksha Patel, Monika Mozere, Mehmet Tekman, Graciana Jaureguiberry, Naomi Issler, Anne Kesselheim, Stephen B. Walsh, Daniel P. Gale, Alexander J. Howie, Joana Raquel Martins, Andrew M. Hall, Michael Kasgharian, Kevin O’Brien, Carlos R. Ferreira, Paldeep S. Atwal, Mahim Jain, Alexander Hammers, Geoff Charles‐Edwards, Chi‐un Choe, Dirk Isbrandt, Alberto Cebrian-Serrano, Benjamin Davies, Richard Sandford, Christopher W. Pugh, David Konecki, Sue Povey, Detlef Böckenhauer, Uta Lichter‐Konecki, William A. Gahl, Robert J. Unwin, Richard Warth, Robert Kleta

    Publicat 2018
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