Neuronal KCNQ potassium channels: physiology and role in disease von Jentsch, T J

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A Potassium Channel Mutation in Neonatal Human Epilepsy von Biervert, Christian, Schroeder, Björn C., Kubisch, Christian, Berkovic, Samuel F., Propping, Peter, Jentsch, Thomas J., Steinlein, Ortrud K.

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Chloride channel diseases resulting from impaired transepithelial transport or vesicular function von Jentsch, Thomas J, Maritzen, Tanja, Zdebik, Anselm A

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ClC-7 expression levels critically regulate bone turnover, but not gastric acid secretion von Supanchart, C, Wartosch, L, Schlack, C, Kühnisch, J, Felsenberg, D, Fuhrmann, J.C, de Vernejoul, M.-C, Jentsch, T.J, Kornak, U

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A constitutively open potassium channel formed by KCNQ1 and KCNE3 von Schroeder, Björn C., Waldegger, Siegfried, Fehr, Susanne, Bleich, Markus, Warth, Richard, Greger, Rainer, Jentsch, Thomas J.

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Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy von Schroeder, Björn C., Kubisch, Christian, Stein, Valentin, Jentsch, Thomas J.

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Mutations in the a3 subunit of the vacuolar H+-ATPase cause infantile malignant osteopetrosis von KORNAK, U, SCHULZ, A, FRIEDRICH, W, UHLHAAS, S, KREMENS, B, VOIT, T, HASAN, C, BODE, U, JENTSCH, T. J, KUBISCH, C

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The CLC chloride channel family von Jentsch, T J, Friedrich, T, Schriever, A, Yamada, H

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Detection and differentiation of sensorineural hearing loss in mice using auditory steady-state responses and transient auditory brainstem responses von Pauli-Magnus, D, Hoch, G, Strenzke, N, Anderson, S, Jentsch, T.J, Moser, T

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Myokymia and Neonatal Epilepsy Caused by a Mutation in the Voltage Sensor of the KCNQ2 K+Channel von Dedek, Karin, Kunath, Bernhard, Kananura, Colette, Reuner, Ulrike, Jentsch, Thomas J., Steinlein, Ortrud K.

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Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias von Wollnik, Bernd, Schroeder, Björn C., Kubisch, Christian, Esperer, Hans D., Wieacker, Peter, Jentsch, Thomas J.

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Inhibition of KCNQ1-4 potassium channels expressed in mammalian cells via M1 muscarinic acetylcholine receptors von Selyanko, A. A., Hadley, J. K., Wood, I. C., Abogadie, F. C., Jentsch, T. J., Brown, D. A.

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Two physically distinct pores in the dimeric CIC-0 chloride channel von Ludewig, Uwe, Pusch, Michael, Jentsch, Thomas J.

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Functional and Structural Analysis of ClC-K Chloride Channels Involved in Renal Disease von Waldegger, Siegfried, Jentsch, Thomas J.

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Localization and induction by dehydration of ClC-K chloride channels in the rat kidney von Vandewalle, A, Cluzeaud, F, Bens, M, Kieferle, S, Steinmeyer, K, Jentsch, T. J

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De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females von Palmer, E E, Stuhlmann, T, Weinert, S, Haan, E, Van Esch, H, Holvoet, M, Boyle, J, Leffler, M, Raynaud, M, Moraine, C, van Bokhoven, H, Kleefstra, T, Kahrizi, K, Najmabadi, H, Ropers, H-H, Delgado, M R, Sirsi, D, Golla, S, Sommer, A, Pietryga, M P, Chung, W K, Wynn, J, Rohena, L, Bernardo, E, Hamlin, D, Faux, B M, Grange, D K, Manwaring, L, Tolmie, J, Joss, S, Cobben, J M, Duijkers, F A M, Goehringer, J M, Challman, T D, Hennig, F, Fischer, U, Grimme, A, Suckow, V, Musante, L, Nicholl, J, Shaw, M, Lodh, S P, Niu, Z, Rosenfeld, J A, Stankiewicz, P, Jentsch, T J, Gecz, J, Field, M, Kalscheuer, V M

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A common molecular basis for three inherited kidney stone diseases von Lloyd, Sarah E., Pearce, Simon H. S., Fisher, Simon E., Steinmeyer, Klaus, Schwappach, Blanche, Scheinman, Steven J., Harding, Brian, Bolino, Alessandra, Devoto, Marcella, Goodyer, Paul, Rigden, Susan P. A., Wrong, Oliver, Jentsch, Thomas J., Craig, Ian W., Thakker, Rajesh V.

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Properties of voltage-gated chloride channels of the ClC gene family von Jentsch, T J, Günther, W, Pusch, M, Schwappach, B

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Reply from L. P. Cid, T. J. Jentsch and F. V. Sepúlveda: intestinal electrolyte and fluid secretion – a model in trouble? von Cid, L. P., Jentsch, T. J., Sepúlveda, F. V.

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ClC-1 Chloride Channel Mutations in Myotonia Congenita: Variable Penetrance of Mutations Shifting the Voltage Dependence von Kubisch, Christian, Schmidt-Rose, Thomas, Fontaine, Bertrand, Bretag, Allan H., Jentsch, Thomas J.

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