Scientific Publications Search Search Author Impact Factor Release Date Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Bader, Michael Prof. Dr. (8) Bähring, Sylvia Dr. (4) Birchmeier, Walter Prof. Dr. (7) Birchmeier-Kohler, Carmen Prof. Dr. (4) Blankenstein, Thomas Prof. Dr. (9) Falcke, Martin Prof. Dr. (1) Fielitz, Jens Dr. (1) Gotthardt, Michael Prof. Dr. (1) Hammes-Lewin, Annette Dr. (1) Höpken, Uta Elisabeth PD Dr. (1) Ivics, Zoltan Dr. (2) Izsvak, Zsuzsanna Dr. (2) Kammertöns, Thomas Dr. (1) Kettenmann, Helmut Prof. Dr. (9) Kettritz, Ralph Prof. Dr. (3) Kühn, Ralf Dr. (3) Leutz, Achim Prof. Dr. (1) Lewin, Gary Prof. Dr. (6) Luft, Friedrich Prof. Dr. (58) Meyer, Irmtraud Margret Prof. Dr. (1) Morano, Ingo Prof. Dr. (8) Müller, Dominik Prof. Dr. (3) Niendorf, Thoralf Prof. Dr. (2) Pezzutto, Antonio Prof. Dr. (2) Rahn, Hans-Peter Dr. (1) Rajewsky, Klaus Prof. Dr. (1) Rajewsky, Nikolaus Prof. Dr. (2) Sander, Maike Prof. Dr. (1) Scheidereit, Claus Prof. Dr. (4) Schlag, Peter M. Prof. Dr. (3) Schulz-Menger, Jeanette Prof. Dr. (1) Sommer, Thomas Prof. Dr. (1) Spuler, Simone Prof. (2) Stein, Ulrike Prof. Dr. (6) Walther, Wolfgang Prof. Dr. (6) Wanker, Erich Prof. Dr. (7) Willimsky, Gerald Dr. (1) Willnow, Thomas Prof. Dr. (2) (-) Jentsch, Thomas Prof. Dr. (13) 1980 - 1989 (22) 1990 (2) 1991 (3) 1992 (3) 1993 (3) 1994 (11) 1995 (9) 1996 (8) 1997 (12) (-) 1998 (13) 1999 (5) 2000 (14) 2001 (11) 2002 (5) 2003 (4) 2004 (5) 2005 (8) 2006 (7) 2007 (4) 2008 (6) 2009 (6) 2011 (4) 2012 (5) 2013 (7) 2014 (10) 2015 (9) 2016 (9) 2017 (6) 2018 (12) 2019 (3) 2020 (10) 2021 (11) 2022 (4) 2023 (5) 2024 (5) 13 Results: Active Filter: Jentsch, Thomas Prof. Dr.1998 Sort: Result score Newest to oldest Oldest to newest November, 1998 / Pathol Biol (Paris) KCNQ2, the first gene found to be mutated in human generalized idiopathic epilepsy O.K. Steinlein T.J. Jentsch December 17, 1998 / Nature Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy B.C. Schroeder C. Kubisch V. Stein T.J. Jentsch December, 1998 / Kidney Int Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease T. Igarashi W. Guenther T. Sekine J. Inatomi H. Shiraga S. Takahashi J. Suzuki N. Tsuru T. Yanagihara M. Shimazu T.J. Jentsch R.V. Thakker September, 1998 / Curr Opin Nephrol Hypertens Molecular physiology of renal chloride channels K. Steinmeyer T.J. Jentsch October, 1998 / Hum Mol Genet ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependence C. Kubisch T. Schmidt-Rose B. Fontaine A.H. Bretag T.J. Jentsch July 07, 1998 / Proc Natl Acad Sci U S A ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells W. Guenther A. Luechow F. Cluzeaud A. Vandewalle T.J. Jentsch 1998 / Hum Mutat Molecular diagnosis of McArdle disease: revised genomic structure of the myophosphorylase gene and identification of a novel mutation C. Kubisch E.M. Wicklein T.J. Jentsch May, 1998 / J Gen Physiol Permeation and block of the skeletal muscle chloride channel, ClC-1, by foreign anions G.Y. Rychkov M. Pusch M.L. Roberts T.J. Jentsch A.H. Bretag June 12, 1998 / J Biol Chem Golgi localization and functionally important domains in the NH2 and COOH terminus of the yeast CLC putative chloride channel Gef1p B. Schwappach S. Stobrawa M. Hechenberger K. Steinmeyer T.J. Jentsch April, 1998 / Am J Physiol Endocrinol Metab Determinants of slow gating in ClC-0, the voltage-gated chloride channel of Torpedo marmorata P. Fong A. Rehfeldt T.J. Jentsch Pagination Current page 1 Page 2 Next page Next › Last page Last »
November, 1998 / Pathol Biol (Paris) KCNQ2, the first gene found to be mutated in human generalized idiopathic epilepsy O.K. Steinlein T.J. Jentsch
December 17, 1998 / Nature Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy B.C. Schroeder C. Kubisch V. Stein T.J. Jentsch
December, 1998 / Kidney Int Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease T. Igarashi W. Guenther T. Sekine J. Inatomi H. Shiraga S. Takahashi J. Suzuki N. Tsuru T. Yanagihara M. Shimazu T.J. Jentsch R.V. Thakker
September, 1998 / Curr Opin Nephrol Hypertens Molecular physiology of renal chloride channels K. Steinmeyer T.J. Jentsch
October, 1998 / Hum Mol Genet ClC-1 chloride channel mutations in myotonia congenita: variable penetrance of mutations shifting the voltage dependence C. Kubisch T. Schmidt-Rose B. Fontaine A.H. Bretag T.J. Jentsch
July 07, 1998 / Proc Natl Acad Sci U S A ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells W. Guenther A. Luechow F. Cluzeaud A. Vandewalle T.J. Jentsch
1998 / Hum Mutat Molecular diagnosis of McArdle disease: revised genomic structure of the myophosphorylase gene and identification of a novel mutation C. Kubisch E.M. Wicklein T.J. Jentsch
May, 1998 / J Gen Physiol Permeation and block of the skeletal muscle chloride channel, ClC-1, by foreign anions G.Y. Rychkov M. Pusch M.L. Roberts T.J. Jentsch A.H. Bretag
June 12, 1998 / J Biol Chem Golgi localization and functionally important domains in the NH2 and COOH terminus of the yeast CLC putative chloride channel Gef1p B. Schwappach S. Stobrawa M. Hechenberger K. Steinmeyer T.J. Jentsch
April, 1998 / Am J Physiol Endocrinol Metab Determinants of slow gating in ClC-0, the voltage-gated chloride channel of Torpedo marmorata P. Fong A. Rehfeldt T.J. Jentsch