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. (12) 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. (24) Kettritz, Ralph Prof. Dr. (3) Kühn, Ralf Dr. (6) 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. (10) Müller, Dominik Prof. Dr. (3) Niendorf, Thoralf Prof. Dr. (2) Pezzutto, Antonio Prof. Dr. (2) Rahn, Hans-Peter Dr. (1) Rajewsky, Klaus Prof. Dr. (4) 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. (7) Walther, Wolfgang Prof. Dr. (7) Wanker, Erich Prof. Dr. (8) Willimsky, Gerald Dr. (1) Willnow, Thomas Prof. Dr. (2) (-) Jentsch, Thomas Prof. Dr. (16) 1980 - 1989 (22) 1990 (2) (-) 1991 (3) 1992 (3) 1993 (3) 1994 (13) 1995 (15) 1996 (8) 1997 (17) (-) 1998 (13) 1999 (6) 2000 (14) 2001 (12) 2002 (9) 2003 (10) 2004 (10) 2005 (12) 2006 (18) 2007 (14) 2008 (20) 2009 (19) 2010 (29) 2011 (11) 2012 (12) 2013 (21) 2014 (22) 2015 (30) 2016 (18) 2019 (12) 2020 (14) 2021 (22) 2022 (18) 2023 (17) 2024 (4) 16 Results: Active Filter: Jentsch, Thomas Prof. Dr.19911998 Sort: Result score Newest to oldest Oldest to newest November 01, 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 01, 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 01, 1998 / Curr Opin Nephrol Hypertens Molecular physiology of renal chloride channels K. Steinmeyer T.J. Jentsch October 01, 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 January 01, 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 01, 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 01, 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 01, 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 01, 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 01, 1998 / Curr Opin Nephrol Hypertens Molecular physiology of renal chloride channels K. Steinmeyer T.J. Jentsch
October 01, 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
January 01, 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 01, 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 01, 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