Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Wirkungsfaktor Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend 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) 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) (-) Falcke, Martin Prof. Dr. (1) (-) Jentsch, Thomas Prof. Dr. (13) Mathematische Zellphysiologie (1) 1980 - 1989 (22) 1990 (2) 1991 (3) 1992 (6) 1993 (3) 1995 (10) 1996 (8) 1997 (15) (-) 1998 (14) 1999 (9) 2000 (20) 2001 (13) 2002 (8) 2003 (10) 2004 (10) 2005 (16) 2006 (8) 2007 (15) 2008 (18) 2009 (15) 2010 (22) 2011 (10) 2012 (19) 2013 (12) 2015 (11) 2016 (22) 2018 (20) 2020 (20) 2021 (32) 2022 (26) 2023 (31) 2024 (16) 14 Ergebnisse: Active Filter: Falcke, Martin Prof. Dr.Jentsch, Thomas Prof. Dr.1998 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste November 1998 / Pathol Biol (Paris) KCNQ2, the first gene found to be mutated in human generalized idiopathic epilepsy O.K. Steinlein T.J. Jentsch 17. Dezember 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 Dezember 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 Oktober 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 07. Juli 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 Mai 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 12. Juni 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 Seitennummerierung Aktuelle Seite 1 Seite 2 Nächste Seite Next › Letzte Seite 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
17. Dezember 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
Dezember 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
Oktober 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
07. Juli 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
Mai 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
12. Juni 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