Scientific Publications Search Search Author Release Date Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Bader, Michael Prof. Dr. (8) Bähring, Sylvia Dr. (5) Birchmeier, Walter Prof. Dr. (5) Birchmeier-Kohler, Carmen Prof. Dr. (7) Blankenstein, Thomas Prof. Dr. (9) Dechend, Ralf Priv. Doz. (4) Falcke, Martin Prof. Dr. (2) Fielitz, Jens Dr. (1) Gerhardt, Holger Prof. Dr. (1) Gotthardt, Michael Prof. Dr. (1) Höpken, Uta Elisabeth PD Dr. (2) Hübner, Norbert Prof. Dr. (5) Ivics, Zoltan Dr. (3) Izsvak, Zsuzsanna Dr. (4) Kettenmann, Helmut Prof. Dr. (15) Kettritz, Ralph Prof. Dr. (1) Klußmann, Enno PD Dr. (2) Kocks, Christine Dr. (1) Kühn, Ralf Dr. (5) Lee, Young-Ae Prof. Dr. (2) Leutz, Achim Prof. Dr. (4) Lewin, Gary Prof. Dr. (5) Luft, Friedrich Prof. Dr. (53) Morano, Ingo Prof. Dr. (11) Müller, Dominik Prof. Dr. (1) Pezzutto, Antonio Prof. Dr. (2) Rahn, Hans-Peter Dr. (1) Rajewsky, Klaus Prof. Dr. (2) Rajewsky, Nikolaus Prof. Dr. (1) Rathjen, Fritz Prof. Dr. (1) Sander, Maike Prof. Dr. (2) Scheidereit, Claus Prof. Dr. (4) Spuler, Simone Prof. (3) Stein, Ulrike Prof. Dr. (7) Walther, Wolfgang Prof. Dr. (7) Wanker, Erich Prof. Dr. (4) Willimsky, Gerald Dr. (1) Willnow, Thomas Prof. Dr. (4) Wolf, Jana Prof. Dr. (2) (-) Jentsch, Thomas Prof. Dr. (12) 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 (13) 2002 (7) 2003 (7) 2004 (9) 2005 (14) 2006 (11) 2007 (5) 2008 (6) 2009 (8) 2010 (16) 2011 (6) 2012 (7) 2013 (8) 2015 (17) 2016 (11) 2017 (7) 2018 (16) 2019 (6) 2020 (21) 2021 (31) 2022 (16) 2023 (14) 2024 (14) 12 Results: Active Filter: Jentsch, Thomas Prof. Dr.1997 Sort: Result score Newest to oldest Oldest to newest October, 1997 / Hum Mol Genet Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias B. Wollnik B.C. Schroeder C. Kubisch H.D. Esperer P. Wieacker T.J. Jentsch August 15, 1997 / J Biol Chem Reconstitution of functional voltage-gated chloride channels from complementary fragments of CLC-1 T. Schmidt-Rose T.J. Jentsch August, 1997 / Hum Mol Genet Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders S.E. Lloyd W. Gunther S.H. Pearce A. Thomson M.L. Bianchi M. Bosio I.W. Craig S.E. Fisher S.J. Scheinman O. Wrong T.J. Jentsch R.V. Thakker August, 1997 / Biophys J Independent gating of single pores in CLC-0 chloride channels U. Ludewig M. Pusch T.J. Jentsch August, 1997 / J Gen Physiol Inward rectification in ClC-0 chloride channels caused by mutations in several protein regions U. Ludewig T.J. Jentsch M. Pusch July 08, 1997 / Proc Natl Acad Sci U S A Transmembrane topology of a CLC chloride channel T. Schmidt-Rose T.J. Jentsch May, 1997 / Am J Physiol Endocrinol Metab Localization and induction by dehydration of ClC-K chloride channels in the rat kidney A. Vandewalle F. Cluzeaud M. Bens S. Kieferle K. Steinmeyer T.J. Jentsch April 01, 1997 / EMBO J Molecular dissection of gating in the ClC-2 chloride channel S.E. Jordt T.J. Jentsch March 01, 1997 / J Clin Invest Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5) S.E. Lloyd S.H. Pearce W. Guenther H. Kawaguchi T. Igarashi T.J. Jentsch R.V. Thakker February 01, 1997 / J Physiol Analysis of a protein region involved in permeation and gating of the voltage-gated Torpedo chloride channel ClC-0 U. Ludewig T.J. Jentsch M. Pusch Pagination Current page 1 Page 2 Next page Next › Last page Last »
October, 1997 / Hum Mol Genet Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias B. Wollnik B.C. Schroeder C. Kubisch H.D. Esperer P. Wieacker T.J. Jentsch
August 15, 1997 / J Biol Chem Reconstitution of functional voltage-gated chloride channels from complementary fragments of CLC-1 T. Schmidt-Rose T.J. Jentsch
August, 1997 / Hum Mol Genet Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders S.E. Lloyd W. Gunther S.H. Pearce A. Thomson M.L. Bianchi M. Bosio I.W. Craig S.E. Fisher S.J. Scheinman O. Wrong T.J. Jentsch R.V. Thakker
August, 1997 / Biophys J Independent gating of single pores in CLC-0 chloride channels U. Ludewig M. Pusch T.J. Jentsch
August, 1997 / J Gen Physiol Inward rectification in ClC-0 chloride channels caused by mutations in several protein regions U. Ludewig T.J. Jentsch M. Pusch
July 08, 1997 / Proc Natl Acad Sci U S A Transmembrane topology of a CLC chloride channel T. Schmidt-Rose T.J. Jentsch
May, 1997 / Am J Physiol Endocrinol Metab Localization and induction by dehydration of ClC-K chloride channels in the rat kidney A. Vandewalle F. Cluzeaud M. Bens S. Kieferle K. Steinmeyer T.J. Jentsch
April 01, 1997 / EMBO J Molecular dissection of gating in the ClC-2 chloride channel S.E. Jordt T.J. Jentsch
March 01, 1997 / J Clin Invest Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5) S.E. Lloyd S.H. Pearce W. Guenther H. Kawaguchi T. Igarashi T.J. Jentsch R.V. Thakker
February 01, 1997 / J Physiol Analysis of a protein region involved in permeation and gating of the voltage-gated Torpedo chloride channel ClC-0 U. Ludewig T.J. Jentsch M. Pusch