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(2) (-) Poulet, James Prof. Dr. (1) (-) Yilmaz, Zekiye Buket Dr. (1) Animal Phenotyping (1) Genetik von Angeborenen Herzerkrankungen (2) Integrative Vaskuläre Biologie (10) Neuronale Schaltkreise und Verhalten (1) 1980 - 1989 (22) 1990 (2) 1991 (3) 1992 (3) 1993 (3) 1994 (11) 1995 (9) 1996 (9) (-) 1997 (13) 1998 (13) 1999 (9) 2000 (20) 2001 (13) 2002 (11) 2003 (12) 2004 (11) 2005 (13) 2006 (14) 2007 (10) (-) 2008 (19) 2009 (15) 2010 (16) 2011 (19) 2012 (14) 2013 (18) 2014 (22) 2015 (25) 2016 (20) 2017 (19) 2018 (25) 2019 (21) 2020 (14) 2021 (22) 2022 (24) 2023 (20) 2024 (5) 32 Ergebnisse: Active Filter: Gerhardt, Holger Prof. Dr.Jentsch, Thomas Prof. Dr.Klaassen, Sabine Prof. Dr. med.Poulet, James Prof. Dr.Yilmaz, Zekiye Buket Dr.19972008 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 01. Januar 2008 Focused Review: Ventricular noncompaction: an update S. Klaassen 01. Oktober 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 15. August 1997 / J Biol Chem Reconstitution of functional voltage-gated chloride channels from complementary fragments of CLC-1 T. Schmidt-Rose T.J. Jentsch 01. 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 01. August 1997 / Biophys J Independent gating of single pores in CLC-0 chloride channels U. Ludewig M. Pusch T.J. Jentsch 01. 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 08. Juli 1997 / Proc Natl Acad Sci U S A Transmembrane topology of a CLC chloride channel T. Schmidt-Rose T.J. Jentsch 01. Mai 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 01. April 1997 / EMBO J Molecular dissection of gating in the ClC-2 chloride channel S.E. Jordt T.J. Jentsch 01. März 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 Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 Nächste Seite Next › Letzte Seite Last »
01. Oktober 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
15. August 1997 / J Biol Chem Reconstitution of functional voltage-gated chloride channels from complementary fragments of CLC-1 T. Schmidt-Rose T.J. Jentsch
01. 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
01. August 1997 / Biophys J Independent gating of single pores in CLC-0 chloride channels U. Ludewig M. Pusch T.J. Jentsch
01. 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
08. Juli 1997 / Proc Natl Acad Sci U S A Transmembrane topology of a CLC chloride channel T. Schmidt-Rose T.J. Jentsch
01. Mai 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
01. April 1997 / EMBO J Molecular dissection of gating in the ClC-2 chloride channel S.E. Jordt T.J. Jentsch
01. März 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