Wissenschaftliche Publikationen Suche Suche Autor/in Veröffentlichungsdatum Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Akalin, Altuna Dr. (3) Alenina, Natalia Dr. (7) Bader, Michael Prof. Dr. (40) Bähring, Sylvia Dr. (5) Begay-Müller, Valerie Dr. (1) Bernert, Carola (1) Birchmeier, Walter Prof. Dr. (12) Birchmeier-Kohler, Carmen Prof. Dr. (19) Blankenstein, Thomas Prof. Dr. (11) Chekulaeva, Marina Dr. (2) Chen, Wei Prof. Dr. (4) Cöl Arslan, Seda Dr. (1) Daniel, Peter Prof. Dr. (7) Daumke, Oliver Prof. Dr. (2) Dechend, Ralf Priv. Doz. 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Mai 2009 / Pflugers Arch Physiological roles of CLC Cl(-)/H (+) exchangers in renal proximal tubules V. Plans G. Rickheit T.J. Jentsch 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 Nächste Seite Next › Letzte Seite Last »
01. Mai 2009 / Pflugers Arch Physiological roles of CLC Cl(-)/H (+) exchangers in renal proximal tubules V. Plans G. Rickheit T.J. Jentsch
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