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März 2006 / Nature ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function P.F. Lange L. Wartosch T.J. Jentsch J.C. Fuhrmann 08. Februar 2006 / EMBO J Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness T. Kharkovets K. Dedek H. Maier M. Schweizer D. Khimich R. Nouvian V. Vardanyan R. Leuwer T. Moser T.J. Jentsch 03. März 2006 / Circ Res Neurogenic mechanisms contribute to hypertension in mice with disruption of the K-Cl cotransporter KCC3 M.B. Rust J. Faulhaber M.K. Budack P. Pfeffer T. Maritzen M. Didie F.X. Beck T. Boettger R. Schubert H. Ehmke T.J. Jentsch C.A. Huebner 01. Juli 1995 / Phys Rev E Cluster formation, standing waves, and stripe patterns in oscillatory active media with local and global coupling M. Falcke H. Engel M. Neufeld 01. Juni 2006 / Phys Rev E Frequency of elemental events of intracellular Ca(2+) dynamics R. Thul M. Falcke 22. Mai 2006 / J Cell Biol M line-deficient titin causes cardiac lethality through impaired maturation of the sarcomere S. Weinert N. Bergmann X. Luo B. Erdmann M. Gotthardt 12. September 2006 / Proc Natl Acad Sci U S A Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6 M. Poet U. Kornak M. Schweizer A.A. Zdebik O. Scheel S. Hoelter W. Wurst A. Schmitt J.C. Fuhrmann R. Planells-Cases S.E. Mole C.A. Huebner T.J. Jentsch 29. Dezember 1995 / J Biol Chem Cloning and functional expression of rat CLC-5, a chloride channel related to kidney disease K. Steinmeyer B. Schwappach M. Bens A. Vandewalle T.J. Jentsch 11. Dezember 1995 / FEBS Lett ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family S. Brandt T.J. Jentsch 01. Dezember 1995 / Neuron Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel M. Pusch K. Steinmeyer M.C. Koch T.J. 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09. März 2006 / Nature ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function P.F. Lange L. Wartosch T.J. Jentsch J.C. Fuhrmann
08. Februar 2006 / EMBO J Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness T. Kharkovets K. Dedek H. Maier M. Schweizer D. Khimich R. Nouvian V. Vardanyan R. Leuwer T. Moser T.J. Jentsch
03. März 2006 / Circ Res Neurogenic mechanisms contribute to hypertension in mice with disruption of the K-Cl cotransporter KCC3 M.B. Rust J. Faulhaber M.K. Budack P. Pfeffer T. Maritzen M. Didie F.X. Beck T. Boettger R. Schubert H. Ehmke T.J. Jentsch C.A. Huebner
01. Juli 1995 / Phys Rev E Cluster formation, standing waves, and stripe patterns in oscillatory active media with local and global coupling M. Falcke H. Engel M. Neufeld
01. Juni 2006 / Phys Rev E Frequency of elemental events of intracellular Ca(2+) dynamics R. Thul M. Falcke
22. Mai 2006 / J Cell Biol M line-deficient titin causes cardiac lethality through impaired maturation of the sarcomere S. Weinert N. Bergmann X. Luo B. Erdmann M. Gotthardt
12. September 2006 / Proc Natl Acad Sci U S A Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6 M. Poet U. Kornak M. Schweizer A.A. Zdebik O. Scheel S. Hoelter W. Wurst A. Schmitt J.C. Fuhrmann R. Planells-Cases S.E. Mole C.A. Huebner T.J. Jentsch
29. Dezember 1995 / J Biol Chem Cloning and functional expression of rat CLC-5, a chloride channel related to kidney disease K. Steinmeyer B. Schwappach M. Bens A. Vandewalle T.J. Jentsch
11. Dezember 1995 / FEBS Lett ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family S. Brandt T.J. Jentsch
01. Dezember 1995 / Neuron Mutations in dominant human myotonia congenita drastically alter the voltage dependence of the CIC-1 chloride channel M. Pusch K. Steinmeyer M.C. Koch T.J. Jentsch