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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 01. 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 01. September 1998 / Curr Opin Nephrol Hypertens Molecular physiology of renal chloride channels K. Steinmeyer T.J. Jentsch 01. 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 01. Januar 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 01. 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 01. 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. 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01. 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
01. 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
01. September 1998 / Curr Opin Nephrol Hypertens Molecular physiology of renal chloride channels K. Steinmeyer T.J. Jentsch
01. 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
01. Januar 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
01. 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
01. 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