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Dezember 1993 / Ann N Y Acad Sci The ClC family of voltage-gated chloride channels: structure and function T.J. Jentsch M. Pusch A. Rehfeldt K. Steinmeyer 01. November 1993 / J Med Genet Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker) M.C. Koch K. Ricker M. Otto F. Wolf B. Zoll C. Lorenz K. Steinmeyer T.J. Jentsch 01. Juni 1993 / Curr Opin Neurobiol Chloride channels T.J. Jentsch 01. September 2021 / Magn Reson Med Simultaneous T(2) and T(2)* mapping of multiple sclerosis lesions with radial RARE-EPI C. Herrmann A. Els L. Boehmert J. Periquito T.W. Eigentler J. Millward S. Waiczies J. Kuchling F. Paul T. Niendorf 05. August 2021 / Am J Hum Genet Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders A.R. Duncan M.M. Polovitskaya H. Gaitán-Peñas S. Bertelli G.E. VanNoy P.E. Grant A. O'Donnell-Luria Z. Valivullah A.K. Lovgren E.M. England E. Agolini J.A. Madden K. Schmitz-Abe A. Kritzer P. Hawley A. Novelli P. Alfieri G.S. Colafati D. Wieczorek K. Platzer J. Luppe M. Koch-Hogrebe R. Abou Jamra J. Neira-Fresneda A. Lehman C.F. Boerkoel K. Seath L. Clarke Y. van Ierland E. Argilli E.H. Sherr A. Maiorana T. Diel M. Hempel T. Bierhals R. Estévez T.J. Jentsch M. Pusch P.B. Agrawal 04. Januar 2021 / J Biol Chem Cellular basis of ClC-2 Cl(-) channel-related brain and testis pathologies C. Göppner A.H. Soria M.B. Hoegg-Beiler T.J. Jentsch 12. Januar 2021 / Cell Rep Variability of an early developmental cell population underlies stochastic laterality defects R. Moreno-Ayala P. Olivares-Chauvet R. Schäfer J.P. Junker 10. August 2021 / Nat Commun Place fields of single spikes in hippocampus involve Kcnq3 channel-dependent entrainment of complex spike bursts X. Gao F. Bender H. Soh C. Chen M. Altafi S. Schütze M. Heidenreich M. Gorbati M.A. Corbu M. Carus-Cadavieco T. Korotkova A.V. Tzingounis T.J. Jentsch A. Ponomarenko 16. November 2021 / Nat Commun Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4 S. Grosche I. Marenholz J. Esparza-Gordillo A. Arnau-Soler E. Pairo-Castineira F. Rüschendorf T.S. Ahluwalia C. Almqvist A. Arnold H. Baurecht H. Bisgaard K. Bønnelykke S.J. Brown M. Bustamante J.A. Curtin A. Custovic S.C. Dharmage A. Esplugues M. Falchi D. Fernandez-Orth M.A.R. Ferreira A. Franke S. Gerdes C. Gieger H. Hakonarson P.G. Holt G. Homuth N. Hubner P.G. Hysi M.R. Jarvelin R. Karlsson G.H. Koppelman S. Lau M. Lutz P.K.E. Magnusson G.B. Marks M. Müller-Nurasyid M.M. Nöthen L. Paternoster C.E. Pennell A. Peters K. Rawlik C.F. Robertson E. Rodriguez S. Sebert A. Simpson P.M.A. Sleiman M. Standl D. Stölzl K. Strauch A. Szwajda A. Tenesa P.J. Thompson V. Ullemar A. Visconti J.M. Vonk C.A. Wang S. Weidinger M. Wielscher C.L. Sargent C.J. Xu Y.A. Lee 01. Januar 2021 / Encyclopedia of Molecular Pharmacology Cl(-) channels and Cl(-)/H(+) exchangers F. Ullrich T.J. 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20. Dezember 1993 / Ann N Y Acad Sci The ClC family of voltage-gated chloride channels: structure and function T.J. Jentsch M. Pusch A. Rehfeldt K. Steinmeyer
01. November 1993 / J Med Genet Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker) M.C. Koch K. Ricker M. Otto F. Wolf B. Zoll C. Lorenz K. Steinmeyer T.J. Jentsch
01. September 2021 / Magn Reson Med Simultaneous T(2) and T(2)* mapping of multiple sclerosis lesions with radial RARE-EPI C. Herrmann A. Els L. Boehmert J. Periquito T.W. Eigentler J. Millward S. Waiczies J. Kuchling F. Paul T. Niendorf
05. August 2021 / Am J Hum Genet Unique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders A.R. Duncan M.M. Polovitskaya H. Gaitán-Peñas S. Bertelli G.E. VanNoy P.E. Grant A. O'Donnell-Luria Z. Valivullah A.K. Lovgren E.M. England E. Agolini J.A. Madden K. Schmitz-Abe A. Kritzer P. Hawley A. Novelli P. Alfieri G.S. Colafati D. Wieczorek K. Platzer J. Luppe M. Koch-Hogrebe R. Abou Jamra J. Neira-Fresneda A. Lehman C.F. Boerkoel K. Seath L. Clarke Y. van Ierland E. Argilli E.H. Sherr A. Maiorana T. Diel M. Hempel T. Bierhals R. Estévez T.J. Jentsch M. Pusch P.B. Agrawal
04. Januar 2021 / J Biol Chem Cellular basis of ClC-2 Cl(-) channel-related brain and testis pathologies C. Göppner A.H. Soria M.B. Hoegg-Beiler T.J. Jentsch
12. Januar 2021 / Cell Rep Variability of an early developmental cell population underlies stochastic laterality defects R. Moreno-Ayala P. Olivares-Chauvet R. Schäfer J.P. Junker
10. August 2021 / Nat Commun Place fields of single spikes in hippocampus involve Kcnq3 channel-dependent entrainment of complex spike bursts X. Gao F. Bender H. Soh C. Chen M. Altafi S. Schütze M. Heidenreich M. Gorbati M.A. Corbu M. Carus-Cadavieco T. Korotkova A.V. Tzingounis T.J. Jentsch A. Ponomarenko
16. November 2021 / Nat Commun Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4 S. Grosche I. Marenholz J. Esparza-Gordillo A. Arnau-Soler E. Pairo-Castineira F. Rüschendorf T.S. Ahluwalia C. Almqvist A. Arnold H. Baurecht H. Bisgaard K. Bønnelykke S.J. Brown M. Bustamante J.A. Curtin A. Custovic S.C. Dharmage A. Esplugues M. Falchi D. Fernandez-Orth M.A.R. Ferreira A. Franke S. Gerdes C. Gieger H. Hakonarson P.G. Holt G. Homuth N. Hubner P.G. Hysi M.R. Jarvelin R. Karlsson G.H. Koppelman S. Lau M. Lutz P.K.E. Magnusson G.B. Marks M. Müller-Nurasyid M.M. Nöthen L. Paternoster C.E. Pennell A. Peters K. Rawlik C.F. Robertson E. Rodriguez S. Sebert A. Simpson P.M.A. Sleiman M. Standl D. Stölzl K. Strauch A. Szwajda A. Tenesa P.J. Thompson V. Ullemar A. Visconti J.M. Vonk C.A. Wang S. Weidinger M. Wielscher C.L. Sargent C.J. Xu Y.A. Lee
01. Januar 2021 / Encyclopedia of Molecular Pharmacology Cl(-) channels and Cl(-)/H(+) exchangers F. Ullrich T.J. Jentsch