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(2) Klein, Christian Dr. (2) Klußmann, Enno PD Dr. (4) Kobelt, Dennis Dr. (1) Kopp, Joachim Dr. (1) Kowenz-Leutz, Elisabeth Dr. (2) Kudryashev, Mikhail Prof. Dr. (3) Lacadie, Scott Allen Dr. (1) Landthaler, Markus Prof. Dr. (3) Lee, Young-Ae Prof. Dr. (4) Leisegang, Matthias Prof. Dr. rer. nat. (1) Leutz, Achim Prof. Dr. (7) Lewin, Gary Prof. Dr. (13) Luft, Friedrich Prof. Dr. (121) Lupianez Garcia, Dario Jesus Dr. (1) Maglione, Marta (1) Marenholz, Ingo Dr. (2) Marg, Andreas Dr. (2) Marko, Lajos Dr. (1) Mastrobuoni, Guido Dr. (4) Mathas, Stephan Dr. (4) Meier, Katja (2) Mertins, Philipp Dr. (1) Meyer, Irmtraud Margret Prof. Dr. (3) Millward, Jason Dr. (1) Morano, Ingo Prof. Dr. (23) Müller, Dominik Prof. Dr. (17) Na, Il-Kang Dr. (2) Niendorf, Thoralf Prof. Dr. (8) Nimptsch, Katharina Dr. (5) Obermayer-Wasserscheid, Benedikt Dr. (3) Panakova, Daniela Dr. (2) Paul, Friedemann Prof. Dr. med. 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Dezember 2011 / Hum Mol Genet The X-chromosome linked intellectual disability protein PQBP1 is a component of neuronal RNA granules and regulates the appearance of stress granules S.A. Kunde L. Musante A. Grimme U. Fischer E. Mueller E.E. Wanker V.M. Kalscheuer 01. März 2011 / J Physiol Astrocytes control GABAergic inhibition of neurons in the mouse barrel cortex B. Benedetti V. Matyash H. Kettenmann 01. April 2011 / J Neurochem Functional importance of inositol-1,4,5-triphosphate-induced intracellular Ca(2+) mobilization in galanin-induced microglial migration M. Ifuku Y. Okuno Y. Yamakawa K. Izumi S. Seifert H. Kettenmann M. Noda 01. Januar 1998 / J Cardiovasc Pharmacol Single-cell characterization of endothelin system gene expression in the cerebellum in situ K.M. Schmidt-Ott S. Tuschick F. Kirchhoff A. Verkhratsky L. Liefeldt H. Kettenmann M. Paul 01. Juli 2011 / PLoS Genet Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes pelizaeus-merzbacher-like disease in humans O. Tress M. Maglione A. Zlomuzica D. May N. Dicke J. Degen E. Dere H. Kettenmann D. Hartmann K. Willecke 01. April 2011 / Gene Ther Allogeneic gene-modified tumor cells (RCC-26/IL-7/CD80) as a vaccine in patients with metastatic renal cell cancer: a clinical phase-I study J. Westermann A. Floercken G. Willimsky A. van Lessen J. Kopp A. Takvorian K. Joehrens A. Lukowsky C. Schoenemann B. Sawitzki H. Pohla R. Frank B. Doerken D.J. Schendel T. Blankenstein A. Pezzutto 01. August 1998 / Biochem Soc Trans Polyglutamine expansion and Huntington's disease G.P. Bates L. Mangiarini E.E. Wanker S.W. Davies 17. April 1998 / FEBS Lett HAP1-huntingtin interactions do not contribute to the molecular pathology in Huntington's disease transgenic mice F. Bertaux A.H. Sharp C.A. Ross H. Lehrach G.P. Bates E.E. Wanker 26. Mai 1998 / Proc Natl Acad Sci U S A Huntingtin aggregation monitored by dynamic light scattering Y. Georgalis E.B. Starikov B. Hollenbach R. Lurz E. Scherzinger W. Saenger H. Lehrach E.E. Wanker 01. Januar 1998 / Mamm Genome IRS-PCR-based genetic mapping of the huntingtin interacting protein gene (HIP1) on mouse chromosome 5 H. Himmelbauer N. Wedemeyer T. Haaf E.E. Wanker L.C. Schalkwyk H. Lehrach Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
15. Dezember 2011 / Hum Mol Genet The X-chromosome linked intellectual disability protein PQBP1 is a component of neuronal RNA granules and regulates the appearance of stress granules S.A. Kunde L. Musante A. Grimme U. Fischer E. Mueller E.E. Wanker V.M. Kalscheuer
01. März 2011 / J Physiol Astrocytes control GABAergic inhibition of neurons in the mouse barrel cortex B. Benedetti V. Matyash H. Kettenmann
01. April 2011 / J Neurochem Functional importance of inositol-1,4,5-triphosphate-induced intracellular Ca(2+) mobilization in galanin-induced microglial migration M. Ifuku Y. Okuno Y. Yamakawa K. Izumi S. Seifert H. Kettenmann M. Noda
01. Januar 1998 / J Cardiovasc Pharmacol Single-cell characterization of endothelin system gene expression in the cerebellum in situ K.M. Schmidt-Ott S. Tuschick F. Kirchhoff A. Verkhratsky L. Liefeldt H. Kettenmann M. Paul
01. Juli 2011 / PLoS Genet Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes pelizaeus-merzbacher-like disease in humans O. Tress M. Maglione A. Zlomuzica D. May N. Dicke J. Degen E. Dere H. Kettenmann D. Hartmann K. Willecke
01. April 2011 / Gene Ther Allogeneic gene-modified tumor cells (RCC-26/IL-7/CD80) as a vaccine in patients with metastatic renal cell cancer: a clinical phase-I study J. Westermann A. Floercken G. Willimsky A. van Lessen J. Kopp A. Takvorian K. Joehrens A. Lukowsky C. Schoenemann B. Sawitzki H. Pohla R. Frank B. Doerken D.J. Schendel T. Blankenstein A. Pezzutto
01. August 1998 / Biochem Soc Trans Polyglutamine expansion and Huntington's disease G.P. Bates L. Mangiarini E.E. Wanker S.W. Davies
17. April 1998 / FEBS Lett HAP1-huntingtin interactions do not contribute to the molecular pathology in Huntington's disease transgenic mice F. Bertaux A.H. Sharp C.A. Ross H. Lehrach G.P. Bates E.E. Wanker
26. Mai 1998 / Proc Natl Acad Sci U S A Huntingtin aggregation monitored by dynamic light scattering Y. Georgalis E.B. Starikov B. Hollenbach R. Lurz E. Scherzinger W. Saenger H. Lehrach E.E. Wanker
01. Januar 1998 / Mamm Genome IRS-PCR-based genetic mapping of the huntingtin interacting protein gene (HIP1) on mouse chromosome 5 H. Himmelbauer N. Wedemeyer T. Haaf E.E. Wanker L.C. Schalkwyk H. Lehrach