Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Adami, Eleonora Dr. (1) Akalin, Altuna Dr. (2) Altmueller, Janine Dr.med. (1) Annibale, Paolo Dr. (2) Bader, Michael Prof. Dr. (1) Bähring, Sylvia Dr. (1) Bartolomaeus, Theda (1) Berruezo Llacuna, Maria (1) Birchmeier-Kohler, Carmen Prof. Dr. (1) Blachut, Susanne (1) Borodina, Tatiana Dr. (1) Carvalho, Silvia Filipa (1) Conrad, Thomas Dr. (1) Diecke, Sebastian Dr. (71) Di Virgilio, Michela Prof. Dr. (1) Escobar Fernandez, Helena Dr. (3) Forslund, Sofia Dr. (1) Frahm-Barske, Silke Dr. (4) Fritsche, Raphaela Dr. (1) Genehr, Carolin (3) Gerhardt, Holger Prof. Dr. (1) Gotthardt, Michael Prof. Dr. (1) Gouti, Mina Dr. (1) Grosswendt, Stefanie Dr. (1) Haucke, Volker Professor (2) Heuser, Arnd Dr. (1) Hinze, Christian Dr. med. Dipl.-Math. 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November 2020 / Front Cell Dev Biol Assessment of ethanol-induced toxicity on iPSC-derived human dopaminergic neurons using a novel high-throughput mitochondrial neuronal health (MNH) assay A. Zink J. Conrad N.S. Telugu S. Diecke A. Heinz E. Wanker J. Priller A. Prigione 20. September 2018 / Cell Mutations in disordered regions can cause disease by creating dileucine motifs K. Meyer M. Kirchner B. Uyar J.Y. Cheng G. Russo L.R. Hernandez-Miranda A. Szymborska H. Zauber I.M. Rudolph T.E. Willnow A. Akalin V. Haucke H. Gerhardt C. Birchmeier R. Kühn M. Krauss S. Diecke J.M. Pascual M. Selbach 01. Juli 2020 / Kidney Int Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome J. Flemming M. Marczenke I.M. Rudolph R. Nielsen T. Storm E. Ilsoe Christensen S. Diecke F. Emma T.E. Willnow 01. Mai 2022 / Stem Cell Res Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T > G or m.8993T > C in the mitochondrial gene MT-ATP6 C. Lorenz A. Zink M.T. Henke S. Staege B. Mlody M. Bünning E. Wanker S. Diecke M. Schuelke A. Prigione 26. März 2021 / Nat Commun Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome G. Inak A. Rybak-Wolf P. Lisowski T.M. Pentimalli R. Jüttner P. Glažar K. Uppal E. Bottani D. Brunetti C. Secker A. Zink D. Meierhofer M.T. Henke M. Dey U. Ciptasari B. Mlody T. Hahn M. Berruezo-Llacuna N. Karaiskos M. Di Virgilio J.A. Mayr S.B. Wortmann J. Priller M. Gotthardt D.P. Jones E. Mayatepek W. Stenzel S. Diecke R. Kühn E.E. Wanker N. Rajewsky M. Schuelke A. Prigione 01. April 2023 / Stem Cell Res Generation of an induced pluripotent stem cell line from a Huntington's disease patient with a long HTT-PolyQ sequence D.C. Miller P. Lisowski C. Genehr E.E. Wanker J. Priller A. Prigione S. Diecke 01. Dezember 2022 / Stem Cell Res Generation of induced pluripotent stem cells from three individuals with Huntington's disease D.C. Miller P. Lisowski S. Lickfett B. Mlody M. Bünning C. Genehr C. Ulrich E.E. Wanker S. Diecke J. Priller A. Prigione
05. November 2020 / Front Cell Dev Biol Assessment of ethanol-induced toxicity on iPSC-derived human dopaminergic neurons using a novel high-throughput mitochondrial neuronal health (MNH) assay A. Zink J. Conrad N.S. Telugu S. Diecke A. Heinz E. Wanker J. Priller A. Prigione
20. September 2018 / Cell Mutations in disordered regions can cause disease by creating dileucine motifs K. Meyer M. Kirchner B. Uyar J.Y. Cheng G. Russo L.R. Hernandez-Miranda A. Szymborska H. Zauber I.M. Rudolph T.E. Willnow A. Akalin V. Haucke H. Gerhardt C. Birchmeier R. Kühn M. Krauss S. Diecke J.M. Pascual M. Selbach
01. Juli 2020 / Kidney Int Induced pluripotent stem cell-based disease modeling identifies ligand-induced decay of megalin as a cause of Donnai-Barrow syndrome J. Flemming M. Marczenke I.M. Rudolph R. Nielsen T. Storm E. Ilsoe Christensen S. Diecke F. Emma T.E. Willnow
01. Mai 2022 / Stem Cell Res Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T > G or m.8993T > C in the mitochondrial gene MT-ATP6 C. Lorenz A. Zink M.T. Henke S. Staege B. Mlody M. Bünning E. Wanker S. Diecke M. Schuelke A. Prigione
26. März 2021 / Nat Commun Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome G. Inak A. Rybak-Wolf P. Lisowski T.M. Pentimalli R. Jüttner P. Glažar K. Uppal E. Bottani D. Brunetti C. Secker A. Zink D. Meierhofer M.T. Henke M. Dey U. Ciptasari B. Mlody T. Hahn M. Berruezo-Llacuna N. Karaiskos M. Di Virgilio J.A. Mayr S.B. Wortmann J. Priller M. Gotthardt D.P. Jones E. Mayatepek W. Stenzel S. Diecke R. Kühn E.E. Wanker N. Rajewsky M. Schuelke A. Prigione
01. April 2023 / Stem Cell Res Generation of an induced pluripotent stem cell line from a Huntington's disease patient with a long HTT-PolyQ sequence D.C. Miller P. Lisowski C. Genehr E.E. Wanker J. Priller A. Prigione S. Diecke
01. Dezember 2022 / Stem Cell Res Generation of induced pluripotent stem cells from three individuals with Huntington's disease D.C. Miller P. Lisowski S. Lickfett B. Mlody M. Bünning C. Genehr C. Ulrich E.E. Wanker S. Diecke J. Priller A. Prigione