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Juni 2018 / Mol Ther Nucleic Acids The antibiotic-free pFAR4 vector paired with the Sleeping Beauty transposon system mediates efficient transgene delivery in human cells M. Pastor S. Johnen N. Harmening M. Quiviger J. Pailloux M. Kropp P. Walter Z. Ivics Z. Izsvák G. Thumann D. Scherman C. Marie 04. März 2018 / RNA Biol Expanding the map of protein-RNA interaction sites via cell fusion followed by PAR-CLIP F. Hinze P. Drewe-Boss M. Milek U. Ohler M. Landthaler M. Gotthardt 01. Januar 2018 / Methods Mol Biol Systematic detection of poly(A)(+) RNA-interacting proteins and their differential binding M. Milek M. Landthaler 16. März 2018 / Mol Ther Methods Clin Dev A combined in vivo HSC transduction/selection approach results in efficient and stable gene expression in peripheral blood cells in mice H. Wang M. Richter N. Psatha C. Li J. Kim J. Liu A. Ehrhardt S.K. Nilsson B. Cao D. Palmer P. Ng Z. Izsvák K.G. Haworth H.P. Kiem T. Papayannopoulou A. Lieber 01. März 2018 / J Thromb Haemost High and long-term von Willebrand factor expression after Sleeping Beauty transposon-mediated gene therapy in a mouse model of severe von Willebrand disease I. Portier K. Vanhoorelbeke S. Verhenne I. Pareyn N. Vandeputte H. Deckmyn D.S. Goldenberg H.B. Samal M. Singh Z. Ivics Z. Izsvák S.F. De Meyer 15. Juni 2018 / Mol Ther Methods Clin Dev Integrating HDAd5/35++ vectors as a new platform for HSC gene therapy of hemoglobinopathies C. Li N. Psatha H. Wang M. Singh H.B. Samal W. Zhang A. Ehrhardt Z. Izsvák T. Papayannopoulou A. Lieber 01. Juni 2018 / Mol Ther Nucleic Acids The antibiotic-free pFAR4 vector paired with the sleeping beauty transposon sSystem mediates efficient transgene delivery in human cells M. Pastor S. Johnen N. Harmening M. Quiviger J. Pailloux M. Kropp P. Walter Z. Ivics Z. Izsvák G. Thumann D. Scherman C. Marie 01. November 2018 / Eur J Med Genet Improved molecular platform for the gene therapy of rare diseases by liver protein secretion M. Quiviger A. Giannakopoulos S. Verhenne C. Marie E.F. Stavrou K. Vanhoorelbeke Z. Izsvák S.F. De Meyer A. Athanassiadou D. Scherman 01. Januar 2020 / Nucleic Acids Res A single amino acid switch converts the sleeping beauty transposase into an efficient unidirectional excisionase with utility in stem cell reprogramming L. Kesselring C. Miskey C. Zuliani I. Querques V. Kapitonov A. Laukó A. Fehér A. Palazzo T. Diem J. Lustig A. Sebe Y. Wang A. Dinnyés Z. Izsvák O. Barabas Z. Ivics 01. Februar 2018 / Mol Metab The RhoGAP Stard13 controls insulin secretion through F-actin remodeling H. Naumann T. Rathjen M.N. Poy F.M. Spagnoli Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 Nächste Seite Next › Letzte Seite Last »
01. Juni 2018 / Mol Ther Nucleic Acids The antibiotic-free pFAR4 vector paired with the Sleeping Beauty transposon system mediates efficient transgene delivery in human cells M. Pastor S. Johnen N. Harmening M. Quiviger J. Pailloux M. Kropp P. Walter Z. Ivics Z. Izsvák G. Thumann D. Scherman C. Marie
04. März 2018 / RNA Biol Expanding the map of protein-RNA interaction sites via cell fusion followed by PAR-CLIP F. Hinze P. Drewe-Boss M. Milek U. Ohler M. Landthaler M. Gotthardt
01. Januar 2018 / Methods Mol Biol Systematic detection of poly(A)(+) RNA-interacting proteins and their differential binding M. Milek M. Landthaler
16. März 2018 / Mol Ther Methods Clin Dev A combined in vivo HSC transduction/selection approach results in efficient and stable gene expression in peripheral blood cells in mice H. Wang M. Richter N. Psatha C. Li J. Kim J. Liu A. Ehrhardt S.K. Nilsson B. Cao D. Palmer P. Ng Z. Izsvák K.G. Haworth H.P. Kiem T. Papayannopoulou A. Lieber
01. März 2018 / J Thromb Haemost High and long-term von Willebrand factor expression after Sleeping Beauty transposon-mediated gene therapy in a mouse model of severe von Willebrand disease I. Portier K. Vanhoorelbeke S. Verhenne I. Pareyn N. Vandeputte H. Deckmyn D.S. Goldenberg H.B. Samal M. Singh Z. Ivics Z. Izsvák S.F. De Meyer
15. Juni 2018 / Mol Ther Methods Clin Dev Integrating HDAd5/35++ vectors as a new platform for HSC gene therapy of hemoglobinopathies C. Li N. Psatha H. Wang M. Singh H.B. Samal W. Zhang A. Ehrhardt Z. Izsvák T. Papayannopoulou A. Lieber
01. Juni 2018 / Mol Ther Nucleic Acids The antibiotic-free pFAR4 vector paired with the sleeping beauty transposon sSystem mediates efficient transgene delivery in human cells M. Pastor S. Johnen N. Harmening M. Quiviger J. Pailloux M. Kropp P. Walter Z. Ivics Z. Izsvák G. Thumann D. Scherman C. Marie
01. November 2018 / Eur J Med Genet Improved molecular platform for the gene therapy of rare diseases by liver protein secretion M. Quiviger A. Giannakopoulos S. Verhenne C. Marie E.F. Stavrou K. Vanhoorelbeke Z. Izsvák S.F. De Meyer A. Athanassiadou D. Scherman
01. Januar 2020 / Nucleic Acids Res A single amino acid switch converts the sleeping beauty transposase into an efficient unidirectional excisionase with utility in stem cell reprogramming L. Kesselring C. Miskey C. Zuliani I. Querques V. Kapitonov A. Laukó A. Fehér A. Palazzo T. Diem J. Lustig A. Sebe Y. Wang A. Dinnyés Z. Izsvák O. Barabas Z. Ivics
01. Februar 2018 / Mol Metab The RhoGAP Stard13 controls insulin secretion through F-actin remodeling H. Naumann T. Rathjen M.N. Poy F.M. Spagnoli