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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 01. Januar 2018 / Diabetes Deletion of protein kinase D1 in pancreatic β-cells impairs insulin secretion in high-fat diet-fed mice V. Bergeron J. Ghislain K. Vivot N. Tamarina L.H. Philipson J. Fielitz V. Poitout 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 16. Mai 2018 / Sci Rep Molecular details of dimerization kinetics reveal negligible populations of transient µ-opioid receptor homodimers at physiological concentrations. D. Meral D. Provasi D. Prada-Gracia J. Möller K. Marino M.J. Lohse M. Filizola 30. Mai 2018 / Sci Rep The C/EBPβ LIP isoform rescues loss of C/EBPβ function in the mouse V. Bégay C. Baumeier K. Zimmermann A. Heuser A. Leutz 10. September 2018 / Dev Cell FACT sets a barrier for cell fate reprogramming in Caenorhabditis elegans and human cells E. Kolundzic A. Ofenbauer S.I. Bulut B. Uyar G. Baytek A. Sommermeier S. Seelk M. He A. Hirsekorn D. Vucicevic A. Akalin S. Diecke S.A. Lacadie B. 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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
01. Januar 2018 / Diabetes Deletion of protein kinase D1 in pancreatic β-cells impairs insulin secretion in high-fat diet-fed mice V. Bergeron J. Ghislain K. Vivot N. Tamarina L.H. Philipson J. Fielitz V. Poitout
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
16. Mai 2018 / Sci Rep Molecular details of dimerization kinetics reveal negligible populations of transient µ-opioid receptor homodimers at physiological concentrations. D. Meral D. Provasi D. Prada-Gracia J. Möller K. Marino M.J. Lohse M. Filizola
30. Mai 2018 / Sci Rep The C/EBPβ LIP isoform rescues loss of C/EBPβ function in the mouse V. Bégay C. Baumeier K. Zimmermann A. Heuser A. Leutz
10. September 2018 / Dev Cell FACT sets a barrier for cell fate reprogramming in Caenorhabditis elegans and human cells E. Kolundzic A. Ofenbauer S.I. Bulut B. Uyar G. Baytek A. Sommermeier S. Seelk M. He A. Hirsekorn D. Vucicevic A. Akalin S. Diecke S.A. Lacadie B. Tursun