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Translational Research : the Journal of Laboratory and Clinical Medicine
|
July 30, 2017
Evaluation of tolerance to lentiviral LV-RPE65 gene therapy vector after subretinal delivery in non-human primates
Alexandre Matet, Corinne Kostic, Alexis-Pierre Bemelmans, et al.
American Journal of Human Genetics
|
September 6, 2023
High-throughput transcriptome analyses from ASPIRO, a phase 1/2/3 study of gene replacement therapy for X-linked myotubular myopathy
Gaia Andreoletti, Oriana Romano, Hsin-Jung Chou, et al.
Molecular Therapy. Nucleic Acids
|
April 24, 2023
Novel lentiviral vectors for gene therapy of sickle cell disease combining gene addition and gene silencing strategies
Mégane Brusson, Anne Chalumeau, Pierre Martinucci, et al.
Blood Advances
|
February 26, 2021
Correction of β-thalassemia by CRISPR/Cas9 editing of the α-globin locus in human hematopoietic stem cells
Giulia Pavani, Anna Fabiano, Marine Laurent, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 14, 2013
Targeted gene addition in human epithelial stem cells by zinc-finger nuclease-mediated homologous recombination
Andrea Coluccio, Francesca Miselli, Angelo Lombardo, et al.
Plos One
|
May 16, 2015
Genome-Wide Definition of Promoter and Enhancer Usage during Neural Induction of Human Embryonic Stem Cells
Valentina Poletti, Alessia Delli Carri, Guidantonio Malagoli Tagliazucchi, et al.
Blood
|
May 18, 2007
Hot spots of retroviral integration in human CD34+ hematopoietic cells
Claudia Cattoglio, Giulia Facchini, Daniela Sartori, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 25, 2006
Retroviral vector integration deregulates gene expression but has no consequence on the biology and function of transplanted T cells
Alessandra Recchia, Chiara Bonini, Zulma Magnani, et al.
Blood
|
August 5, 2009
Integration of retroviral vectors induces minor changes in the transcriptional activity of T cells from ADA-SCID patients treated with gene therapy
Barbara Cassani, Eugenio Montini, Giulietta Maruggi, et al.
Molecular Therapy. Methods & Clinical Development
|
November 14, 2019
Biosafety Studies of a Clinically Applicable Lentiviral Vector for the Gene Therapy of Artemis-SCID
Sabine Charrier, Chantal Lagresle-Peyrou, Valentina Poletti, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 87) with videos related to
Sort By:
Page
of 9
Translational Research : the Journal of Laboratory and Clinical Medicine
|
July 30, 2017
Evaluation of tolerance to lentiviral LV-RPE65 gene therapy vector after subretinal delivery in non-human primates
Alexandre Matet, Corinne Kostic, Alexis-Pierre Bemelmans, et al.
American Journal of Human Genetics
|
September 6, 2023
High-throughput transcriptome analyses from ASPIRO, a phase 1/2/3 study of gene replacement therapy for X-linked myotubular myopathy
Gaia Andreoletti, Oriana Romano, Hsin-Jung Chou, et al.
Molecular Therapy. Nucleic Acids
|
April 24, 2023
Novel lentiviral vectors for gene therapy of sickle cell disease combining gene addition and gene silencing strategies
Mégane Brusson, Anne Chalumeau, Pierre Martinucci, et al.
Blood Advances
|
February 26, 2021
Correction of β-thalassemia by CRISPR/Cas9 editing of the α-globin locus in human hematopoietic stem cells
Giulia Pavani, Anna Fabiano, Marine Laurent, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 14, 2013
Targeted gene addition in human epithelial stem cells by zinc-finger nuclease-mediated homologous recombination
Andrea Coluccio, Francesca Miselli, Angelo Lombardo, et al.
Plos One
|
May 16, 2015
Genome-Wide Definition of Promoter and Enhancer Usage during Neural Induction of Human Embryonic Stem Cells
Valentina Poletti, Alessia Delli Carri, Guidantonio Malagoli Tagliazucchi, et al.
Blood
|
May 18, 2007
Hot spots of retroviral integration in human CD34+ hematopoietic cells
Claudia Cattoglio, Giulia Facchini, Daniela Sartori, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 25, 2006
Retroviral vector integration deregulates gene expression but has no consequence on the biology and function of transplanted T cells
Alessandra Recchia, Chiara Bonini, Zulma Magnani, et al.
Blood
|
August 5, 2009
Integration of retroviral vectors induces minor changes in the transcriptional activity of T cells from ADA-SCID patients treated with gene therapy
Barbara Cassani, Eugenio Montini, Giulietta Maruggi, et al.
Molecular Therapy. Methods & Clinical Development
|
November 14, 2019
Biosafety Studies of a Clinically Applicable Lentiviral Vector for the Gene Therapy of Artemis-SCID
Sabine Charrier, Chantal Lagresle-Peyrou, Valentina Poletti, et al.
Page
of 9