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Thierry VandenDriessche

Showing results (31-40 of 85) with videos related to

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Gene Therapy|October 19, 2019
Distinct transduction of muscle tissue in mice after systemic delivery of AAVpo1 vectorsWarut Tulalamba, Jonas Weinmann, Quang Hong Pham, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 9, 2021
Comprehensive transcriptome-wide analysis of spliceopathy correction of myotonic dystrophy using CRISPR-Cas9 in iPSCs-derived cardiomyocytesSumitava Dastidar, Debanjana Majumdar, Jaitip Tipanee, et al.
Human Gene Therapy|March 18, 2003
Efficiency of onco-retroviral and lentiviral gene transfer into primary mouse and human B-lymphocytes is pseudotype dependentWim Janssens, Marinee K L Chuah, Luigi Naldini, et al.
Blood|July 20, 2002
Lentiviral vectors containing the human immunodeficiency virus type-1 central polypurine tract can efficiently transduce nondividing hepatocytes and antigen-presenting cells in vivoThierry VandenDriessche, Lieven Thorrez, Luigi Naldini, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 16, 2010
Retroviral vectors induce epigenetic chromatin modifications and IL-10 production in transduced B cells via activation of toll-like receptor 2Roxana R Ahangarani, Wim Janssens, Vincent Carlier, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 31, 2018
Efficient In Vivo Liver-Directed Gene Editing Using CRISPR/Cas9Kshitiz Singh, Hanneke Evens, Nisha Nair, et al.
Human Gene Therapy|July 18, 2025
Long-Term Functional Correction of Pompe Disease and Increased α-Glucosidase Expression after Gene Therapy with Novel Combinations of Muscle-Targeted Transcriptional <i>Cis</i>-Regulatory ElementsQuang Hong Pham, Venkata Anudeep Bheemsetty, Phuong Anh Nguyen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 6, 2006
Angiogenesis enhances factor IX delivery and persistence from retrievable human bioengineered muscle implantsLieven Thorrez, Herman Vandenburgh, Nico Callewaert, et al.
Blood Advances|July 2, 2026
Increased Gene Therapy Efficacy Through the Use of Extended Half-Life Clotting FactorsDries De Wolf, Phuong Anh Nguyen, Nisha Nair, et al.
Research and Practice in Thrombosis and Haemostasis|June 18, 2020
Hemophilia gene therapy knowledge and perceptions: Results of an international surveyFlora Peyvandi, David Lillicrap, Johnny Mahlangu, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
Gene Therapy|October 19, 2019
Distinct transduction of muscle tissue in mice after systemic delivery of AAVpo1 vectorsWarut Tulalamba, Jonas Weinmann, Quang Hong Pham, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 9, 2021
Comprehensive transcriptome-wide analysis of spliceopathy correction of myotonic dystrophy using CRISPR-Cas9 in iPSCs-derived cardiomyocytesSumitava Dastidar, Debanjana Majumdar, Jaitip Tipanee, et al.
Human Gene Therapy|March 18, 2003
Efficiency of onco-retroviral and lentiviral gene transfer into primary mouse and human B-lymphocytes is pseudotype dependentWim Janssens, Marinee K L Chuah, Luigi Naldini, et al.
Blood|July 20, 2002
Lentiviral vectors containing the human immunodeficiency virus type-1 central polypurine tract can efficiently transduce nondividing hepatocytes and antigen-presenting cells in vivoThierry VandenDriessche, Lieven Thorrez, Luigi Naldini, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 16, 2010
Retroviral vectors induce epigenetic chromatin modifications and IL-10 production in transduced B cells via activation of toll-like receptor 2Roxana R Ahangarani, Wim Janssens, Vincent Carlier, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 31, 2018
Efficient In Vivo Liver-Directed Gene Editing Using CRISPR/Cas9Kshitiz Singh, Hanneke Evens, Nisha Nair, et al.
Human Gene Therapy|July 18, 2025
Long-Term Functional Correction of Pompe Disease and Increased α-Glucosidase Expression after Gene Therapy with Novel Combinations of Muscle-Targeted Transcriptional <i>Cis</i>-Regulatory ElementsQuang Hong Pham, Venkata Anudeep Bheemsetty, Phuong Anh Nguyen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 6, 2006
Angiogenesis enhances factor IX delivery and persistence from retrievable human bioengineered muscle implantsLieven Thorrez, Herman Vandenburgh, Nico Callewaert, et al.
Blood Advances|July 2, 2026
Increased Gene Therapy Efficacy Through the Use of Extended Half-Life Clotting FactorsDries De Wolf, Phuong Anh Nguyen, Nisha Nair, et al.
Research and Practice in Thrombosis and Haemostasis|June 18, 2020
Hemophilia gene therapy knowledge and perceptions: Results of an international surveyFlora Peyvandi, David Lillicrap, Johnny Mahlangu, et al.
Pageof 9