Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Thierry VandenDriessche

Showing results (21-30 of 85) with videos related to

Pageof 9
Sort By:
Expert Opinion on Biological Therapy|June 12, 2012
Recent developments in transposon-mediated gene therapyMario Di Matteo, Eyayu Belay, Marinee K Chuah, et al.
Current Gene Therapy|August 26, 2011
Transposon-mediated gene transfer into adult and induced pluripotent stem cellsEyayu Belay, Sumitava Dastidar, Thierry VandenDriessche, et al.
Blood|May 28, 2009
Emerging potential of transposons for gene therapy and generation of induced pluripotent stem cellsThierry VandenDriessche, Zoltán Ivics, Zsuzsanna Izsvák, et al.
Methods (San Diego, Calif.)|July 21, 2009
Efficient stable gene transfer into human cells by the Sleeping Beauty transposon vectorsZsuzsanna Izsvák, Marinee K L Chuah, Thierry Vandendriessche, et al.
Current Gene Therapy|July 1, 2015
Pluripotent Stem Cells for Gene Therapy of Degenerative Muscle DiseasesMariana Loperfido, Heather B Steele-Stallard, Francesco Saverio Tedesco, et al.
Seminars in Thrombosis and Hemostasis|May 1, 2004
Onco-retroviral and lentiviral vector-based gene therapy for hemophilia: preclinical studiesAn Van Damme, Marinee K L Chuah, Désiré Collen, et al.
Molecular Therapy. Methods & Clinical Development|December 10, 2024
Comprehensive analysis of off-target and on-target effects resulting from liver-directed CRISPR-Cas9-mediated gene targeting with AAV vectorsKshitiz Singh, Raffaele Fronza, Hanneke Evens, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 17, 2022
Universal allogeneic CAR T cells engineered with Sleeping Beauty transposons and CRISPR-CAS9 for cancer immunotherapyJaitip Tipanee, Ermira Samara-Kuko, Thierry Gevaert, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 28, 2012
PiggyBac toolboxMario Di Matteo, Janka Mátrai, Eyayu Belay, et al.
Biomaterials|October 12, 2007
Growth, differentiation, transplantation and survival of human skeletal myofibers on biodegradable scaffoldsLieven Thorrez, Janet Shansky, Lin Wang, et al.
Pageof 9

Showing results (21-30 of 85) with videos related to

Sort By:
Pageof 9
Expert Opinion on Biological Therapy|June 12, 2012
Recent developments in transposon-mediated gene therapyMario Di Matteo, Eyayu Belay, Marinee K Chuah, et al.
Current Gene Therapy|August 26, 2011
Transposon-mediated gene transfer into adult and induced pluripotent stem cellsEyayu Belay, Sumitava Dastidar, Thierry VandenDriessche, et al.
Blood|May 28, 2009
Emerging potential of transposons for gene therapy and generation of induced pluripotent stem cellsThierry VandenDriessche, Zoltán Ivics, Zsuzsanna Izsvák, et al.
Methods (San Diego, Calif.)|July 21, 2009
Efficient stable gene transfer into human cells by the Sleeping Beauty transposon vectorsZsuzsanna Izsvák, Marinee K L Chuah, Thierry Vandendriessche, et al.
Current Gene Therapy|July 1, 2015
Pluripotent Stem Cells for Gene Therapy of Degenerative Muscle DiseasesMariana Loperfido, Heather B Steele-Stallard, Francesco Saverio Tedesco, et al.
Seminars in Thrombosis and Hemostasis|May 1, 2004
Onco-retroviral and lentiviral vector-based gene therapy for hemophilia: preclinical studiesAn Van Damme, Marinee K L Chuah, Désiré Collen, et al.
Molecular Therapy. Methods & Clinical Development|December 10, 2024
Comprehensive analysis of off-target and on-target effects resulting from liver-directed CRISPR-Cas9-mediated gene targeting with AAV vectorsKshitiz Singh, Raffaele Fronza, Hanneke Evens, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 17, 2022
Universal allogeneic CAR T cells engineered with Sleeping Beauty transposons and CRISPR-CAS9 for cancer immunotherapyJaitip Tipanee, Ermira Samara-Kuko, Thierry Gevaert, et al.
Methods in Molecular Biology (Clifton, N.J.)|February 28, 2012
PiggyBac toolboxMario Di Matteo, Janka Mátrai, Eyayu Belay, et al.
Biomaterials|October 12, 2007
Growth, differentiation, transplantation and survival of human skeletal myofibers on biodegradable scaffoldsLieven Thorrez, Janet Shansky, Lin Wang, et al.
Pageof 9