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Gene Therapy
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October 7, 2025
Codon changes challenge PCR-based gene doping detection
Die Wu, Shengqian Ding, Nian Liu, et al.
Gene Therapy
|
September 26, 2025
Overcoming matrix effects in AAV neutralization assays with a constant serum concentration approach
Beatrix Kovács, Viktória Szabó, Domonkos Horváth, et al.
Gene Therapy
|
January 5, 2020
Integrating gene delivery and gene-editing technologies by adenoviral vector transfer of optimized CRISPR-Cas9 components
Ignazio Maggio, Hidde A Zittersteijn, Qian Wang, et al.
Gene Therapy
|
September 12, 2020
Overexpression of miR-144-3p alleviates polycystic ovaries syndrome through targeting expression of HSP-70
Bing Qu, Qinghong Zhao, Qinglian Ma, et al.
Gene Therapy
|
October 1, 2020
Easy and robust electrotransfection protocol for efficient ectopic gene expression and genome editing in human B cells
Reynand Jay Canoy, Franck André, Anna Shmakova, et al.
Gene Therapy
|
March 24, 2020
Reactivation of FMR1 gene expression is a promising strategy for fragile X syndrome therapy
Ekaterina M Shitik, Anastasia A Velmiskina, Alexander A Dolskiy, et al.
Gene Therapy
|
July 26, 2023
Correction: Site-specific modifications to AAV8 capsid yields enhanced brain transduction in the neonatal MPS IIIB mouse
Janine A Gilkes, Benjamin L Judkins, Brontie N Herrera, et al.
Gene Therapy
|
June 1, 2022
Splicing mutations in the CFTR gene as therapeutic targets
Karine Deletang, Magali Taulan-Cadars
Gene Therapy
|
January 12, 2021
Double viral vector technology for selective manipulation of neural pathways with higher level of efficiency and safety
Yoshinori Koshimizu, Kaoru Isa, Kenta Kobayashi, et al.
Gene Therapy
|
May 27, 2021
The transformative potential of HSC gene therapy as a genetic medicine
Pervinder Sagoo, H Bobby Gaspar
Page
of 489
Search research articles
Search
Showing results (31-40 of 4,883) with videos related to
Sort By:
Page
of 489
Gene Therapy
|
October 7, 2025
Codon changes challenge PCR-based gene doping detection
Die Wu, Shengqian Ding, Nian Liu, et al.
Gene Therapy
|
September 26, 2025
Overcoming matrix effects in AAV neutralization assays with a constant serum concentration approach
Beatrix Kovács, Viktória Szabó, Domonkos Horváth, et al.
Gene Therapy
|
January 5, 2020
Integrating gene delivery and gene-editing technologies by adenoviral vector transfer of optimized CRISPR-Cas9 components
Ignazio Maggio, Hidde A Zittersteijn, Qian Wang, et al.
Gene Therapy
|
September 12, 2020
Overexpression of miR-144-3p alleviates polycystic ovaries syndrome through targeting expression of HSP-70
Bing Qu, Qinghong Zhao, Qinglian Ma, et al.
Gene Therapy
|
October 1, 2020
Easy and robust electrotransfection protocol for efficient ectopic gene expression and genome editing in human B cells
Reynand Jay Canoy, Franck André, Anna Shmakova, et al.
Gene Therapy
|
March 24, 2020
Reactivation of FMR1 gene expression is a promising strategy for fragile X syndrome therapy
Ekaterina M Shitik, Anastasia A Velmiskina, Alexander A Dolskiy, et al.
Gene Therapy
|
July 26, 2023
Correction: Site-specific modifications to AAV8 capsid yields enhanced brain transduction in the neonatal MPS IIIB mouse
Janine A Gilkes, Benjamin L Judkins, Brontie N Herrera, et al.
Gene Therapy
|
June 1, 2022
Splicing mutations in the CFTR gene as therapeutic targets
Karine Deletang, Magali Taulan-Cadars
Gene Therapy
|
January 12, 2021
Double viral vector technology for selective manipulation of neural pathways with higher level of efficiency and safety
Yoshinori Koshimizu, Kaoru Isa, Kenta Kobayashi, et al.
Gene Therapy
|
May 27, 2021
The transformative potential of HSC gene therapy as a genetic medicine
Pervinder Sagoo, H Bobby Gaspar
Page
of 489