Search research articles
Contact Us
Filters
Showing results (21-30 of 36) with videos related to
Page
of 4
Sort By:
Frontiers in Genetics
|
September 12, 2022
Comprehensive exploration of tumor immune microenvironment feature and therapeutic response in colorectal cancer based on a novel immune-related long non-coding RNA prognostic signature
Xueliang Zhou, Batuer Aikemu, Shuchun Li, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 23, 2008
Recombinant AAV serotype and capsid mutant comparison for pulmonary gene transfer of alpha-1-antitrypsin using invasive and noninvasive delivery
Rejean Liqun Wang, Thomas McLaughlin, Travis Cossette, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 8, 2012
Long-term correction of very long-chain acyl-coA dehydrogenase deficiency in mice using AAV9 gene therapy
Allison M Keeler, Thomas Conlon, Glenn Walter, et al.
Cancer Letters
|
July 14, 2022
Tumor-derived exosomes in the cancer immune microenvironment and cancer immunotherapy
Qiushi Tang, Shuo Yang, Guangpeng He, et al.
Biorxiv : the Preprint Server for Biology
|
July 14, 2025
A Compact Base Editor Rescues AATD-associated Liver and Lung Disease in Mouse Models
Jenny Gao, Nathan Bamidele, Debora Pires-Ferreira, et al.
Molecular Therapy. Methods & Clinical Development
|
March 6, 2024
Biodistribution and safety of a single rAAV3B-AAT vector for silencing and replacement of alpha-1 antitrypsin in <i>Cynomolgus macaques</i>
Meghan Blackwood, Alisha M Gruntman, Qiushi Tang, et al.
Human Gene Therapy
|
March 31, 2018
In Vivo Genome Editing Partially Restores Alpha1-Antitrypsin in a Murine Model of AAT Deficiency
Chun-Qing Song, Dan Wang, Tingting Jiang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 17, 2017
Survival Advantage of Both Human Hepatocyte Xenografts and Genome-Edited Hepatocytes for Treatment of α-1 Antitrypsin Deficiency
Florie Borel, Qiushi Tang, Gwladys Gernoux, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
June 27, 2007
In vivo post-transcriptional gene silencing of alpha-1 antitrypsin by adeno-associated virus vectors expressing siRNA
Pedro E Cruz, Christian Mueller, Travis L Cossette, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 28, 2005
Localized gene expression following administration of adeno-associated viral vectors via pancreatic ducts
Scott A Loiler, Qiushi Tang, Tracy Clarke, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 36) with videos related to
Sort By:
Page
of 4
Frontiers in Genetics
|
September 12, 2022
Comprehensive exploration of tumor immune microenvironment feature and therapeutic response in colorectal cancer based on a novel immune-related long non-coding RNA prognostic signature
Xueliang Zhou, Batuer Aikemu, Shuchun Li, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 23, 2008
Recombinant AAV serotype and capsid mutant comparison for pulmonary gene transfer of alpha-1-antitrypsin using invasive and noninvasive delivery
Rejean Liqun Wang, Thomas McLaughlin, Travis Cossette, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 8, 2012
Long-term correction of very long-chain acyl-coA dehydrogenase deficiency in mice using AAV9 gene therapy
Allison M Keeler, Thomas Conlon, Glenn Walter, et al.
Cancer Letters
|
July 14, 2022
Tumor-derived exosomes in the cancer immune microenvironment and cancer immunotherapy
Qiushi Tang, Shuo Yang, Guangpeng He, et al.
Biorxiv : the Preprint Server for Biology
|
July 14, 2025
A Compact Base Editor Rescues AATD-associated Liver and Lung Disease in Mouse Models
Jenny Gao, Nathan Bamidele, Debora Pires-Ferreira, et al.
Molecular Therapy. Methods & Clinical Development
|
March 6, 2024
Biodistribution and safety of a single rAAV3B-AAT vector for silencing and replacement of alpha-1 antitrypsin in <i>Cynomolgus macaques</i>
Meghan Blackwood, Alisha M Gruntman, Qiushi Tang, et al.
Human Gene Therapy
|
March 31, 2018
In Vivo Genome Editing Partially Restores Alpha1-Antitrypsin in a Murine Model of AAT Deficiency
Chun-Qing Song, Dan Wang, Tingting Jiang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 17, 2017
Survival Advantage of Both Human Hepatocyte Xenografts and Genome-Edited Hepatocytes for Treatment of α-1 Antitrypsin Deficiency
Florie Borel, Qiushi Tang, Gwladys Gernoux, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology
|
June 27, 2007
In vivo post-transcriptional gene silencing of alpha-1 antitrypsin by adeno-associated virus vectors expressing siRNA
Pedro E Cruz, Christian Mueller, Travis L Cossette, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 28, 2005
Localized gene expression following administration of adeno-associated viral vectors via pancreatic ducts
Scott A Loiler, Qiushi Tang, Tracy Clarke, et al.
Page
of 4