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Cell Death and Differentiation|February 16, 2022
Regulation of sclerostin by the SIRT1 stabilization pathway in osteocytesJung-Min Kim, Yeon-Suk Yang, Jun Xie, et al.
Molecular Therapy. Methods & Clinical Development|May 15, 2020
Bone-Targeting AAV-Mediated Gene Silencing in Osteoclasts for Osteoporosis TherapyYeon-Suk Yang, Jun Xie, Sachin Chaugule, et al.
Molecular Therapy. Methods & Clinical Development|September 13, 2021
Efficacious, safe, and stable inhibition of corneal neovascularization by AAV-vectored anti-VEGF therapeuticsWenqi Su, Shuo Sun, Bo Tian, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 11, 2025
Nature-inspired IL-1 targeted therapy to treat chronic inflammatory diseasesYeon-Suk Yang, Mi-Jeong Kim, Sachin Chaugule, et al.
Human Gene Therapy|March 31, 2018
In Vivo Genome Editing Partially Restores Alpha1-Antitrypsin in a Murine Model of AAT DeficiencyChun-Qing Song, Dan Wang, Tingting Jiang, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 29, 2015
AAV9 delivering a modified human Mullerian inhibiting substance as a gene therapy in patient-derived xenografts of ovarian cancerDavid Pépin, Amanda Sosulski, Lihua Zhang, et al.
Human Gene Therapy|October 26, 2018
Intrathecal Adeno-Associated Viral Vector-Mediated Gene Delivery for AdrenomyeloneuropathyYi Gong, Anna Berenson, Fiza Laheji, et al.
European Journal of Immunology|February 13, 2008
Single-dose immunogenicity and protective efficacy of simian adenoviral vectors against Plasmodium bergheiArturo Reyes-Sandoval, Saranya Sridhar, Tamara Berthoud, et al.
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