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Human Gene Therapy|October 3, 2017
Systemic SMAD7 Gene Therapy Increases Striated Muscle Mass and Enhances Exercise Capacity in a Dose-Dependent MannerJoseph W Maricelli, Yemeserach M Bishaw, Bo Wang, et al.Human Gene Therapy|February 22, 2018
Micro-Dystrophin Gene Therapy Goes Systemic in Duchenne Muscular Dystrophy PatientsDongsheng DuanHuman Gene Therapy|February 16, 2018
Recent Advances in Therapeutic Genome Editing in ChinaYang Yang, Qingnan Wang, Qian Li, et al.Human Gene Therapy|January 17, 2018
Development of Gene Therapeutics for Head and Neck Cancer in China: From Bench to BedsideWei Guo, Hao SongHuman Gene Therapy|January 31, 2018
Severe Toxicity in Nonhuman Primates and Piglets Following High-Dose Intravenous Administration of an Adeno-Associated Virus Vector Expressing Human SMNChristian Hinderer, Nathan Katz, Elizabeth L Buza, et al.Human Gene Therapy|January 12, 2018
Transducing Airway Basal Cells with a Helper-Dependent Adenoviral Vector for Lung Gene TherapyHuibi Cao, Hong Ouyang, Hartmut Grasemann, et al.Human Gene Therapy|February 3, 2018
Preclinical Models in Chimeric Antigen Receptor-Engineered T-Cell TherapyElizabeth Louise Siegler, Pin WangHuman Gene Therapy|December 12, 2018
Pretreatment of rAAV-Mediated Expression of Myostatin Propeptide Lowers Type 2 Diabetes Incidence in C57BL/6 Mice on a High-Fat DietHui Yan, Jiejie Meng, Shasha Zhang, et al.Human Gene Therapy|March 23, 2018
Efficient Non-Viral T-Cell Engineering by Sleeping Beauty Minicircles Diminishing DNA Toxicity and miRNAs Silencing the Endogenous T-Cell ReceptorsJulian Clauss, Matthias Obenaus, Csaba Miskey, et al.Human Gene Therapy|March 31, 2018
Seamless Genetic Conversion of SMN2 to SMN1 via CRISPR/Cpf1 and Single-Stranded Oligodeoxynucleotides in Spinal Muscular Atrophy Patient-Specific Induced Pluripotent Stem CellsMiaojin Zhou, Zhiqing Hu, Liyan Qiu, et al.Pageof 413