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Human Gene Therapy|December 26, 2024
Vectorized Human Antibody-Mediated Anti-Eosinophil Gene TherapyMaria Gioulvanidou, Selenay Sarklioglu, Xinlei Chen, et al.
Human Gene Therapy|October 25, 2024
Adeno-Associated Virus Gene Transfer Ameliorates Progression of Skeletal Lesions in Mucopolysaccharidosis IVA MiceAngélica María Herreño-Pachón, Kazuki Sawamoto, Molly Stapleton, et al.
Human Gene Therapy|February 18, 2025
Minimally Humanized Ezh2 Exon-18 Mouse Cell Lines Validate Preclinical CRISPR/Cas9 Approach to Treat Weaver SyndromeWilliam T Gibson, Tess C Lengyell, Andrea J Korecki, et al.
Human Gene Therapy|February 24, 2025
A Comprehensive Review of Clinically Applied Adeno-Associated Virus-Based Gene Therapies for Ocular DiseaseValerie G Hinsch, Sanford L Boye, Shannon E Boye
Human Gene Therapy|February 20, 2025
Analysis of HIV-1-Based Lentiviral Vector Particle Composition by PacBio Long-Read Nucleic Acid SequencingSaqlain Suleman, Mohammad S Khalifa, Serena Fawaz, et al.
Human Gene Therapy|February 20, 2025
Adeno-Associated Virus Gene Therapy Development: Early Planning and Regulatory Considerations to Advance the Platform Vector Gene Therapy ProgramRicha Madan Lomash, Jean Dehdashti, Oleg A Shchelochkov, et al.
Human Gene Therapy|January 1, 1991
Molecular analysis of retroviral transduction in chronic myelogenous leukemiaD Claxton, S P Suh, M Filaccio, et al.
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