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Gene Therapy|March 22, 2021
Functional expression of complement factor I following AAV-mediated gene delivery in the retina of mice and human cellsAnna K Dreismann, Michelle E McClements, Alun R Barnard, et al.Immunological Reviews|November 12, 2022
Gene targeting as a therapeutic avenue in diseases mediated by the complement alternative pathwayAnna K Dreismann, Thomas M Hallam, Lawrence Cs Tam, et al.Human Gene Therapy|July 9, 2021
Adeno-Associated Virus Vector Gene Delivery Elevates Factor I Levels and Downregulates the Complement Alternative Pathway In VivoAmina Ahmad, Mawj Mandwie, Anna K Dreismann, et al.Pageof 1