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Methods in Molecular Biology (Clifton, N.J.)|February 21, 2019
AAV-Mediated Gene Delivery to the Liver: Overview of Current Technologies and MethodsBrett Palaschak, Roland W Herzog, David M MarkusicMolecular Therapy. Methods & Clinical Development|May 9, 2017
An Immune-Competent Murine Model to Study Elimination of AAV-Transduced Hepatocytes by Capsid-Specific CD8<sup>+</sup> T CellsBrett Palaschak, Damien Marsic, Roland W Herzog, et al.Frontiers in Immunology|July 17, 2020
B Cell Depletion Eliminates FVIII Memory B Cells and Enhances AAV8-coF8 Immune Tolerance Induction When Combined With RapamycinMoanaro Biswas, Brett Palaschak, Sandeep R P Kumar, et al.Molecular Therapy. Methods & Clinical Development|October 15, 2016
Potential for cellular stress response to hepatic factor VIII expression from AAV vectorIrene Zolotukhin, David M Markusic, Brett Palaschak, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|September 26, 2017
Gene Therapy-Induced Antigen-Specific Tregs Inhibit Neuro-inflammation and Reverse Disease in a Mouse Model of Multiple SclerosisGeoffrey D Keeler, Sandeep Kumar, Brett Palaschak, et al.Journal of Translational Medicine|May 3, 2017
Evaluation of engineered AAV capsids for hepatic factor IX gene transfer in murine and canine modelsDavid M Markusic, Timothy C Nichols, Elizabeth P Merricks, et al.Pageof 1