Brett Palaschak

AAV-Mediated Gene Delivery to the Liver: Overview of Current Technologies and Methods.

R. Herzog, D. Markusic, Brett Palaschak, 2019, Methods in molecular biology.

Potential for cellular stress response to hepatic factor VIII expression from AAV vector

R. Herzog, I. Zolotukhin, D. Markusic, 2016, Molecular therapy. Methods & clinical development.

Evaluation of engineered AAV capsids for hepatic factor IX gene transfer in murine and canine models

S. Zolotukhin, R. Herzog, A. Srivastava, 2017, Journal of Translational Medicine.

B Cell Depletion Eliminates FVIII Memory B Cells and Enhances AAV8-coF8 Immune Tolerance Induction When Combined With Rapamycin

D. Markusic, J. Rana, Brett Palaschak, 2020, Frontiers in Immunology.

Gene Therapy-Induced Antigen-Specific Tregs Inhibit Neuro-inflammation and Reverse Disease in a Mouse Model of Multiple Sclerosis

D. Markusic, Brett Palaschak, B. Hoffman, 2017, Molecular therapy : the journal of the American Society of Gene Therapy.

An Immune-Competent Murine Model to Study Elimination of AAV-Transduced Hepatocytes by Capsid-Specific CD8+ T Cells

S. Zolotukhin, R. Herzog, D. Markusic, 2017, Molecular therapy. Methods & clinical development.

Evaluation of engineered AAV capsids for hepatic factor IX gene transfer in murine and canine models

S. Zolotukhin, R. Herzog, T. Nichols, 2017, Journal of Translational Medicine.