Optimized AAV Vectors for TMC1 Gene Therapy in a Humanized Mouse Model of DFNB7/11

por Marcovich, Irina, Baer, Nicholas K., Shubina-Oleinik, Olga, Eclov, Rachel, Beard, Clayton W., Holt, Jeffrey R.
Publicado 2022

OR25-01 Durable CYP21A2 Gene Therapy in Non-Human Primates for Treatment of Congenital Adrenal Hyperplasia

por Eclov, Rachel J, Lewis, Terra E W, Kapadia, Mayank, Scott, David W, McCoy, Daniel D, Rouse, Jeremy L, Romero, Kirsten B, Beard, Clayton W, Mansfield, Gary S
Publicado 2020

Inhibition of FOXP3 by stapled alpha-helical peptides dampens regulatory T cell function

por Hawley, Katrina M., Eclov, Rachel J., Schnorenberg, Mathew R., Tian, Yu, Shah, Rhea N., Thomas-Toth, Anika T., Fefferman, Marie, Bird, Gregory H., Walensky, Loren D., Tirrell, Matthew V., LaBelle, James L.
Publicado 2022