A System to Enrich for Primitive Streak-Derivatives, Definitive Endoderm and Mesoderm, from Pluripotent Cells in Culture

por Vassilieva, Svetlana, Goh, Hwee Ngee, Lau, Kevin X., Hughes, James N., Familari, Mary, Rathjen, Peter D., Rathjen, Joy
Publicado 2012

CRISPR/Cas9-generated mouse model with humanizing single-base substitution in the Gnao1 for safety studies of RNA therapeutics

por Polikarpova, Anna V., Egorova, Tatiana V., Lunev, Evgenii A., Tsitrina, Alexandra A., Vassilieva, Svetlana G., Savchenko, Irina M., Silaeva, Yuliya Y., Deykin, Alexey V., Bardina, Maryana V.
Publicado 2023

CRISPR/Cas9-generated mouse model of Duchenne muscular dystrophy recapitulating a newly identified large 430 kb deletion in the human DMD gene

por Egorova, Tatiana V., Zotova, Evgenia D., Reshetov, Denis A., Polikarpova, Anna V., Vassilieva, Svetlana G., Vlodavets, Dmitry V., Gavrilov, Alexey A., Ulianov, Sergey V., Buchman, Vladimir L., Deykin, Alexei V.
Publicado 2019

In-Frame Deletion of Dystrophin Exons 8–50 Results in DMD Phenotype

por Egorova, Tatiana V., Galkin, Ivan I., Velyaev, Oleg A., Vassilieva, Svetlana G., Savchenko, Irina M., Loginov, Vyacheslav A., Dzhenkova, Marina A., Korshunova, Diana S., Kozlova, Olga S., Ivankov, Dmitry N., Polikarpova, Anna V.
Publicado 2023

CRISPR-Cas9 correction in the DMD mouse model is accompanied by upregulation of Dp71f protein

por Egorova, Tatiana V., Polikarpova, Anna V., Vassilieva, Svetlana G., Dzhenkova, Marina A., Savchenko, Irina M., Velyaev, Oleg A., Shmidt, Anna A., Soldatov, Vladislav O., Pokrovskii, Mikhail V., Deykin, Alexey V., Bardina, Maryana V.
Publicado 2023

Therapeutic potential of highly functional codon-optimized microutrophin for muscle-specific expression

por Starikova, Anna V., Skopenkova, Victoria V., Polikarpova, Anna V., Reshetov, Denis A., Vassilieva, Svetlana G., Velyaev, Oleg A., Shmidt, Anna A., Savchenko, Irina M., Soldatov, Vladislav O., Egorova, Tatiana V., Bardina, Maryana V.
Publicado 2022