Assembly of CRISPR ribonucleoproteins with biotinylated oligonucleotides via an RNA aptamer for precise gene editing

por Carlson-Stevermer, Jared, Abdeen, Amr A., Kohlenberg, Lucille, Goedland, Madelyn, Molugu, Kaivalya, Lou, Meng, Saha, Krishanu
Publicado 2017

iPSC-derived hepatocytes generated from NASH donors provide a valuable platform for disease modeling and drug discovery

por Gurevich, Igor, Burton, Sarah A., Munn, Christie, Ohshima, Makiko, Goedland, Madelyn E., Czysz, Katherine, Rajesh, Deepika
Publicado 2020

High-Content Analysis of CRISPR-Cas9 Gene-Edited Human Embryonic Stem Cells

por Carlson-Stevermer, Jared, Goedland, Madelyn, Steyer, Benjamin, Movaghar, Arezoo, Lou, Meng, Kohlenberg, Lucille, Prestil, Ryan, Saha, Krishanu
Publicado 2016

Design of efficacious somatic cell genome editing strategies for recessive and polygenic diseases

por Carlson-Stevermer, Jared, Das, Amritava, Abdeen, Amr A., Fiflis, David, Grindel, Benjamin I, Saxena, Shivani, Akcan, Tugce, Alam, Tausif, Kletzien, Heidi, Kohlenberg, Lucille, Goedland, Madelyn, Dombroe, Micah J., Saha, Krishanu
Publicado 2020