Explore how CRISPR and stem cell technologies are transforming medicine by enabling precise genetic corrections for diseases like sickle cell anemia and cancer.
Explore how microRNAs and Ago2 protein work together as cellular traffic controllers to guide stem cell fate through genome-wide binding mapping.
Discover how the KOLF2.1J reference iPSC line is solving the reproducibility crisis in stem cell research and enabling large-scale collaborative studies.
Explore how mouse embryonic stem cells employ unique strategies to preserve their genomic integrity against constant DNA damage threats.
Exploring how CRISPR/Cas9 and synthetic DNA are used to create NPHP1 knockout stem cells for studying kidney diseases.