Exploring the revolutionary frontier of programmable CRISPR-responsive smart materials that sense disease markers and respond intelligently.
Exploring how CRISPR/Cas9 and synthetic DNA are used to create NPHP1 knockout stem cells for studying kidney diseases.
Explore how CRISPR/Cas9 genome editing is revolutionizing agriculture by creating climate-resilient, nutrient-dense crops to address global food security challenges.
Exploring the breakthroughs and ethical challenges of CRISPR gene editing technology through the case study of Baby KJ's treatment and global socio-bioethics considerations
Exploring CRISPR-mediated gamma globin activation in HEK293 cells as a revolutionary approach for treating blood disorders like sickle cell disease and beta-thalassemia.
Understanding the hidden risks of gene editing and how scientists are creating safer genetic medicines with CRISPR technology.
Explore how CRISPR gene editing is transforming the treatment of inherited blindness through groundbreaking clinical trials and innovative therapies.
Explore how CRISPR-Cas9 is transforming hematology, from curing sickle cell disease to personalized gene therapies for rare blood disorders.
Exploring how knowledge and values influence attitudes toward gene editing technologies among farmers, scientists, policymakers, and the public.
An in-depth look at the CRISPR baby scandal, its ethical implications, and the future of human gene editing