Exploring how CRISPR gene editing challenges traditional distinctions between therapy and enhancement through groundbreaking medical cases.
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.
How CRISPR/Cas9 gene-editing technology offers hope for curing Duchenne Muscular Dystrophy by correcting the root genetic cause of this devastating disorder.
Exploring the revolutionary technologies transforming ophthalmology in 2025 - from AI diagnostics to gene therapy and smart wearables.