Research Articles
The Gene Editing Revolution: Healing Humanity Without Losing Our Souls
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
Unlocking the Body's Fetal Blueprint: CRISPR Reactivation of Gamma Globin in HEK293 Cells
Exploring CRISPR-mediated gamma globin activation in HEK293 cells as a revolutionary approach for treating blood disorders like sickle cell disease and beta-thalassemia.
The Unseen Side Effects of Genetic Scissors: Hunting CRISPR's Off-Target Effects
Understanding the hidden risks of gene editing and how scientists are creating safer genetic medicines with CRISPR technology.
Seeing the Light: How CRISPR Gene Editing Is Revolutionizing the Fight Against Blindness
Explore how CRISPR gene editing is transforming the treatment of inherited blindness through groundbreaking clinical trials and innovative therapies.
The Genetic Scissors Revolution: How CRISPR Is Rewriting the Future of Blood Disease Treatment
Explore how CRISPR-Cas9 is transforming hematology, from curing sickle cell disease to personalized gene therapies for rare blood disorders.
The Gene Gap: How Knowledge and Values Shape Our Views on CRISPR Crops and Designer Babies
Exploring how knowledge and values influence attitudes toward gene editing technologies among farmers, scientists, policymakers, and the public.
The CRISPR Baby Scandal: Science, Ethics, and the Future of Humanity
An in-depth look at the CRISPR baby scandal, its ethical implications, and the future of human gene editing
Unlocking Cancer's Origins: How CRISPR-Edited Mini-Organs Decode Mutational Mysteries
Discover how CRISPR-edited organoids are revolutionizing cancer research by decoding mutational signatures and revealing cancer origins.
CRISPR Cluckers: Rewriting the Chicken Embryo Genome
How CRISPR is transforming chicken embryos into sophisticated genetic models, advancing fields from immunology to sustainable agriculture.
CRISPR's Precision Scissors: Rewriting the Genetic Code of Duchenne Muscular Dystrophy
How CRISPR/Cas9 gene-editing technology offers hope for curing Duchenne Muscular Dystrophy by correcting the root genetic cause of this devastating disorder.