Research Articles
Bone Marrow Delivery: Revolutionizing Genetically Modified Stem Cell Transplantation
Discover how bone marrow delivery of genetically modified CD34+ HSPCs improves homing and engraftment of short-term progenitors over long-term repopulating hematopoietic stem cells.
Red Blood Cell Revolution: Advances in Transfusion Therapy and Emerging Treatments for Sickle Cell Disease
Exploring the latest advances in transfusion therapy, pharmacological treatments, and groundbreaking gene therapies for sickle cell disease.
CRISPR and Beyond: How French Scientists Are Revolutionizing Gene Therapy
Explore how French researchers are advancing genome editing technologies for gene therapy applications, tackling genetic disorders with innovative CRISPR-based approaches.
Rewriting Our Defense Code: How CRISPR and Adenoviruses Are Revolutionizing HIV Treatment
Explore how adenovirus-delivered CRISPR/Cas9 gene editing technology is revolutionizing HIV treatment by targeting the CCR5 receptor.
Genetic Packages: How Lipid Nanoparticles Are Revolutionizing Gene Therapy
Explore how lipid nanoparticles are transforming gene therapy, enabling safe DNA delivery and targeted treatments for chronic diseases like diabetes, cancer, and heart conditions.
Unlocking the Code: Gene Editing Revolutionizes Veterinary Cancer Care
How CRISPR gene editing and advanced gene therapies are transforming veterinary oncology by targeting cancer at its genetic roots.
Redefining Human Potential: How CRISPR Shatters the Therapy-Enhancement Divide
Exploring how CRISPR gene editing challenges traditional distinctions between therapy and enhancement through groundbreaking medical cases.
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.
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.