Research Articles
The Secret Highway of Our Cells: How Francesca Bottanelli is Rewriting the Textbooks
Discover how Francesca Bottanelli's groundbreaking research revealed the ARF1 compartment, a previously unknown cellular structure revolutionizing our understanding of intracellular transport.
The CRISPR Revolution: Rewriting the Code of Life
Explore how CRISPR-Cas genome editing technology is revolutionizing genetic engineering, from basic mechanisms to real-world applications in medicine and biotechnology.
Rewriting Cancer's Code: How AI Decodes Leukemia's Secrets
Discover how neurosymbolic AI is revolutionizing pediatric acute myeloid leukemia research by predicting cell fate decisions and enabling personalized treatments.
Unlocking Safer Cancer Therapy: How Tumour-Specific Promoters Are Revolutionizing Armoured CAR T-Cells
Discover how tumour-specific promoters and CRISPR technology are creating safer, more effective armoured CAR T-cell therapies for cancer treatment.
Unlocking Pancreatic Cancer's Secret Weapon: A Surprising Metabolic Twist
Discover how pancreatic cancer rewires its metabolism through HDAC1 deletion and fatty acid oxidation, revealing new therapeutic opportunities.
The Gene Editors: How Molecular Genetics is Rewriting the Code of Insect Life
Explore how molecular genetics is transforming our understanding and manipulation of insects through CRISPR, gene drives, and other revolutionary technologies.
Harnessing Nature's Scissors: How CRISPR is Revolutionizing Bacillus Biotechnology
Explore how CRISPR-based tools are reprogramming Bacillus bacteria and their phages, opening new frontiers in biotechnology, medicine, and sustainable manufacturing.
Restoring Vision: How Gene Therapy is Revolutionizing Treatment for Retinal Ciliopathies
Explore how gene therapy is transforming treatment for retinal ciliopathies, genetic disorders affecting cellular antennae in the eyes that cause progressive vision loss.
CRISPR and the Quest for a Cure: Rewriting the Genetic Code of Duchenne Muscular Dystrophy
Explore how CRISPR/Cas9 gene editing technology is revolutionizing the treatment of Duchenne Muscular Dystrophy by correcting the genetic mutations responsible for this devastating condition.
The Heart's Silent Scaffold: How a Tiny Flaw Unravels the Engine of Life
Discover how titin mutations cause dilated cardiomyopathy through sarcomere insufficiency in lab-grown heart cells