Research Articles
AI and Biology: Programming the Future of Life Sciences
Explore how artificial intelligence is revolutionizing biological sciences, from DNA analysis to drug discovery and protein design.
The Green Scissors: How Precision Genome Editing is Revolutionizing Agriculture and Challenging the Precautionary Principle
Explore how precision genome editing technologies like CRISPR are transforming agriculture while navigating regulatory frameworks and the precautionary principle.
Tangeria: How Gene Editing Became Africa's Answer to the Climate Crisis
Exploring how gene editing technology offers solutions to climate change impacts on agriculture in Africa
The Gene Editor's Toolkit: How Scientists Are Rewriting the Code of Life to Unlock Disease Mysteries
Explore how gene editing technologies like CRISPR are revolutionizing biomedical research and enabling scientists to study gene function and disease mechanisms with unprecedented precision.
Grand Challenges in Analytical Science: How Cutting-Edge Technology is Solving World's Biggest Problems
Explore how analytical science tackles global challenges through innovations in pathogen detection, food safety, and miniaturization with AI integration.
Delivering the Goods: The Scientific Quest to Perfect CRISPR Gene Editing
Explore the groundbreaking research making CRISPR-Cas gene editing more targeted and efficient through nanotechnology and advanced delivery systems.
The Molecular Machines That Awaken Bacterial Genes: How ATP Powers Transcription
Explore how bacterial enhancer-binding proteins harness ATP energy to activate gene transcription through sophisticated molecular mechanisms.
Cracking the Code of Life: How Scientists Are Modeling Infertility One SNP at a Time
Explore how scientists are developing innovative in vitro platforms to model infertility-causing SNPs, combining computational biology with gene editing to revolutionize reproductive medicine.
Rewriting Life's Code: How CRISPR Gene Editing is Revolutionizing Treatment for Blood Diseases
Explore how CRISPR-mediated genome editing of hematopoietic stem and progenitor cells is transforming treatment for genetic blood disorders like sickle cell disease and beta thalassemia.
Cracking the Code: How Exome Sequencing Solved a Genetic Mystery Linking Spine Abnormalities and Muscle Weakness
Discover how exome sequencing identified DYNC1H1 variants associated with spinal muscular atrophy and vertebral abnormalities, revolutionizing genetic diagnosis.