Research Articles
The Gatekeeper's Secret: How a Tiny Mouse Receptor Controls Inflammation and Healing
Discover how IL-22RA1, a molecular receptor in mice, bridges immunity and tissue repair through its unique genomic features and inducible expression patterns.
Beyond Metabolism: The Secret Life of GAPDH in HeLa Cells
Exploring the multifaceted roles of GAPDH in HeLa cells beyond its metabolic functions, including DNA repair, cell survival, and transcriptional complexity.
The Silent Invader: How a Crafty Fungus Thrives in Termite Metropolises
Discover how Pseudoxylaria, a crafty fungus, survives in termite colonies through genomic downsizing, metabolic stealth, and chemical warfare.
The Genetic Treasure Hunt: Unlocking Rice's Hidden Potential Against Salinity
Discover how genome-wide association studies (GWAS) are revolutionizing rice breeding to combat salinity stress in a changing climate.
Unlocking Evolutionary Secrets: How a Splice Variant's "Molecular Fossils" Rewrite Primate History
Discover how SP100 splice variant's molecular fossils are rewriting primate evolutionary history through genetic archaeology.
The Cellular Tightrope: How Chfr and Kif22 Dance to Prevent Genetic Chaos
Exploring the crucial interaction between Chfr and Kif22 proteins in maintaining genomic stability during cell division and its implications for cancer research.
Building Better Blood Vessels: The Rise of Humanized ECFCs in Regenerative Medicine
Exploring the breakthrough of humanized ECFCs for blood vessel regeneration in cardiovascular diseases and regenerative medicine.
The Tiny Titans: How Soybean Genetics Are Revolutionizing Your Dinner Plate
Discover how soybean genetics are transforming global food supply through breakthroughs in seed size and yield characteristics.
The Secret Life of Rice Genomes: Unmasking Active Transposons in the Wild
Discover how active transposable elements in naturally growing rice plants are reshaping our understanding of genome evolution and crop improvement.
Rewriting Genetic Destiny: How CRISPR Revolutionized Treatment for a Baby's Rare Metabolic Disorder
Breakthrough CRISPR treatment saves newborn with CPS1 deficiency through personalized gene editing in just six months.