Discover how copy number variations (CNVs) influence congenital heart defects through groundbreaking genomic research and advanced diagnostic techniques.
Exploring novel signaling pathways in renal ischemia-reperfusion injury (IRI) and emerging therapeutic strategies.
Explore how genetic research is revolutionizing our understanding of type 2 diabetes, revealing eight distinct subtypes and paving the way for personalized treatment approaches.
Discover how bacteriophages from hospital wastewater are being used to combat antibiotic-resistant Pseudomonas aeruginosa infections through cutting-edge research.
Exploring how AIR technology revolutionizes our understanding of alternative splicing and gene annotation
Exploring how Dicer and Drosha enzymes influence ovarian cancer prognosis and potential therapeutic applications.
Discover how POT1 genetic variations dramatically increase thyroid cancer risk in childhood cancer survivors through telomere dysfunction.
Discover how scientists cracked the genomic code of XiangQingCai, revealing the genetic secrets behind its signature vanilla-like aroma and evolutionary history.
Exploring how modern genomics is decoding BPD's genetic architecture and transforming our understanding of premature lung disease.
Exploring how microsatellites escape genomic detection and their crucial role in evolution, adaptation, and disease.