Exploring the role of the androgen receptor gene in hypospadias development through recent scientific research and genetic analysis.
Discover how the Ryanodine Receptor 1 gene mutation affects anesthesia response and leads to malignant hyperthermia, with recent scientific breakthroughs explained.
Exploring the expanding genetic spectrum of heritable polyposis syndromes and colorectal cancer, from new gene discoveries to clinical applications.
Explore the fascinating phenomenon of recurrent centromere seeding, where chromosomes can form new centromeres at specific hotspot locations, challenging our understanding of genetics.
Discover how the Fli-1 gene and its Fli-1b isoform regulate blood development and contribute to diseases through alternative promoters and differential splicing.
Discover how exome sequencing in multiplex families provides compelling evidence for the NMDA receptor hypofunction hypothesis of schizophrenia and its implications for treatment.
Explore how scientists are redesigning genome-wide association studies (GWAS) to be more efficient, powerful, and useful in understanding our genetic blueprint.
Discover how B chromosomes, the genomic rebels, challenge our understanding of genetics with their selfish inheritance strategies and potential biological significance.
Explore the fascinating world of mitochondrial introns - from their classification and functions to their evolutionary journey across organisms.
Exploring rare genetic variants in acute promyelocytic leukemia that challenge standard treatment approaches and require advanced diagnostic techniques.