Explore how KLF14 genetic variations function as master regulators in metabolic diseases, with sex-specific effects and therapeutic potential.
Explore the genetic factors, diagnostic approaches, and prevention strategies for inherited Alzheimer's disease risk.
Explore the fascinating story of the bronze-mutable 4 mutation in maize, a natural genetic experiment that revealed how transposable elements create diversity.
Explore how ghrelin, the hunger hormone, and its genetic variants influence type 2 diabetes risk, complications, and potential treatments.
Discover how breaking the ATF4 gene in mice creates resistance to fatty liver disease even on high-carb diets, revealing new therapeutic pathways for human health.
Discover how SLC2A9 isoforms mediate electrogenic urate transport with different characteristics in the presence of hexoses and their implications for human health.
Explore how genetic predisposition and circadian misalignment interact to influence obesity risk and metabolic health.
Discover how fructose uniquely hijacks your body's fat-making genes in intestines and kidneys, leading to increased fat storage through fascinating scientific experiments.
Explore how CRISPR-Cas9 technology is revolutionizing genetic engineering, from bacterial defense systems to groundbreaking medical applications.
Exploring the controversial Trp64Arg mutation research in Japanese men and how scientific understanding of obesity genetics evolved through conflicting studies.