Low dose of aspirin cuts recurrence risk in colorectal cancer with genetic mutation
A Swedish-led research team at Karolinska Institutet and Karolinska University Hospital has shown in a new randomized clinical…
Genetic mutation in some East Asians linked to aldehyde storm and increased liver disease risk
Researchers have identified the mechanism by which a common genetic mutation increases liver disease risk. Their findings suggest…
Zebrafish study reveals how environment influences social behaviors in autism
Researchers from Brain Research Institute, Niigata University, Japan have revealed that environment influences social behaviors in autism. By…
A novel MCMDC2 variant causes meiotic arrest and non-obstructive azoospermia in a consanguineous Chinese family
Cerván-MartÃn M, Castilla JA, Palomino-Morales RJ, Carmona FD. Genetic landscape of nonobstructive azoospermia and new perspectives for the…
Insights into clinical features and genetic variants of Cornelia de Lange syndrome in China
Cornelia de Lange syndrome (CdLS) is a rare genetic disorder with symptoms, including facial anomalies (such as fused…
Prime editing reverses symptoms of severe childhood neurological disease
Scientists use a precise form of gene editing called prime editing to correct the most common genetic mutations…
$5.5 million federal grant funds research to improve measurement of FXTAS treatments
UC Davis Health Professor of Psychiatry and Behavioral Sciences David Hessl will help lead a major research project…
Researchers classify how specific genetic mutations correspond to rare disorders
The NF-κB signaling pathway plays a pivotal role in how our bodies fight infection, heal, and regulate inflammation.…
Rare coexistence of APC and KRAS mutations observed in patient with FAP and endometrial cancer
Researchers have discovered an unusual case where two well-known cancer-related mutations-APC and KRAS-coexisted in a woman with familial…