A recent publication in Genes & Diseases has delivered a compelling synthesis of the latest insights into the cellular ...

A recent publication in Genes & Diseases has delivered a compelling synthesis of the latest insights into the cellular ...

Amyotrophic lateral sclerosis (ALS) is a relatively rare but very serious disease of the nervous system. A cure is not yet ...

Focal cortical dysplasia (FCD) type 2 is a congenital malformation of the cerebral cortex that is often associated with ...

Sclerosteosis is a rare genetic disorder that causes excessive bone growth, leading to life-altering complications, including hearing loss and facial paralysis.

Sclerosteosis arises from mutations in the SOST gene, causing abnormally high bone mass and skeletal overgrowth, which can lead to severe health issues such as hearing loss and increased intracranial ...

Shin Dong-yeop, a professor of hematologic oncology at Seoul National University Hospital, recently won the Senior Researcher ...

Here, we discover lysophospholipids as endogenous pannexin activators, using activity-guided fractionation of mouse tissue extracts combined with untargeted metabolomics and electrophysiology. We show ...

A landmark review in Nature Reviews Genetics dissects the rare and common genetic variants that shape human height. The paper ...

Neha Dole, an assistant  professor in the departments of Physiology and Cell Biology, Orthopaedic Surgery and Pediatrics at the University of Arkansas for Medical Sciences, will speak at 12:55 p.m.

The stock has managed to close above the Doji formation, signaling buyer dominance. The price has managed to trade above the major EMA further confirming the uptrend. The RSI is moving in the ...