Scientists have uncovered a hidden layer of genetic regulation that helps explain why individuals with the same blood type can differ so dramatically at the molecular level.

Researchers at University of California San Diego School of Medicine, the Salk Institute and Sanford Burnham Prebys have ...

Researchers discovered that suppressing BMP signaling in astrocytes reduces seizures and restores brain balance in Fragile X syndrome models.

In vitro transcribed mRNA has lived up to its potential as a game-changing disruptive vaccine modality during the COVID-19 ...

A research university emphasizes entrepreneurial science—and spawns start-ups in fields as varied as genetic medicine, ...

Genome editing is revolutionizing the medical landscape by offering new therapeutic possibilities for genetic diseases, which collectively affect hundreds ...

Research uncovers new genetic pathways linking lipid metabolites to cardiovascular disease and diabetes risk in the Indian ...

On 25 April 1953, Watson and Crick published an article, in the acclaimed journal “Nature” titled “Molecular structure of nucleic acids: A structure for deoxyribonucleic acid”. The one-page article ...

Fragile X syndrome (FXS) is an inherited genetic developmental condition that strongly impacts brain development. Despite the ...

Roizman reshaped the field of virology through his work on the herpes simplex virus, laying the groundwork for efforts to ...

Responding to reports from peer reviewers is a crucial part of scientific publishing, but early-career researchers are rarely taught about this process.

A study conducted in an Indian population has identified new molecular pathways that contribute to cardiovascular disease, ...