Genetics

Discovery unravels the mystery of a rare bone disease

A McGill-led team of researchers has made an important discovery shedding light on the genetic basis of a rare skeletal disorder. The study, published in Nature Communications, reveals that a defect in a specific gene (heterozygous ...

Diseases, Conditions, Syndromes

Study shows T cells can tackle new 'Pirola' SARS-CoV-2 variant

In August, researchers detected a new SARS-CoV-2 "variant of concern" in patients in Israel and Denmark. Since then, this variant, dubbed BA.2.86 or "Pirola," has made its way around the globe. The Pirola variant has raised ...

page 4 from 40