Their data suggests that tweaking the expression of FDX2 could make up for the loss of frataxin, the protein tied to FA's development.
Scientists discovered that the protein RPA plays a critical and previously unconfirmed role in stimulating telomerase to ...
With a rate of mutation 35 percent higher than random chance, this previously unknown weakness could be a major vector for ...
European fertility clinics used cancer-causing sperm for 17 years, prompting urgent calls for genetic screening reforms and ...
After more than 50 years of research, scientists still don't know exactly what causes autism. But the data make clear that ...
Every winter, respiratory viruses, especially influenza, SARS-CoV-2 and RSV, put huge pressure on healthcare systems throughout Europe. In a typical season, flu causes up to 50 million symptomatic ...
Although the COVID pandemic led to a better understanding of the coronaviruses, viruses, and vaccines, a backlash emerged to ...
Researchers at the Department of Cell and Molecular Biology, Karolinska Institutet have captured the first detailed molecular ...
Financing includes participation from leading institutional investors including Janus Henderson Investors, Brahma Capital, Biotrack Capital, Cormorant Asset Management, OrbiMed, Plaisance Capital ...
An international research team involving the German Primate Center—Leibniz Institute for Primate Research (DPZ), Hannover ...
A sperm donor with a rare genetic mutation linked to an increased risk of developing cancer fathered at least 197 children across Europe, some of whom have already died from the disease, according to ...
Scientists have uncovered a surprising genetic workaround that helps cells cope with Friedreich’s ataxia, a rare and devastating disorder.
Some results have been hidden because they may be inaccessible to you
Show inaccessible results