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Mutation

Prime editing offers promising path to permanent treatment for cystic fibrosis

Cystic fibrosis is one of the most common genetic disorders, causing thick...

Novel antiviral protein SAMD9L blocks HIV-1 and other lentiviruses

In a recent study published in the journal PLOS Biology, researchers in...

Pacific Northwest Research Institute uncovers hidden DNA mechanisms of rare genetic diseases

Researchers at the Pacific Northwest Research Institute (PNRI) and collaborating institutions have made a...

New therapeutic target discovered for treatment-resistant melanoma

An international research team led by scientists from the University of Liège...

How 1301B7 Could Contribute To Advanced Vaccine Development

In the ongoing Omicron era, a new COVID-19 antibody could renew optimism for urgently required SARS-CoV-2 monoclonal therapies. Over the last three years, various...

Family’s rare telomere mutation reveals new insights into telomere flexibility and disease

In a recent study published in the journal Nature Communications, researchers discovered...

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