Experts hailed exciting news for some people with sickle cell disease in England as the health watchdog decided to grant ...

Image source: Getty Images. Several companies are using CRISPR to edit human genomes in an attempt to treat (and even cure) genetic diseases. Their therapies either use an ex vivo approach or an ...

CRISPR technology has revolutionized genetic testing and disease detection, offering precise, rapid, and cost-effective diagnostic solutions. This gene-editing tool has been adapted for molecular ...

In December 2023, the FDA approved the first Crispr-based therapy for sickle cell disease. That approach required taking bone marrow cells out of the body, making a disabling cut in a particular ...

For example, we manipulate a pathway to prevent mosquitoes from transmitting viral diseases. We also develop diagnostics so that people can detect in the field if an insect is infected with a pathogen ...

Algen Biotechnologies fuses cutting-edge gene editing clustered regularly interspaced short palindromic repeat (CRISPR ... biology of cancer and other diseases to find novel, high-confidence ...

The CRISPR/Cas9 technology is among the most exciting developments in biotechnology in recent years, a revolutionary technique which will allow faulty genes linked to any inherited disease to be ...

But it’s a slippery slope. When does reducing the risk of inherited breast cancer, diabetes, or Alzheimer’s disease edge into “designer baby” territory? As scientists grapple with the implications of ...

CRISPR is a technology that can be used to edit genes and, as such, will likely change the world. The essence of CRISPR is simple: it’s a way of finding a specific bit of DNA inside a cell.

CRISPR Therapeutics (Nasdaq: CRSP), a biopharmaceutical company focused on creating transformative gene-based medicines for serious diseases, today highlighted its strategic priorities and ...