The personalized CRISPR treatment could be the future of gene therapy, but hurdles remain before everyone has access.

An international group of gene editing leaders has put out a call for a 10-year ban on heritable human genome editing (HHGE), ...

Broad Institute researchers have developed a way to edit the genetic sequences at the root of Huntington's disease and ...

Released Tuesday, the 2025 Sunscreen Guide lists the most effective sunscreens available for purchase in 2025.

Somatic hypermutation (SHM) of immunoglobulin variable (V) regions modulates antibody-antigen affinity is initiated by activation-induced cytidine deaminase (AID) on single-stranded DNA (ssDNA).

David Liu and Richard Merkin of the Broad Institute of MIT and Harvard, along with Columbia professor Sam Sternberg, have ...

Global health stories including rare illnesses, climate change, hypertension, and more, with a focus on little KJ Muldoon's ...

“This is the first step towards the use of gene editing therapies to treat a wide variety of rare genetic disorders for which ...

Editas Medicine reports successful gene editing levels in stem cells, supporting potential treatment for sickle cell disease and beta thalassemia. Editas Medicine announced promising new data on ...

Full list of extinct animals being brought back from extinction As the power of gene editing becomes more advanced, ideas that once seemed like science fiction are rapidly becoming a possibility.Now, ...

In the study, researchers used CRISPR/Cas9 gene-editing to modify a type of immune cell called tumor-infiltrating lymphocytes (TILs). By deactivating a gene called CISH, the researchers found that ...