Most current approaches rely on adding nuclear localization signal (NLS) motifs to the ends of Cas9 to facilitate nuclear entry. However, this method is inefficient, and much of the Cas9 that is ...
A company’s plan to edit the genomes of human embryos worries some researchers — but it might reflect the changing attitudes ...
In a world first, a bespoke gene-editing therapy benefitted one child. Now reseachers plan to launch a clinical trial of the ...
Advances in cancer immunotherapy from immune checkpoint modulation to adoptive cell transfer of tumour-infiltrating ...
NEW YORK, NY – Two prominent biotechnology companies, Vertex Pharmaceuticals and CRISPR Therapeutics, both led by Indian American CEOs, have been named to TIME’s 2025 list of the 100 Most Influential ...
Northwestern Medicine scientists have discovered how a specific transcription factor promotes genetic reprogramming and ...
In a separate 2024 study, researchers also made mice temporarily transparent. The study, published in Science, showed that ...
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