New gene-editing system precisely inserts large DNA sequences into cellular DNA
Researchers identify and develop new CRISPR-associated transposase system for targeted integration of DNA, adding key capabilities to gene-editing technology.
Researchers identify and develop new CRISPR-associated transposase system for targeted integration of DNA, adding key capabilities to gene-editing technology.
CRISPR team harnesses new Cas12b enzyme for use in eukaryotic cells, adding to the CRISPR toolbox.
Enzyme can target almost half of the genome’s “ZIP codes” and could enable editing of many more disease-specific mutations.
With SHERLOCK, a strip of paper can now indicate presence of pathogens, tumor DNA, or any genetic signature of interest.
Department of Biology kicks off IAP seminar series with a lecture by synthetic-biology visionary George Church.
“REPAIR” system edits RNA, rather than DNA; has potential to treat diseases without permanently affecting the genome.
MIT associate professor and member of the Broad Institute and McGovern Institute recognized for commitment to invention, collaboration, and mentorship.
Five recipients honored for their fundamental and complementary accomplishments related to CRISPR-Cas9.
New system adapts tool known for gene editing; to be used in rapid, inexpensive disease diagnosis.
MIT professor and NAS report committee co-chair Richard Hynes gives insight into the report’s recommendations.
MIT and Broad Institute scientist shares recognition with four other scientists for developing CRISPR gene-editing systems.
PhD student Tim Wang uses CRISPR to take a big-picture approach to cancer research.
Broad Institute/MIT scientist among three honored for CRISPR contributions.
Scientists program C2c2, discovered in bacteria as a viral defense mechanism, to manipulate cellular RNA.
Broad/MIT scientist among five honored as pioneers of CRISPR-Cas9 system.