High-precision technique stores cellular “memory” in DNA
Engineers program human and bacterial cells to keep a record of complex molecular events.
Search Stories
Speeding up drug discovery for brain diseases
Whitehead Institute team finds drugs that activate a key brain gene; initial tests in cells and mice show promise for rare, untreatable neurodevelopmental disorder.
New CRISPR platform expands RNA editing capabilities
The new system, dubbed RESCUE, allows RNA edits to be made that were not previously possible.
Machine learning for everyone
A new EECS course on applications of machine learning teaches students from a variety of disciplines about one of today’s hottest topics.
Using gene editing, neuroscientists develop a new model for autism
By introducing a gene variant associated with autism into monkeys, researchers hope to study treatment options for severe neurodevelopmental disorders.
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.
Nanoparticles take a fantastic, magnetic voyage
Tiny robots powered by magnetic fields could help drug-delivery nanoparticles reach their targets.
The complex world of carbohydrate chemistry
Drawn to MIT by its “amazing women who were doing science,” Professor Laura Kiessling explores sugar-protein interactions that influence cell behavior.
How our gray matter tackles gray areas
Marshall Scholar Katie O’Nell investigates how the brain resolves complicated questions involving morality and generosity.
The evolving definition of a gene
Professor Gerald Fink, a pioneer in the field of genetics, delivers the annual Killian Lecture.
Keeping genetic engineering localized
Researchers are developing a so-called "daisy-chain" gene-drive system that provides controls for genetic engineering of certain populations.
Academic institutions grant commercial license for CRISPR-based SHERLOCK diagnostic technology in developed world
Rights are protected for broad use in developing world and for public health needs.
Scientists engineer new CRISPR platform for DNA targeting
CRISPR team harnesses new Cas12b enzyme for use in eukaryotic cells, adding to the CRISPR toolbox.
New CRISPR tool opens up more of the genome for editing
Enzyme can target almost half of the genome’s “ZIP codes” and could enable editing of many more disease-specific mutations.
Feng Zhang wins 2018 Keio Medical Science Prize
McGovern Institute scientist is recognized with award for outstanding and creative achievements made in the life and medical sciences.