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.
Fluorescent tagging system can expedite the process of designing genes and personalizing medicine.
Study finds shallow bodies of water were probably more suitable for Earth’s first life forms.
Professor Gerald Fink, a pioneer in the field of genetics, delivers the annual Killian Lecture.
Rights are protected for broad use in developing world and for public health needs.
Studies could speed the development of new treatments for liver disease.
CRISPR team harnesses new Cas12b enzyme for use in eukaryotic cells, adding to the CRISPR toolbox.
Patients with lung disease could find relief by breathing in messenger RNA molecules.
Researchers refine a method to quantify protein production, show that the precision with which bacteria and eukaryotes tune their gene expression is remarkably similar.
Together, cell growth rate and gene expression shed light on why some tumor cells survive treatment.
Enzyme can target almost half of the genome’s “ZIP codes” and could enable editing of many more disease-specific mutations.
Biological engineers design RNA circuits that enable precise control over the dose of therapeutic protein a patient receives.
Biophysicist will investigate the biology of RNA aggregation.
Scientists leverage one step, unbiased method to characterize the binding preferences of more than 70 human RNA-binding proteins.
Scientists identify the first known network consisting of three types of regulatory RNAs.