AI Powered CRISPR: The Next Generation of Gene Editing Tools Gene editing has relied on tools discovered in nature, but a new wave of innovation is changing how we create proteins by harnessing artificial intelligence. Scientists can now design custom CRISPR sy... artificial intelligence CRISPR gene editing genome engineering immunogenicity precision medicine protein design synthetic biology
Yale’s Antibody-RNA Therapy: Tackling Treatment Resistant Cancers Recent advances at Yale are reshaping the fight against some of the toughest cancers. Researchers have engineered a unique antibody-RNA therapy that offers renewed hope for patients where traditional ... antibody-RNA cancer therapy clinical trials immunotherapy precision medicine resistant tumors Yale research
Unveiling Hidden Cell Subtypes to Transform Cancer Research CellLENS is a groundbreaking artificial intelligence tool developed by a multidisciplinary team led by MIT designed to precisely identify which immune cells are fighting, helping, or hindering tumors,... artificial intelligence biomarkers cancer research cell subtypes deep learning immunotherapy precision medicine
Yale Scientists Triple Precision and Reach in Human Gene Editing Yale genome engineers are dramatically expanding the capacity and accuracy of gene editing. The work recently published in Nature , may change how we approach gene editing across research and personal... biotechnology CRISPR disease research gene editing genome engineering precision medicine Yale research
AI Powers Precision Gene Delivery Systems For Brain and Spinal Cord Therapy Thanks to innovative gene delivery systems developed by NIH-funded teams, we may soon be able to deliver genetic instructions directly and precisely to select cells within the brain or spinal cord. Th... AAV vectors brain research gene therapy neurological disorders neuroscience NIH BRAIN Initiative precision medicine
Personalized Gene Therapy: A Lifesaving Advance for Infants with Rare Diseases Picture the heartbreak of learning your newborn has a rare, life-threatening genetic disorder with no proven cure. Now, imagine that within months, a customized therapy could rewrite that child’s dest... CRISPR gene therapy infant health liver disorders NIH research precision medicine rare diseases