| abstract |
The present invention relates to a method for delivering a nucleic acid to a cell, a tissue, an organ, and a patient, a method for inducing a cell to express a protein using nucleic acid, Methods, kits and devices for transfection, gene editing, and regrouping of cells, and cells, organisms, therapeutic agents, and cosmetics produced using these methods, kits, and devices. Methods and products for modifying the DNA sequence of a cell, and methods and products for inducing the expression of proteins, including cells in vivo, using synthetic RNA molecules, are described. Therapeutic agents comprising a nucleic acid encoding a gene-editing protein are also described. |