Outside Publication
May 31, 2022
The lately printed e book, Regulation of Genome Editing in Human iPS Cells, examines two situations for the long run therapy of hereditary ailments—both germ line therapies or somatic cell/gene therapies. Genome enhancing—particularly by means of clustered recurrently interspaced brief palindromic repeats (CRISPR)/CRISPR-associated proteins and induced pluripotent stem cells (iPSCs)—kinds the important scientific and technological elements of these two therapeutic approaches.
Partner Kathy Sanzo authored the US chapter of the e book, noting the United States is a “world leader in the field of cell and gene therapies,” which is “mirrored by the US regulatory framework which fosters research on, as well as development, application and marketing of, cell and gene therapy (CGT) products without compromising their safety, efficacy and quality.”
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