CRISPR Corrects Disease Mutation in Human Embryos

04:49 EDT 3 Aug 2017 | Genetic Engineering News

You may want your children to inherit your blue eyes, your sharp wit, or your athletic prowess. You may not, however, wish to pass on your genetic mutations that are associated with chronic disease and mortality. With the help of CRISPR and a bait-and-switch of genetic material, scientists may soon be able to halt the inheritance of gene-based diseases across generations. In the near-term, investigators are specifically looking at how genes can be repaired to avoid disease. The technique would likely be reserved for serious conditions that have few existing treatment options; researchers have not yet evaluated the clinical applicability of “designer babies,” wherein parents pick and choose the traits they would like their children to possess. "This research significantly advances scientific understanding of the procedures that would be necessary to ensure the safety and efficacy of germline gene correction," said Daniel Dorsa, Ph.D., senior vice president ...

Original Article: CRISPR Corrects Disease Mutation in Human Embryos


More From BioPortfolio on "CRISPR Corrects Disease Mutation in Human Embryos"

Quick Search

Relevant Topics

Pediatrics is the general medicine of childhood. Because of the developmental processes (psychological and physical) of childhood, the involvement of parents, and the social management of conditions at home and at school, pediatrics is a specialty. With ...

Ophthalmology is the branch of medicine that is devoted to the study and treatment of eye diseases. As well as mild visual defects correctable by lenses, ophthalmology is concerned with glaucoma, uveitis and other serious conditions affecting the eye, ...

Bioinformatics is the application of computer software and hardware to the management of biological data to create useful information. Computers are used to gather, store, analyze and integrate biological and genetic information which can then be applied...