Every year, approximately 8 million children are born with a serious genetic disorder, and 3 million of them die before the age of 5. This disease burden is about to change. In this episode, we launch the CRISPR Chronicles series that will run throughout season 3. Since the pivotal paper by Doudna and Charpentier in 2012, CRISPR has taken the world by storm. Scientists have used this genome engineering tool in the lab to quickly and easily create mutants to study gene function in laboratory animals. But more importantly, the power of CRISPR gene editing as a biomedical intervention to cure diseases has been realized. Currently, dozens of clinical trials are ongoing or on the verge of being launched to cure everything from genetic blindness and sickle cell anemia, to cancers and HIV. In fact, the Sickle Cell Disease treatment, exa-cel is poised to become the first CRISPR gene editing therapy to be approved by the FDA. Due to its far-reaching impacts, Doudna and Charpentier won the Nobel Prize in chemistry in 2020 for discovery of CRISPR-Cas9 gene editing; thereby, breaking the boundary as dual female winners of this prize.
In this series we will explore:
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Hear directly from Sickle Cell Disease patients who were cured during the clinical trial: Victoria Gray and Jimi Olaghere
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Reach out to Fatu:
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Music from Pixabay: Future Artificial Intelligence Technology 130 by TimMoor
Music from https://freemusicarchive.org/music/Scott_Holmes: Hotshot by ScottHolmesMusic