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CRISPR is a tool that allows one to go into a person’s genome–which is the complete set of genes in a cell–and manipulate it to add, subtract or change a person’s genes.
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The Code Breaker profiles Jennifer Doudna, a Nobel Prize-winning biochemist key to the development of CRISPR, and examines the technology's exciting possibilities and need for oversight.
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Since receiving a landmark treatment with the gene-editing tool CRISPR, a sickle cell patient has the strength to care for herself and her children — while navigating the pandemic.
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He Jiankui announced in November 2018 that he had created the world's first gene-edited babies. Scientists are concerned about unintended side effects that could be passed down to future generations.