Labs around the world are trying to turn cells into autobiographers, tracking their own development from embryos to adults.
Progress in the quest to help progeria patients suggests that gene editing techniques may help treat other ultrarare conditions.
Much as ChatGPT generates poetry, a new A.I. system devises blueprints for microscopic mechanisms that can edit your DNA.
There is no clear path for African patients to get access to the treatments, which have multimillion-dollar price tags and are highly complex to manufacture and deliver.
People with the genetic disease have new opportunities to eliminate their symptoms, but the treatments come with obstacles that limit their reach.
The first treatment that relies on CRISPR is expected to receive U.S. approval next month. But it may cost millions of dollars per patient.
The decision by an advisory committee may lead to Food and Drug Administration approval of the first treatment for humans that uses the CRISPR gene-editing system.
The treatment from the company Vertex would be the first medicine to use the gene editing tool CRISPR.
We may be on the cusp of an era of astonishing innovation — the limits of which aren’t even clear yet.
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