Bill Alpert
CRISPR’s biggest challenge is addressing complex hereditary ailments like cystic fibrosis — but progress is being made
Treatments based on the Nobel-prize winning Crispr gene-editing approach can make permanent changes to a genetic flaw— but those edits ...
Gene transfer therapies are the ‘next big thing’ in medicine. Here’s how gene editing works and the companies behind it
The breakthroughs made possible by gene editing were shown in the Jan. 6 news that base editing had repaired a ...
