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A major drawback of CRISPR-Cas9-mediated genome editing is that not

Genetically modified immune cells successfully target specific cancer cells that

Breakthrough findings were presented at the 2022 ASCO Annual Meeting

It is a pity that non integrating lentiviral vectors are

In a recent study, a team of researchers used a

With a $17 million grant, UCSF Benioff Children’s Hospital in

The FDA has granted accelerated designation to PRGN-3006 for the

Mucopolysaccharidosis I is caused by mutations in the gene for

In the process of engineering CAR T cells, if the