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Many drugs cannot cross the blood-brain barrier (BBB), which also

GC012F is an autologous, genetically engineered, bispecific CAR-T that targets

Jin-Soo Kim’s team has discovered how to edit the mitochondrial

Researchers have shown that a synthetic IL-9 receptor allows anti-cancer

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