AI Networking Cookbook: Practical recipes for AI-assisted network automation and development
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A multiplex prime-editing platform is developed that converts commonly used immunosuppressive drugs into tools for in vivo control of T-cell therapies via defined, pathway-specific drug resistance, enabling selective in vivo modulation in settings where immunosuppression cannot be withdrawn.
The spectrum of genetic lesions that result in activation of NF‑κB in mature B‑cell malignancies is expanded and highlights the incomplete understanding of NF‑κB drivers in mature B‑cell malignancies.
It is concluded from preliminary data that gene therapy using BE HSPCs appear very promising for achieving an earlier and more robust multi-lineage immune reconstitution in adult patients using BE HSPCs.
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