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A New Way to Deliver Gene Editing Therapies for Blood Disorders #medicine #biotech #innovation
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Scientists have taken a major step towards creating genetically modified babies, successfully editing DNA in human embryos for the first time. Researchers say the technique could one day eliminate inherited diseases by removing harmful mutations before birth. But critics warn the breakthrough raises serious ethical concerns, including the prospect of so-called
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CRISPR… but make it ✨precise✨ Forget cutting DNA—CRISPR base editing is here to re-write the genetic script! 🎯✍️ 💡 Instead of breaking the double helix to make edits (knock-outs or knock-ins), base editors chemically convert one base to another—like A ➡️ G or C ➡️ T. 👩‍🔬 Scientists disable to the ✂️ function of the Cas9 protein and FUSE it to a protein that processes this chemical conversion (deaminase) 🧠 Think: molecular pencil ✏️, not scissors! CRISPR base editing is perfect for fixing po
146.8K viewsJun 15, 2025
TikToksciencewithspice
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