This paves the way for correcting gene defects anywhere in the body. 🙄 engineering
. Now, in a major breakthrough, researchers at University College London injected CRISPR into the blood of six people with a genetic condition. Three of them showed promising results, paving way for further trials using this approach.
The deposits occur over the years and symptoms can appear anywhere between the age of 20 to 70. The condition occursMost CRISPR-related treatments involve treatment of the cellsin-vivo Researchers at Regeneron Pharmaceuticals and Intellia Therapeutics developed an injectable CRISPR treatment with a simple operation. They used messenger RNAs , which carry instructions for making proteins. Since the host cell can use the mRNAs to make its own proteins, researchers simply needed to send enough information to enable CRISPR editing inside the cell.
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