With the power to rewrite the genetic code underlying countless diseases, CRISPR holds immense promise to revolutionize medicine. But until scientists can deliver its gene-editing machinery safely and efficiently into relevant cells and tissues, that promise will remain out of reach.



Summary

CRISPR technology offers revolutionary potential for treating genetic diseases by rewriting faulty DNA. However, realizing this potential hinges on developing effective delivery methods. Currently, the gene-editing machinery struggles to reach the specific cells and tissues where it’s needed, safely and efficiently. Overcoming this delivery challenge is crucial for translating CRISPR’s theoretical promise into tangible medical breakthroughs. The future of CRISPR medicine depends on solving this critical hurdle.

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