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CRISPR: The gene-editing tool revolutionizing biomedical research
A new tool could be the key to treating genetic diseases and may be the most consequential discovery in biomedicine this century. Bill Whitaker reports.
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Inaugurated the new advanced Gene translational facility at #CSIR-Institute of Genomics & Integrated Biology #IGIB, New Delhi. Congratulations CSIR -IGIB, for successfully accomplishing a breakthrough in developing India’s first indegenous therapy for Genetic cure of Sickle Cell Disease. The therapy is based on #CRISPR technology , that is, “Clustered Regularly Interspaced Short Palindromic Repeats” is a technology for editing genomes, derived from a natural defense system in bacteria. The most
Inaugurated the new advanced Gene translational facility at #CSIR-Institute of Genomics & Integrated Biology #IGIB, New Delhi. Congratulations CSIR -IGIB, for successfully accomplishing a breakthrough in developing India’s first indegenous therapy for Genetic cure of Sickle Cell Disease. The therapy is based on #CRISPR technology , that is, “Clustered Regularly Interspaced Short Palindromic Repeats” is a technology for editing genomes, derived from a natural defense system in bacteria. The most
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