Gene therapy to repair damaged heart muscle is most likely to succeed if it can be injected at the site of ischemia where there is viable myocardium with reduced contractile ability, and a new ...
Mixed headlines have plagued the cell and gene therapy space of late. We believe that a renewed case of optimism is not only ...
The problem of antibiotic resistance gene (ARG) pollution in the environment has become one of the most severe public health ...
CSIR-IGIB and Serum Institute of India sign a tech transfer pact to develop an indigenous, affordable CRISPR-based gene-editing therapy for sickle cell disease ...
IIIF provides researchers rich metadata and media viewing options for comparison of works across cultural heritage collections. Visit the IIIF page to learn more. This shadow box display demonstrates ...
The launch of BIRSA 101 marks a major breakthrough in CRISPR gene-editing technology, positioning India to deliver affordable ...
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