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Editorial Article

What next for CRISPR after first therapeutic approvals?

As we celebrate the first regulatory approval of a gene-editing based therapeutic, Casgevy™, for the treatment of sickle cell disease and transfusion-dependent β-thalassemia, we consider the gene-editing challenges that must be overcome before CRISPR gene-editing technology becomes a common treatment modality






















Industry News

Synthetic mucus can mimic the real thing

An MIT team has created polymers that replicate the structure of mucins, the molecules that give mucus its unique antimicrobial properties