A new variation of the CRISPR-Cas9 gene editing system makes it easier to re-engineer massive quantities of cells for therapeutic applications. The approach, developed at Gladstone Institutes and UC ...

The successes seen in a number of clinical studies on viral vector-based gene therapies (AAV, retroviral, and lentiviral vectors) are well documented, with an ever-broadening pipeline of products ...

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When most people think of technology, iPhones and laptops may come to mind. But what about a canoe? Or a longhouse? That's the question University of Saskatchewan Engineering professor Sean Maw is ...