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Precise, high-efficiency editing of stem cells to probe human biology and model disease
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Discover how combining two nobel-prize winning technologies—cell reprogramming and CRISPR gene editing—creates a powerful platform to study basic cell biology, development, and disease. You'll learn how this technology overcomes problems with more traditional immortalized cell models and see how it is already being used to study neurodegenerative diseases.
This webinar is presented by Bill Skarnes, Professor of Cellular Engineering at The Jackson Laboratory.
Follow Bill and The Jackson Laboratory on Twitter.
Click here to view the full presentation of this webinar.
Browse all episodes of the Listen In Series here: https://listen-in.bitesizebio.com/
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