Center-Authored Papers
Filters: Author is Khan, Iram F [Clear All Filters]
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2016. High efficiency CRISPR/Cas9-mediated gene editing in primary human T-cells using mutant adenoviral E4orf6/E1b55k "helper" proteins.. Molecular therapy : the journal of the American Society of Gene Therapy. Abstract
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2015. Efficient modification of CCR5 in primary human hematopoietic cells using a megaTAL nuclease and AAV donor template.. Science translational medicine. 7(307):307ra156. Abstract
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