A reprogramming human T cell function and specificity with non-viral genome targeting
Abstract
This article decries a CRISPR-Cas9 genome-targeting system that does not require viral vectors, allowing rapid and efficient insertion of large DNA sequences at specific sites in the genomes of primary human T cells, while preserving cell viability and...
Paper Details
Title
A reprogramming human T cell function and specificity with non-viral genome targeting
Published Date
Sep 12, 2019
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Notes
History