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Using the power of CRISPR to engineer better, stronger, longer-lived T cells

New approach using CRISPR can engineer massive quantities of cells for therapeutic applications

A new variation of the CRISPR-Cas9 gene editing system makes it easier to re-engineer massive quantities of cells for therapeutic applications.

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High-yield CRISPR without viral vectors

High-yield CRISPR without viral vectors
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Jonathan-esensten
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Institute-of-genomic-immunology
Division-of-hematology
Gladstone-institutes
Genomic-immunology
Nature-biotechnology
Brian-shy

A Cellular Engineering Breakthrough: High-Yield CRISPR Without Viral Vectors

/PRNewswire/ A new variation of the CRISPR-Cas9 gene editing system makes it easier to re-engineer massive quantities of cells for therapeutic applications..

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A Cellular Engineering Breakthrough: High-Yield CRISPR Without Viral Vectors

A Cellular Engineering Breakthrough: High-Yield CRISPR Without Viral Vectors
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