Combining CRISPR and transposon-based technologies for improved sdAb-based CAR-T therapies
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Optimizing plasmid DNA purification: strategies for reliable and expandable processes
Christy Franco, Jasmina Puc
Making robust choices: evaluating materials in your AAV process
Michael Bodo, Birgit Rogell
Actionable insights for overcoming CMC challenges in TIL therapy: GRIT’s strategic approach
Alex Lei, Sabrina Carmichael
Exploring the advantages of ready-to-use lipid-based gene delivery for gene-modified cell therapy
Chesney Michels, Claire Guéguen