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Optimizing AAV manufacturing: a scalable harvest protocol

ImmuSignature™ MLR: Rapid high-throughput assessment of therapeutic immunogenicity

Assessing the epigenetics of T cell exhaustion using CRISPR screens

Base editing and stem-cell based therapies

Addressing the challenges in solid tumor therapy with base editing

Finding the right technology for your genome engineering project

Generating a clonal HAP1LIG4(-) Cas9(+) cell line – an expert interview

CRISPR-derived base editing technology: The what, the how, and the why

AAV vectors: Pursuing a one-time therapy for ocular diseases

Innovative approaches for advancing genetic payload development

History of immunotherapy and CAT T-cells

The historical development of the hemacytometer


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