Gene Therapy Delivery Systems: Evaluating the Latest Methods for Effective Gene Therapy Delivery
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Keywords

CRISPR-Cas9
hematological
Adenoviral
endocytosis
encapsulated

Abstract

Gene therapy has emerged as a promising approach for treating genetic disorders, cancers, and various diseases. However, effective delivery of therapeutic genes to target cells remains a significant challenge. This review discusses the latest methods in gene therapy delivery systems, evaluating their mechanisms, efficiency, and clinical applications. We categorize these systems into viral and non-viral vectors, highlighting recent advancements, challenges, and future directions.

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