Transgene

In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration

The dTAG system for immediate and target-specific protein degradation

ARGOS 8 variants generated by CRISPR ‐Cas9 improve maize grain yield under field drought stress conditions

Efficient and transgene-free genome editing in wheat through transient expression of CRISPR/Cas9 DNA or RNA

Development of broad virus resistance in non‐transgenic cucumber using CRISPR/Cas9 technology

Reprogramming human T cell function and specificity with non-viral genome targeting

Adeno-Associated Virus Engineering and Load Strategy for Tropism Modification, Immune Evasion and Enhanced Transgene Expression

Clinical and Translational Landscape of Viral Gene Therapies

Clinical Pharmacology Perspective on Development of Adeno‐Associated Virus Vector‐Based Retina Gene Therapy

Therapeutic in vivo genome editing: innovations and challenges in rAAV vector-based CRISPR delivery

Current and Emerging Issues in Adeno-Associated Virus Vector-Mediated Liver-Directed Gene Therapy

miRNA modules for precise, tunable control of gene expression