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Research Frontiers in CRISPR-Based Viral Gene Editing Therapeutics

Development of CRISPR-Cas9 systems to directly target and edit viral genomes within infected cells for therapeutic intervention.

Viral Genome Editing in Persistent Latent Infections
Off-Target Effects in CRISPR-Modified Viral Therapeutics
Escape Mutations Against Engineered CRISPR Targeting
Multiplex CRISPR Strategies for Polyploid Viral Genomes
In Vivo Delivery of CRISPR Across the Blood-Brain Barrier
Epigenetic Reactivation of Silenced CRISPR-Edited Viruses
Immunogenicity of CRISPR-Modified Viral Antigens
Precision Excision of Integrated Viral DNA Elements
CRISPR-Mediated Viral Attenuation for Live Vaccine Development
RNA Virus Editing at Sub-Population Quasispecies Level

All Virology PhD categories