Stephen Gray

Precise and Heritable Genome Editing in Evolutionarily Diverse Nematodes Using TALENs and CRISPR/Cas9 to Engineer Insertions and Deletions

Hypothesis: RNA and DNA Viral Sequence Integration into the Mammalian Host Genome Supports Long-Term B Cell and T Cell Adaptive Immunity

Hepatocellular carcinoma

Playing the End Game: DNA Double-Strand Break Repair Pathway Choice

Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects

Hydrolytic function of Exo1 in mammalian mismatch repair

Advances in genome editing through control of DNA repair pathways

Repair of Strand Breaks by Homologous Recombination

Search-and-replace genome editing without double-strand breaks or donor DNA

Genome editing with CRISPR–Cas nucleases, base editors, transposases and prime editors

Inflammation-Induced Cell Proliferation Potentiates DNA Damage-Induced Mutations In Vivo

Coupling of Human DNA Excision Repair and the DNA Damage Checkpoint in a Defined in Vitro System

Noncanonical views of homology-directed DNA repair

Biology and Applications of CRISPR Systems: Harnessing Nature’s Toolbox for Genome Engineering

Microhomology-Mediated End Joining: A Back-up Survival Mechanism or Dedicated Pathway?

NF-κB, inflammation, immunity and cancer: coming of age

MammalianExo1encodes both structural and catalytic functions that play distinct roles in essential biological processes

End-resection at DNA double-strand breaks in the three domains of life

Simultaneous precise editing of multiple genes in human cells

CRISPR-Cas guides the future of genetic engineering

Bidirectional resection of DNA double-strand breaks by Mre11 and Exo1