CAS9 is a genome mutator by directly disrupting DNA-PK dependent DNA repair pathway

Author Correction: Gene and mutation independent therapy via CRISPR-Cas9 mediated cellular reprogramming in rod photoreceptors

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Wild-Type p53 Promotes Cancer Metabolic Switch by Inducing PUMA-Dependent Suppression of Oxidative Phosphorylation

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Ctrl-Alt-inDel: genome editing to reprogram a cell in the clinic

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Repair of double-strand breaks induced by CRISPR–Cas9 leads to large deletions and complex rearrangements

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p53 inhibits CRISPR–Cas9 engineering in human pluripotent stem cells

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CRISPR–Cas9 genome editing induces a p53-mediated DNA damage response

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Artemisitene suppresses tumorigenesis by inducing DNA damage through deregulating c-Myc-topoisomerase pathway

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Evolved Cas9 variants with broad PAM compatibility and high DNA specificity

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Precision gene editing technology and applications in nephrology

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Programmed DNA destruction by miniature CRISPR-Cas14 enzymes

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APOBEC3 induces mutations during repair of CRISPR–Cas9-generated DNA breaks

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APOBEC3 induces mutations during repair of CRISPR–Cas9-generated DNA breaks

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CRISPR/Cas9 β-globin gene targeting in human haematopoietic stem cells

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Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System

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Stemness factor Sall4 is required for DNA damage response in embryonic stem cells

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DNA-PK: A dynamic enzyme in a versatile DSB repair pathway

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Off-target assessment of CRISPR-Cas9 guiding RNAs in human iPS and mouse ES cells

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Cas9 as a versatile tool for engineering biology

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New Tools to Study DNA Double-Strand Break Repair Pathway Choice

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Multiplex Genome Engineering Using CRISPR/Cas Systems

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A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity

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Modeling Disease in Human ESCs Using an Efficient BAC-Based Homologous Recombination System

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