A Review on Advanced CRISPR-Based Genome-Editing Tools: Base Editing and Prime Editing

[1] Doudna JA(2014)The new frontier of genome engineering with CRISPR-Cas9 Science 346 1258096-405

[2] Charpentier E(2018)Repair of a site-specific DNA cleavage: Old-school lessons for Cas9-mediated gene editing ACS Chemical Biology 13 397-8106

[3] Gallagher DN(1994)Introduction of double-strand breaks into the genome of mouse cells by expression of a rare-cutting endonuclease Molecular and Cellular Biology 14 8096-355

[4] Haber JE(2014)CRISPR-Cas systems for editing, regulating and targeting genomes Nature Biotechnology 32 347-1771

[5] Rouet P(2008)Comparison of nonhomologous end joining and homologous recombination in human cells DNA Repair 7 1765-60

[6] Smih F(2017)Optimizing the DNA donor template for homology-directed repair of double-strand breaks Molecular Therapy-Nucleic Acids 7 53-6454

[7] Jasin M(2018)How to create state-of-the-art genetic model systems: Strategies for optimal CRISPR-mediated genome editing Nucleic Acids Research 46 6435-36

[8] Sander JD(2017)CRISPR-based technologies for the manipulation of eukaryotic genomes Cell 168 20-471

[9] Joung JK(2016)Targeted nucleotide editing using hybrid prokaryotic and vertebrate adaptive immune systems Science 353 aaf8729-424

[10] Mao Z(2017)Programmable base editing of A• T to G• C in genomic DNA without DNA cleavage Nature 551 464-157

[1] Doudna JA(2014)The new frontier of genome engineering with CRISPR-Cas9 Science 346 1258096-405

[2] Charpentier E(2018)Repair of a site-specific DNA cleavage: Old-school lessons for Cas9-mediated gene editing ACS Chemical Biology 13 397-8106

[3] Gallagher DN(1994)Introduction of double-strand breaks into the genome of mouse cells by expression of a rare-cutting endonuclease Molecular and Cellular Biology 14 8096-355

[4] Haber JE(2014)CRISPR-Cas systems for editing, regulating and targeting genomes Nature Biotechnology 32 347-1771

[5] Rouet P(2008)Comparison of nonhomologous end joining and homologous recombination in human cells DNA Repair 7 1765-60

[6] Smih F(2017)Optimizing the DNA donor template for homology-directed repair of double-strand breaks Molecular Therapy-Nucleic Acids 7 53-6454

[7] Jasin M(2018)How to create state-of-the-art genetic model systems: Strategies for optimal CRISPR-mediated genome editing Nucleic Acids Research 46 6435-36

[8] Sander JD(2017)CRISPR-based technologies for the manipulation of eukaryotic genomes Cell 168 20-471

[9] Joung JK(2016)Targeted nucleotide editing using hybrid prokaryotic and vertebrate adaptive immune systems Science 353 aaf8729-424

[10] Mao Z(2017)Programmable base editing of A• T to G• C in genomic DNA without DNA cleavage Nature 551 464-157