相关参考文献
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Baohong Zhang
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MOLECULAR THERAPY-NUCLEIC ACIDS (2020)
Cytosine base editor generates substantial off-target single-nucleotide variants in mouse embryos
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SCIENCE (2019)
DNA double-strand break repair-pathway choice in somatic mammalian cells
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Search-and-replace genome editing without double-strand breaks or donor DNA
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Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutants
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BMC BIOLOGY (2018)
Generation and validation of homozygous fluorescent knock-in cells using CRISPR-Cas9 genome editing
Birgit Koch et al.
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Covalent linkage of the DNA repair template to the CRISPR-Cas9 nuclease enhances homology-directed repair
Natasa Savic et al.
ELIFE (2018)
Efficient SSA-mediated precise genome editing using CRISPR/Cas9
Xinyi Li et al.
FEBS JOURNAL (2018)
Efficient, footprint-free human iPSC genome editing by consolidation of Cas9/CRISPR and piggyBac technologies
Gang Wang et al.
NATURE PROTOCOLS (2017)
Enhanced CRISPR/Cas9-mediated biallelic genome targeting with dual surrogate reporter-integrated donors
Yun Wu et al.
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Enhancing CRISPR/Cas9-mediated homology-directed repair in mammalian cells by expressing Saccharomyces cerevisiae Rad52
Simin Shao et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2017)
In trans paired nicking triggers seamless genome editing without double-stranded DNA cutting
Xiaoyu Chen et al.
NATURE COMMUNICATIONS (2017)
Cell cycle-dependent control of homologous recombination
Xin Zhao et al.
ACTA BIOCHIMICA ET BIOPHYSICA SINICA (2017)
Efficient precise knockin with a double cut HDR donor after CRISPR/Cas9-mediated double-stranded DNA cleavage
Jian-Ping Zhang et al.
GENOME BIOLOGY (2017)
Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9
Dominik Paquet et al.
NATURE (2016)
Genome editing using CRISPR-Cas9 to create the HPFH genotype in HSPCs: An approach for treating sickle cell disease and β-thalassemia
Lin Ye et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2016)
Improved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickase
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Dual-reporter surrogate systems for efficient enrichment of genetically modified cells
Chonghua Ren et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2015)
Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells
Van Trung Chu et al.
NATURE BIOTECHNOLOGY (2015)
A novel two-step genome editing strategy with CRISPR-Cas9 provides new insights into telomerase action and TERT gene expression
Linghe Xi et al.
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Development and Applications of CRISPR-Cas9 for Genome Engineering
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CELL (2014)
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Optimization of scarless human stem cell genome editing
Luhan Yang et al.
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RNA-Guided Human Genome Engineering via Cas9
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Multiplex Genome Engineering Using CRISPR/Cas Systems
Le Cong et al.
SCIENCE (2013)
Taking a Back Door to Target Myc
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SCIENCE (2012)
Mice Lacking a Myc Enhancer That Includes Human SNP rs6983267 Are Resistant to Intestinal Tumors
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A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity
Martin Jinek et al.
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Breaking the Code of DNA Binding Specificity of TAL-Type III Effectors
Jens Boch et al.
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Conservative homologous recombination preferentially repairs DNA double-strand breaks in the S phase of the cell cycle in human cells
N Saleh-Gohari et al.
NUCLEIC ACIDS RESEARCH (2004)
Enhancing gene targeting with designed zinc finger nucleases
M Bibikova et al.
SCIENCE (2003)