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Insertional Mutagenesis by CRISPR/Cas9 Ribonucleoprotein Gene Editing in Cells Targeted for Point Mutation Repair Directed by Short Single-Stranded DNA Oligonucleotides.

机译：通过CRIspR / Cas9核糖核蛋白基因编辑的插入突变，针对由短单链DNa寡核苷酸指导的点突变修复。

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Natalia Rivera-Torres; Kelly Banas; Pawel Bialk; Kevin M Bloh; Eric B Kmiec;
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1. Mutagenesis and homologous recombination in Drosophila cell lines using CRISPR/Cas9 Mutagenesis and homologous recombination in Drosophila cell lines using CRISPR/Cas9 Mutagenesis and homologous recombination in Drosophila cell lines using CRISPR/Cas9 [J] . Chris P. Ponting, Charlotte Tibbit, Andrew R. Bassett, Biology Open . 2014,第1期

机译：使用CRISPR / Cas9的果蝇细胞系的诱变和同源重组使用CRISPR / Cas9的果蝇细胞系的诱变和同源重组使用CRISPR / Cas9的果蝇细胞系的诱变和同源重组。
2. Analyses of point mutation repair and allelic heterogeneity generated by CRISPR/Cas9 and single-stranded DNA oligonucleotides [J] . Pawel Bialk, Brett Sansbury, Natalia Rivera-Torres, Scientific reports. . 2016,第1期

机译：CRISPR / CAS9和单链DNA寡核苷酸产生的点突变修复和等位基因异质性分析
3. Generation of a gene edited hemophilia A patient-derived iPSC cell line, YCMi001-B-1, by targeted insertion of coagulation factor FVIII using CRISPR/Cas9 [J] . Jin Jea Sung, Sanghyun Park, Sang-Hwi Choi, Stem cell research . 2020,第2期

机译：产生基因编辑血友病患者衍生的IPSC细胞系，YCMI001-B-1，通过CRISPR / CAS9靶向插入凝血因子FVIII
4. Targeted genome editing in potato protoplast via optical delivery of CRISPR/Cas9 ribonucleoproteins [C] . Anke Londenberg, Frederik-Matti Bartels, Joseph Kpakpo Quaye, Nanophotonics Conference . 2020

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5. Developing an In Vitro System to Elucidate the Mechanism and Regulation of CRISPR-Directed Gene Editing and the Responding DNA Damage Repair Pathways [D] . Sansbury, Brett M. 2020

机译：开发体外系统以阐明CrispR-Pirected Gene编辑的机制和调节和响应DNA损伤修复途径
6. Insertional Mutagenesis by CRISPR/Cas9 Ribonucleoprotein Gene Editing in Cells Targeted for Point Mutation Repair Directed by Short Single-Stranded DNA Oligonucleotides [O] . Natalia Rivera-Torres, Kelly Banas, Pawel Bialk, -1

机译：CRISPR / Cas9核糖核酸蛋白基因编辑在靶向短突变单链DNA寡核苷酸指导点突变修复的细胞中的插入诱变
7. Insertional Mutagenesis by CRISPR/Cas9 Ribonucleoprotein Gene Editing in Cells Targeted for Point Mutation Repair Directed by Short Single-Stranded DNA Oligonucleotides. [O] . Natalia Rivera-Torres, Kelly Banas, Pawel Bialk, 2017

机译：通过CRIspR / Cas9核糖核蛋白基因编辑的插入突变，针对由短单链DNa寡核苷酸指导的点突变修复。

Insertional Mutagenesis by CRISPR/Cas9 Ribonucleoprotein Gene Editing in Cells Targeted for Point Mutation Repair Directed by Short Single-Stranded DNA Oligonucleotides.

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