scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1035773610 |
P356 | DOI | 10.1186/S12934-016-0605-5 |
P8608 | Fatcat ID | release_bef6go75ozgqbgs5gsnzpwtfci |
P932 | PMC publication ID | 5134288 |
P698 | PubMed publication ID | 27908280 |
P50 | author | Changhao Bi | Q88194344 |
P2093 | author name string | Jing Li | |
Dongdong Zhao | |||
Bin Xiong | |||
Xueli Zhang | |||
Lijun Ye | |||
Hongnian Sun | |||
Shenli Yuan | |||
P2860 | cites work | De novo-engineered transcription activator-like effector (TALE) hybrid nuclease with novel DNA binding specificity creates double-strand breaks | Q24624851 |
RNA-guided editing of bacterial genomes using CRISPR-Cas systems | Q24630389 | ||
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A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity | Q24669850 | ||
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products | Q27860842 | ||
Programming cells by multiplex genome engineering and accelerated evolution | Q28253066 | ||
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CRISPR/Cas, the immune system of bacteria and archaea | Q29614423 | ||
An efficient recombination system for chromosome engineering in Escherichia coli | Q29615038 | ||
Genome-scale CRISPR-Cas9 knockout screening in human cells | Q29616044 | ||
Transfection of Escherichia coli spheroplasts. V. Activity of recBC nuclease in rec+ and rec minus spheroplasts measured with different forms of bacteriophage DNA | Q30450610 | ||
A one pot, one step, precision cloning method with high throughput capability | Q33382728 | ||
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CRISPR/Cas9 advances engineering of microbial cell factories. | Q34045724 | ||
Genome-scale promoter engineering by coselection MAGE | Q34224602 | ||
Targeted chromosomal cleavage and mutagenesis in Drosophila using zinc-finger nucleases | Q34615432 | ||
j5 DNA assembly design automation software | Q34708680 | ||
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Genome editing with RNA-guided Cas9 nuclease in zebrafish embryos | Q36739960 | ||
Minimizing acetate formation in E. coli fermentations. | Q36898780 | ||
Efficient generation of large-scale genome-modified mice using gRNA and CAS9 endonuclease | Q37271124 | ||
Consequences of Cas9 cleavage in the chromosome of Escherichia coli | Q38883743 | ||
Coupling the CRISPR/Cas9 System with Lambda Red Recombineering Enables Simplified Chromosomal Gene Replacement in Escherichia coli | Q41251787 | ||
PaR-PaR laboratory automation platform | Q44484599 | ||
PR-PR: cross-platform laboratory automation system | Q46080807 | ||
Multiplex metabolic pathway engineering using CRISPR/Cas9 in Saccharomyces cerevisiae. | Q46414542 | ||
An improved recombineering approach by adding RecA to lambda Red recombination | Q46871203 | ||
Combining metabolic engineering and metabolic evolution to develop nonrecombinant strains of Escherichia coli C that produce succinate and malate | Q46922472 | ||
Metabolic engineering of Escherichia coli using CRISPR-Cas9 meditated genome editing. | Q52423793 | ||
Engineering central metabolic modules of Escherichia coli for improving β-carotene production. | Q54315207 | ||
DNA double-strand break repair by homologous recombination | Q64387340 | ||
P433 | issue | 1 | |
P921 | main subject | Escherichia coli | Q25419 |
CRISPR | Q412563 | ||
Cas9 | Q16965677 | ||
CRISPR-Cas method | Q17310682 | ||
P304 | page(s) | 205 | |
P577 | publication date | 2016-12-01 | |
P1433 | published in | Microbial Cell Factories | Q15766995 |
P1476 | title | Development of a fast and easy method for Escherichia coli genome editing with CRISPR/Cas9. | |
P478 | volume | 15 |
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