scholarly article | Q13442814 |
P50 | author | Joakim Näsvall | Q45792385 |
P2093 | author name string | Joakim Näsvall | |
P2860 | cites work | Precise and nearly-precise excision of the symmetrical inverted repeats of Tn 5; common features of recA-independent deletion events in Escherichia coli | Q67234650 |
Transducing fragments in generalized transduction by phage P1. I. Molecular origin of the fragments | Q72706367 | ||
Instability of palindromic DNA in Escherichia coli | Q72911645 | ||
Excision of unstable artificial gene-specific inverted repeats mediates scar-free gene deletions in Escherichia coli | Q86063539 | ||
Simple and highly efficient BAC recombineering using galK selection | Q24794075 | ||
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 | ||
An efficient recombination system for chromosome engineering in Escherichia coli | Q29615038 | ||
Single-stranded heteroduplex intermediates in lambda Red homologous recombination | Q33644920 | ||
Rapid and highly efficient method for scarless mutagenesis within the Salmonella enterica chromosome | Q33802758 | ||
High efficiency mutagenesis, repair, and engineering of chromosomal DNA using single-stranded oligonucleotides | Q33948878 | ||
Lambda red recombineering in Escherichia coli occurs through a fully single-stranded intermediate. | Q34285766 | ||
Real-time evolution of new genes by innovation, amplification, and divergence | Q34307457 | ||
Positive and negative selection using the tetA-sacB cassette: recombineering and P1 transduction in Escherichia coli | Q34383416 | ||
Engineered CRISPR-Cas9 nucleases with altered PAM specificities | Q34481737 | ||
The no-SCAR (Scarless Cas9 Assisted Recombineering) system for genome editing in Escherichia coli | Q34497847 | ||
A highly precise and portable genome engineering method allows comparison of mutational effects across bacterial species | Q35925574 | ||
Markerless Escherichia coli rrn Deletion Strains for Genetic Determination of Ribosomal Binding Sites | Q36383088 | ||
Inverted DNA repeats: a source of eukaryotic genomic instability | Q36698685 | ||
Compensating the Fitness Costs of Synonymous Mutations | Q36904243 | ||
Mutagenic inverted repeat assisted genome engineering (MIRAGE). | Q37041800 | ||
Improved seamless mutagenesis by recombineering using ccdB for counterselection | Q38257003 | ||
The enzymatic basis of processivity in lambda exonuclease | Q39744726 | ||
A new Vibrio fischeri lux gene precedes a bidirectional termination site for the lux operon | Q39951996 | ||
Duplication-Insertion Recombineering: a fast and scar-free method for efficient transfer of multiple mutations in bacteria. | Q40450325 | ||
Evidence for two mechanisms of palindrome-stimulated deletion in Escherichia coli: single-strand annealing and replication slipped mispairing. | Q42132539 | ||
Phage P22-mutants with increased or decreased transduction abilities | Q45252565 | ||
Activation of cryptic aminoglycoside resistance in Salmonella enterica | Q45792333 | ||
Two-step red-mediated recombination for versatile high-efficiency markerless DNA manipulation in Escherichia coli | Q45856655 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | e0184126 | |
P577 | publication date | 2017-08-30 | |
P1433 | published in | PLOS One | Q564954 |
P1476 | title | Direct and Inverted Repeat stimulated excision (DIRex): Simple, single-step, and scar-free mutagenesis of bacterial genes | |
P478 | volume | 12 |
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