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WO2015144691A   [0006]  [0010]  [0046] 
WO2006024954A   [0006]  [0011]  [0046]  [0047]  [0047]  [0048] 
WO2016184860A   [0009]  [0020] 
WO2014106123A   [0012] 
EP3312192A   [0020] 
WO2005004908A   [0026] 

Annu.Rev.Microbiol.   [0002]  [0003]  [0003] 
Microbiol.Mol.Biol.Rev.   [0002] 
Micrbiol.Mol.Biol.Rev.   [0003] 
Discovery Medicine   [0004] 
Vaccine   [0004] 
J. Immunol.   [0004] 
Hum. Vaccines.Immunother.   [0004] 
Inn.Immun.   [0004] 
Cell.Miocrobiol.   [0004] 
PNAS   [0004]  [0006] 
Infect Immun.   [0005] 
Immunol. Clinical Microbiol.   [0005] 
Int.J.Med.Microbiol.   [0005] 
J. Immunol.   [0005] 
NIPH Ann.   [0006] 
Clin.Infect.Dis.   [0006] 
Meningococcal vaccinations   [0006] 
Proteomics   [0006]  [0006] 
J. Bacteriol.   [0006] 
Journal of Extracellular Vesicles   [0006]  [0006]  [0046] 
Nat. Commun.   [0006] 
Mol. Microbiol.   [0006] 
Mol. Microbiol.   [0006] 
Molecular System Biology   [0006] 
PLos ONE   [0006] 
PlosOne   [0006] 
J.Biol.Chem.   [0006]  [0046] 
Vaccine   [0006] 
Mol.Cell.Proteomics   [0006]  [0043]  [0043]  [0045]  [0046]  [0048] 
Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection   [0007]  [0032] 
Genome Res   [0007] 
Nat Biotechnol   [0007] 
Mol Microbiol   [0007] 
Science   [0007] 
Biotechnol Appl Biochem   [0007] 
Methods Mol Biol   [0007] 
J Biosci Bioeng   [0007] 
Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: The Keio collection   [0016] 
An efficient recombination system for chromosome engineering in Escherichia coli   [0018]  [0036] 
RNA-guided editing of bacterial genomes using CRISPR-Cas systems   [0018]  [0037] 
Gram negative promiscuous lipoproteins keep surface topology when transplanted from one species to another and can deliver foreign polypeptides to the bacterial surface   [0032] 
A new logic for DNA engineering using recombination in Escherichia coli   [0034] 
A set of recombineering plasmids for gram-negative bacteria   [0034] 
Use of bacteriophage lambda recombination functions to promote gene replacement in Escherichia coli   [0034] 
Rapid modification of bacterial artificial chromosomes by ET-recombination   [0034] 
High efficiency mutagenesis, repair, and engineering of chromosomal DNA using single-stranded oligonucleotides   [0034] 
Recombineering with overlapping single-stranded DNA oligonucleotides: testing a recombination intermediate   [0036] 
Genome editing. The new frontier of genome engineering with CRISPR-Cas9   [0037] 
Expanding the Biologist's Toolkit with CRISPR-Cas9   [0037] 
Exploring the potential of genome editing CRISPR-Cas9 technology   [0037] 
Recombineering: highly efficient in vivo genetic engineering using single-strand oligos   [0038] 
PLoS Pathog.   [0047] 
Cell Host Microbe   [0047] 
Microbiol Mol Biol Rev.   [0047] 
Proc Natl Acad Sci USA   [0047] 
Br J Cancer   [0047] 
Frontiers in Oncology   [0048]  [0048]