128 related articles for article (PubMed ID: 8036169)
1. In vivo excision and amplification of large segments of the Escherichia coli genome.
Pósfai G; Koob M; Hradecná Z; Hasan N; Filutowicz M; Szybalski W
Nucleic Acids Res; 1994 Jun; 22(12):2392-8. PubMed ID: 8036169
[TBL] [Abstract][Full Text] [Related]
2. Cre/loxP-mediated excision and amplification of large segments of the Escherichia coli genome.
Yoon YG; Cho JH; Kim SC
Genet Anal; 1998 Jan; 14(3):89-95. PubMed ID: 9526700
[TBL] [Abstract][Full Text] [Related]
3. A broad-host-range in vivo pop-out and amplification system for generating large quantities of 50- to 100-kb genomic fragments for direct DNA sequencing.
Wild J; Hradecná Z; Pósfai G; Szybalski W
Gene; 1996 Nov; 179(1):181-8. PubMed ID: 8955645
[TBL] [Abstract][Full Text] [Related]
4. Cre/loxP-mediated in vivo excision of large segments from yeast genome and their amplification based on the 2microm plasmid-derived system.
Yoon YG; Pósfai G; Szybalski W; Kim SC
Gene; 1998 Nov; 223(1-2):67-76. PubMed ID: 9858689
[TBL] [Abstract][Full Text] [Related]
5. Targeting and retrofitting pre-existing libraries of transposon insertions with FRT and oriV elements for in-vivo generation of large quantities of any genomic fragment.
Wild J; Sektas M; Hradecná Z; Szybalski W
Gene; 1998 Nov; 223(1-2):55-66. PubMed ID: 9858684
[TBL] [Abstract][Full Text] [Related]
6. Escherichia coli genome targeting, I. Cre-lox-mediated in vitro generation of ori- plasmids and their in vivo chromosomal integration and retrieval.
Hasan N; Koob M; Szybalski W
Gene; 1994 Dec; 150(1):51-6. PubMed ID: 7959062
[TBL] [Abstract][Full Text] [Related]
7. A novel approach for Escherichia coli genome editing combining in vivo cloning and targeted long-length chromosomal insertion.
Hook CD; Samsonov VV; Ublinskaya AA; Kuvaeva TM; Andreeva EV; Gorbacheva LY; Stoynova NV
J Microbiol Methods; 2016 Nov; 130():83-91. PubMed ID: 27567891
[TBL] [Abstract][Full Text] [Related]
8. Convenient and reversible site-specific targeting of exogenous DNA into a bacterial chromosome by use of the FLP recombinase: the FLIRT system.
Huang LC; Wood EA; Cox MM
J Bacteriol; 1997 Oct; 179(19):6076-83. PubMed ID: 9324255
[TBL] [Abstract][Full Text] [Related]
9. An Escherichia coli system for assay of F1p site-specific recombination on substrate plasmids.
Snaith MR; Kilby NJ; Murray JA
Gene; 1996 Nov; 180(1-2):225-7. PubMed ID: 8973372
[TBL] [Abstract][Full Text] [Related]
10. In vivo excision and amplification of large human genomic segments using the Cre/loxP-and large T antigen/SV40 ori-mediated machinery.
Min Kim J; Young Choi J; Sun Kim M; Chang Kim S
J Biotechnol; 2004 Jun; 110(3):227-33. PubMed ID: 15163513
[TBL] [Abstract][Full Text] [Related]
11. Chromosomal integration of heterologous DNA in Escherichia coli with precise removal of markers and replicons used during construction.
Martinez-Morales F; Borges AC; Martinez A; Shanmugam KT; Ingram LO
J Bacteriol; 1999 Nov; 181(22):7143-8. PubMed ID: 10559184
[TBL] [Abstract][Full Text] [Related]
12. The Flp double cross system a simple efficient procedure for cloning DNA fragments.
Sadowski PD
BMC Biotechnol; 2003 Jul; 3():9. PubMed ID: 12871598
[TBL] [Abstract][Full Text] [Related]
13. Replicon-free and markerless methods for genomic insertion of DNAs in phage attachment sites and controlled expression of chromosomal genes in Escherichia coli.
Chiang CJ; Chen PT; Chao YP
Biotechnol Bioeng; 2008 Dec; 101(5):985-95. PubMed ID: 18553504
[TBL] [Abstract][Full Text] [Related]
14. Improvement of a yeast self-excising integrative vector by prevention of expression leakage of the intronated Cre recombinase gene during plasmid maintenance in Escherichia coli.
Agaphonov MO
FEMS Microbiol Lett; 2017 Dec; 364(22):. PubMed ID: 29069450
[TBL] [Abstract][Full Text] [Related]
15. Genetic system for reversible integration of DNA constructs and lacZ gene fusions into the Escherichia coli chromosome.
Platt R; Drescher C; Park SK; Phillips GJ
Plasmid; 2000 Jan; 43(1):12-23. PubMed ID: 10610816
[TBL] [Abstract][Full Text] [Related]
16. Gene disruption in Escherichia coli: TcR and KmR cassettes with the option of Flp-catalyzed excision of the antibiotic-resistance determinant.
Cherepanov PP; Wackernagel W
Gene; 1995 May; 158(1):9-14. PubMed ID: 7789817
[TBL] [Abstract][Full Text] [Related]
17. Dual-In/Out strategy for genes integration into bacterial chromosome: a novel approach to step-by-step construction of plasmid-less marker-less recombinant E. coli strains with predesigned genome structure.
Minaeva NI; Gak ER; Zimenkov DV; Skorokhodova AY; Biryukova IV; Mashko SV
BMC Biotechnol; 2008 Aug; 8():63. PubMed ID: 18699991
[TBL] [Abstract][Full Text] [Related]
18. Marker-free chromosomal expression of foreign and native genes in Escherichia coli.
Chiang CJ; Chen PT; Chen SY; Chao YP
Methods Mol Biol; 2011; 765():113-23. PubMed ID: 21815090
[TBL] [Abstract][Full Text] [Related]
19. A broad-host-range Flp-FRT recombination system for site-specific excision of chromosomally-located DNA sequences: application for isolation of unmarked Pseudomonas aeruginosa mutants.
Hoang TT; Karkhoff-Schweizer RR; Kutchma AJ; Schweizer HP
Gene; 1998 May; 212(1):77-86. PubMed ID: 9661666
[TBL] [Abstract][Full Text] [Related]
20. Site-specific bacterial chromosome engineering mediated by IntA integrase from Rhizobium etli.
Hernández-Tamayo R; Torres-Tejerizo G; Brom S; Romero D
BMC Microbiol; 2016 Jun; 16(1):133. PubMed ID: 27357704
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]