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Cited by 953

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Harnessing homologous recombination in vitro to generate recombinant DNA via SLIC

Li, Mamie Z, Elledge, Stephen J·2007·Nature Methods
DOI 10.1038/nmeth1010
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Research works printed but not linked: 22

  1. Smith, H.O. & Wilcox, K.W. A restriction enzyme from Hemophilus influenzae. I. Purification and general properties. J. Mol. Biol. 51, 379–391 (1970). · DOI · Paper page
  2. Danna, K. & Nathans, D. Specific cleavage of simian virus 40 DNA by restriction endonuclease of Hemophilus influenzae. Proc. Natl. Acad. Sci. USA 68, 2913–2917 (1971). · DOI · Paper page
  3. Cohen, S.N., Chang, A.C., Boyer, H.W. & Helling, R.B. Construction of biologically functional bacterial plasmids in vitro. Proc. Natl. Acad. Sci. USA 70, 3240–3244 (1973). · DOI · Paper page
  4. Backman, K. & Ptashne, M. Maximizing gene expression on a plasmid using recombination in vitro. Cell 13, 65–71 (1978). · DOI
  5. Hutchison, C.A. et al. Mutagenesis at a specific position in a DNA sequence. J. Biol. Chem. 253, 6551–6560 (1978). · DOI · Paper page
  6. Rumsby, G. An introduction to PCR techniques. PCR Methods Mol. Biol. 324, 75–89 (2006).
  7. Ho, S.N., Hunt, H.D., Horton, R.M., Pullen, J.K. & Pease, L.R. Site-directed mutagenesis by overlap extension using the polymerase chain reaction. Gene 77, 51–59 (1989). · DOI · Paper page
  8. Liu, Q., Li, M.Z., Liebham, D., Cortez, D. & Elledge, S.J. The univector plasmid fusion system, a method for rapid construction of recombinant DNA without restriction enzymes. Curr. Biol. 8, 1300–1309 (1998). · DOI · Paper page
  9. Hartley, J.L., Temple, G.F. & Brasch, M.A. DNA cloning using in vitro site-specific recombination. Genome Res. 10, 1788–1795 (2000). · DOI · Paper page
  10. Walhout, A.J. et al. GATEWAY recombinational cloning: application to the cloning of large numbers of open reading frames or ORFeomes. Methods Enzymol. 328, 575–592 (2000). · DOI · Paper page
  11. Bethke, B. & Sauer, B. Segmental genomic replacement by Cre-mediated recombination: Genotoxic stress activation of the p53 promoter in single-copy transformants. Nucleic Acids Res. 25, 2828–2834 (1997). · doi:10.1093/nar/25.14.2828
  12. Nebert, D.W., Dalton, T.P., Stuart, G.W. & Carvan, M.J. Gene-swap knock-in cassette in mice to study allelic differences in human genes. Ann. NY Acad. Sci. 919, 148–170 (2000). · DOI
  13. Siegel, R.W. et al. Recombinatorial cloning using heterologous lox sites. Genome Res. 14, 1119–1129 (2004). · DOI
  14. Li, M.Z. & Elledge, S.J. MAGIC: An in vivo genetic method for the rapid construction of recombinant DNA molecules. Nat. Genet. 37, 311–319 (2005). · DOI
  15. Amundsen, S.K. & Smith, G.R. Interchangeable parts of the Escherichia coli recombination machinery. Cell 112, 741–744 (2003). · DOI
  16. Kuzminov, A. Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda. Microbiol. Mol. Biol. Rev. 63, 751–813 (1999). · DOI · Paper page
  17. Konforti, B.B. & Davis, R.W. 3′ homologous free ends are required for stable joint molecule formation by the RecA and single-stranded binding proteins of Escherichia coli. Proc. Natl. Acad. Sci. USA 84, 690–694 (1987). · doi:10.1073/pnas.84.3.690
  18. Tillett, D. & Neilan, B.A. Enzyme-free cloning: A rapid method to clone PCR products independent of vector restriction enzyme sites. Nucleic Acids Res. 27, e26 (1999). · DOI
  19. Aslanidis, C. & de Jong, P.J. Ligation-independent cloning of PCR products (LIC-PCR). Nucleic Acids Res. 18, 6069–6074 (1990). · DOI · Paper page
  20. Haun, R.S., Servanti, I.M. & Moss, J. Rapid, reliable ligation-independent cloning of PCR products using modified plasmid vectors. Biotechniques 13, 515–518 (1992).
  21. Aslanidis, C., de Jong, P.J. & Schmitz, G. Minimal length requirement of the single-stranded tails for ligation-independent cloning (LIC) of PCR products. PCR Methods Appl. 4, 172–177 (1994). · DOI
  22. Cheo, D.L. et al. Concerted assembly and cloning of multiple DNA fragments using in vitro site-specific recombination: Functional analysis of multi-site expression clones. Gen. Res. 14, 2111–2120 (2004). · DOI

Cited by

Metadata

Authors
Li, M. Z., & Elledge, S. J.
Venue
Nature Methods
Publisher
Springer Science and Business Media LLC
Published
2007-02-11
Volume
4
Issue
3
Pages
251-256
ISSN
  • 1548-7091 (ISSN-L)
  • 1548-7105
DOI
10.1038/nmeth1010
OpenAlex
W2102440675
Cited by
953
References
1
FWCI
6.82
Type
journal article
Language
en
Open access
closed
Licence
www.springer.com/tdm (tdm)

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