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. 1995 Jan 3;92(1):83–85. doi: 10.1073/pnas.92.1.83

From mutation mapping to phenotype cloning.

J J Jonsson 1, S M Weissman 1
PMCID: PMC42820  PMID: 7816851

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Au K. G., Welsh K., Modrich P. Initiation of methyl-directed mismatch repair. J Biol Chem. 1992 Jun 15;267(17):12142–12148. [PubMed] [Google Scholar]
  2. Barnes W. M. PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates. Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2216–2220. doi: 10.1073/pnas.91.6.2216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bhattacharyya A., Lilley D. M. Single base mismatches in DNA. Long- and short-range structure probed by analysis of axis trajectory and local chemical reactivity. J Mol Biol. 1989 Oct 20;209(4):583–597. doi: 10.1016/0022-2836(89)90596-2. [DOI] [PubMed] [Google Scholar]
  4. Collins F. S. Positional cloning: let's not call it reverse anymore. Nat Genet. 1992 Apr;1(1):3–6. doi: 10.1038/ng0492-3. [DOI] [PubMed] [Google Scholar]
  5. Cooper D. N., Smith B. A., Cooke H. J., Niemann S., Schmidtke J. An estimate of unique DNA sequence heterozygosity in the human genome. Hum Genet. 1985;69(3):201–205. doi: 10.1007/BF00293024. [DOI] [PubMed] [Google Scholar]
  6. Cotton R. G., Rodrigues N. R., Campbell R. D. Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations. Proc Natl Acad Sci U S A. 1988 Jun;85(12):4397–4401. doi: 10.1073/pnas.85.12.4397. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dodgson J. B., Wells R. D. Action of single-strand specific nucleases on model DNA heteroduplexes of defined size and sequence. Biochemistry. 1977 May 31;16(11):2374–2379. doi: 10.1021/bi00630a010. [DOI] [PubMed] [Google Scholar]
  8. Kunkel L. M., Monaco A. P., Middlesworth W., Ochs H. D., Latt S. A. Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Proc Natl Acad Sci U S A. 1985 Jul;82(14):4778–4782. doi: 10.1073/pnas.82.14.4778. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Lisitsyn N. A., Segre J. A., Kusumi K., Lisitsyn N. M., Nadeau J. H., Frankel W. N., Wigler M. H., Lander E. S. Direct isolation of polymorphic markers linked to a trait by genetically directed representational difference analysis. Nat Genet. 1994 Jan;6(1):57–63. doi: 10.1038/ng0194-57. [DOI] [PubMed] [Google Scholar]
  10. Lisitsyn N., Lisitsyn N., Wigler M. Cloning the differences between two complex genomes. Science. 1993 Feb 12;259(5097):946–951. doi: 10.1126/science.8438152. [DOI] [PubMed] [Google Scholar]
  11. Nelson S. F., McCusker J. H., Sander M. A., Kee Y., Modrich P., Brown P. O. Genomic mismatch scanning: a new approach to genetic linkage mapping. Nat Genet. 1993 May;4(1):11–18. doi: 10.1038/ng0593-11. [DOI] [PubMed] [Google Scholar]
  12. Rosenberg M., Przybylska M., Straus D. "RFLP subtraction": a method for making libraries of polymorphic markers. Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):6113–6117. doi: 10.1073/pnas.91.13.6113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Sanda A. I., Ford J. P. Genomic analysis I: inheritance units and genetic selection in the rapid discovery of locus linked DNA markers. Nucleic Acids Res. 1986 Sep 25;14(18):7265–7283. doi: 10.1093/nar/14.18.7265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Shenk T. E., Rhodes C., Rigby P. W., Berg P. Biochemical method for mapping mutational alterations in DNA with S1 nuclease: the location of deletions and temperature-sensitive mutations in simian virus 40. Proc Natl Acad Sci U S A. 1975 Mar;72(3):989–993. doi: 10.1073/pnas.72.3.989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Solaro P. C., Birkenkamp K., Pfeiffer P., Kemper B. Endonuclease VII of phage T4 triggers mismatch correction in vitro. J Mol Biol. 1993 Apr 5;230(3):868–877. doi: 10.1006/jmbi.1993.1207. [DOI] [PubMed] [Google Scholar]
  16. Thomas D. C., Kunkel T. A., Casna N. J., Ford J. P., Sancar A. Activities and incision patterns of ABC excinuclease on modified DNA containing single-base mismatches and extrahelical bases. J Biol Chem. 1986 Nov 5;261(31):14496–14505. [PubMed] [Google Scholar]
  17. West S. C. Enzymes and molecular mechanisms of genetic recombination. Annu Rev Biochem. 1992;61:603–640. doi: 10.1146/annurev.bi.61.070192.003131. [DOI] [PubMed] [Google Scholar]
  18. Youil R., Kemper B. W., Cotton R. G. Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII. Proc Natl Acad Sci U S A. 1995 Jan 3;92(1):87–91. doi: 10.1073/pnas.92.1.87. [DOI] [PMC free article] [PubMed] [Google Scholar]

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