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. 1967 Feb;57(2):277–283. doi: 10.1073/pnas.57.2.277

THE STRUCTURAL GENE FOR λ EXONUCLEASE*

Charles M Radding 1,2, Josiane Szpirer 1,2,, René Thomas 1,2
PMCID: PMC335501  PMID: 16591465

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Selected References

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

  1. Campbell A. The steric effect in lysogenization by bacteriophage lambda. II. Chromosomal attachment of the b2 mutant. Virology. 1965 Nov;27(3):340–345. doi: 10.1016/0042-6822(65)90113-3. [DOI] [PubMed] [Google Scholar]
  2. Eisen H. A., Fuerst C. R., Siminovitch L., Thomas R., Lambert L., Pereira da Silva L., Jacob F. Genetics and physiology of defective lysogeny in K12 (lambda): studies of early mutants. Virology. 1966 Oct;30(2):224–241. doi: 10.1016/0042-6822(66)90098-5. [DOI] [PubMed] [Google Scholar]
  3. JORDAN E. THE LOCATION OF THE B2 DELETION OF BACTERIOPHAGE LAMBDA. J Mol Biol. 1964 Nov;10:341–344. doi: 10.1016/s0022-2836(64)80052-8. [DOI] [PubMed] [Google Scholar]
  4. KAISER A. D., JACOB F. Recombination between related temperate bacteriophages and the genetic control of immunity and prophage localization. Virology. 1957 Dec;4(3):509–521. doi: 10.1016/0042-6822(57)90083-1. [DOI] [PubMed] [Google Scholar]
  5. KELLENBERGER G., ZICHICHI M. L., WEIGLE J. A mutation affecting the DNA content of bacteriophage lambda and its lysogenizing properties. J Mol Biol. 1961 Aug;3:399–408. doi: 10.1016/s0022-2836(61)80053-3. [DOI] [PubMed] [Google Scholar]
  6. MATSUSHIRO A. Specialized transduction of tryptophan markers in Escherichia coli K12 by bacteriophage phi-80. Virology. 1963 Apr;19:475–482. doi: 10.1016/0042-6822(63)90041-2. [DOI] [PubMed] [Google Scholar]
  7. Protass J. J., Korn D. Function of the N cistron of bacteriophage lambda. Proc Natl Acad Sci U S A. 1966 May;55(5):1089–1095. doi: 10.1073/pnas.55.5.1089. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. RADDING C. M. NUCLEASE ACTIVITY IN DEFECTIVE LYSOGENS OF PHAGE MU. II. A HYPERACTIVE MUTANT. Proc Natl Acad Sci U S A. 1964 Oct;52:965–973. doi: 10.1073/pnas.52.4.965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Radding C. M. Regulation of lambda exonuclease. I. Properties of lambda exonuclease purified from lysogens of lambda T11 and wild type. J Mol Biol. 1966 Jul;18(2):235–250. doi: 10.1016/s0022-2836(66)80243-7. [DOI] [PubMed] [Google Scholar]
  10. Radding C. M., Shreffler D. C. Regulation of lambda exonuclease. II. Joint regulation of exonuclease and a new lambda antigen. J Mol Biol. 1966 Jul;18(2):251–261. doi: 10.1016/s0022-2836(66)80244-9. [DOI] [PubMed] [Google Scholar]
  11. SIGNER E. R. RECOMBINATION BETWEEN COLIPHAGES LAMBDA AND PHI-80. Virology. 1964 Apr;22:650–651. doi: 10.1016/0042-6822(64)90090-x. [DOI] [PubMed] [Google Scholar]
  12. Signer E. R. Interaction of prophages at the att80 site with the chromosome of Escherichia coli. J Mol Biol. 1966 Jan;15(1):243–255. doi: 10.1016/s0022-2836(66)80224-3. [DOI] [PubMed] [Google Scholar]
  13. ZICHICHI M. L., KELLENBERGER G. Two distinct functions in the lysogenization process: the repression of phage multiplication and incorporation of the prophage in the bacterial genome. Virology. 1963 Apr;19:450–460. doi: 10.1016/0042-6822(63)90038-2. [DOI] [PubMed] [Google Scholar]

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