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. 1969 Feb;3(2):278–281. doi: 10.1128/jvi.3.2.278-281.1969

Variations in sedimentation patterns among deoxyribonucleic acids synthesized after infection of Escherichia coli by different amber mutants of bacteriophage T7.

R Hausmann, K LaRue
PMCID: PMC375763  PMID: 4886657

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Selected References

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

  1. Bode V. C., Kaiser A. D. Changes in the structure and activity of lambda DNA in a superinfected immune bacterium. J Mol Biol. 1965 Dec;14(2):399–417. doi: 10.1016/s0022-2836(65)80190-5. [DOI] [PubMed] [Google Scholar]
  2. Botstein D., Levine M. Synthesis and maturation of phage P22 DNA. II. Properties of temperature-sensitive phage mutants defective in DNA metabolism. J Mol Biol. 1968 Jun 28;34(3):643–654. doi: 10.1016/0022-2836(68)90186-1. [DOI] [PubMed] [Google Scholar]
  3. Botstein D. Synthesis and maturation of phage P22 DNA. I. Identification of intermediates. J Mol Biol. 1968 Jun 28;34(3):621–641. doi: 10.1016/0022-2836(68)90185-x. [DOI] [PubMed] [Google Scholar]
  4. Carlson K. Intracellular fate of deoxyribonucleic acid from T7 bacteriophages. J Virol. 1968 Oct;2(10):1230–1233. doi: 10.1128/jvi.2.10.1230-1233.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Frankel F. R. Evidence for long DNA strands in the replicating pool after T4 infection. Proc Natl Acad Sci U S A. 1968 Jan;59(1):131–138. doi: 10.1073/pnas.59.1.131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Frankel F. R. Studies on the nature of replicating DNA in T4-infected Escherichia coli. J Mol Biol. 1966 Jun;18(1):127–143. doi: 10.1016/s0022-2836(66)80081-5. [DOI] [PubMed] [Google Scholar]
  7. Frankel F. R. Studies on the nature of the replicating DNA in Escherichia coli infected with certain amber mutants of phage T4. J Mol Biol. 1966 Jun;18(1):144–155. doi: 10.1016/s0022-2836(66)80082-7. [DOI] [PubMed] [Google Scholar]
  8. Hausmann R., Gomez B. Amber mutants of bacteriophages T3 and T7 defective in phage-directed deoxyribonucleic acid synthesis. J Virol. 1967 Aug;1(4):779–792. doi: 10.1128/jvi.1.4.779-792.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hausmann R. Sedimentation analysis of phage T7-directed DNA synthesized in the presence of a dominant conditional lethal phage gene. Biochem Biophys Res Commun. 1968 May 23;31(4):609–615. doi: 10.1016/0006-291x(68)90522-6. [DOI] [PubMed] [Google Scholar]
  10. Rhoades M., Thomas C. A., Jr The P22 bacteriophage DNA molecule. II. Circular intracellular forms. J Mol Biol. 1968 Oct 14;37(1):41–61. doi: 10.1016/0022-2836(68)90072-7. [DOI] [PubMed] [Google Scholar]
  11. Salzman L. A., Weissbach A. Deoxyribonucleic acid replication in lambda bacteriophage mutants. J Virol. 1968 Feb;2(2):118–123. doi: 10.1128/jvi.2.2.118-123.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Smith M. G., Burton K. Fractionation of deoxyribonucleic acid from phage-infected bacteria. Biochem J. 1966 Jan;98(1):229–241. doi: 10.1042/bj0980229. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Smith M. G., Skalka A. Some properties of DNA from phage-infected bacteria. J Gen Physiol. 1966 Jul;49(6):127–142. doi: 10.1085/jgp.49.6.127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Streisinger G., Emrich J., Stahl M. M. Chromosome structure in phage t4, iii. Terminal redundancy and length determination. Proc Natl Acad Sci U S A. 1967 Feb;57(2):292–295. doi: 10.1073/pnas.57.2.292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Young E. T., 2nd, Sinsheimer R. L. Vegetative lambda DNA. 3. Pulse-labeled components. J Mol Biol. 1968 Apr 14;33(1):49–59. doi: 10.1016/0022-2836(68)90280-5. [DOI] [PubMed] [Google Scholar]

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