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. 1966 Nov;56(5):1441–1448. doi: 10.1073/pnas.56.5.1441

MANIFESTATION OF LINEAR ORGANIZATION IN MOLECULES OF PNEUMOCOCCAL TRANSFORMING DNA*

Magda Gabor 1,†, Rollin D Hotchkiss 1
PMCID: PMC219994  PMID: 16591391

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Selected References

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

  1. ALEXANDER H. E., LEIDY G., HAHN E. Studies on the nature of hemophilus influenzae cells susceptible to heritable changes by desoxyribonucleic acids. J Exp Med. 1954 Jun 1;99(6):505–533. doi: 10.1084/jem.99.6.505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BERNS K. I., THOMAS C. A., Jr ISOLATION OF HIGH MOLECULAR WEIGHT DNA FROM HEMOPHILUS INFLUENZAE. J Mol Biol. 1965 Mar;11:476–490. doi: 10.1016/s0022-2836(65)80004-3. [DOI] [PubMed] [Google Scholar]
  3. Bodmer W. F. Integration of deoxyribonuclease-treated DNA in bacillus subtilis transformation. J Gen Physiol. 1966 Jul;49(6):233–258. doi: 10.1085/jgp.49.6.233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Ephrussi-Taylor H., Sicard A. M., Kamen R. Genetic Recombination in DNA-Induced Transformation of Pneumococcus. I. the Problem of Relative Efficiency of Transforming Factors. Genetics. 1965 Mar;51(3):455–475. doi: 10.1093/genetics/51.3.455. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. FOX M. S., ALLEN M. K. ON THE MECHANISM OF DEOXYRIBONUCLEATE INTEGRATION IN PNEUMOCOCCAL TRANSFORMATION. Proc Natl Acad Sci U S A. 1964 Aug;52:412–419. doi: 10.1073/pnas.52.2.412. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. FOX M. S. Deoxyribonucleic acid incorporation by transformed bacteria. Biochim Biophys Acta. 1957 Oct;26(1):83–85. doi: 10.1016/0006-3002(57)90056-2. [DOI] [PubMed] [Google Scholar]
  7. FOX M. S., HOTCHKISS R. D. Initiation of bacterial transformation. Nature. 1957 Jun 29;179(4574):1322–1325. doi: 10.1038/1791322a0. [DOI] [PubMed] [Google Scholar]
  8. GOODGAL S. H. Studies on transformations of Hemophilus influenzae. IV. Linked and unlinked transformations. J Gen Physiol. 1961 Nov;45:205–228. doi: 10.1085/jgp.45.2.205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. GUILD W. R., ROBINSON M. Evidence for message reading from a unique strand of pneumococcal DNA. Proc Natl Acad Sci U S A. 1963 Jul;50:106–112. doi: 10.1073/pnas.50.1.106. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. HERSHEY A. D., BURGI E. COMPLEMENTARY STRUCTURE OF INTERACTING SITES AT THE ENDS OF LAMBDA DNA MOLECULES. Proc Natl Acad Sci U S A. 1965 Feb;53:325–328. doi: 10.1073/pnas.53.2.325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Herriott R. M. Structure of the hybrid transforming unit. Genetics. 1965 Dec;52(6):1235–1246. doi: 10.1093/genetics/52.6.1235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Hotchkiss R. D. CYCLICAL BEHAVIOR IN PNEUMOCOCCAL GROWTH AND TRANSFORMABILITY OCCASIONED BY ENVIRONMENTAL CHANGES. Proc Natl Acad Sci U S A. 1954 Feb;40(2):49–55. doi: 10.1073/pnas.40.2.49. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. KENT J. L., HOTCHKISS R. D. KINETIC ANALYSIS OF MULTIPLE, LINKED RECOMBINATIONS IN PNEUMOCOCCAL TRANSFORMATION. J Mol Biol. 1964 Aug;9:308–322. doi: 10.1016/s0022-2836(64)80209-6. [DOI] [PubMed] [Google Scholar]
  14. KENT J. L., ROGER M., HOTCHKISS R. D. ON THE ROLE OF INTEGRITY OF DNA PARTICLES IN GENETIC RECOMBINATION DURING PNEUMOCOCCAL TRANSFORMATION. Proc Natl Acad Sci U S A. 1963 Oct;50:717–725. doi: 10.1073/pnas.50.4.717. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. LACKS S. Molecular fate of DNA in genetic transformation of Pneumococcus. J Mol Biol. 1962 Jul;5:119–131. doi: 10.1016/s0022-2836(62)80067-9. [DOI] [PubMed] [Google Scholar]
  16. LERMAN L. S., TOLMACH L. J. Genetic transformation. I. Cellular incorporation of DNA accompanying transformation in Pneumococcus. Biochim Biophys Acta. 1957 Oct;26(1):68–82. doi: 10.1016/0006-3002(57)90055-0. [DOI] [PubMed] [Google Scholar]
  17. LEVINE J. S., STRAUSS N. LAG PERIOD CHARACTERIZING THE ENTRY OF TRANSFORMING DEOXYRIBONUCLEIC ACID INTO BACILLUS SUBTILIS. J Bacteriol. 1965 Feb;89:281–287. doi: 10.1128/jb.89.2.281-287.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lacks S. Integration efficiency and genetic recombination in pneumococcal transformation. Genetics. 1966 Jan;53(1):207–235. doi: 10.1093/genetics/53.1.207. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Marmur J., Lane D. STRAND SEPARATION AND SPECIFIC RECOMBINATION IN DEOXYRIBONUCLEIC ACIDS: BIOLOGICAL STUDIES. Proc Natl Acad Sci U S A. 1960 Apr;46(4):453–461. doi: 10.1073/pnas.46.4.453. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Notani N., Goodgal S. H. On the nature of recombinants formed during transformation in Hemophilus influenzae. J Gen Physiol. 1966 Jul;49(6):197–209. doi: 10.1085/jgp.49.6.197. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. OPARA-KUBINSKA Z., KUBINSKI H., SZYBALSKI W. INTERACTION BETWEEN DENATURED DNA, POLYRIBONUCLEOTIDES, AND RIBOSOMAL RNA: ATTEMPTS AT PREPARATIVE SEPARATION OF THE COMPLEMENTARY DNA STRANDS. Proc Natl Acad Sci U S A. 1964 Oct;52:923–930. doi: 10.1073/pnas.52.4.923. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. RAVIN A. W., IYER V. N. Genetic mapping of DNA: influence of the mutated configuration on the frequency of recombination along the length of the molecule. Genetics. 1962 Oct;47:1369–1384. doi: 10.1093/genetics/47.10.1369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Roger M., Beckmann C. O., Hotchkiss R. D. Fractionation of denatured pneumococcal DNA: evidence for resolution of complementary strands. J Mol Biol. 1966 Jun;18(1):174–194. doi: 10.1016/s0022-2836(66)80084-0. [DOI] [PubMed] [Google Scholar]
  24. Roger M., Beckmann C. O., Hotchkiss R. D. Separation of native and denatured fractions from partially denatured pneumococcal DNA. J Mol Biol. 1966 Jun;18(1):156–173. doi: 10.1016/s0022-2836(66)80083-9. [DOI] [PubMed] [Google Scholar]
  25. STRACK H. B., KAISER A. D. ON THE STRUCTURE OF THE ENDS OF LAMBADA DNA. J Mol Biol. 1965 May;12:36–49. doi: 10.1016/s0022-2836(65)80280-7. [DOI] [PubMed] [Google Scholar]
  26. STRAUSS N. CONFIGURATION OF TRANSFORMING DEOXYRIBONUCLEIC ACID DURING ENTRY INTO BACILLUS SUBTILIS. J Bacteriol. 1965 Feb;89:288–293. doi: 10.1128/jb.89.2.288-293.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. STUY J. H., STERN D. THE KINETICS OF DNA UPTAKE BY HAEMOPHILUS INFLUENZAE. J Gen Microbiol. 1964 Jun;35:391–400. doi: 10.1099/00221287-35-3-391. [DOI] [PubMed] [Google Scholar]
  28. THOMAS R. Recherches sur la cinétique des transformations bactériennes. Biochim Biophys Acta. 1955 Dec;18(4):467–481. doi: 10.1016/0006-3002(55)90137-2. [DOI] [PubMed] [Google Scholar]

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