Skip to main content
Bacteriological Reviews logoLink to Bacteriological Reviews
. 1968 Jun;32(2):127–137. doi: 10.1128/br.32.2.127-137.1968

Recent progress in poxvirus research.

B Woodson
PMCID: PMC378301  PMID: 4873813

Full text

PDF
127

Selected References

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

  1. ABEL P. REACTIVATION OF HEATED VACCINIA VIRUS IN VITRO. Z Vererbungsl. 1963 Nov 21;94:249–252. doi: 10.1007/BF00894768. [DOI] [PubMed] [Google Scholar]
  2. ABEL P., TRAUTNER T. A. FORMATION OF AN ANIMAL VIRUS WITHIN A BACTERIUM. Z Vererbungsl. 1964 Apr 10;95:66–72. doi: 10.1007/BF00898185. [DOI] [PubMed] [Google Scholar]
  3. APPLEYARD G., WESTWOOD J. C. THE GROWTH OF RABBITPOX VIRUS IN TISSUE CULTURE. J Gen Microbiol. 1964 Dec;37:391–401. doi: 10.1099/00221287-37-3-391. [DOI] [PubMed] [Google Scholar]
  4. APPLEYARD G., ZWARTOUW H. T., WESTWOOD J. C. A PROTECTIVE ANTIGEN FROM THE POX-VIRUSES. I. REACTION WITH NEUTRALIZING ANTIBODY. Br J Exp Pathol. 1964 Apr;45:150–161. [PMC free article] [PubMed] [Google Scholar]
  5. Babbar O. P., Chowdhury B. L., Rani G. Pock formation by vaccinia virus deoxyribonucleic acid after passage through Escherichia coli spheroplasts. Acta Virol. 1966 Jan;10(1):15–19. [PubMed] [Google Scholar]
  6. Chang L. M., Hodes M. E. Induction of DNA nucleotidyltransferase by the Shope fibroma virus. Virology. 1967 Jun;32(2):258–266. doi: 10.1016/0042-6822(67)90275-9. [DOI] [PubMed] [Google Scholar]
  7. Cohen G. H., Wilcox W. C. Soluble antigens of vaccinia-infected mammalian cells. I. Separation of virus-induced soluble antigens into two classes on the basis of physical characteristics. J Bacteriol. 1966 Sep;92(3):676–686. doi: 10.1128/jb.92.3.676-686.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. DALES S., KAJIOKA R. THE CYCLE OF MULTIPLICATION OF VACCINIA VIRUS IN EARLE'S STRAIN L CELLS. I. UPTAKE AND PENETRATION. Virology. 1964 Nov;24:278–294. doi: 10.1016/0042-6822(64)90167-9. [DOI] [PubMed] [Google Scholar]
  9. DALES S. The uptake and development of vaccinia virus in strain L cells followed with labeled viral deoxyribonucleic acid. J Cell Biol. 1963 Jul;18:51–72. doi: 10.1083/jcb.18.1.51. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dales S. Effects of streptovitacin A on the initial events in the replication of vaccinia and reovirus. Proc Natl Acad Sci U S A. 1965 Aug;54(2):462–468. doi: 10.1073/pnas.54.2.462. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dales S. Pentration of animal viruses into cells. Prog Med Virol. 1965;7:1–43. [PubMed] [Google Scholar]
  12. EASTERBROOK K. B. Interference with the maturation of vaccinia virus by isatin beta-thiosemicarbazone. Virology. 1962 Jun;17:245–251. doi: 10.1016/0042-6822(62)90114-9. [DOI] [PubMed] [Google Scholar]
  13. Easterbrook K. B. Controlled degradation of vaccinia virions in vitro: an electron microscopic study. J Ultrastruct Res. 1966 Mar;14(5):484–496. doi: 10.1016/s0022-5320(66)80077-1. [DOI] [PubMed] [Google Scholar]
  14. Easterbrook K. B. Morphology of deoxyribonucleic acid extracted from cores of vaccinia virus. J Virol. 1967 Jun;1(3):643–645. doi: 10.1128/jvi.1.3.643-645.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Fenner F., Sambrook J. F. Conditional lethal mutants of rabbitpox virus. II. Mutants (p) that fail to multiply in PK-2a cells. Virology. 1966 Apr;28(4):600–609. doi: 10.1016/0042-6822(66)90245-5. [DOI] [PubMed] [Google Scholar]
  16. Friesen J. D., Dale B., Bode W. Presence of T4 "early" messenger RNA on polysomes late in infection. J Mol Biol. 1967 Sep 28;28(3):413–422. doi: 10.1016/s0022-2836(67)80090-1. [DOI] [PubMed] [Google Scholar]
  17. Gafford L. G., Randall C. C. The high molecular weight of the fowlpox virus genome. J Mol Biol. 1967 Jun 14;26(2):303–310. doi: 10.1016/0022-2836(67)90299-9. [DOI] [PubMed] [Google Scholar]
  18. Hyde J. M., Gafford L. G., Randall C. C. Molecular weight determination of fowlpox virus DNA by electron microscopy. Virology. 1967 Sep;33(1):112–120. doi: 10.1016/0042-6822(67)90099-2. [DOI] [PubMed] [Google Scholar]
  19. JOKLIK W. K., BECKER Y. THE REPLICATION AND COATING OF VACCINIA DNA. J Mol Biol. 1964 Dec;10:452–474. doi: 10.1016/s0022-2836(64)80066-8. [DOI] [PubMed] [Google Scholar]
  20. JOKLIK W. K. THE INTRACELLULAR FATE OF RABBITPOX VIRUS RENDERED NONINFECTIOUS BY VARIOUS REAGENTS. Virology. 1964 Apr;22:620–633. doi: 10.1016/0042-6822(64)90084-4. [DOI] [PubMed] [Google Scholar]
  21. JOKLIK W. K. THE INTRACELLULAR UNCOATING OF POXVIRUS DNA. I. THE FATE OF RADIOACTIVELY-LABELED RABBITPOX VIRUS. J Mol Biol. 1964 Feb;8:263–276. doi: 10.1016/s0022-2836(64)80136-4. [DOI] [PubMed] [Google Scholar]
  22. JOKLIK W. K. THE INTRACELLULAR UNCOATING OF POXVIRUS DNA. II. THE MOLECULAR BASIS OF THE UNCOATING PROCESS. J Mol Biol. 1964 Feb;8:277–288. doi: 10.1016/s0022-2836(64)80137-6. [DOI] [PubMed] [Google Scholar]
  23. JOKLIK W. K. The purification fo four strains of poxvirus. Virology. 1962 Sep;18:9–18. doi: 10.1016/0042-6822(62)90172-1. [DOI] [PubMed] [Google Scholar]
  24. Joklik W. K., Becker Y. Studies on the genesis of polyribosomes. II. The association of nascent messenger RNA with the 40 S subribosomal particle. J Mol Biol. 1965 Sep;13(2):511–520. doi: 10.1016/s0022-2836(65)80113-9. [DOI] [PubMed] [Google Scholar]
  25. Joklik W. K., Merigan T. C. Concerning the mechanism of action of interferon. Proc Natl Acad Sci U S A. 1966 Aug;56(2):558–565. doi: 10.1073/pnas.56.2.558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Joklik W. K. The poxviruses. Bacteriol Rev. 1966 Mar;30(1):33–66. doi: 10.1128/br.30.1.33-66.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Jungwirth C., Dawid I. B. Vaccinia DNA: separation of viral from host cell DNA. Arch Gesamte Virusforsch. 1967;20(4):464–468. doi: 10.1007/BF01275228. [DOI] [PubMed] [Google Scholar]
  28. Jungwirth C., Joklik W. K. Studies on "early" enzymes in HeLa cells infected with vaccinia virus. Virology. 1965 Sep;27(1):80–93. doi: 10.1016/0042-6822(65)90145-5. [DOI] [PubMed] [Google Scholar]
  29. Kates J. R., McAuslan B. R. Messenger RNA synthesis by a "coated" viral genome. Proc Natl Acad Sci U S A. 1967 Feb;57(2):314–320. doi: 10.1073/pnas.57.2.314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Kates J. R., McAuslan B. R. Poxvirus DNA-dependent RNA polymerase. Proc Natl Acad Sci U S A. 1967 Jul;58(1):134–141. doi: 10.1073/pnas.58.1.134. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Kates J. R., McAuslan B. R. Relationship between protein synthesis and viral deoxyribonucleic acid synthesis. J Virol. 1967 Feb;1(1):110–114. doi: 10.1128/jvi.1.1.110-114.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Kim K. S., Sharp D. G. Multiplicity reactivation of vaccinia virus particles treated with nitrogen mustard. J Virol. 1967 Feb;1(1):45–49. doi: 10.1128/jvi.1.1.45-49.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. MCAUSLAN B. R. THE INDUCTION AND REPRESSION OF THYMIDINE KINASE IN THE POXVIRUS-INFECTED HELA CELL. Virology. 1963 Nov;21:383–389. doi: 10.1016/0042-6822(63)90199-5. [DOI] [PubMed] [Google Scholar]
  34. Magee W. E., Miller O. V. Immunological evidence for the appearance of a new DNA-polymerase in cells infected with vaccinia virus. Virology. 1967 Jan;31(1):64–69. doi: 10.1016/0042-6822(67)90008-6. [DOI] [PubMed] [Google Scholar]
  35. Maitra U., Cohen S. N., Hurwitz J. Specificity of initiation and synthesis of RNA from DNA templates. Cold Spring Harb Symp Quant Biol. 1966;31:113–122. doi: 10.1101/sqb.1966.031.01.018. [DOI] [PubMed] [Google Scholar]
  36. McCrea J. F., Lipman M. B. Strand-length measurements of normal and 5-iodo-2'-deoxyuridine-treated vaccinia virus deoxyribonucleic acid released by the Kleinschmidt method. J Virol. 1967 Oct;1(5):1037–1044. doi: 10.1128/jvi.1.5.1037-1044.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Munyon W. H., Kit S. Induction of cytoplasmic ribonucleic acid (RNA) synthesis in vaccinia-infected LM cells during inhibition of protein synthesis. Virology. 1966 Jun;29(2):303–309. doi: 10.1016/0042-6822(66)90037-7. [DOI] [PubMed] [Google Scholar]
  38. Munyon W., Paoletti E., Grace J. T., Jr RNA polymerase activity in purified infectious vaccinia virus. Proc Natl Acad Sci U S A. 1967 Dec;58(6):2280–2287. doi: 10.1073/pnas.58.6.2280. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Oda K. I., Joklik W. K. Hybridization and sedimentation studies on "early" and "late" vaccinia messenger RNA. J Mol Biol. 1967 Aug 14;27(3):395–419. doi: 10.1016/0022-2836(67)90047-2. [DOI] [PubMed] [Google Scholar]
  40. Ptashne M. ISOLATION OF THE lambda PHAGE REPRESSOR. Proc Natl Acad Sci U S A. 1967 Feb;57(2):306–313. doi: 10.1073/pnas.57.2.306. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Pène J. J., Marmur J. Deoxyribonucleic acid replication and expression of early and late bacteriophage functions in Bacillus subtilis. J Virol. 1967 Feb;1(1):86–91. doi: 10.1128/jvi.1.1.86-91.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. RANDALL C. C., GAFFORD L. G., DARLINGTON R. W., HYDE J. COMPOSITION OF FOWLPOX VIRUS AND INCLUSION MATRIX. J Bacteriol. 1964 Apr;87:939–944. doi: 10.1128/jb.87.4.939-944.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Randall C. C., Gafford L. G., Soehner R. L., Hyde J. M. Physicochemical properties of fowlpox virus deoxyribonucleic acid and its anomalous infectious behavior. J Bacteriol. 1966 Jan;91(1):95–100. doi: 10.1128/jb.91.1.95-100.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Rodriguez-Burgos A., Chordi A., Diaz R., Tormo J. Immunoelectrophoretic analysis of vaccinia virus. Virology. 1966 Nov;30(3):569–572. doi: 10.1016/0042-6822(66)90133-4. [DOI] [PubMed] [Google Scholar]
  45. Rosenkranz H. S., Rose H. M., Morgan C., Hsu K. C. The effect of hydroxyurea on virus development. II. Vaccinia virus. Virology. 1966 Apr;28(4):510–519. doi: 10.1016/0042-6822(66)90235-2. [DOI] [PubMed] [Google Scholar]
  46. SHATKIN A. J. The formation of vaccinia virus protein in the presence of 5-fluorodeoxyuridine. Virology. 1963 Jun;20:292–301. doi: 10.1016/0042-6822(63)90118-1. [DOI] [PubMed] [Google Scholar]
  47. Salzman N. P., Sebring E. D. Sequential formation of vaccinia virus proteins and viral deoxyribonucleic acid replication. J Virol. 1967 Feb;1(1):16–23. doi: 10.1128/jvi.1.1.16-23.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Sambrook J. F., Padgett B. L., Tomkins J. K. Conditional lethal mutants of rabbitpox virus. I. Isolation of host cell-dependent and temperature-dependent mutants. Virology. 1966 Apr;28(4):592–599. doi: 10.1016/0042-6822(66)90244-3. [DOI] [PubMed] [Google Scholar]
  49. Sarov I., Becker Y. Studies on vaccinia virus DNA. Virology. 1967 Nov;33(3):369–375. doi: 10.1016/0042-6822(67)90112-2. [DOI] [PubMed] [Google Scholar]
  50. Sebring E. D., Salzman N. P. Metabolic properties of early and late vaccinia virus messenger ribonucleic acid. J Virol. 1967 Jun;1(3):550–558. doi: 10.1128/jvi.1.3.550-558.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Sharp D. G., Kim K. S. Multiplicity reactivation and radiation survival of aggregated vaccinia virus. Calculation of plaque titer based on MR and particle aggregation seen in the electron microscope. Virology. 1966 Jul;29(3):359–366. doi: 10.1016/0042-6822(66)90211-x. [DOI] [PubMed] [Google Scholar]
  52. Skalka A., Butler B., Echols H. Genetic control of transcription during development of phage gamma. Proc Natl Acad Sci U S A. 1967 Aug;58(2):576–583. doi: 10.1073/pnas.58.2.576. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Smadel J. E., Hoagland C. L. ELEMENTARY BODIES OF VACCINIA. Bacteriol Rev. 1942 Jun;6(2):79–110. doi: 10.1128/br.6.2.79-110.1942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Takehara M., Schwerdt C. E. Infective subviral particles from cell cultures infected with myxoma and fibroma viruses. Virology. 1967 Jan;31(1):163–166. doi: 10.1016/0042-6822(67)90020-7. [DOI] [PubMed] [Google Scholar]
  55. WESTWOOD J. C., ZWARTOUW H. T., APPLEYARD G., TITMUSS D. H. COMPARISON OF THE SOLUBLE ANTIGENS AND VIRUS PARTICLE ANTIGENS OF VACCINIA VIRUS. J Gen Microbiol. 1965 Jan;38:47–53. doi: 10.1099/00221287-38-1-47. [DOI] [PubMed] [Google Scholar]
  56. Wilcox W. C., Cohen G. H. Soluble antigens of vaccinia-infected mammalian cells. II. Time course of synthesis of soluble antigens and virus structural proteins. J Virol. 1967 Jun;1(3):500–508. doi: 10.1128/jvi.1.3.500-508.1967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Woodson B., Joklik W. K. The inhibition of vaccinia virus multiplication by isatin-beta-thiosemicarbazone. Proc Natl Acad Sci U S A. 1965 Sep;54(3):946–953. doi: 10.1073/pnas.54.3.946. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Woodson B. Vaccinia mRNA synthesis under conditions which prevent uncoating. Biochem Biophys Res Commun. 1967 Apr 20;27(2):169–175. doi: 10.1016/s0006-291x(67)80057-3. [DOI] [PubMed] [Google Scholar]

Articles from Bacteriological Reviews are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES