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. 1966 Aug;56(2):558–565. doi: 10.1073/pnas.56.2.558

Concerning the mechanism of action of interferon.

W K Joklik, T C Merigan
PMCID: PMC224409  PMID: 5229977

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Selected References

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

  1. BECKER Y., JOKLIK W. K. MESSENGER RNA IN CELLS INFECTED WITH VACCINIA VIRUS. Proc Natl Acad Sci U S A. 1964 Apr;51:577–585. doi: 10.1073/pnas.51.4.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. DE SOMER P., PRINZIE A., DENYS P., Jr, SCHONNE E. Mechanism of action of interferon. I. Relationship with viral ribonucleic acid. Virology. 1962 Jan;16:63–70. doi: 10.1016/0042-6822(62)90202-7. [DOI] [PubMed] [Google Scholar]
  3. EAGLE H. Amino acid metabolism in mammalian cell cultures. Science. 1959 Aug 21;130(3373):432–437. doi: 10.1126/science.130.3373.432. [DOI] [PubMed] [Google Scholar]
  4. FRIEDMAN R. M. ROLE OF INTERFERON IN VIRAL INTERFERENCE. Nature. 1964 Feb 22;201:848–849. doi: 10.1038/201848a0. [DOI] [PubMed] [Google Scholar]
  5. FRIEDMAN R. M., SONNABEND J. A. INHIBITION OF INTERFERON ACTION BY P-FLUOROPHENYLALANINE. Nature. 1964 Jul 25;203:366–367. doi: 10.1038/203366a0. [DOI] [PubMed] [Google Scholar]
  6. FRIEDMAN R. M., SONNABEND J. A., MCDEVITT H. INTERFERON INHIBITION OF CYTOPLASMIC DNA ACCUMULATION IN VACCINIA VIRUS INFECTION. A RADIOAUTOGRAPHIC STUDY. Proc Soc Exp Biol Med. 1965 Jun;119:551–553. doi: 10.3181/00379727-119-30235. [DOI] [PubMed] [Google Scholar]
  7. Friedman R. M., Sonnabend J. A. Inhibition by interferon of production of double-stranded Semliki forest virus ribonucleic acid. Nature. 1965 May 1;206(983):532–532. doi: 10.1038/206532a0. [DOI] [PubMed] [Google Scholar]
  8. Gauntt C. J., Lockart R. Z., Jr Inhibition of Mengo virus by interferon. J Bacteriol. 1966 Jan;91(1):176–182. doi: 10.1128/jb.91.1.176-182.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gordon I., Chenault S. S., Stevenson D., Acton J. D. Effect of interferon on polymerization of single-stranded and double-stranded mengovirus ribonucleic acid. J Bacteriol. 1966 Mar;91(3):1230–1238. doi: 10.1128/jb.91.3.1230-1238.1966. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. HELLER E. ENHANCEMENT OF CHIKUNGUNYA VIRUS REPLICATION AND INHIBITION OF INTERFERON PRODUCTION BY ACTINOMYCIN D. Virology. 1963 Dec;21:652–656. doi: 10.1016/0042-6822(63)90239-3. [DOI] [PubMed] [Google Scholar]
  11. 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]
  12. JOKLIK W. K. The preparation and characteristics of highly purified radioactively labelled poxvirus. Biochim Biophys Acta. 1962 Aug 20;61:290–301. doi: 10.1016/0926-6550(62)90091-9. [DOI] [PubMed] [Google Scholar]
  13. 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]
  14. JUNGWIRTH C., BODO G. BESTIMMUNG DES MOLEKULARGEWICHTES VON INTERFERON DURCH GELFILTRATION. Biochem Z. 1964 Mar 12;339:382–389. [PubMed] [Google Scholar]
  15. Joklik W. K., Becker Y. Studies on the genesis of polyribosomes. I. Origin and significance of the subribosomal particles. J Mol Biol. 1965 Sep;13(2):496–510. doi: 10.1016/s0022-2836(65)80112-7. [DOI] [PubMed] [Google Scholar]
  16. 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]
  17. 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]
  18. LEVINE S. EFFECT OF ACTINOMYCIN D AND PUROMYCIN DIHYDROCHLORIDE ON ACTION OF INTERFERON. Virology. 1964 Dec;24:586–588. doi: 10.1016/0042-6822(64)90211-9. [DOI] [PubMed] [Google Scholar]
  19. LEVY H. B. STUDIES ON THE MECHANISM OF INTERFERON ACTION. II. THE EFFECT OF INTERFERON ON SOME EARLY EVENTS IN MENGO VIRUS INFECTION IN L CELLS. Virology. 1964 Apr;22:575–579. doi: 10.1016/0042-6822(64)90079-0. [DOI] [PubMed] [Google Scholar]
  20. Levy H. B., Snellbaker L. F., Baron S. Effect of interferon on RNA synthesis in Sindbis virus infected cells. Proc Soc Exp Biol Med. 1966 Feb;121(2):630–632. doi: 10.3181/00379727-121-30848. [DOI] [PubMed] [Google Scholar]
  21. Oxman M. N., Black P. H. Inhibition of SV40 T antigen formation by interferon. Proc Natl Acad Sci U S A. 1966 May;55(5):1133–1140. doi: 10.1073/pnas.55.5.1133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Penman S., Summers D. Effects on host cell metabolism following synchronous infection with poliovirus. Virology. 1965 Dec;27(4):614–620. doi: 10.1016/0042-6822(65)90187-x. [DOI] [PubMed] [Google Scholar]
  23. Taylor J. Inhibition of interferon action by actinomycin. Biochem Biophys Res Commun. 1964;14:447–451. doi: 10.1016/0006-291x(64)90084-1. [DOI] [PubMed] [Google Scholar]
  24. WAGNER R. R. INHIBITION OF INTERFERON BIOSYNTHESIS BY ACTINOMYCIN D. Nature. 1964 Oct 3;204:49–51. doi: 10.1038/204049a0. [DOI] [PubMed] [Google Scholar]
  25. 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]

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