Skip to main content
NCBI home page
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1965 Aug;54(2):551–558. doi: 10.1073/pnas.54.2.551

Kinetics of x-ray and heat inactivation of phi-x174 RF-DNA.

W Ginoza, R C Miller
PMCID: PMC219703  PMID: 5217442

Full text

PDF
552

Selected References

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

  1. GINOZA W., HOELLE C. J., VESSEY K. B., CARMACK C. MECHANISMS OF INACTIVATION OF SINGLE-STRANDED VIRUS NUCLEIC ACIDS BY HEAT. Nature. 1964 Aug 8;203:606–609. doi: 10.1038/203606a0. [DOI] [PubMed] [Google Scholar]
  2. GINOZA W. RADIOSENSITIVE MOLECULAR WEIGHT OF SINGLE-STRANDED VIRUS NUCLEIC ACIDS. Nature. 1963 Aug 3;199:453–456. doi: 10.1038/199453a0. [DOI] [PubMed] [Google Scholar]
  3. GINOZA W., ZIMM B. H. Mechanisms of inactivation of deoxyribonucleic acids by heat. Proc Natl Acad Sci U S A. 1961 May 15;47:639–652. doi: 10.1073/pnas.47.5.639. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. KLEINSCHMIDT A. K., BURTON A., SINSHEIMER R. L. ELECTRON MICROSCOPY OF THE REPLICATIVE FORM OF THE DNA OF THE BACTERIOPHAGE PHI-X174. Science. 1963 Nov 15;142(3594):961–961. doi: 10.1126/science.142.3594.961. [DOI] [PubMed] [Google Scholar]
  5. KOZINSKI A. W. Fragmentary transfer of P32-labeled parental DNA to progeny phage. Virology. 1961 Jan;13:124–134. doi: 10.1016/0042-6822(61)90039-3. [DOI] [PubMed] [Google Scholar]
  6. KOZINSKI A. W., SZYBALSKI W. Dispersive transfer of the parental DNA molecule to the progeny of phage phiX-174. Virology. 1959 Oct;9:260–274. doi: 10.1016/0042-6822(59)90119-9. [DOI] [PubMed] [Google Scholar]
  7. ROGER M., HOTCHKISS R. D. Selective heat inactivation of pneumococcal transforming deoxyribonucleate. Proc Natl Acad Sci U S A. 1961 May 15;47:653–669. doi: 10.1073/pnas.47.5.653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. SINSHEIMER R. L., STARMAN B., NAGLER C., GUTHRIE S. The process of infection with bacteriophage phi-XI74. I. Evidence for a "replicative form". J Mol Biol. 1962 Mar;4:142–160. doi: 10.1016/s0022-2836(62)80047-3. [DOI] [PubMed] [Google Scholar]
  9. TESSMAN I. Some unusual properties of the nucleic acid in bacteriophages S13 and phi X174. Virology. 1959 Mar;7(3):263–275. doi: 10.1016/0042-6822(59)90197-7. [DOI] [PubMed] [Google Scholar]
  10. WEIL R., VINOGRAD J. THE CYCLIC HELIX AND CYCLIC COIL FORMS OF POLYOMA VIRAL DNA. Proc Natl Acad Sci U S A. 1963 Oct;50:730–738. doi: 10.1073/pnas.50.4.730. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. YARUS M., SINSHEIMER R. L. THE U.V.-RESISTANCE OF DOUBLE-STRANDED PHIX174 DNA. J Mol Biol. 1964 Apr;8:614–615. doi: 10.1016/s0022-2836(64)80018-8. [DOI] [PubMed] [Google Scholar]
  12. ZIMMERMANN F., KROEGER H., HAGEN U., KECK K. THE EFFECT OF X-IRRADIATION ON THE PRIMING ABILITY OF DNA IN THE RNA POLYMERASE SYSTEM. Biochim Biophys Acta. 1964 May 18;87:160–162. doi: 10.1016/0926-6550(64)90058-1. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES