Skip to main content

. 1964 Dec;52(6):1449–1455. doi: 10.1073/pnas.52.6.1449

ELECTRON MICROSCOPE STUDIES ON REOVIRUS RNA^{^*}

Peter J Gomatos ¹, Walther Stoeckenius ¹

PMCID: PMC300468 PMID: 14243517

1453

Images in this article

Image
on p.1450

Image
on p.1451

Selected References

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

BEER M., ZOBEL C. R. Electron stains. II: Electron microscopic studies on the visibility of stained DNA molecules. J Mol Biol. 1961 Dec;3:717–726. doi: 10.1016/s0022-2836(61)80076-4. [DOI] [PubMed] [Google Scholar]
BURGI E., HERSHEY A. D. A relative molecular weight series derived from the nucleic acid of bacteriophage T2. J Mol Biol. 1961 Aug;3:458–472. doi: 10.1016/s0022-2836(61)80058-2. [DOI] [PubMed] [Google Scholar]
BURGI E., HERSHEY A. D. Sedimentation rate as a measure of molecular weight of DNA. Biophys J. 1963 Jul;3:309–321. doi: 10.1016/s0006-3495(63)86823-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
ELLEM K. A., COLTER J. S. The interaction of infections ribonucleic acid with a mammalian cell line. I. Relationship between the osmotic pressure of the medium and the production of infectious centers. Virology. 1960 Jun;11:434–443. doi: 10.1016/0042-6822(60)90085-4. [DOI] [PubMed] [Google Scholar]
Gomatos P. J., Tamm I. THE SECONDARY STRUCTURE OF REOVIRUS RNA. Proc Natl Acad Sci U S A. 1963 May;49(5):707–714. doi: 10.1073/pnas.49.5.707. [DOI] [PMC free article] [PubMed] [Google Scholar]
HALL C. E., CAVALIERI L. F. Four-stranded DNA as determined by electron microscopy. J Biophys Biochem Cytol. 1961 Jul;10:347–351. doi: 10.1083/jcb.10.3.347. [DOI] [PMC free article] [PubMed] [Google Scholar]
HALL C. E. Method for the observation of macromolecules with the electron microscope illustrated with micrographs of DNA. J Biophys Biochem Cytol. 1956 Sep 25;2(5):625–628. doi: 10.1083/jcb.2.5.625. [DOI] [PMC free article] [PubMed] [Google Scholar]
KLEINSCHMIDT A. K., LANG D., JACHERTS D., ZAHN R. K. [Preparation and length measurements of the total desoxyribonucleic acid content of T2 bacteriophages]. Biochim Biophys Acta. 1962 Dec 31;61:857–864. [PubMed] [Google Scholar]
LANGRIDGE R., GOMATOS P. J. The structure of RNA. Reovirus RNA and transfer RNA have similar three-dimensional structures, which differ from DNA. Science. 1963 Aug 23;141(3582):694–698. doi: 10.1126/science.141.3582.694. [DOI] [PubMed] [Google Scholar]
MACHATTIE L. A., THOMAS C. A., Jr DNA FROM BACTERIOPHAGE LAMBDA: MOLECULAR LENGTH AND CONFORMATION. Science. 1964 May 29;144(3622):1142–1144. doi: 10.1126/science.144.3622.1142. [DOI] [PubMed] [Google Scholar]
NELSON J. B., TARNOWSKI G. S. An oncolytic virus recovered from Swiss mice during passage of an ascites tumour. Nature. 1960 Dec 3;188:866–867. doi: 10.1038/188866a0. [DOI] [PubMed] [Google Scholar]
PFAU C. J., MCCREA J. F. STUDIES ON THE DEOXYRIBONUCLEIC ACID OF VACCINIA VIRUS. III. CHARACTERIZATION OF DNA ISOLATED BY DIFFERENT METHODS AND ITS RELATION TO VIRUS STRUCTURE. Virology. 1963 Nov;21:425–435. doi: 10.1016/0042-6822(63)90204-6. [DOI] [PubMed] [Google Scholar]
PFAU C. J., McCREA J. F. Release of deoxyribonucleic acid from vaccinia virus by 2-mercaptoethanol and pronase. Nature. 1962 Jun 2;194:894–895. doi: 10.1038/194894a0. [DOI] [PubMed] [Google Scholar]
STOECKENIUS W. Electron microscopy of DNA molecules "stained" with heavy metal salts. J Biophys Biochem Cytol. 1961 Nov;11:297–310. doi: 10.1083/jcb.11.2.297. [DOI] [PMC free article] [PubMed] [Google Scholar]
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]

ACTIONS

RESOURCES