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Evidence of precursors of defective measles virus

dc.contributor.authorKiley, Michael P.en_US
dc.contributor.authorPayne, Francis E.en_US
dc.date.accessioned2006-09-11T19:04:54Z
dc.date.available2006-09-11T19:04:54Z
dc.date.issued1974-11en_US
dc.identifier.citationKiley, Michael P.; Payne, Francis E.; (1974). "Evidence of precursors of defective measles virus." Medical Microbiology and Immunology 160 (2-3): 91-97. <http://hdl.handle.net/2027.42/47527>en_US
dc.identifier.issn1432-1831en_US
dc.identifier.issn0300-8584en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47527
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=4444687&dopt=citationen_US
dc.description.abstractCytoplasmic extracts of Vero cells infected with wild strain Edmonston measles virus were found to contain at least two distinct nucleocapsid species. The two most prominent species of nucleocapsids sedimented at 200S and 110S and contained RNA of molecular weight 6.0×10 6 and 0.6×10 6 daltons respectively. Both species of nucleocapsids had a density of 1.31 g/cm 3 in CsCl. A third species sedimenting at 170S was not present in all experiments and was not characterized in detail. Infection of cells with undiluted-passage virus usually resulted in production of mostly 110S nucleocapsids while both 110S and 200S species were found when diluted-passage virus was used. These results suggest that measles virus may produce distinct classes of defective virus which contain segments of RNA representing as little as 10% of the complete viral genome.en_US
dc.format.extent346550 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherMedical Microbiologyen_US
dc.subject.otherImmunologyen_US
dc.subject.otherBiomedicineen_US
dc.titleEvidence of precursors of defective measles virusen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumVirus Laboratory, Department of Epidemiology, School of Public Health, The University of Michigan, 48104, Ann Arbor, Michiganen_US
dc.contributor.affiliationumVirus Laboratory, Department of Epidemiology, School of Public Health, The University of Michigan, 48104, Ann Arbor, Michiganen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid4444687en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47527/1/430_2005_Article_BF02121716.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF02121716en_US
dc.identifier.sourceMedical Microbiology and Immunologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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