dc.creatorMello M.L.S.
dc.creatorPudney M.
dc.date1987
dc.date2015-06-30T13:40:29Z
dc.date2015-11-26T14:36:40Z
dc.date2015-06-30T13:40:29Z
dc.date2015-11-26T14:36:40Z
dc.date.accessioned2018-03-28T21:40:39Z
dc.date.available2018-03-28T21:40:39Z
dc.identifier
dc.identifierGenetica. Kluwer Academic Publishers, v. 74, n. 2, p. 131 - 136, 1987.
dc.identifier166707
dc.identifier10.1007/BF00055224
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0023656607&partnerID=40&md5=1fd2b6141fca040f0de160b3f5b15b8d
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/98146
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/98146
dc.identifier2-s2.0-0023656607
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1248851
dc.descriptionThe cytophotometric evaluation of the Feulgen-DNA content of the BTC-32 cells at passage 160 after 6 days of growth demonstrated that polyploidy is relatively frequent in this cell line. 4C values were assumed to pertain to diploid nuclei at the S or G2 phases but also to polyploid nuclei at the G1 phase. Polyploidy in 4C nuclei is assumed to be attained by endomitosis. However, there are morphological indications that polyploidization in cells with an 8C-128C Feulgen-DNA content could result from cellular and nuclear fusions, possibly mediated by viral particles present in the cell culture. Micronucleation was also frequent; it was assumed to be promoted by viral action or deficiency in some culture medium nutrient. These nuclear characteristics should be considered when using the BTC-32 cell line for monitoring the action of infective agents or their products. © 1987 Dr W. Junk Publishers.
dc.description74
dc.description2
dc.description131
dc.description136
dc.languageen
dc.publisherKluwer Academic Publishers
dc.relationGenetica
dc.rightsfechado
dc.sourceScopus
dc.titlePolyploidization Of The Btc-32 Cell Line From Triatoma Infestans (hemiptera, Reduviidae)
dc.typeArtículos de revistas


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