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dc.contributor.authorBenício, Daniela Ferreira Araújopt_BR
dc.contributor.authorPereira, Luciana Oliveirapt_BR
dc.contributor.authorSilva, Izabel Cristina Rodrigues dapt_BR
dc.contributor.authorAzevedo, Ricardo Bentespt_BR
dc.contributor.authorBezerra, Ana Cristina Barretopt_BR
dc.date.accessioned2019-01-02T13:54:57Z-
dc.date.available2019-01-02T13:54:57Z-
dc.date.issued2018pt_BR
dc.identifier.citationBENÍCIO, Daniela Ferreira Araújo et al. Culture of human dental pulp cells at variable times post-tooth extraction. Brazilian Oral Research, São Paulo, v. 32, e003, 2018. DOI: http://dx.doi.org/10.1590/1807-3107bor-2018.vol32.0003. Disponível em: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242018000100202&lng=en&nrm=iso. Acesso em: 30 jan. 2019. Epub Feb 01, 2018.pt_BR
dc.identifier.urihttp://repositorio.unb.br/handle/10482/33615-
dc.language.isoenpt_BR
dc.publisherSociedade Brasileira de Pesquisa Odontológica - SBPqOpt_BR
dc.rightsAcesso Abertopt_BR
dc.titleCulture of human dental pulp cells at variable times post-tooth extractionpt_BR
dc.typeArtigopt_BR
dc.subject.keywordCélulas-troncopt_BR
dc.subject.keywordPolpa dentáriapt_BR
dc.rights.licenseBrazilian Oral Research - (CC BY) - This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Fonte: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242018000100202&lng=en&nrm=iso&tlng=en. Acesso em: 30 jan. 2019.-
dc.identifier.doihttp://dx.doi.org/10.1590/1807-3107bor-2018.vol32.0003pt_BR
dc.description.abstract1The aim of this study was to investigate the viability of human dental pulp cells from extracted teeth kept at standard room temperature and atmospheric pressure for different periods of time. Twenty-one healthy permanent teeth were used. They were divided into five groups according to the expected time from extraction to processing. One group was tested immediately after extraction; the other groups were each tested at one of the following time points: 30 minutes, 1 hour, 2 hours, and 5 hours post-extraction. Cell morphology was analysed by light microscopy; cell proliferation was analysed using MTT assay and by counting the viable cells in a haemocytometer. Similar results were observed in all groups (p < 0.05). A delay of up to five hours for tooth processing and tissue collection does not preclude the establishment of dental pulp cell cultures, affect the morphology of these cells, or reduce their proliferative potential.-
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