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dc.contributor.authorSchvartzman, Jorge Bernardo 
dc.contributor.authorMartínez, Víctor
dc.contributor.authorHernández, Pablo
dc.contributor.authorKrimer, Dora B
dc.contributor.authorFernández Nestosa, María José
dc.contributor.otherUniversidad Nacional de Asunción - Facultad Politécnicaes
dc.date.accessioned2022-04-24T03:37:46Z
dc.date.available2022-04-24T03:37:46Z
dc.date.issued2021
dc.identifier.urihttp://hdl.handle.net/20.500.14066/3307
dc.description.abstractMost of the methods used to analyze DNA, including electrophoresis, electron microscopy or atomic force microscopy, involve de-proteinization, and it is well known that the removal of proteins affects DNA topology. After de-proteinization in vitro, the topology of replication intermediates changes significantly. A comprehensive analysis of the topological changes introduced during DNA isolation (de-proteinization) is important to get a better understanding of DNA topology in vivo. The topology of replication intermediates examined by electrophoresis, electron microscopy or atomic force microscopy in vitro does not necessarily represent the situation in vivo.es
dc.description.sponsorshipCONACYT - Consejo Nacional de Ciencias y Tecnologíaes
dc.language.isoenges
dc.subject.classification1303 I+D en relación con las Ciencias médicases
dc.subject.otherBIOLOGIA MOLECULARes
dc.subject.otherADNes
dc.subject.otherGENETICA HUMANAes
dc.subject.otherBIOINFORMATICAes
dc.titleChanges in the Topology of DNA Replication Intermediates: In vivo vs In vitroes
dc.typeconference posteres
dc.conference.date2021-09
dc.conference.placeVirtuales
dc.conference.titleEMBO WorkshopDNA Topology in genomic transactionses
dc.description.fundingtextPROCIENCIAes
dc.relation.projectCONACYTPINV15-573es
dc.rights.accessRightsopen accesses


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