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dc.contributor.authorToro-Ascuy, Daniela
dc.contributor.authorGaete-Argel, Aracelly
dc.contributor.authorRojas-Celis, Victoria
dc.contributor.authorValiente-Echeverría, Fernando
dc.date.accessioned2020-12-01T13:07:14Z
dc.date.available2020-12-01T13:07:14Z
dc.date.issued2020-11-18
dc.identifier10.1007/978-1-0716-0935-4_19
dc.identifier.issn10643745
dc.identifier.urihttps://hdl.handle.net/20.500.12728/7802
dc.description.abstractThe mechanisms involved in the posttranscriptional control of the replicative cycle of the human immunodeficiency virus (HIV), specifically the molecular events which allow the interaction between the viral genomic RNA (gRNA) and the cellular machinery for the transport, translation, or intracellular packaging, have not been yet elucidated. In this chapter, we describe the in situ hybridization-proximity ligation assay (ISH-PLA) to characterize interactions between the genomic RNA (gRNA) of HIV-1 and viral proteins or host proteins involved in nuclear export and translation initiation. We also present data that validate the ISH-PLA as a simple and useful tool to study HIV-1 gRNA-protein interactions within cells.es_ES
dc.language.isoenes_ES
dc.publisherHumana Press Inc.es_ES
dc.subjectAIDSes_ES
dc.subjectHIV-1es_ES
dc.subjectHIV-1 RNAes_ES
dc.subjectISH-PLAes_ES
dc.subjectProximity ligation assayes_ES
dc.subjectRNA-protein interactiones_ES
dc.titleIn Situ Hybridization-Proximity Ligation Assay (ISH-PLA) to Study the Interaction of HIV-1 RNA and Remodeling Proteinses_ES
dc.typeArticlees_ES


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