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dc.contributor.authorCabezón Navarro, María Elena 
dc.contributor.authorArechaga Iturregui, Ignacio María 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2021-01-27T11:10:04Z
dc.date.available2021-01-27T11:10:04Z
dc.date.issued2020
dc.identifier.issn2296-889X
dc.identifier.urihttp://hdl.handle.net/10902/20582
dc.description.abstractThe current outbreak of SARS-CoV-2 virus has caused a large increase in mortality and morbidity associated with respiratory diseases. Huge efforts are currently ongoing to develop a vaccine against this virus. However, alternative approaches could be considered in the fight against this disease. Among other strategies, structural-based drug design could be an effective approach to generate specific molecules against SARS-CoV-2, thus reducing viral burden in infected patients. Here, in addition to this structural approach, we also revise several therapeutic strategies to fight against this viral threat. Furthermore, we report ACE-2 genetic polymorphic variants affecting residues involved in close contacts with SARS-CoV-2 that might be associated to different infection risks. These analyses could provide valuable information to predict the course of the disease.es_ES
dc.format.extent11 p.es_ES
dc.language.isoenges_ES
dc.publisherFrontiers Mediaes_ES
dc.rightsAttribution 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceFrontiers in molecular biosciences 2020; 7: 204es_ES
dc.subject.otherCoronaviruses_ES
dc.subject.otherSARS-CoV-2es_ES
dc.subject.otherCovid-19es_ES
dc.subject.otherSpikees_ES
dc.subject.otherDrugses_ES
dc.subject.otherACE-2es_ES
dc.subject.otherPolymorphismses_ES
dc.titleDrug weaponry to fight against SARS-CoV-2es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps//DOI: 10.3389/fmolb.2020.00204es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.3389/fmolb.2020.00204
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International