dc.creatorRojas, Armando
dc.creatorMorales, Miguel
dc.creatorGonzález-Bonet, Ileana
dc.creatorAraya, Paulina
dc.date2019-05-14T13:38:01Z
dc.date2019-05-14T13:38:01Z
dc.date2019
dc.date.accessioned2019-11-20T15:11:10Z
dc.date.available2019-11-20T15:11:10Z
dc.identifierhttp://repositorio.ucm.cl/handle/ucm/2086
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3033894
dc.descriptionThe Receptor for Advanced Glycation End Products (RAGE) is an important cell surface receptor, which belongs to the IgG super family and is now considered as a pattern recognition receptor. Because of its relevance in many human clinical settings, it is now pursued as a very attractive therapeutic target. However, particular features of this receptor such as a wide repertoire of ligands with different binding domains, the existence of many RAGE variants as well as the presence of cytoplasmatic adaptors leading a diverse signaling, are important limitations in the search for successful pharmacological approaches to inhibit RAGE signaling. Therefore, the present review aimed to display the most promising approaches to inhibit RAGE signaling, and provide an up to date review of progress in this area.
dc.languageen
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.sourceCurrent Drug Targets, 20(3), 340-346
dc.subjectAdvanced glycation end products
dc.subjectCytoplasmatic adaptors
dc.subjectInhibitors
dc.subjectIntracellular signaling
dc.titleInhibition of RAGE Axis signaling: A pharmacological challenge
dc.typeArtículos de revistas


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