dc.creatorErlejman, Alejandra Giselle
dc.creatorLagadari, Mariana
dc.creatorGaligniana, Mario Daniel
dc.date.accessioned2016-02-11T13:34:19Z
dc.date.accessioned2018-11-06T12:29:09Z
dc.date.available2016-02-11T13:34:19Z
dc.date.available2018-11-06T12:29:09Z
dc.date.created2016-02-11T13:34:19Z
dc.date.issued2013-04
dc.identifierErlejman, Alejandra Giselle; Lagadari, Mariana; Galigniana, Mario Daniel; Hsp90-binding immunophilins as a potential new platform for drug treatment; Future Science; Future Medicinal Chemistry; 5; 5; 4-2013; 591-607
dc.identifier1756-8919
dc.identifierhttp://hdl.handle.net/11336/4128
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1867169
dc.description.abstractImmunophilins are proteins that contain a PPIase domain as a family signature. Low-molecular-weight immunophilins were first described associated to immunosuppressive action and protein folding. Recent studies of other members of the family have led to the identification of their participation in basic processes such as protein-protein interactions, signal transduction cascades, cell differentiation, cell cycle progression, metabolic activity, apoptosis mechanisms, microorganisms infection, cancer, neurotrophism and neuroprotection, among several other physiological and pathophysiological processes. Due to all these emerging features, the development of specific ligands for immunophilins appears to have promising perspectives, in particular in the fields of cancer biology and neuroregeneration fields. We review the emerging role of immunophilins in protein transport, transcription regulation, malignancies development and neurotrophic action, in addition to a number of biological properties that transform these proteins in potential targets for novel therapeutic strategies.
dc.languageeng
dc.publisherFuture Science
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.future-science.com/doi/abs/10.4155/fmc.13.7
dc.relationinfo:eu-repo/semantics/altIdentifier/issn/1756-8919
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://dx.doi.org/doi:10.4155/fmc.13.7
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectFKBP52
dc.subjectFKBP51
dc.subjectCICLOFILINAS
dc.subjectPEPTIDILPROLIL ISOMERASA
dc.titleHsp90-binding immunophilins as a potential new platform for drug treatment
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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