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dc.contributor.authorHajjari, SN
dc.contributor.authorMehdizadeh, M
dc.contributor.authorSadigh-Eteghad, S
dc.contributor.authorShanehbandi, D
dc.contributor.authorTeimourian, S
dc.contributor.authorBaradaran, B
dc.date.accessioned2018-08-26T04:57:28Z
dc.date.available2018-08-26T04:57:28Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/38637
dc.description.abstractAmyloid-? (A?) as a crucial factor in pathogenesis of Alzheimer's disease (AD) is derived from amyloid precursor protein (APP) through a proteolytic process catalyzing by ?- and ?-secretase-in amyloidogenesis pathway. Products of ?-secretase cleavage also have protective effects against A? toxicity. According to existing evidences, microRNAs (miRNAs) show a unique pattern of expression in AD. Moreover, miRNAs regulatory effects on expression of secretases and their main components have been demonstrated in AD. The miRNAs levels may be changed in preclinical conditions and may be considered as diagnostic biomarkers in AD. Therefore, in this paper, we review the miRNAs involved in APP cleavage pathways and the formation of A? in order to evaluate the potential diagnostic biomarkers in AD.
dc.language.isoEnglish
dc.relation.ispartofNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
dc.subjectAlzheimer Disease
dc.subjectAmyloid Precursor Protein Secretases
dc.subjectAnimals
dc.subjectBiomarkers
dc.subjectHumans
dc.subjectMicroRNAs
dc.titleSecretases-related miRNAs in Alzheimer's disease: new approach for biomarker discovery.
dc.typearticle
dc.citation.volume38
dc.citation.issue11
dc.citation.spage1921
dc.citation.epage1926
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1007/s10072-017-3086-3


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