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dc.contributor.authorCardo, Lucía F.-
dc.contributor.authorCoto García, Eliecer-
dc.contributor.authorMiar, Ana B.-
dc.contributor.authorDíaz, Marta-
dc.contributor.authorCorao, Ana I.-
dc.contributor.authorAlonso, Belén-
dc.contributor.authorRibacoba, René-
dc.contributor.authorSalvador, Carlos-
dc.contributor.authorMenéndez, Manuel-
dc.contributor.authorMorís, Germán-
dc.contributor.authorÁlvarez, Victoria-
dc.date.accessioned2010-12-17T08:32:14Z-
dc.date.available2010-12-17T08:32:14Z-
dc.date.issued2010-
dc.identifier.urihttps://ria.asturias.es/RIA/handle/123456789/706-
dc.description.abstractDNA variation at the FGF20 gene has been associated with Parkinson´s disease (PD). In particular, SNP rs12720208 in the 3´ untranslated region (3´UTR) was linked to PD-risk through a mechanism that would implicate a differential binding to micro RNA – 433 (miR-433). The reduction of the affinity of miR-433 to the 3´UTR would result in increased FGF20 expression and upregulation of alpha-synuclein, that could in turn promote dopaminergic neurons degeneration. We genotyped the rs12720208 SNP in a total of 512 PD patients and 258 healthy controls from Spain, and searched for miR-433 variants in the patients. We did not find significant differences in allele and genotype frequencies between patients and controls. None of the patients had miR-433 variants. In conclusion, our work did not confirm the association between rs12720208 and PD, or an effect of miR-433 variants on this disease.eng
dc.description.sponsorshipThis work was supported by grants from the Spanish Fondo de Investigaciones Sanitarias-Fondos FEDER European Union (FIS-05/008 and 08/0915). LDM is a predoctoral fellow of FICYT-Principado de Asturias. AIC is the recipient of a Contrato de Apoyo a la Investigación- Fondo de Investigaciones Sanitarias.eng
dc.language.isoengeng
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
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dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/deed.eseng
dc.subjectParkinson's diseaseeng
dc.subjectDNA polymorphismseng
dc.subjectGenetic riskeng
dc.titleFGF20 rs12720208 SNP and microRNA-433 variation: noeng
dc.typepostprinteng
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