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dc.contributor.authorVallejo Diez, Sara-
dc.contributor.authorAguillón Niño, David Fernando-
dc.contributor.authorFleischer, Aarne-
dc.contributor.authorMartín Fernández, Jose María-
dc.contributor.authorSánchez Gilabert, Almudena-
dc.contributor.authorCastresana Jáuregui, Mónica-
dc.contributor.authorVillegas Lanau, Carlos Andrés-
dc.contributor.authorMastronardi, Claudio A.-
dc.contributor.authorEspinosa Aroca, Lady Giovanna-
dc.contributor.authorArcos Burgos, Oscar Mauricio-
dc.contributor.authorDel Pozo, Ángel-
dc.contributor.authorHerrán, Enara-
dc.contributor.authorGainza, Eusebio-
dc.contributor.authorIsaza Ruget, Mario-
dc.contributor.authorLopera, Francisco-
dc.contributor.authorBachiller, Daniel-
dc.date.accessioned2023-03-23T23:06:21Z-
dc.date.available2023-03-23T23:06:21Z-
dc.date.issued2019-
dc.identifier.issn1876-7753-
dc.identifier.urihttps://hdl.handle.net/10495/34211-
dc.description.abstractABSTRACT: The mutation E280A in PSEN1 (presenilin-1) is the most common cause of early-onset familial Alzheimer's Disease (fAD). It presents autosomal dominant inheritance and frequently leads to the manifestation of the disease in relatively young individuals. Here we report the generation of one PSEN1 E280A iPSC line derived from an early-onset patient. OriP/EBNA1-based episomal plasmids containing OCT3/4, SOX2, KLF4, L-MYC, LIN28, BCL-xL and shp53 were used to reprogram oral mucosa fibroblasts. The iPSC line generated has normal karyotype, carry the E280A mutation, is free of plasmid integration, express high levels of pluripotency markers and can differentiate into all three germ layers.spa
dc.format.extent5spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherElsevierspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.titleGeneration of one iPSC line (IMEDEAi006-A) from an Early-onset Familial Alzheimer's Disease (fAD) Patient Carrying the E280A Mutation in the PSEN1 Genespa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGrupo de Neurociencias de Antioquiaspa
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1873-5061-
oaire.citationtitleStem Cell Researchspa
oaire.citationstartpage1spa
oaire.citationendpage5spa
oaire.citationvolume37spa
thesis.degree.disciplinesin facultad - programaspa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-nd/4.0/spa
dc.publisher.placePaises Bajosspa
dc.type.coarhttp://purl.org/coar/resource_type/c_18wsspa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsInduced Pluripotent Stem Cells-
dc.subject.decsCélulas Madre Pluripotentes Inducidas-
dc.subject.decsAlzheimer Disease-
dc.subject.decsEnfermedad de Alzheimer-
dc.subject.decsMutation-
dc.subject.decsMutación-
dc.identifier.urlhttp://doi.org/10.1016/j.scr.2019.101440spa
dc.description.researchgroupidCOL0010744spa
dc.description.researchgroupidCOL0029147spa
dc.relation.ispartofjournalabbrevStem Cell Resspa
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