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dc.contributor.authorMontes, Rosa
dc.contributor.authorMollinedo, Pilar
dc.contributor.authorPerales, Sonia
dc.contributor.authorGonzález-Lamuño Leguina, Domingo 
dc.contributor.authorRamos-Mejía, Veronica
dc.contributor.authorFernandez-Luna, Jose L.
dc.contributor.authorReal, Pedro J.
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2020-02-07T18:56:20Z
dc.date.available2020-02-07T18:56:20Z
dc.date.issued2019
dc.identifier.issn1873-5061
dc.identifier.issn1876-7753
dc.identifier.urihttp://hdl.handle.net/10902/18123
dc.description.abstractADNP syndrome is an intellectual disability associated with Autism spectrum disorder caused by mutations in ADNP. We generated an iPSC line from an ADNP syndrome pediatric patient harboring the mutation p.Trp719* (GENYOi004-A). Peripheral blood mononuclear cells were reprogrammed using a non-transmissible form of Sendai viruses expressing the four Yamanaka factors (Oct3/4, SOX2, KLF4 and c-MYC). Characterization of GENYOi004-A included mutation analysis of ADNP by allele-specific PCR, genetic identity by Short Tandem Repeats polymorphism profiling, alkaline phosphatase enzymatic activity, expression of pluripotency-associated factors and pluripotency studies in vivo. GENYOi004-A will be useful to evaluate ADNP syndrome alterations at early developmental stages.es_ES
dc.description.sponsorshipThis work was supported by the Postdoctoral Subprogramme Juan de la Cierva (JCI_2012_12666) to RM and Ramon y Cajal (RYC-2015-18382) to PJR founded by the Ministry of Economy and Competitiveness; the Instituto de Salud Carlos III-FEDER (CP12/03175 and CPII17/00032) to V.R-M. and (PI12/1598, CPII15/00018 and PI16/01340) to PJR; the Instituto de Investigación Valdecilla (IDIVAL) 2014.041 to JLF-L and DG-L and APG/03 to JLF-L.es_ES
dc.format.extent5 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rights© 2019 Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceStem Cell Res. 2019 May;37:101446es_ES
dc.titleGENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutationes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.scr.2019.101446es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.scr.2019.101446
dc.type.versionpublishedVersiones_ES


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© 2019 Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND licenseExcepto si se señala otra cosa, la licencia del ítem se describe como © 2019 Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license