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dc.contributor.authorLópez Onieva, Lourdes 
dc.contributor.authorMontes, Rosa
dc.contributor.authorLamolda, Mar
dc.contributor.authorRomero, Tamara
dc.contributor.authorAyllon, Verónica
dc.contributor.authorLozano, María Luisa
dc.contributor.authorVicente, Vicente
dc.contributor.authorRivera, José
dc.contributor.authorRamos Mejía, Verónica 
dc.contributor.authorReal Luna, Pedro José 
dc.date.accessioned2025-01-10T11:41:21Z
dc.date.available2025-01-10T11:41:21Z
dc.date.issued2016-05
dc.identifier.citationLopez-Onieva L, Montes R, Lamolda M, Romero T, Ayllon V, Lozano ML, Vicente V, Rivera J, Ramos-Mejía V, Real PJ. Generation of induced pluripotent stem cells (iPSCs) from a Bernard-Soulier syndrome patient carrying a W71R mutation in the GPIX gene. Stem Cell Res. 2016 May;16(3):692-5. doi: 10.1016/j.scr.2016.04.013. Epub 2016 Apr 15. Erratum in: Stem Cell Res. 2016 Sep;17(2):462. doi: 10.1016/j.scr.2016.07.008. PMID: 27346198.es_ES
dc.identifier.urihttps://hdl.handle.net/10481/98864
dc.description.abstractWe generated an induced pluripotent stem cell (iPSC) line from a Bernard-Soulier Syndrome (BSS) patient carrying the mutation p.Trp71Arg in the GPIX locus (BSS1-PBMC-iPS4F4). Peripheral blood mononuclear cells (PBMCs) were reprogrammed using heat sensitive non-integrative Sendai viruses containing the reprogramming factors Oct3/4, SOX2, KLF4 and c-MYC. Successful silencing of the exogenous reprogramming factors was checked by RT-PCR. Characterization of BSS1-PBMC-iPS4F4 included mutation analysis of GPIX locus, Short Tandem Repeats (STR) profiling, alkaline phosphatase enzymatic activity, analysis of conventional pluripotency-associated factors at mRNA and protein level and in vivo differentiation studies. BSS1-PBMC-iPS4F4 will provide a powerful tool to study BSS.es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleGeneration of induced pluripotent stem cells (iPSCs) from a Bernard-Soulier syndrome patient carrying a W71R mutation in the GPIX genees_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1016/j.scr.2016.07.008


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