Publication: Generation of induced pluripotent stem cells (iPSCs) from a Bernard-Soulier syndrome patient carrying a W71R mutation in the GPIX gene.
dc.contributor.author | Lopez-Onieva, Lourdes | |
dc.contributor.author | Montes, Rosa | |
dc.contributor.author | Lamolda, Mar | |
dc.contributor.author | Romero, Tamara | |
dc.contributor.author | Ayllon, Verónica | |
dc.contributor.author | Lozano, Maria Luisa | |
dc.contributor.author | Vicente, Vicente | |
dc.contributor.author | Rivera, José | |
dc.contributor.author | Ramos-Mejía, Verónica | |
dc.contributor.author | Real, Pedro J | |
dc.date.accessioned | 2023-01-25T08:33:46Z | |
dc.date.available | 2023-01-25T08:33:46Z | |
dc.date.issued | 2016-04-15 | |
dc.description.abstract | We 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. | |
dc.identifier.doi | 10.1016/j.scr.2016.04.013 | |
dc.identifier.essn | 1876-7753 | |
dc.identifier.pmid | 27346198 | |
dc.identifier.unpaywallURL | https://doi.org/10.1016/j.scr.2016.04.013 | |
dc.identifier.uri | http://hdl.handle.net/10668/10219 | |
dc.issue.number | 3 | |
dc.journal.title | Stem cell research | |
dc.journal.titleabbreviation | Stem Cell Res | |
dc.language.iso | en | |
dc.organization | Centro Pfizer-Universidad de Granada-Junta de Andalucía de Genómica e Investigación Oncológica-GENYO | |
dc.page.number | 692-5 | |
dc.pubmedtype | Journal Article | |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Bernard-Soulier Syndrome | |
dc.subject.mesh | Cell Differentiation | |
dc.subject.mesh | Cells, Cultured | |
dc.subject.mesh | Cellular Reprogramming | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Induced Pluripotent Stem Cells | |
dc.subject.mesh | Karyotype | |
dc.subject.mesh | Kruppel-Like Factor 4 | |
dc.subject.mesh | Leukocytes, Mononuclear | |
dc.subject.mesh | Mice | |
dc.subject.mesh | Mice, Inbred NOD | |
dc.subject.mesh | Mice, SCID | |
dc.subject.mesh | Mutation | |
dc.subject.mesh | Platelet Glycoprotein GPIb-IX Complex | |
dc.subject.mesh | Teratoma | |
dc.subject.mesh | Transcription Factors | |
dc.title | Generation of induced pluripotent stem cells (iPSCs) from a Bernard-Soulier syndrome patient carrying a W71R mutation in the GPIX gene. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 16 | |
dspace.entity.type | Publication |