Publication:
Generation of induced pluripotent stem cells (iPSCs) from a Bernard-Soulier syndrome patient carrying a W71R mutation in the GPIX gene.

dc.contributor.authorLopez-Onieva, Lourdes
dc.contributor.authorMontes, Rosa
dc.contributor.authorLamolda, Mar
dc.contributor.authorRomero, Tamara
dc.contributor.authorAyllon, Verónica
dc.contributor.authorLozano, Maria Luisa
dc.contributor.authorVicente, Vicente
dc.contributor.authorRivera, José
dc.contributor.authorRamos-Mejía, Verónica
dc.contributor.authorReal, Pedro J
dc.date.accessioned2023-01-25T08:33:46Z
dc.date.available2023-01-25T08:33:46Z
dc.date.issued2016-04-15
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.
dc.identifier.doi10.1016/j.scr.2016.04.013
dc.identifier.essn1876-7753
dc.identifier.pmid27346198
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.scr.2016.04.013
dc.identifier.urihttp://hdl.handle.net/10668/10219
dc.issue.number3
dc.journal.titleStem cell research
dc.journal.titleabbreviationStem Cell Res
dc.language.isoen
dc.organizationCentro Pfizer-Universidad de Granada-Junta de Andalucía de Genómica e Investigación Oncológica-GENYO
dc.page.number692-5
dc.pubmedtypeJournal Article
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.meshAnimals
dc.subject.meshBernard-Soulier Syndrome
dc.subject.meshCell Differentiation
dc.subject.meshCells, Cultured
dc.subject.meshCellular Reprogramming
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshInduced Pluripotent Stem Cells
dc.subject.meshKaryotype
dc.subject.meshKruppel-Like Factor 4
dc.subject.meshLeukocytes, Mononuclear
dc.subject.meshMice
dc.subject.meshMice, Inbred NOD
dc.subject.meshMice, SCID
dc.subject.meshMutation
dc.subject.meshPlatelet Glycoprotein GPIb-IX Complex
dc.subject.meshTeratoma
dc.subject.meshTranscription Factors
dc.titleGeneration of induced pluripotent stem cells (iPSCs) from a Bernard-Soulier syndrome patient carrying a W71R mutation in the GPIX gene.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number16
dspace.entity.typePublication

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