Publication: GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant.
dc.contributor.author | Lamolda, Mar | |
dc.contributor.author | Montes, Rosa | |
dc.contributor.author | Simón, Iris | |
dc.contributor.author | Perales, Sonia | |
dc.contributor.author | Martínez-Navajas, Gonzalo | |
dc.contributor.author | Lopez-Onieva, Lourdes | |
dc.contributor.author | Ríos-Pelegrina, Rosa | |
dc.contributor.author | Del Moral, Raimundo García | |
dc.contributor.author | Griñan-Lison, Carmen | |
dc.contributor.author | Marchal, Juan A | |
dc.contributor.author | Lozano, Maria L | |
dc.contributor.author | Ramos-Mejia, Veronica | |
dc.contributor.author | Rivera, Jose | |
dc.contributor.author | Bastida, Jose M | |
dc.contributor.author | Real, Pedro J | |
dc.date.accessioned | 2023-02-08T14:37:14Z | |
dc.date.available | 2023-02-08T14:37:14Z | |
dc.date.issued | 2019-10-15 | |
dc.description.abstract | Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) is a rare platelet disorder caused by mutations in RUNX1. We generated an iPSC line (GENYOi005-A) from a FPDMM patient with a non-previously reported variant p.Thr196Ala. Non-integrative Sendai viruses expressing the Yamanaka reprogramming factors were used to reprogram peripheral blood mononuclear cells from this FPDMM patient. Characterization of GENYOi005-A included genetic analysis of RUNX1 locus, Short Tandem Repeats profiling, alkaline phosphatase enzymatic activity, expression of pluripotency-associated factors and differentiation studies in vitro and in vivo. This iPSC line will provide a powerful tool to study developmental alterations of FPDMM patients. | |
dc.identifier.doi | 10.1016/j.scr.2019.101603 | |
dc.identifier.essn | 1876-7753 | |
dc.identifier.pmid | 31698193 | |
dc.identifier.unpaywallURL | https://doi.org/10.1016/j.scr.2019.101603 | |
dc.identifier.uri | http://hdl.handle.net/10668/14652 | |
dc.journal.title | Stem cell research | |
dc.journal.titleabbreviation | Stem Cell Res | |
dc.language.iso | en | |
dc.organization | IBS | |
dc.page.number | 101603 | |
dc.pubmedtype | Journal Article | |
dc.pubmedtype | Research Support, Non-U.S. Gov't | |
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 | Blood Coagulation Disorders, Inherited | |
dc.subject.mesh | Blood Platelet Disorders | |
dc.subject.mesh | Cell Differentiation | |
dc.subject.mesh | Cells, Cultured | |
dc.subject.mesh | Cellular Reprogramming | |
dc.subject.mesh | Core Binding Factor Alpha 2 Subunit | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Induced Pluripotent Stem Cells | |
dc.subject.mesh | Leukemia, Myeloid, Acute | |
dc.subject.mesh | Leukocytes, Mononuclear | |
dc.subject.mesh | Middle Aged | |
dc.subject.mesh | Mutation | |
dc.title | GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 41 | |
dspace.entity.type | Publication |