Publication: GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation.
dc.contributor.author | Montes, Rosa | |
dc.contributor.author | Mollinedo, Pilar | |
dc.contributor.author | Perales, Sonia | |
dc.contributor.author | Gonzalez-Lamuño, Domingo | |
dc.contributor.author | Ramos-Mejía, Veronica | |
dc.contributor.author | Fernandez-Luna, Jose L | |
dc.contributor.author | Real, Pedro J | |
dc.date.accessioned | 2023-01-25T13:33:00Z | |
dc.date.available | 2023-01-25T13:33:00Z | |
dc.date.issued | 2019-04-22 | |
dc.description.abstract | ADNP 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. | |
dc.identifier.doi | 10.1016/j.scr.2019.101446 | |
dc.identifier.essn | 1876-7753 | |
dc.identifier.pmid | 31035039 | |
dc.identifier.unpaywallURL | https://doi.org/10.1016/j.scr.2019.101446 | |
dc.identifier.uri | http://hdl.handle.net/10668/13890 | |
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 | 101446 | |
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 | Animals | |
dc.subject.mesh | Autism Spectrum Disorder | |
dc.subject.mesh | Cell Differentiation | |
dc.subject.mesh | Cells, Cultured | |
dc.subject.mesh | Cellular Reprogramming | |
dc.subject.mesh | Child | |
dc.subject.mesh | Female | |
dc.subject.mesh | Homeodomain Proteins | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Induced Pluripotent Stem Cells | |
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 | Nerve Tissue Proteins | |
dc.subject.mesh | Phenotype | |
dc.subject.mesh | Teratoma | |
dc.title | GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 37 | |
dspace.entity.type | Publication |