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.authorMontes, Rosa
dc.contributor.authorMollinedo, Pilar
dc.contributor.authorPerales, Sonia
dc.contributor.authorGonzalez-Lamuño, Domingo
dc.contributor.authorRamos-Mejía, Veronica
dc.contributor.authorFernandez-Luna, Jose L
dc.contributor.authorReal, Pedro J
dc.date.accessioned2023-01-25T13:33:00Z
dc.date.available2023-01-25T13:33:00Z
dc.date.issued2019-04-22
dc.description.abstractADNP 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.doi10.1016/j.scr.2019.101446
dc.identifier.essn1876-7753
dc.identifier.pmid31035039
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.scr.2019.101446
dc.identifier.urihttp://hdl.handle.net/10668/13890
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.number101446
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
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.meshAutism Spectrum Disorder
dc.subject.meshCell Differentiation
dc.subject.meshCells, Cultured
dc.subject.meshCellular Reprogramming
dc.subject.meshChild
dc.subject.meshFemale
dc.subject.meshHomeodomain Proteins
dc.subject.meshHumans
dc.subject.meshInduced Pluripotent Stem Cells
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.meshNerve Tissue Proteins
dc.subject.meshPhenotype
dc.subject.meshTeratoma
dc.titleGENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number37
dspace.entity.typePublication

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