GENYOi004-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with autism-related ADNP syndrome carrying a pTyr719* mutation
Ver/ Abrir
Registro completo
Mostrar el registro completo DCAutoría
Montes, Rosa; Mollinedo, Pilar; Perales, Sonia; González-Lamuño Leguina, Domingo
Fecha
2019Derechos
© 2019 Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license
Publicado en
Stem Cell Res. 2019 May;37:101446
Editorial
Elsevier
Enlace a la publicación
Resumen/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.
Colecciones a las que pertenece
- D06 Artículos [595]