Publication details.

Paper

Year:2019
Author(s):S. Vallejo-Diez, A. Fleischer, J. Martín-Fernández, A. Sánchez-Gilabert, M. Castresana, D. Aguillón, A. Villegas, C. Mastronardi, L. Espinosa, M. Arcos-Burgos, Á. del Pozo, E. Herrán, E. Gainza, M. Isaza-Ruget, F. Lopera, D. Bachiller
Title:Generation of one iPSC line (IMEDEAi006-A) from an early-onset familial Alzheimer's Disease (fAD) patient carrying the E280A mutation in the PSEN1 gene
Journal:Stem Cell Research
ISSN:1873-5061
JCR Impact Factor:4.489
Volume:37
Pages:101440
D.O.I.:10.1016/j.scr.2019.101440
Web:https://dx.doi.org/10.1016/j.scr.2019.101440
Abstract:© 2019The mutation E280A in PSEN1 (presenilin-1) is the most common cause of early-onset familial Alzheimer's Disease (fAD). It presents autosomal dominant inheritance and frequently leads to the manifestation of the disease in relatively young individuals. Here we report the generation of one PSEN1 E280A iPSC line derived from an early-onset patient. OriP/EBNA1-based episomal plasmids containing OCT3/4, SOX2, KLF4, L-MYC, LIN28, BCL-xL and shp53 were used to reprogram oral mucosa fibroblasts. The iPSC line generated has normal karyotype, carry the E280A mutation, is free of plasmid integration, express high levels of pluripotency markers and can differentiate into all three germ layers.

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  • Sara Vallejo Diez
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