TY - JOUR
T1 - Generation of an integration-free iPSC line, ICCSICi006-A, derived from a male Alzheimer's disease patient carrying the PSEN1-G206D mutation
AU - Díaz-Guerra, Eva
AU - Oria-Muriel, Manuel A.
AU - Moreno-Jiménez, Elena P.
AU - de Rojas, Itziar
AU - Rodríguez, César
AU - Rodríguez-Traver, Eva
AU - Orera, María
AU - Hernández, Isabel
AU - Ruiz, Agustín
AU - Vicario, Carlos
N1 - Publisher Copyright:
© 2019 The Authors
PY - 2019/10
Y1 - 2019/10
N2 - The familial form of Alzheimer's disease (FAD), which is caused by mutations in PRESENILIN 1 (PSEN1) and amyloid precursor protein (APP) genes, represents less than 5% of all AD cases and has an early-onset. We report the generation and characterization of an iPSC line derived from a FAD patient carrying the PSEN1-G206D mutation. The iPSC line maintained the original genotype, a normal karyotype, was free from Sendai viral vectors and reprogramming factors (OCT4, SOX2, KLF4 and c-MYC), presented a typical morphology, expressed endogenous pluripotency markers, and could be differentiated into ectodermal, mesodermal and endodermal cells, confirming its pluripotency.
AB - The familial form of Alzheimer's disease (FAD), which is caused by mutations in PRESENILIN 1 (PSEN1) and amyloid precursor protein (APP) genes, represents less than 5% of all AD cases and has an early-onset. We report the generation and characterization of an iPSC line derived from a FAD patient carrying the PSEN1-G206D mutation. The iPSC line maintained the original genotype, a normal karyotype, was free from Sendai viral vectors and reprogramming factors (OCT4, SOX2, KLF4 and c-MYC), presented a typical morphology, expressed endogenous pluripotency markers, and could be differentiated into ectodermal, mesodermal and endodermal cells, confirming its pluripotency.
UR - http://www.scopus.com/inward/record.url?scp=85073272641&partnerID=8YFLogxK
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U2 - 10.1016/j.scr.2019.101574
DO - 10.1016/j.scr.2019.101574
M3 - Article
C2 - 31627126
AN - SCOPUS:85073272641
SN - 1873-5061
VL - 40
JO - Stem Cell Research
JF - Stem Cell Research
M1 - 101574
ER -