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Corrigendum to “Generation and characterization of a human iPSC line (UAMi004-A) from a patient with propionic acidemia due to defects in the PCCB gene”

Autor (es)
López-Márquez, Arístides; Alonso-Barroso, Esmeralda; Cerro-Tello, Gema; Bravo-Alonso, I.; Arribas-Carreira, L.; Briso-Montiano, Álvaro; Navarrete, Rosa; Pérez-Cerdá, C.; Ugarte, Magdalena; Pérez, Belén; Ruiz Desviat, LourdesAutoridad UAM; Richard Rodríguez, Eva MaríaAutoridad UAM
Entidad
UAM. Departamento de Biología Molecular
Editor
Elsevier BV
Fecha de edición
2019-08-01
Cita
Stem Cell Research 2019.39 (2019): 101516
ISSN
1873-5061
DOI
10.1016/j.scr.2019.101513
Financiado por
This study was funded in part by the Australian National Health and Medical Research Council (NHMRC) project grants (GNT1044175 and GNT1098255) awarded to E.G.S, M.B.D, I.S and P.J.L. K.B is supported by an E.H. Flack Fellowship and P.J.L is supported by the Vincent Chiodo Foundation. Additional infrastructure funding to the Murdoch Children's Research Institute was provided by the Australian Government NHMRC Independent Research Institute Infrastructure Support Scheme and the Victorian Government's Operational Infrastructure Support Program. The MCRI iPSC Core Facility is supported by the Stafford Fox Medical Research Foundation. M.B and E.G.S are Research Fellows, and I.S is a Practitioner Fellow, of the NHMRC
Versión del editor
https://doi.org/10.1016/j.scr.2019.101516
Materias
Mononuclear cells; Peripheral blood mononuclear cells (PBMCs); Autism Spectrum Disorder (ASD); Biología y Biomedicina / Biología
URI
http://hdl.handle.net/10486/690956
Derechos
© 2019 The Author(s)

Licencia Creative Commons
Esta obra está bajo una Licencia Creative Commons Atribución 4.0 Internacional.

Resumen

We have generated and characterized seven human induced pluripotent stem cell (iPSC) lines derived from peripheral blood mononuclear cells (PBMCs) from a single family, including unaffected and affected individuals clinically diagnosed with Autism Spectrum Disorder (ASD). The reprogramming of the PBMCs was performed using non-integrative Sendai virus containing the reprogramming factors POU5F1 (OCT4), SOX2, KLF4 and MYC. All iPSC lines exhibited a normal karyotype and pluripotency was validated by immunofluorescence, flow cytometry and their ability to differentiate into the three embryonic germ layers. These iPSC lines are a valuable resource to study the molecular mechanisms underlying ASD
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Google™ Scholar:López-Márquez, Arístides - Alonso-Barroso, Esmeralda - Cerro-Tello, Gema - Bravo-Alonso, I. - Arribas-Carreira, L. - Briso-Montiano, Álvaro - Navarrete, Rosa - Pérez-Cerdá, C. - Ugarte, Magdalena - Pérez, Belén - Ruiz Desviat, Lourdes - Richard Rodríguez, Eva María

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