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Generation of a human iPSC line from a patient with Leigh syndrome

dc.contributor.authorGalera-Monge, Teresa
dc.contributor.authorZurita-Díaz, Francisco
dc.contributor.authorGonzález-Páramos, Cristina
dc.contributor.authorMoreno-Izquierdo, Ana
dc.contributor.authorFraga, Mario F.
dc.contributor.authorFernández, Agustin F.
dc.contributor.authorGaresse, Rafael
dc.contributor.authorGallardo, M. Esther
dc.date.accessioned2026-02-05T14:11:30Z
dc.date.available2026-02-05T14:11:30Z
dc.date.issued2016-01-10
dc.identifier.citationGalera, T., Zurita, F., González-Páramos, C., Moreno-Izquierdo, A., Fraga, M. F., Fernández, A. F., Garesse, R., & Gallardo, M. E. (2015). Generation of a human iPSC line from a patient with Leigh syndrome. Stem Cell Research, 16(1), 63-66. https://doi.org/10.1016/j.scr.2015.12.005es
dc.identifier.issn1873-5061
dc.identifier.urihttps://hdl.handle.net/20.500.12412/7083
dc.description.abstractHuman iPSC line LND554SV.3 was generated from heteroplasmic fibroblasts of a patient with Leigh syndrome carrying a mutation in the MT-ND5 gene (m.13513G > A; p.D393N). Reprogramming factors Oct3/4, Sox2, Klf4, and cMyc were delivered using a non-integrative methodology that involves the use of Sendai virus.es
dc.language.isoenges
dc.titleGeneration of a human iPSC line from a patient with Leigh syndromees
dc.typearticlees
dc.identifier.doi10.1016/j.scr.2015.12.005
dc.journal.titleStem Cell Researches
dc.page.initial63es
dc.page.final66es
dc.rights.accessRightsopenAccesses
dc.volume.number16es


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