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Generation of a human iPSC line from a patient with a defect of intergenomic communication

dc.contributor.authorZurita-Díaz, Francisco
dc.contributor.authorGalera-Monge, Teresa
dc.contributor.authorGonzález-Páramos, Cristina
dc.contributor.authorMoreno-Izquierdo, Ana
dc.contributor.authorSchneiderat, Peter
dc.contributor.authorFraga, Mario F.
dc.contributor.authorFernández, Agustin F.
dc.contributor.authorGaresse, Rafael
dc.contributor.authorGallardo, M. Esther
dc.date.accessioned2026-02-05T13:55:33Z
dc.date.available2026-02-05T13:55:33Z
dc.date.issued2016-01-10
dc.identifier.citationZurita, F., Galera, T., González-Páramos, C., Moreno-Izquierdo, A., Schneiderat, P., Fraga, M. F., Fernández, A. F., Garesse, R., & Gallardo, M. E. (2015). Generation of a human iPSC line from a patient with a defect of intergenomic communication. Stem Cell Research, 16(1), 120-123. https://doi.org/10.1016/j.scr.2015.12.016es
dc.identifier.issn1873-5061
dc.identifier.urihttps://hdl.handle.net/20.500.12412/7081
dc.description.abstractHuman iPSC line PG64SV.2 was generated from fibroblasts of a patient with a defect of intergenomic communication. This patient harbored a homozygous mutation (c.2243G>C; p.Trp748Ser) in the gene encoding the catalytic subunit of the mitochondrial DNA polymerase gamma gene (POLG). 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 a defect of intergenomic communicationes
dc.typearticlees
dc.identifier.doi10.1016/j.scr.2015.12.016
dc.journal.titleStem Cell Researches
dc.page.initial120es
dc.page.final123es
dc.rights.accessRightsopenAccesses
dc.volume.number16es


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