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Generation of a human iPSC line from a patient with Leigh syndrome caused by a mutation in the MT-ATP6 gene.

Stem cell research - 1 May 2016

Galera-Monge Teresa, Zurita-Díaz Francisco, González-Páramos Cristina, Moreno-Izquierdo Ana, Fraga Mario F, Fernández Agustin F, Garesse Rafael, Gallardo M Esther

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 27346203
DOI: 10.1016/j.scr.2016.04.012

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Generation of a human iPSC line from a patient with Leigh syndrome caused by a mutation in the MT-ATP6 gene.PMID 27346203Read ↗

Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T > G or m.8993T > C in the mitochondrial gene MT-ATP6.Semantic proximity Read ↗

Generation of two mother-child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations.Semantic proximity Read ↗

Reprogramming of two induced pluripotent stem cell clones from a patient with a novel MT-ATP6/8 mutation (m.8570 T > C).Semantic proximity Read ↗

Characterization of two iPSC lines from patients with maternally inherited leigh (MILS) and neuropathy, ataxia, and retinitis pigmentosa (NARP) syndrome carrying the MT-ATP6 m.8993 T>G mutation at different degrees of heteroplasmy.Semantic proximity Read ↗

RNA-based generation of iPSCs from a boy carrying the mutation m.9185 T>C in the mitochondrial gene MT-ATP6 and from his healthy mother.Semantic proximity Read ↗

Generation of a human induced pluripotent stem cell line NTUHi004-A from a patient with Leigh syndrome harboring a homozygous missense mutation c.836 T > G (p.Met279Arg) in NDUFAF5 gene.Semantic proximity Read ↗

Self-replicative mRNA-mediated generation of induced pluripotent stem cell line from a 1-year-old Leigh syndrome patient with mitochondrial DNA cytochrome b mutation.Semantic proximity Read ↗

Generation of an iPSC line IUFi004-A-13 with homozygous NDUFS1 mutation for the study of Leigh syndrome.Semantic proximity Read ↗

Human iPSC-derived cerebral organoids model features of Leigh Syndrome and reveal abnormal corticogenesisSemantic proximity Read ↗

Striking pathology in Leigh syndrome associated with the MTATP6 T8993G mutation.Semantic proximity Read ↗

Human iPSC-derived cerebral organoids model features of Leigh syndrome and reveal abnormal corticogenesis.Semantic proximity Read ↗

Metabolic rescue in pluripotent cells from patients with mtDNA disease.Semantic proximity Read ↗

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