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Article

Establishment of a human iPSC line (IISHDOi001-A) from a patient with McArdle disease.

Stem cell research - 1 Aug 2017

Ortuño-Costela María Del Carmen, Rodríguez-Mancera Nathalie, García-López Marta, Zurita-Díaz Francisco, Moreno-Izquierdo Ana, Lucía Alejandro, Martín Miguel Ángel, Garesse Rafael, Gallardo M Esther

Abstract excerpt

Human iPSC line IISHDOi001-A was generated from fibroblasts of a patient with McArdle disease harbouring the mutation, c.148C>T; p.Arg50Ter, in the PYGM gene. Reprogramming factors Oct3/4, Sox2, Klf4, and c-Myc were delivered using Sendai virus.

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Source

Identifiers

PMID: 28925366
DOI: 10.1016/j.scr.2017.07.020

Genes

PYGM

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

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Research trail→

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Establishment of a human iPSC line (IISHDOi001-A) from a patient with McArdle disease.PMID 28925366Read ↗

Generation of the iPSC line IISHDOi007-A from peripheral blood mononuclear cells from a patient with McArdle disease harbouring the mutation c.2392 T > C; p.Trp798Arg.Semantic proximity Read ↗

Establishment of a human DOA 'plus' iPSC line, IISHDOi003-A, with the mutation in the OPA1 gene: c.1635C>A; p.Ser545Arg.Semantic proximity Read ↗

Establishment of a human iPSC line, IISHDOi004-A, from a patient with Usher syndrome associated with the mutation c.2276G>T; p.Cys759Phe in the USH2A gene.Semantic proximity Read ↗

Generation of the human induced pluripotent stem cell line PUMCi005-A from a patient with Perrault syndrome.Semantic proximity Read ↗

Generation and characterization of iPSC lines (UOHi003-A, UOHi002-A) from a patient with SHANK3 mutation and her healthy mother.Semantic proximity Read ↗

Generation of a human iPSC line (MPIi008-A) from a patient with Denys-Drash syndrome.Semantic proximity Read ↗

Generation and characterization of iPSC lines (UOHi001-A, UOHi002-A) From a patient with SHANK3 mutation and her healthy motherSemantic proximity Read ↗

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Generation of a human iPSC line (MPIi006-A) from a patient with Pelizaeus-Merzbacher disease.Semantic proximity Read ↗

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