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Biomedicines|September 28, 2023
Creation of an iPSC-Based Skeletal Muscle Model of McArdle Disease Harbouring the Mutation c.2392T>C (p.Trp798Arg) in the <i>PYGM</i> GeneVictoria Cerrada, Inés García-Consuegra, Joaquín Arenas, et al.Journal of Cellular and Molecular Medicine|April 2, 2019
iPSCs: A powerful tool for skeletal muscle tissue engineeringMaría Del Carmen Ortuño-Costela, Marta García-López, Victoria Cerrada, et al.International Journal of Molecular Sciences|December 19, 2019
The Challenge of Bringing iPSCs to the PatientMaría Del Carmen Ortuño-Costela, Victoria Cerrada, Marta García-López, et al.Stem Cell Research|December 29, 2020
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.Trp798ArgVictoria Cerrada, Marta García-López, Sofía Alvarez-Galeano, et al.Stem Cell Research|March 22, 2019
Derivation of an aged mouse induced pluripotent stem cell line, IISHDOi005-AMaría Del Carmen Ortuño-Costela, Victoria Cerrada, Marta García-López, et al.Stem Cell Research|September 12, 2019
Derivation of a human DOA iPSC line, IISHDOi006-A, with a mutation in the ACO2 gene: c.1999G>A; p.Glu667LysVictoria Cerrada, Marta García-López, Ana Moreno-Izquierdo, et al.International Journal of Molecular Sciences|November 26, 2022
Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC TechnologyMaría Del Carmen Ortuño-Costela, Victoria Cerrada, Ana Moreno-Izquierdo, et al.Pageof 1