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Genes|January 22, 2021
Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D ApproachesMarta García-López, Joaquín Arenas, M Esther GallardoInternational 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.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.Journal of Shoulder and Elbow Surgery|October 2, 2022
Plasma rich in growth factors versus corticosteroid injections for management of chronic rotator cuff tendinopathy: a prospective double-blind randomized controlled trial with 1 year of follow-upVíctor Vaquerizo, Marta García-López, Araceli Mena-Rosón, 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|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|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|July 13, 2024
Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the <i>OPA1</i> GeneMarta García-López, Lydia Jiménez-Vicente, Raquel González-Jabardo, et al.Stem Cell Research|September 20, 2017
Establishment of a human iPSC line (IISHDOi001-A) from a patient with McArdle diseaseMaría Del Carmen Ortuño-Costela, Nathalie Rodríguez-Mancera, Marta García-López, et al.Pageof 1