María Esther Gallardo
9PUBLICATIONS
17CO-AUTHORS
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Publications (9)
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|Jul 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 OPA1 Gene.Marta García-López, Lydia Jiménez-Vicente, Raquel González-Jabardo
|Jan 22, 2024
Hereditary Optic Neuropathies: A Systematic Review on the Interplay between Biomaterials and Induced Pluripotent Stem Cells.Miguel Ladero, Jose Alberto Reche-Sainz, M Esther Gallardo
|Sep 28, 2023
Creation of an iPSC-Based Skeletal Muscle Model of McArdle Disease Harbouring the Mutation c.2392T>C (p.Trp798Arg) in the PYGM Gene.Victoria Cerrada, Inés García-Consuegra, Joaquín Arenas
|Nov 26, 2022
Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology.María Del Carmen Ortuño-Costela, Victoria Cerrada, Ana Moreno-Izquierdo
|Jan 22, 2021
Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches.Marta García-López, Joaquín Arenas, M Esther Gallardo
|May 06, 2020
Mitochondrial Dysfunction and Calcium Dysregulation in Leigh Syndrome Induced Pluripotent Stem Cell Derived Neurons.Teresa Galera-Monge, Francisco Zurita-Díaz, Isaac Canals
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Frequent Collaborators
2 joint publications
Miguel Ángel Martín
1 joint publications
Isaac Canals
1 joint publications
Eskil Elmér
1 joint publications
Henrik Ahlenius
1 joint publications
Miguel Ladero
1 joint publications
María Del Carmen Ortuño-Costela
1 joint publications
Camille Laberthonnière
1 joint publications
Mégane Delourme
1 joint publications
Carla Fuster García
1 joint publications
Gema García García
