M. ESTHER GALLARDO PEREZ

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Miguel Servet II Researcher; Head of the Traslational Research with iPS Cells Group

Instituto de Investigación Hospital 12 de Octubre

Spain

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About

M. Esther Gallardo Perez is a Miguel Servet II Researcher and the Head of the Translational Research with iPS Cells Group at Instituto de Investigación Sanitaria Hospital 12 de Octubre (i+12), Spain. Her research primarily focuses on induced pluripotent stem cells (iPSCs) and their application in modeling hereditary diseases, particularly optic neuropathies and skeletal muscle disorders. Recent work includes the development of iPSC-based models for McArdle disease and dominant optic atrophy, along with studies on biocatalysis involving glycerol and rosin.

Recent Grants

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TerDOABiomiPS: Nuevas aproximaciones terapéuticas para DOA basadas en tecnología de iPSCs y biomateriales texturizados

Open Date: 2023-07-01

Close Date: 2024-07-01

Grant: Close

bioTEP-DOA: Generación de RGCs candidatas a terapia celular para la DOA por diferenciación de iPSCs sobre biomateriales escalables

Open Date: 2022-11-01

Close Date: 2024-01-01

Grant: Close

bioMAT4EYE: Neoteric Biomaterials for hiPSCs Monitorized Differentiation to RGCs: Creation, Microfabrication & Microfluidics

Open Date: 2022-09-01

Close Date: 2025-09-01

Grant: Close

Dominant optic atrophy: iPSCs as a model of disease, diagnostic improvement and therapeutic approach

Open Date: 2022-01-01

Close Date: 2024-12-01

Grant: Close

Generation of a human model of RGCs for the search of therapies against dominant optic atrophy

Open Date: 2021-11-01

Close Date: 2022-11-01

Articles (11)

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2025

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2024

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2024

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2023

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2022

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2022

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2022

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2021

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2020

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2020

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2020

Collaborators (3)

Carmen Ayuso

SPAIN

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Miguel Ladero

Associate Professor

Complutense University

SPAIN

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Frederique Magdinier

FRANCE

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M. ESTHER GALLARDO PEREZ

Research Interests

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Recent Grants

Articles (11)

Esterification of Glycerol and Rosin Catalyzed by Irganox 1425: A Kinetic Comparison to the Thermal Process

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

Hereditary Optic Neuropathies: A Systematic Review on the Interplay between Biomaterials and Induced Pluripotent Stem Cells

Creation of an iPSC-Based Skeletal Muscle Model of McArdle Disease Harbouring the Mutation c.2392T>C (p.Trp798Arg) in the PYGM Gene

Lipozyme® TL IM Biocatalyst for Castor Oil FAME and Triacetin Production by Interesterification: Activity, Stability, and Kinetics

Synthesis of Ibuprofen Monoglyceride Using Novozym®435: Biocatalyst Activation and Stabilization in Multiphasic Systems

Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology

Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches

Mitochondrial Dysfunction and Calcium Dysregulation in Leigh Syndrome Induced Pluripotent Stem Cell Derived Neurons

Erratum: Enhanced tumorigenicity by mitochondrial DNA mild mutations (Oncotarget (2015) 6 (13628-13643) DOI: 10.18632/oncotarget.3698)

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

Collaborators (3)

Carmen Ayuso

Miguel Ladero

Frederique Magdinier

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M. ESTHER GALLARDO PEREZ

Research Interests

Explore related searches

Contact this professor

About

Recent Grants

Articles (11)

Esterification of Glycerol and Rosin Catalyzed by Irganox 1425: A Kinetic Comparison to the Thermal Process

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

Hereditary Optic Neuropathies: A Systematic Review on the Interplay between Biomaterials and Induced Pluripotent Stem Cells

Creation of an iPSC-Based Skeletal Muscle Model of McArdle Disease Harbouring the Mutation c.2392T>C (p.Trp798Arg) in the PYGM Gene

Lipozyme® TL IM Biocatalyst for Castor Oil FAME and Triacetin Production by Interesterification: Activity, Stability, and Kinetics

Synthesis of Ibuprofen Monoglyceride Using Novozym®435: Biocatalyst Activation and Stabilization in Multiphasic Systems

Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology

Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches

Mitochondrial Dysfunction and Calcium Dysregulation in Leigh Syndrome Induced Pluripotent Stem Cell Derived Neurons

Erratum: Enhanced tumorigenicity by mitochondrial DNA mild mutations (Oncotarget (2015) 6 (13628-13643) DOI: 10.18632/oncotarget.3698)

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

Collaborators (3)

Carmen Ayuso

Miguel Ladero

Frederique Magdinier

Make your next move.

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