Alejandra Cabrera-Lopez

Sevilla, AN, Spain

Last Updated: 09/26/2026

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Found 12 publications

Pathophysiology, biological models and new therapeutic approaches in β-Propeller Associated Neurodegeneration.

Pathophysiology, biological models and new therapeutic approaches in β-Propeller Associated Neurodegeneration.

Journal: International review of cell and molecular biology

Published: June 16, 2026

Mitochondrial Unfolded Protein Response (mtUPR) Activation Improves Pathological Alterations in Cellular Models of Ethylmalonic Encephalopathy.

Mitochondrial Unfolded Protein Response (mtUPR) Activation Improves Pathological Alterations in Cellular Models of Ethylmalonic Encephalopathy.

Journal: Antioxidants (Basel, Switzerland)

Published: April 21, 2025

Alpha-lipoic acid supplementation improves pathological alterations in cellular models of Friedreich ataxia.

Alpha-lipoic acid supplementation improves pathological alterations in cellular models of Friedreich ataxia.

Journal: Orphanet journal of rare diseases

Published: April 17, 2025

Biotin Induces Inactive Chromosome X Reactivation and Corrects Physiopathological Alterations in Beta-Propeller-Protein-Associated Neurodegeneration.

Biotin Induces Inactive Chromosome X Reactivation and Corrects Physiopathological Alterations in Beta-Propeller-Protein-Associated Neurodegeneration.

Journal: International journal of molecular sciences

Published: January 11, 2025

Polydatin and Nicotinamide Prevent Iron Accumulation and Lipid Peroxidation in Cellular Models of Mitochondrial Diseases.

Polydatin and Nicotinamide Prevent Iron Accumulation and Lipid Peroxidation in Cellular Models of Mitochondrial Diseases.

Journal: Antioxidants (Basel, Switzerland)

Published: December 22, 2024

Iron Accumulation and Lipid Peroxidation in Cellular Models of Nemaline Myopathies.

Iron Accumulation and Lipid Peroxidation in Cellular Models of Nemaline Myopathies.

Journal: International journal of molecular sciences

Published: November 23, 2024

Mitochondrial dysfunction, iron accumulation, lipid peroxidation, and inflammasome activation in cellular models derived from patients with multiple sclerosis.

Mitochondrial dysfunction, iron accumulation, lipid peroxidation, and inflammasome activation in cellular models derived from patients with multiple sclerosis.

Journal: Aging

Published: September 10, 2024

A Multi-Target Pharmacological Correction of a Lipoyltransferase LIPT1 Gene Mutation in Patient-Derived Cellular Models.

A Multi-Target Pharmacological Correction of a Lipoyltransferase LIPT1 Gene Mutation in Patient-Derived Cellular Models.

Journal: Antioxidants (Basel, Switzerland)

Published: July 19, 2024

Polydatin and Nicotinamide Rescue the Cellular Phenotype of Mitochondrial Diseases by Mitochondrial Unfolded Protein Response (mtUPR) Activation.

Polydatin and Nicotinamide Rescue the Cellular Phenotype of Mitochondrial Diseases by Mitochondrial Unfolded Protein Response (mtUPR) Activation.

Journal: Biomolecules

Published: April 15, 2024

Mitochondrial Quality Control via Mitochondrial Unfolded Protein Response (mtUPR) in Ageing and Neurodegenerative Diseases.

Mitochondrial Quality Control via Mitochondrial Unfolded Protein Response (mtUPR) in Ageing and Neurodegenerative Diseases.

Journal: Biomolecules

Published: November 18, 2023

Actin Polymerization Defects Induce Mitochondrial Dysfunction in Cellular Models of Nemaline Myopathies.

Actin Polymerization Defects Induce Mitochondrial Dysfunction in Cellular Models of Nemaline Myopathies.

Journal: Antioxidants (Basel, Switzerland)

Published: October 24, 2023

Patient-Derived Cellular Models for Polytarget Precision Medicine in Pantothenate Kinase-Associated Neurodegeneration.

Patient-Derived Cellular Models for Polytarget Precision Medicine in Pantothenate Kinase-Associated Neurodegeneration.

Journal: Pharmaceuticals (Basel, Switzerland)

Published: September 04, 2023

Showing 1-12 of 12

Last Updated: 09/26/2026