Irene
Villalón García
Researcher in the period 2018-2022
Publications (26) Irene Villalón García publications
2023
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Alpha-lipoic acid supplementation corrects pathological alterations in cellular models of pantothenate kinase-associated neurodegeneration with residual PANK2 expression levels
Orphanet journal of rare diseases, Vol. 18, Núm. 1, pp. 80
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Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration
Neural Regeneration Research, Vol. 18, Núm. 6, pp. 1196-1202
2022
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Activation of the Mitochondrial Unfolded Protein Response: A New Therapeutic Target?
Biomedicines, Vol. 10, Núm. 7
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Modeling Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome Using Patient-Derived Induced Neurons Generated by Direct Reprogramming
Cellular reprogramming, Vol. 24, Núm. 5, pp. 294-303
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Pantothenate and L-Carnitine Supplementation Improves Pathological Alterations in Cellular Models of KAT6A Syndrome
Genes, Vol. 13, Núm. 12
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Pterostilbene in Combination With Mitochondrial Cofactors Improve Mitochondrial Function in Cellular Models of Mitochondrial Diseases
Frontiers in Pharmacology, Vol. 13
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Therapeutic approach with commercial supplements for pantothenate kinase-associated neurodegeneration with residual PANK2 expression levels
Orphanet journal of rare diseases, Vol. 17, Núm. 1, pp. 311
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UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases
Orphanet Journal of Rare Diseases, Vol. 17, Núm. 1
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Vitamin E prevents lipid peroxidation and iron accumulation in PLA2G6-Associated Neurodegeneration
Neurobiology of Disease, Vol. 165
2021
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Coenzyme q10 analogues: Benefits and challenges for therapeutics
Antioxidants, Vol. 10, Núm. 2, pp. 1-20
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Down regulation of the expression of mitochondrial phosphopantetheinyl-proteins in pantothenate kinase-associated neurodegeneration: pathophysiological consequences and therapeutic perspectives
Orphanet Journal of Rare Diseases, Vol. 16, Núm. 1
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From mitochondria to atherosclerosis: The inflammation path
Biomedicines, Vol. 9, Núm. 3, pp. 1-24
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Generation of three human iPSC lines from PLAN (PLA2G6-associated neurodegeneration) patients
Stem Cell Research, Vol. 53
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Mitochondria and antibiotics: For good or for evil?
Biomolecules, Vol. 11, Núm. 7
2020
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Advances in mt-tRNA Mutation-Caused Mitochondrial Disease Modeling: Patients’ Brain in a Dish
Frontiers in Genetics, Vol. 11
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Coenzyme q10: Novel formulations and medical trends
International Journal of Molecular Sciences, Vol. 21, Núm. 22, pp. 1-23
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PLA2G6-associated neurodegeneration (PLAN): characterization of patients and drug screening
Biosaia: Revista de los másteres de Biotecnología Sanitaria y Biotecnología Ambiental, Industrial y Alimentaria, Núm. 9
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Parkin-mediated mitophagy and autophagy flux disruption in cellular models of MERRF syndrome
Biochimica et Biophysica Acta - Molecular Basis of Disease, Vol. 1866, Núm. 6
2019
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Atherosclerosis and coenzyme q10
International Journal of Molecular Sciences, Vol. 20, Núm. 20
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Pantothenate Rescues Iron Accumulation in Pantothenate Kinase-Associated Neurodegeneration Depending on the Type of Mutation
Molecular Neurobiology, Vol. 56, Núm. 5, pp. 3638-3656