Fisiología, Anatomía y Biología Celular
Department


Centro Andaluz de Biología del Desarrollo
Sevilla, EspañaPublications in collaboration with researchers from Centro Andaluz de Biología del Desarrollo (57)
2025
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Biotin Induces Inactive Chromosome X Reactivation and Corrects Physiopathological Alterations in Beta-Propeller-Protein-Associated Neurodegeneration
International Journal of Molecular Sciences, Vol. 26, Núm. 3
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Files: The sequence of a complete bacteriophage (DgiS1ag)
Zenodo
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Innate antiviral systems are major defensome components that influence prophage distribution in Acinetobacter baumannii
Zenodo
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Iron Accumulation and Lipid Peroxidation in Cellular Models of Nemaline Myopathies
International Journal of Molecular Sciences, Vol. 26, Núm. 4
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Polydatin and Nicotinamide Prevent Iron Accumulation and Lipid Peroxidation in Cellular Models of Mitochondrial Diseases
Antioxidants, Vol. 14, Núm. 2
2024
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A Multi-Target Pharmacological Correction of a Lipoyltransferase LIPT1 Gene Mutation in Patient-Derived Cellular Models
Antioxidants, Vol. 13, Núm. 8
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A therapeutic approach to pantothenate kinase associated neurodegeneration: a pilot study
Orphanet Journal of Rare Diseases , Vol. 19, Núm. 1
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Mitochondria and liver disease.
Biosaia: Revista de los másteres de Biotecnología Sanitaria y Biotecnología Ambiental, Industrial y Alimentaria, Núm. 13
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Monosaccharides improve symptoms of an animal model for type III galactosemia, through the activation of the insulin pathway
Biomedicine and Pharmacotherapy, Vol. 181
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Polydatin and Nicotinamide Rescue the Cellular Phenotype of Mitochondrial Diseases by Mitochondrial Unfolded Protein Response (mtUPR) Activation
Biomolecules, Vol. 14, Núm. 5
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The impact and future of artificial intelligence in medical genetics and molecular medicine: an ongoing revolution
Functional and Integrative Genomics, Vol. 24, Núm. 4
2023
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Actin Polymerization Defects Induce Mitochondrial Dysfunction in Cellular Models of Nemaline Myopathies
Antioxidants, Vol. 12, Núm. 12
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Mitochondrial Quality Control via Mitochondrial Unfolded Protein Response (mtUPR) in Ageing and Neurodegenerative Diseases
Biomolecules, Vol. 13, Núm. 12
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Neurodegeneration, Mitochondria, and Antibiotics
Metabolites, Vol. 13, Núm. 3
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Patient-Derived Cellular Models for Polytarget Precision Medicine in Pantothenate Kinase-Associated Neurodegeneration
Pharmaceuticals, Vol. 16, Núm. 10
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Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration
Neural Regeneration Research, Vol. 18, Núm. 6, pp. 1196-1202
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mtUPR Modulation as a Therapeutic Target for Primary and Secondary Mitochondrial Diseases
International Journal of Molecular Sciences, Vol. 24, Núm. 2
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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Pterostilbene in Combination With Mitochondrial Cofactors Improve Mitochondrial Function in Cellular Models of Mitochondrial Diseases
Frontiers in Pharmacology, Vol. 13