J. M. Suárez-Rivero

发表

Coenzyme Q10 Analogues: Benefits and Challenges for Therapeutics

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Carmen J. Pastor-Maldonado, 2021, Antioxidants.

Activation of the Mitochondrial Unfolded Protein Response: A New Therapeutic Target?

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Carmen J. Pastor-Maldonado, 2022, Biomedicines.

UPRmt activation improves pathological alterations in cellular models of mitochondrial diseases

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Carmen J. Pastor-Maldonado, 2022, Orphanet Journal of Rare Diseases.

Vitamin E prevents lipid peroxidation and iron accumulation in PLA2G6-Associated Neurodegeneration

J. Salas, A. Rodríguez-Moreno, J. Armengol, 2022, Neurobiology of Disease.

Intracellular cholesterol accumulation and coenzyme Q10 deficiency in Familial Hypercholesterolemia.

J. Salas, M. Cordero, J. Sánchez-Alcázar, 2018, Biochimica et biophysica acta. Molecular basis of disease.

Therapeutic approach with commercial supplements for pantothenate kinase-associated neurodegeneration with residual PANK2 expression levels

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Suleva Povea-Cabello, 2022, Orphanet Journal of Rare Diseases.

Precision Medicine in Rare Diseases

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Suleva Povea-Cabello, 2020, Diseases.

Mitochondrial Dynamics in Mitochondrial Diseases

J. Sánchez-Alcázar, I. de Lavera, D. Cotán, 2016, Diseases.

Dynamic Reorganization of the Cytoskeleton during Apoptosis: The Two Coffins Hypothesis

J. Sánchez-Alcázar, P. Ybot‐González, D. Cotán, 2017, International journal of molecular sciences.

Pantothenate and L-Carnitine Supplementation Improves Pathological Alterations in Cellular Models of KAT6A Syndrome

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Suleva Povea-Cabello, 2022, Genes.

Mitochondria and Antibiotics: For Good or for Evil?

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Carmen J. Pastor-Maldonado, 2021, Biomolecules.

From Mitochondria to Atherosclerosis: The Inflammation Path

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Carmen J. Pastor-Maldonado, 2021, Biomedicines.

Parkin-mediated mitophagy and autophagy flux disruption in cellular models of MERRF syndrome.

A. Rodríguez-Moreno, S. Jackson, J. Sánchez-Alcázar, 2020, Biochimica et biophysica acta. Molecular basis of disease.

Vicious cycle of lipid peroxidation and iron accumulation in neurodegeneration

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Suleva Povea-Cabello, 2022, Neural regeneration research.

Pantothenate Rescues Iron Accumulation in Pantothenate Kinase-Associated Neurodegeneration Depending on the Type of Mutation

Antonio J. Pérez-Pulido, J. Salas, A. Díaz-Quintana, 2018, Molecular Neurobiology.

Neurodegeneration, Mitochondria, and Antibiotics

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Suleva Povea-Cabello, 2023, Metabolites.

NLRP1 inflammasome modulates senescence and senescence-associated secretory phenotype

B. Ryffel, Andrea Gallardo-Orihuela, T. von Zglinicki, 2023, bioRxiv.

Mitochondrial Dysfunction in Lysosomal Storage Disorders

G. Tiscornia, I. de Lavera, D. Cotán, 2016, Diseases.

Advances in mt-tRNA Mutation-Caused Mitochondrial Disease Modeling: Patients’ Brain in a Dish

J. Sánchez-Alcázar, Marina Villanueva-Paz, J. M. Suárez-Rivero, 2021, Frontiers in Genetics.

Coenzyme Q10: Novel Formulations and Medical Trends

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Suleva Povea-Cabello, 2020, International journal of molecular sciences.

mtUPR Modulation as a Therapeutic Target for Primary and Secondary Mitochondrial Diseases

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Suleva Povea-Cabello, 2023, International journal of molecular sciences.

Pterostilbene in Combination With Mitochondrial Cofactors Improve Mitochondrial Function in Cellular Models of Mitochondrial Diseases

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Suleva Povea-Cabello, 2022, Frontiers in Pharmacology.

Modeling Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome Using Patient-Derived Induced Neurons Generated by Direct Reprogramming.

A. Rodríguez-Moreno, J. Armengol, Y. Andrade-Talavera, 2022, Cellular reprogramming.

Down regulation of the expression of mitochondrial phosphopantetheinyl-proteins in pantothenate kinase-associated neurodegeneration: pathophysiological consequences and therapeutic perspectives

J. Salas, J. Sánchez-Alcázar, J. M. Suárez-Rivero, 2021, Orphanet Journal of Rare Diseases.

Alpha-lipoic acid supplementation corrects pathological alterations in cellular models of pantothenate kinase-associated neurodegeneration with residual PANK2 expression levels

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Suleva Povea-Cabello, 2023, Orphanet Journal of Rare Diseases.

3697G>A in MT-ND1 is a causative mutation in mitochondrial disease.

Hugo Naya, L. Spangenberg, C. Robello, 2016, Mitochondrion.

Pathophysiological characterization of MERRF patient-specific induced neurons generated by direct reprogramming.

S. Jackson, J. Sánchez-Alcázar, Marina Villanueva-Paz, 2019, Biochimica et biophysica acta. Molecular cell research.

Coenzyme Q10 partially restores pathological alterations in a macrophage model of Gaucher disease

G. Tiscornia, J. Sánchez-Alcázar, I. de Lavera, 2017, Orphanet Journal of Rare Diseases.

Atherosclerosis and Coenzyme Q10

M. Munuera, J. Sánchez-Alcázar, Marina Villanueva-Paz, 2019, International journal of molecular sciences.

NLRP1 inflammasome modulates senescence and senescence-associated secretory phenotype

B. Ryffel, Andrea Gallardo-Orihuela, T. Zglinicki, 2023, bioRxiv.

Precision medicine in pantothenate kinase-associated neurodegeneration

J. Sánchez-Alcázar, J. Abril-Jaramillo, Marina Villanueva-Paz, 2019, Neural regeneration research.

Precision medicine in pantothenate kinase-associated neurodegeneration

J. Sánchez-Alcázar, J. Abril-Jaramillo, Marina Villanueva-Paz, 2019, Neural regeneration research.

Pantothenate Rescues Iron Accumulation in Pantothenate Kinase-Associated Neurodegeneration Depending on the Type of Mutation

Antonio J. Pérez-Pulido, J. Salas, A. Díaz-Quintana, 2018, Molecular Neurobiology.

Human natural killer cells can activate NLRP1 and NLRP3 inflammasomes and drives pyroptosis

J. M. Suárez-Rivero, Juan López-Pérez, Inés Muela-Zarzuela, 2024, bioRxiv.

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

J. Sánchez-Alcázar, J. M. Suárez-Rivero, Mónica Álvarez-Córdoba, 2024, Biomolecules.