Fisiología, Anatomía y Biología Celular
Department
Universidad de Zaragoza
Zaragoza, EspañaPublications in collaboration with researchers from Universidad de Zaragoza (14)
2022
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Multicentric Standardization of Protocols for the Diagnosis of Human Mitochondrial Respiratory Chain Defects
Antioxidants, Vol. 11, Núm. 4
2021
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
2019
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Muscle involvement in a large cohort of pediatric patients with genetic diagnosis of mitochondrial disease
Journal of Clinical Medicine, Vol. 8, Núm. 1
2017
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Structural basis of mitochondrial dysfunction in response to cytochrome c phosphorylation at tyrosine 48
Proceedings of the National Academy of Sciences of the United States of America, Vol. 114, Núm. 15, pp. E3041-E3050
2016
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A statistical algorithm showing coenzyme Q10 and citrate synthase as biomarkers for mitochondrial respiratory chain enzyme activities
Scientific Reports, Vol. 6, Núm. 1
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Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356
Autophagy
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Autophagy, Vol. 12, Núm. 1, pp. 1-222
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Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders
Mitochondrion, Vol. 30, pp. 51-58
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Severe encephalopathy associated to pyruvate dehydrogenase mutations and unbalanced coenzyme Q 10 content
European Journal of Human Genetics, Vol. 24, Núm. 3, pp. 367-372
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The CoQH2/CoQ Ratio Serves as a Sensor of Respiratory Chain Efficiency
Cell Reports, Vol. 15, Núm. 1, pp. 197-209
2013
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Coenzyme Q10 deficiency in mitochondrial DNA depletion syndromes
Mitochondrion, Vol. 13, Núm. 4, pp. 337-341
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Supercomplex assembly determines electron flux in the mitochondrial electron transport chain
Science, Vol. 340, Núm. 6140, pp. 1567-1570
2009
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Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: A case report
Clinical Biochemistry, Vol. 42, Núm. 7-8, pp. 742-745