María Ángeles
Rodríguez Hernández
Researcher in the period 2011-2016
Publications (23) María Ángeles Rodríguez Hernández publications
2017
2016
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Antitumoral gene-based strategy involving nitric oxide synthase type III overexpression in hepatocellular carcinoma
Gene Therapy, Vol. 23, Núm. 1, pp. 67-77
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Free-thiamine is a potential biomarker of Thiamine transporter-2 deficiency: A treatable cause of Leigh syndrome
Brain, Vol. 139, Núm. 1, pp. 31-38
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Regulation of apoptosis and cell proliferation by Sorafenib in Hepatocellular carcinoma
Biosaia: Revista de los másteres de Biotecnología Sanitaria y Biotecnología Ambiental, Industrial y Alimentaria, Núm. 5
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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
2015
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Nitric Oxide Synthase Type III Overexpression By Gene Therapy Exerts Antitumoral Activity In Mouse Hepatocellular Carcinoma
Redox biology, Vol. 5, pp. 420-421
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Primary coenzyme Q 10 deficiency presenting as fatal neonatal multiorgan failure
European Journal of Human Genetics, Vol. 23, Núm. 9, pp. 1254-1258
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Regulation of cell death receptor S-nitrosylation and apoptotic signaling by Sorafenib in hepatoblastoma cells
Redox Biology, Vol. 6, pp. 174-182
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Regulation of cell death signaling by nitric oxide in cancer cells
Nitric Oxide and Cancer: Pathogenesis and Therapy (Springer International Publishing), pp. 247-258
2014
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Mitophagy Plays a Protective Role in Fibroblasts from Patients with Coenzyme Q10 Deficiency
Autophagy: Cancer, Other Pathologies, Inflammation, Immunity, Infection, and Aging (Elsevier Inc.), pp. 131-144
2013
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Supercomplex assembly determines electron flux in the mitochondrial electron transport chain
Science, Vol. 340, Núm. 6140, pp. 1567-1570
2012
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Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency
Journal of Medical Genetics, Vol. 49, Núm. 3, pp. 187-191
2011
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Apoptotic microtubule network organization and maintenance depend on high cellular ATP levels and energized mitochondria
Apoptosis, Vol. 16, Núm. 4, pp. 404-424
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Secondary coenzyme Q 10 deficiency triggers mitochondria degradation by mitophagy in MELAS fibroblasts
FASEB Journal, Vol. 25, Núm. 8, pp. 2669-2687
2009
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Coenzyme Q deficiency triggers mitochondria degradation by mitophagy
Autophagy, Vol. 5, Núm. 1, pp. 19-32
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Coenzyme Q10 and alpha-tocopherol protect against amitriptyline toxicity
Toxicology and Applied Pharmacology, Vol. 235, Núm. 3, pp. 329-337
2008
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Analysis of Coenzyme Q10 in muscle and fibroblasts for the diagnosis of CoQ10 deficiency syndromes
Clinical Biochemistry, Vol. 41, Núm. 9, pp. 697-700
2007
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Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis
Human Molecular Genetics, Vol. 16, Núm. 9, pp. 1091-1097
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The apoptotic microtubule network preserves plasma membrane integrity during the execution phase of apoptosis
Apoptosis, Vol. 12, Núm. 7, pp. 1195-1208