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index medicus (21) 21
coenzyme q (16) 16
mutation (14) 14
ubiquinone (14) 14
ubiquinone - genetics (13) 13
cell biology (12) 12
humans (12) 12
mitochondria (12) 12
ubiquinone - metabolism (11) 11
biosynthesis (10) 10
oxidative stress (10) 10
saccharomyces cerevisiae - genetics (9) 9
biochemistry & molecular biology (8) 8
saccharomyces cerevisiae - metabolism (8) 8
saccharomyces-cerevisiae (8) 8
ubiquinone - analogs & derivatives (8) 8
yeast (8) 8
article (7) 7
biochemistry (7) 7
cells (7) 7
electron transport (7) 7
mitochondria - enzymology (7) 7
saccharomyces cerevisiae - enzymology (7) 7
ubiquinone - biosynthesis (7) 7
animals (6) 6
biophysics (6) 6
chemistry (6) 6
culture media (6) 6
enzymes (6) 6
hela cells (6) 6
microbiology (6) 6
mitochondria - metabolism (6) 6
phosphorylation (6) 6
respiration (6) 6
antioxidants - metabolism (5) 5
beer (5) 5
cell membrane - metabolism (5) 5
child, preschool (5) 5
coenzyme q10 (5) 5
compositions thereof (5) 5
enzymology (5) 5
fermentation or enzyme-using processes to synthesise a desiredchemical compound or composition or to separate optical isomersfrom a racemic mixture (5) 5
general tagging of cross-sectional technologies spanning over several sections of the ipc (5) 5
general tagging of new technological developments (5) 5
life sciences (5) 5
metallurgy (5) 5
microorganisms or enzymes (5) 5
mitochondrial proteins - genetics (5) 5
mutation or genetic engineering (5) 5
other alcoholic beverages (5) 5
oxidation-reduction (5) 5
physiological aspects (5) 5
preparation thereof (5) 5
processes using microorganisms (5) 5
propagating, preserving or maintaining microorganisms (5) 5
reduction of greenhouse gas [ghg] emissions, related to energygeneration, transmission or distribution (5) 5
saccharomyces cerevisiae (5) 5
spirits (5) 5
technical subjects covered by former uspc cross-reference art collections [xracs] and digests (5) 5
technologies or applications for mitigation or adaptation againstclimate change (5) 5
ubiquinone - deficiency (5) 5
ubiquinone biosynthesis (5) 5
vinegar (5) 5
wine (5) 5
amino acid sequence (4) 4
ascorbic acid - metabolism (4) 4
bioenergetics (4) 4
coenzymes (4) 4
genes (4) 4
geriatrics & gerontology (4) 4
mitochondria - genetics (4) 4
mitochondrial proteins - metabolism (4) 4
molecular biology (4) 4
phosphatase (4) 4
saccharomyces cerevisiae - growth & development (4) 4
saccharomyces cerevisiae proteins - metabolism (4) 4
ubiquinone - pharmacology (4) 4
ubiquinone - physiology (4) 4
ataxia (3) 3
ataxia - genetics (3) 3
cerebellar-ataxia (3) 3
coenzyme q deficiency (3) 3
expression (3) 3
fibroblasts (3) 3
fibroblasts - metabolism (3) 3
gene (3) 3
kinase (3) 3
metabolism (3) 3
mitochondria - pathology (3) 3
mitochondrial diseases (3) 3
mitochondrial diseases - genetics (3) 3
molecular sequence data (3) 3
muscle biopsy (3) 3
muscle weakness - genetics (3) 3
nephrotic syndrome (3) 3
plasma membrane (3) 3
protein (3) 3
rats (3) 3
research (3) 3
research article (3) 3
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1. Full Text COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
by Heeringa, SF and Chernin, G and Chaki, M and Zhou, WB and Sloan, AJ and Ji, ZM and Xie, LX and Salviati, L and Hurd, TW and Vega-Warner, V and Killen, PD and Raphael, Y and Ashraf, S and Ovunc, B and Schoeb, DS and McLaughlin, HM and Airik, R and Vlangos, CN and Gbadegesin, R and Hinkes, B and Saisawat, P and Trevisson, E and Doimo, M and Casarin, A and Pertegato, V and Giorgi, G and Prokisch, H and Rotig, A and Nurnberg, G and Becker, C and Wang, S and Ozaltin, F and Topaloglu, R and Bakkaloglu, A and Bakkaloglu, SA and Muller, D and Beissert, A and Mir, S and Berdeli, A and Ozen, S and Zenker, M and Matejas, V and Santos-Ocana, C and Navas, P and Kusakabe, T and Kispert, A and Akman, S and Soliman, NA and Krick, S and Mundel, P and Reiser, J and Nurnberg, P and Clarke, CF and Wiggins, RC and Faul, C and Hildebrandt, F
JOURNAL OF CLINICAL INVESTIGATION, ISSN 0021-9738, 05/2011, Volume 121, Issue 5, pp. 2013 - 2024
Steroid-resistant nephrotic syndrome (SRNS) is a frequent cause of end-stage renal failure. Identification of single-gene causes of SRNS has generated some... 
MEDICINE, RESEARCH & EXPERIMENTAL | OXIDATIVE STRESS | GENE | COENZYME-Q BIOSYNTHESIS | DIPHOSPHATE SYNTHASE SUBUNIT-2 | NPHS2 | GLOMERULAR PROTEIN | UBIQUINONE BIOSYNTHESIS | COQ DEFICIENCY | FOCAL SEGMENTAL GLOMERULOSCLEROSIS | SACCHAROMYCES-CEREVISIAE | Deafness | Gene mutations | Genetic aspects | Nephrotic syndrome | Research | Health aspects | Risk factors
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2. Full Text Is coenzyme Q a key factor in aging?
by López-Lluch, Guillermo and Rodríguez-Aguilera, Juan Carlos and Santos-Ocaña, Carlos and Navas, Plácido
Mechanisms of Ageing and Development, ISSN 0047-6374, 2010, Volume 131, Issue 4, pp. 225 - 235
Coenzyme Q (Q) is a key component for bioenergetics and antioxidant protection in the cell. During the last years, research on diseases linked to Q-deficiency... 
Aging | Coenzyme Q | Ataxia | Bioenergetics | Neurodegeneration | RAT-LIVER | PERMEABILITY TRANSITION PORE | LIFE-SPAN | OXIDATIVE STRESS | COA REDUCTASE INHIBITORS | LOW-DENSITY-LIPOPROTEIN | CELL BIOLOGY | GERIATRICS & GERONTOLOGY | ELECTRON-TRANSPORT CHAIN | LIVER PLASMA-MEMBRANE | CAENORHABDITIS-ELEGANS | AGE-RELATED-CHANGES | Antioxidants - metabolism | Aging - drug effects | Rats | Ubiquinone - metabolism | Antioxidants - pharmacology | Neurodegenerative Diseases - metabolism | Ubiquinone - pharmacology | Brain - metabolism | Animals | Lipids - pharmacology | Biological Transport | Diet | Ubiquinone - physiology | Energy Metabolism - physiology | Muscles - metabolism | Dietary Supplements
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3. Full Text Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiency
by Doimo, Mara and Trevisson, Eva and Airik, Rannar and Bergdoll, Marc and Santos-Ocaña, Carlos and Hildebrandt, Friedhelm and Navas, Placido and Pierrel, Fabien and Salviati, Leonardo
BBA - Molecular Basis of Disease, ISSN 0925-4439, 01/2014, Volume 1842, Issue 1, pp. 1 - 6
Human encodes a monooxygenase which is responsible for the C5-hydroxylation of the quinone ring of coenzyme Q (CoQ). Mutations in cause primary CoQ deficiency,... 
Coenzyme Q | Vanillic acid | Steroid-resistant nephrotic syndrome | COQ6 | Mitochondria - enzymology | Saccharomyces cerevisiae - genetics | Humans | Ubiquinone - deficiency | Molecular Sequence Data | Ubiquinone - metabolism | Saccharomyces cerevisiae - drug effects | Muscle Weakness - genetics | Vanillic Acid - pharmacology | Hydroxybenzoates - pharmacology | Muscle Weakness - enzymology | Mitochondria - genetics | Ataxia - drug therapy | Ataxia - genetics | Mitochondrial Diseases - genetics | Amino Acid Sequence | Mitochondrial Diseases - drug therapy | Gene Expression | Ubiquinone - analogs & derivatives | Models, Molecular | Ubiquinone - genetics | Mitochondria - drug effects | Saccharomyces cerevisiae Proteins - genetics | Mitochondrial Diseases - enzymology | Sequence Homology, Amino Acid | Sequence Alignment | Ataxia - enzymology | Muscle Weakness - drug therapy | Saccharomyces cerevisiae Proteins - metabolism | Aminobenzoates - pharmacology | Saccharomyces cerevisiae - enzymology | Mutation | Ubiquinone - chemistry | Saccharomyces cerevisiae Proteins - chemistry
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4. Full Text Genetic Rescue of Mitochondrial and Skeletal Muscle Impairment in an Induced Pluripotent Stem Cells Model of Coenzyme Q10 Deficiency
by Romero‐Moya, Damià and Santos‐Ocaña, Carlos and Castaño, Julio and Garrabou, Gloria and Rodríguez‐Gómez, José A and Ruiz‐Bonilla, Vanesa and Bueno, Clara and González‐Rodríguez, Patricia and Giorgetti, Alessandra and Perdiguero, Eusebio and Prieto, Cristina and Moren‐Nuñez, Constanza and Fernández‐Ayala, Daniel J and Victoria Cascajo, Maria and Velasco, Iván and Canals, Josep Maria and Montero, Raquel and Yubero, Delia and Jou, Cristina and López‐Barneo, José and Cardellach, Francesc and Muñoz‐Cánoves, Pura and Artuch, Rafael and Navas, Plácido and Menendez, Pablo
STEM CELLS, ISSN 1066-5099, 07/2017, Volume 35, Issue 7, pp. 1687 - 1703
Coenzyme Q10 (CoQ10) plays a crucial role in mitochondria as an electron carrier within the mitochondrial respiratory chain (MRC) and is an essential... 
COQ4 | Induced pluripotent stem cell | Dopaminergic and motor neurons | Coenzyme Q10 | CRISPR‐Cas9 | Skeletal muscle | CRISPR-Cas9 | Antioxidants | Enzymes | Neurons | Analysis | Genes | Stem cells | Muscles | Mental illness | Brain | Biosynthesis | Rhabdomyolysis | Motor task performance | Tissues | Defects | Mitochondria | Fibroblasts | Dopamine receptors | CRISPR | Motor neurons | Dopamine | Metabolism | Disease control | Musculoskeletal system | Energy demand | Mutation | Respiration | Electron transport | Differentiation | Pluripotency | Inhibitory postsynaptic potentials
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5. Full Text Structural basis of mitochondrial dysfunction in response to cytochrome c phosphorylation at tyrosine 48
by Moreno-Beltrán, Blas and Guerra-Castellano, Alejandra and Díaz-Quintana, Antonio and Conte, Rebecca Del and García-Mauriño, Sofía M and Díaz-Moreno, Sofía and González-Arzola, Katiuska and Santos-Ocaña, Carlos and Velázquez-Campoy, Adrián and De la Rosa, Miguel A and Turano, Paola and Díaz-Moreno, Irene
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 04/2017, Volume 114, Issue 15, pp. E3041 - E3050
Regulation ofmitochondrial activity allows cells to adapt to changing conditions and to control oxidative stress, and its dysfunction can lead to... 
Cytochrome c | Phosphorylation | Mitochondrial dysfunction | Nuclear magnetic resonance | Respiratory supercomplexes | CARDIOLIPIN | MULTIDISCIPLINARY SCIENCES | mitochondrial dysfunction | nuclear magnetic resonance | TRANSIENT COMPLEX | FERRICYTOCHROME-C | respiratory supercomplexes | PROGRAMMED CELL-DEATH | CHAIN | OXIDASE | REDOX REGULATION | cytochrome c | BINDING-SITES | phosphorylation | RESPIRATORY COMPLEXES | NATIVE-LIKE | Phenylalanine - metabolism | Reactive Oxygen Species - metabolism | Magnetic Resonance Spectroscopy | Oxidative Stress | Phenylalanine - analogs & derivatives | Signal Transduction | Cytochromes c - metabolism | Humans | Cytochromes c - genetics | Mitochondria - metabolism | Mitochondria - pathology | Cytochromes c - chemistry | Tyrosine - metabolism | Phenylalanine - chemistry | Peroxidases - metabolism | Protein Conformation | Mutation | Tyrosine - chemistry | Tyrosine - genetics | Tyrosine | Physiological aspects | Observations | Biological Sciences | PNAS Plus
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6. Full Text Molecular characterization of the human COQ5 C-methyltransferase in coenzyme Q10 biosynthesis
by Nguyen, Theresa P.T and Casarin, Alberto and Desbats, Maria Andrea and Doimo, Mara and Trevisson, Eva and Santos-Ocaña, Carlos and Navas, Placido and Clarke, Catherine F and Salviati, Leonardo
BBA - Molecular and Cell Biology of Lipids, ISSN 1388-1981, 11/2014, Volume 1841, Issue 11, pp. 1628 - 1638
Coq5 catalyzes the only -methylation involved in the biosynthesis of coenzyme Q (Q or ubiquinone) in humans and yeast . As one of eleven polypeptides required... 
Q-biosynthetic intermediate | Mitochondrial metabolism | Protein complex | Human COQ gene | Ubiquinone | Saccharomyces cerevisiae
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7. Full Text Regulation of coenzyme Q biosynthesis in yeast: A new complex in the block
by González‐Mariscal, Isabel and García‐Testón, Elena and Padilla, Sergio and Martín‐Montalvo, Alejandro and Pomares‐Viciana, Teresa and Vazquez‐Fonseca, Luis and Gandolfo‐Domínguez, Pablo and Santos‐Ocaña, Carlos
IUBMB Life, ISSN 1521-6543, 02/2014, Volume 66, Issue 2, pp. 63 - 70
Coenzyme Q (CoQ) is an isoprenylated benzoquinone found in mitochondria, which functions mainly as an electron carrier from complex I or II to complex III in... 
ubiquinone | phosphoprotein | mitochondria | respiration | phosphatase | mitochondrial complex | coenzyme Q | MULTISUBUNIT COMPLEX | BIOCHEMISTRY & MOLECULAR BIOLOGY | ESCHERICHIA-COLI | SACCHAROMYCES-CEREVISIAE | PROTEIN-KINASES | DEFICIENCY | PHOSPHORYLATION SITES | CELL BIOLOGY | UBIQUINONE BIOSYNTHESIS | GENETIC-EVIDENCE | POLYPEPTIDE | Saccharomyces cerevisiae - metabolism | Mitochondria - enzymology | Phosphorylation | Mitochondria - genetics | Saccharomyces cerevisiae - genetics | Antioxidants - metabolism | Saccharomyces cerevisiae - enzymology | Ubiquinone - metabolism | Ubiquinone - genetics | Mutation | Mitochondrial Membranes - metabolism | Ubiquinone - biosynthesis | Physiological aspects | Enzymes | Mitochondrial DNA | Questions and answers
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8. Full Text Generation, genome edition and characterization of iPSC lines from a patient with coenzyme Q10 deficiency harboring a heterozygous mutation in COQ4 gene
by Romero-Moya, Damià and Castaño, Julio and Santos-Ocaña, Carlos and Navas, Plácido and Menendez, Pablo
Stem Cell Research, ISSN 1873-5061, 10/2017, Volume 24, Issue C, pp. 144 - 147
We report the generation, CRISPR/Cas9-edition and characterization of induced pluripotent stem cell (iPSC) lines from a patient with coenzyme Q deficiency... 
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9. Full Text Functional characterization of human COQ4, a gene required for Coenzyme Q10 biosynthesis
by Casarin, Alberto and Jimenez-Ortega, Jose Carlos and Trevisson, Eva and Pertegato, Vanessa and Doimo, Mara and Ferrero-Gomez, Maria Lara and Abbadi, Sara and Artuch, Rafael and Quinzii, Catarina and Hirano, Michio and Basso, Giuseppe and Ocaña, Carlos Santos and Navas, Placido and Salviati, Leonardo
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 07/2008, Volume 372, Issue 1, pp. 35 - 39
Defects in genes involved in coenzyme Q (CoQ) biosynthesis cause primary CoQ deficiency, a severe multisystem disorders presenting as progressive... 
Coenzyme Q | Biosynthesis | Ubiquinone | deficiency | Isoenzymes - analysis | Mitochondria - enzymology | Ubiquinone - analysis | Humans | Molecular Sequence Data | Green Fluorescent Proteins - genetics | Mitochondrial Proteins - genetics | Genetic Complementation Test | Ubiquinone - biosynthesis | Chromosomes, Human, Pair 9 - genetics | Mitochondrial Proteins - metabolism | Cloning, Molecular | Transcription, Genetic | Amino Acid Sequence | Green Fluorescent Proteins - analysis | Mitochondrial Proteins - analysis | Isoenzymes - genetics | Ubiquinone - analogs & derivatives | Ubiquinone - genetics | Saccharomyces cerevisiae Proteins - genetics | Blotting, Northern | Transcription Initiation Site | HeLa Cells | Mutation | Isoenzymes - biosynthesis | Coenzyme Q10 deficiency | Coenzyme Q10
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10. Full Text Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis
by López-Martín, José M and Salviati, Leonardo and Trevisson, Eva and Montini, Giovanni and DiMauro, Salvatore and Quinzii, Catarina and Hirano, Michio and Rodriguez-Hernandez, Angeles and Cordero, Mario D and Sánchez-Alcázar, José A and Santos-Ocaña, Carlos and Navas, Plácido
Human Molecular Genetics, ISSN 0964-6906, 05/2007, Volume 16, Issue 9, pp. 1091 - 1097
Coenzyme Q10 (CoQ10) deficiency has been associated with an increasing number of clinical phenotypes that respond to CoQ10 supplementation. In two siblings... 
RESPIRATORY-CHAIN | COMPLEX | MITOCHONDRIAL ENCEPHALOMYOPATHY | CEREBELLAR-ATAXIA | BIOSYNTHESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | UBIQUINONE | MYOPATHY | COENZYME Q DEFICIENCY | TRANSFERASE | Coenzymes - pharmacology | Saccharomyces cerevisiae - genetics | Humans | Alkyl and Aryl Transferases - metabolism | Molecular Sequence Data | Ubiquinone - metabolism | Immunoblotting | Mutation, Missense | Pyrimidines - biosynthesis | Genetic Complementation Test | Pyrimidines - metabolism | Ubiquinone - biosynthesis | Ubiquinone - pharmacology | Coenzymes - metabolism | Alkyl and Aryl Transferases - genetics | Base Sequence | Energy Metabolism - genetics | Fibroblasts - metabolism | Cell Division - genetics | Amino Acid Sequence | Coenzymes - biosynthesis | Ubiquinone - analogs & derivatives | Cells, Cultured | Mitochondria - metabolism | Enzyme Activation - drug effects | Cell Division - drug effects | Uridine - pharmacology | Sequence Alignment | Fibroblasts - drug effects | Saccharomyces cerevisiae - enzymology | Fibroblasts - cytology | HeLa Cells | Saccharomyces cerevisiae - growth & development
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11. Full Text Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency
by Salviati, Leonardo and Trevisson, Eva and Rodriguez Hernandez, Maria Angeles and Casarin, Alberto and Pertegato, Vanessa and Doimo, Mara and Cassina, Matteo and Agosto, Caterina and Desbats, Maria Andrea and Sartori, Geppo and Sacconi, Sabrina and Memo, Luigi and Zuffardi, Orsetta and Artuch, Rafael and Quinzii, Catarina and DiMauro, Salvatore and Hirano, Michio and Santos-Ocaña, Carlos and Navas, Plácido
Journal of Medical Genetics, ISSN 0022-2593, 03/2012, Volume 49, Issue 3, pp. 187 - 191
BackgroundCOQ4 encodes a protein that organises the multienzyme complex for the synthesis of coenzyme Q10 (CoQ10). A 3.9 Mb deletion of chromosome 9q34.13 was... 
Electron Transport | Fibroblasts - enzymology | Saccharomyces cerevisiae - genetics | Humans | Ubiquinone - analogs & derivatives | Ubiquinone - deficiency | Child, Preschool | Male | Abnormalities, Multiple - drug therapy | Mitochondrial Proteins - genetics | Haploinsufficiency | Ubiquinone - pharmacology | Comparative Genomic Hybridization | Mitochondrial Proteins - metabolism | Electron Transport Chain Complex Proteins - metabolism | Abnormalities, Multiple - enzymology | Saccharomyces cerevisiae - enzymology | Ubiquinone - therapeutic use | Transcription, Genetic | Cell Proliferation - drug effects | HeLa Cells | Abnormalities, Multiple - genetics | Fibroblasts - metabolism | Yeast | Dehydrogenases | Genes | Fibroblasts | Ataxia | Skin | Mutation | Bioavailability | Chromosomes | Patients | Deoxyribonucleic acid--DNA | Cell Proliferation | Abnormalities, Multiple | Mitochondrial Proteins | Life Sciences | Ubiquinone | Development Biology | Saccharomyces cerevisiae | Electron Transport Chain Complex Proteins
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12. Full Text The Regulation of Coenzyme Q Biosynthesis in Eukaryotic Cells: All That Yeast Can Tell Us
by González-Mariscal, Isabel and García-Testón, Elena and Padilla, Sergio and Martín-Montalvo, Alejandro and Pomares Viciana, Teresa and Vazquez-Fonseca, Luis and Gandolfo Domínguez, Pablo and Santos-Ocaña, Carlos
Molecular Syndromology, ISSN 1661-8769, 07/2014, Volume 5, Issue 3-4, pp. 107 - 118
Coenzyme Q (CoQ) is a mitochondrial lipid, which functions mainly as an electron carrier from complex I or II to complex III at the mitochondrial inner... 
Further Section | Protein complex | Coenzyme Q | Mitochondria | Ubiquinone | Yeast | Respiration | June, 2014 | Published online
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13. Full Text The phosphatase Ptc7 induces coenzyme Q biosynthesis by activating the hydroxylase Coq7 in yeast
by Martín-Montalvo, Alejandro and González-Mariscal, Isabel and Pomares-Viciana, Teresa and Padilla-López, Sergio and Ballesteros, Manuel and Vazquez-Fonseca, Luis and Gandolfo, Pablo and Brautigan, David L and Navas, Placido and Santos-Ocaña, Carlos
Journal of Biological Chemistry, ISSN 0021-9258, 09/2013, Volume 288, Issue 39, pp. 28126 - 28137
The study of the components of mitochondrial metabolism has potential benefits for health span and lifespan because the maintenance of efficient mitochondrial... 
PROTEIN PHOSPHATASE | GENE | METABOLISM | PHOSPHORYLATION | RESPIRATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | KINASE | IDENTIFICATION | SACCHAROMYCES-CEREVISIAE | EXPRESSION | Gene Expression Regulation, Fungal | Mitochondria - enzymology | Protein Phosphatase 2 - physiology | Phosphorylation | Oxidation-Reduction | Oxidative Stress | Signal Transduction | Antioxidants - metabolism | Isoelectric Focusing | Ubiquinone - metabolism | Mixed Function Oxygenases - metabolism | Plasmids - metabolism | Ubiquinone - biosynthesis | Alleles | Protein Phosphatase 2 - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Saccharomyces cerevisiae - enzymology | Saccharomyces cerevisiae Proteins - physiology | Enzyme Activation | Coenzyme Q | Yeast | Bioenergetics | Phosphatase | Respiratory Chain | Mitochondrial Metabolism
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14. Molecular diagnosis of coenzyme Q10 deficiency: an update
by Yubero, Delia and Montero, Raquel and Santos-Ocaña, Carlos and Salviati, Leonardo and Navas, Placido and Artuch, Rafael
Expert Review of Molecular Diagnostics, ISSN 1473-7159, 06/2018, Volume 18, Issue 6, pp. 491 - 498
deficiency syndromes | Coenzyme Q | mitochondrial diseases | muscle biopsy | next generation sequencing | oxidative phosphorylation
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15. Full Text Structural basis of mitochondrial dysfunction in response to cytochromecphosphorylation at tyrosine 48
by Moreno-Beltrán, Blas and Guerra-Castellano, Alejandra and Díaz-Quintana, Antonio and Del Conte, Rebecca and García-Mauriño, Sofía M and Díaz-Moreno, Sofía and González-Arzola, Katiuska and Santos-Ocaña, Carlos and Velázquez-Campoy, Adrián and De la Rosa, Miguel A and Turano, Paola and Díaz-Moreno, Irene
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 04/2017, Volume 114, Issue 15, pp. E3041 - E3050
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