Electron-transferring-flavoprotein dehydrogenase (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Electron-transferring-flavoprotein dehydrogenase" in English language version.

refsWebsite

Global rank English rank

21nih.gov

4^th place

16doi.org

2^nd place

4semanticscholar.org

11^th place

8^th place

2harvard.edu

18^th place

17^th place

1nbn-resolving.de

3,251^st place

7,630^th place

doi.org

Ghisla S, Thorpe C (Feb 2004). "Acyl-CoA dehydrogenases. A mechanistic overview". European Journal of Biochemistry. 271 (3): 494–508. doi:10.1046/j.1432-1033.2003.03946.x. PMID 14728676.
He M, Rutledge SL, Kelly DR, Palmer CA, Murdoch G, Majumder N, Nicholls RD, Pei Z, Watkins PA, Vockley J (Jul 2007). "A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency". American Journal of Human Genetics. 81 (1): 87–103. doi:10.1086/519219. PMC 1950923. PMID 17564966.
Watmough NJ, Frerman FE (Dec 2010). "The electron transfer flavoprotein: ubiquinone oxidoreductases". Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1797 (12): 1910–6. doi:10.1016/j.bbabio.2010.10.007. PMID 20937244.
Vianey-Liaud C, Divry P, Gregersen N, Mathieu M (1987). "The inborn errors of mitochondrial fatty acid oxidation". Journal of Inherited Metabolic Disease. 10 (Suppl 1): 159–200. doi:10.1007/bf01812855. PMID 3119938. S2CID 9771779.
Zhang J, Frerman FE, Kim JJ (Oct 2006). "Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool". Proceedings of the National Academy of Sciences of the United States of America. 103 (44): 16212–7. Bibcode:2006PNAS..10316212Z. doi:10.1073/pnas.0604567103. PMC 1637562. PMID 17050691.
Ramsay RR, Steenkamp DJ, Husain M (Feb 1987). "Reactions of electron-transfer flavoprotein and electron-transfer flavoprotein: ubiquinone oxidoreductase". The Biochemical Journal. 241 (3): 883–92. doi:10.1042/bj2410883. PMC 1147643. PMID 3593226.
Beckmann JD, Frerman FE (Jul 1985). "Reaction of electron-transfer flavoprotein with electron-transfer flavoprotein-ubiquinone oxidoreductase". Biochemistry. 24 (15): 3922–5. doi:10.1021/bi00336a017. PMID 2996585.
Watmough NJ, Loehr JP, Drake SK, Frerman FE (Feb 1991). "Tryptophan fluorescence in electron-transfer flavoprotein:ubiquinone oxidoreductase: fluorescence quenching by a brominated pseudosubstrate". Biochemistry. 30 (5): 1317–23. doi:10.1021/bi00219a023. PMID 1991113.
Frerman, F. E.; Goodman, S. I. (1985). "Deficiency of Electron Transfer Flavoprotein or Electron Transfer Flavoprotein:Ubiquinone Oxidoreductase in Glutaric Acidemia Type II Fibroblasts". Proceedings of the National Academy of Sciences. 82 (13): 4517–4520. Bibcode:1985PNAS...82.4517F. doi:10.1073/pnas.82.13.4517. PMC 391133. PMID 2989828.
Galloway JH, Cartwright IJ, Bennett MJ (Mar 1987). "Abnormal myocardial lipid composition in an infant with type II glutaric aciduria". Journal of Lipid Research. 28 (3): 279–84. doi:10.1016/S0022-2275(20)38707-1. PMID 3572253.
Singla M, Guzman G, Griffin AJ, Bharati S (Mar 2008). "Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature". Pediatric Cardiology. 29 (2): 446–51. doi:10.1007/s00246-007-9119-6. PMID 17912479. S2CID 370626.
Turnbull DM, Bartlett K, Eyre JA, Gardner-Medwin D, Johnson MA, Fisher J, Watmough NJ (Oct 1988). "Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy". Developmental Medicine and Child Neurology. 30 (5): 667–72. doi:10.1111/j.1469-8749.1988.tb04806.x. PMID 3229565. S2CID 33989343.
Liang WC, Ohkuma A, Hayashi YK, López LC, Hirano M, Nonaka I, Noguchi S, Chen LH, Jong YJ, Nishino I (Mar 2009). "ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency". Neuromuscular Disorders. 19 (3): 212–6. doi:10.1016/j.nmd.2009.01.008. PMC 10409523. PMID 19249206. S2CID 28328495.
Goodman SI, Binard RJ, Woontner MR, Frerman FE (2002). "Glutaric acidemia type II: gene structure and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) gene". Molecular Genetics and Metabolism. 77 (1–2): 86–90. doi:10.1016/S1096-7192(02)00138-5. PMID 12359134.
Olsen RK, Olpin SE, Andresen BS, Miedzybrodzka ZH, Pourfarzam M, Merinero B, Frerman FE, Beresford MW, Dean JC, Cornelius N, Andersen O, Oldfors A, Holme E, Gregersen N, Turnbull DM, Morris AA (Aug 2007). "ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency". Brain. 130 (Pt 8): 2045–54. doi:10.1093/brain/awm135. PMID 17584774.
Rhead W, Roettger V, Marshall T, Amendt B (Feb 1993). "Multiple acyl-coenzyme A dehydrogenation disorder responsive to riboflavin: substrate oxidation, flavin metabolism, and flavoenzyme activities in fibroblasts". Pediatric Research. 33 (2): 129–35. doi:10.1203/00006450-199302000-00008. PMID 8433888.

harvard.edu

ui.adsabs.harvard.edu

Zhang J, Frerman FE, Kim JJ (Oct 2006). "Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool". Proceedings of the National Academy of Sciences of the United States of America. 103 (44): 16212–7. Bibcode:2006PNAS..10316212Z. doi:10.1073/pnas.0604567103. PMC 1637562. PMID 17050691.
Frerman, F. E.; Goodman, S. I. (1985). "Deficiency of Electron Transfer Flavoprotein or Electron Transfer Flavoprotein:Ubiquinone Oxidoreductase in Glutaric Acidemia Type II Fibroblasts". Proceedings of the National Academy of Sciences. 82 (13): 4517–4520. Bibcode:1985PNAS...82.4517F. doi:10.1073/pnas.82.13.4517. PMC 391133. PMID 2989828.

nbn-resolving.de

Ghisla S, Thorpe C (Feb 2004). "Acyl-CoA dehydrogenases. A mechanistic overview". European Journal of Biochemistry. 271 (3): 494–508. doi:10.1046/j.1432-1033.2003.03946.x. PMID 14728676.

nih.gov

pubmed.ncbi.nlm.nih.gov

Ghisla S, Thorpe C (Feb 2004). "Acyl-CoA dehydrogenases. A mechanistic overview". European Journal of Biochemistry. 271 (3): 494–508. doi:10.1046/j.1432-1033.2003.03946.x. PMID 14728676.
He M, Rutledge SL, Kelly DR, Palmer CA, Murdoch G, Majumder N, Nicholls RD, Pei Z, Watkins PA, Vockley J (Jul 2007). "A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency". American Journal of Human Genetics. 81 (1): 87–103. doi:10.1086/519219. PMC 1950923. PMID 17564966.
Watmough NJ, Frerman FE (Dec 2010). "The electron transfer flavoprotein: ubiquinone oxidoreductases". Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1797 (12): 1910–6. doi:10.1016/j.bbabio.2010.10.007. PMID 20937244.
Vianey-Liaud C, Divry P, Gregersen N, Mathieu M (1987). "The inborn errors of mitochondrial fatty acid oxidation". Journal of Inherited Metabolic Disease. 10 (Suppl 1): 159–200. doi:10.1007/bf01812855. PMID 3119938. S2CID 9771779.
Zhang J, Frerman FE, Kim JJ (Oct 2006). "Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool". Proceedings of the National Academy of Sciences of the United States of America. 103 (44): 16212–7. Bibcode:2006PNAS..10316212Z. doi:10.1073/pnas.0604567103. PMC 1637562. PMID 17050691.
Ramsay RR, Steenkamp DJ, Husain M (Feb 1987). "Reactions of electron-transfer flavoprotein and electron-transfer flavoprotein: ubiquinone oxidoreductase". The Biochemical Journal. 241 (3): 883–92. doi:10.1042/bj2410883. PMC 1147643. PMID 3593226.
Beckmann JD, Frerman FE (Jul 1985). "Reaction of electron-transfer flavoprotein with electron-transfer flavoprotein-ubiquinone oxidoreductase". Biochemistry. 24 (15): 3922–5. doi:10.1021/bi00336a017. PMID 2996585.
Watmough NJ, Loehr JP, Drake SK, Frerman FE (Feb 1991). "Tryptophan fluorescence in electron-transfer flavoprotein:ubiquinone oxidoreductase: fluorescence quenching by a brominated pseudosubstrate". Biochemistry. 30 (5): 1317–23. doi:10.1021/bi00219a023. PMID 1991113.
Frerman, F. E.; Goodman, S. I. (1985). "Deficiency of Electron Transfer Flavoprotein or Electron Transfer Flavoprotein:Ubiquinone Oxidoreductase in Glutaric Acidemia Type II Fibroblasts". Proceedings of the National Academy of Sciences. 82 (13): 4517–4520. Bibcode:1985PNAS...82.4517F. doi:10.1073/pnas.82.13.4517. PMC 391133. PMID 2989828.
Galloway JH, Cartwright IJ, Bennett MJ (Mar 1987). "Abnormal myocardial lipid composition in an infant with type II glutaric aciduria". Journal of Lipid Research. 28 (3): 279–84. doi:10.1016/S0022-2275(20)38707-1. PMID 3572253.
Singla M, Guzman G, Griffin AJ, Bharati S (Mar 2008). "Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature". Pediatric Cardiology. 29 (2): 446–51. doi:10.1007/s00246-007-9119-6. PMID 17912479. S2CID 370626.
Turnbull DM, Bartlett K, Eyre JA, Gardner-Medwin D, Johnson MA, Fisher J, Watmough NJ (Oct 1988). "Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy". Developmental Medicine and Child Neurology. 30 (5): 667–72. doi:10.1111/j.1469-8749.1988.tb04806.x. PMID 3229565. S2CID 33989343.
Liang WC, Ohkuma A, Hayashi YK, López LC, Hirano M, Nonaka I, Noguchi S, Chen LH, Jong YJ, Nishino I (Mar 2009). "ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency". Neuromuscular Disorders. 19 (3): 212–6. doi:10.1016/j.nmd.2009.01.008. PMC 10409523. PMID 19249206. S2CID 28328495.
Goodman SI, Binard RJ, Woontner MR, Frerman FE (2002). "Glutaric acidemia type II: gene structure and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) gene". Molecular Genetics and Metabolism. 77 (1–2): 86–90. doi:10.1016/S1096-7192(02)00138-5. PMID 12359134.
Olsen RK, Olpin SE, Andresen BS, Miedzybrodzka ZH, Pourfarzam M, Merinero B, Frerman FE, Beresford MW, Dean JC, Cornelius N, Andersen O, Oldfors A, Holme E, Gregersen N, Turnbull DM, Morris AA (Aug 2007). "ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency". Brain. 130 (Pt 8): 2045–54. doi:10.1093/brain/awm135. PMID 17584774.
Rhead W, Roettger V, Marshall T, Amendt B (Feb 1993). "Multiple acyl-coenzyme A dehydrogenation disorder responsive to riboflavin: substrate oxidation, flavin metabolism, and flavoenzyme activities in fibroblasts". Pediatric Research. 33 (2): 129–35. doi:10.1203/00006450-199302000-00008. PMID 8433888.

ncbi.nlm.nih.gov

He M, Rutledge SL, Kelly DR, Palmer CA, Murdoch G, Majumder N, Nicholls RD, Pei Z, Watkins PA, Vockley J (Jul 2007). "A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency". American Journal of Human Genetics. 81 (1): 87–103. doi:10.1086/519219. PMC 1950923. PMID 17564966.
Zhang J, Frerman FE, Kim JJ (Oct 2006). "Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool". Proceedings of the National Academy of Sciences of the United States of America. 103 (44): 16212–7. Bibcode:2006PNAS..10316212Z. doi:10.1073/pnas.0604567103. PMC 1637562. PMID 17050691.
Ramsay RR, Steenkamp DJ, Husain M (Feb 1987). "Reactions of electron-transfer flavoprotein and electron-transfer flavoprotein: ubiquinone oxidoreductase". The Biochemical Journal. 241 (3): 883–92. doi:10.1042/bj2410883. PMC 1147643. PMID 3593226.
Frerman, F. E.; Goodman, S. I. (1985). "Deficiency of Electron Transfer Flavoprotein or Electron Transfer Flavoprotein:Ubiquinone Oxidoreductase in Glutaric Acidemia Type II Fibroblasts". Proceedings of the National Academy of Sciences. 82 (13): 4517–4520. Bibcode:1985PNAS...82.4517F. doi:10.1073/pnas.82.13.4517. PMC 391133. PMID 2989828.
Liang WC, Ohkuma A, Hayashi YK, López LC, Hirano M, Nonaka I, Noguchi S, Chen LH, Jong YJ, Nishino I (Mar 2009). "ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency". Neuromuscular Disorders. 19 (3): 212–6. doi:10.1016/j.nmd.2009.01.008. PMC 10409523. PMID 19249206. S2CID 28328495.

semanticscholar.org

api.semanticscholar.org

Vianey-Liaud C, Divry P, Gregersen N, Mathieu M (1987). "The inborn errors of mitochondrial fatty acid oxidation". Journal of Inherited Metabolic Disease. 10 (Suppl 1): 159–200. doi:10.1007/bf01812855. PMID 3119938. S2CID 9771779.
Singla M, Guzman G, Griffin AJ, Bharati S (Mar 2008). "Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature". Pediatric Cardiology. 29 (2): 446–51. doi:10.1007/s00246-007-9119-6. PMID 17912479. S2CID 370626.
Turnbull DM, Bartlett K, Eyre JA, Gardner-Medwin D, Johnson MA, Fisher J, Watmough NJ (Oct 1988). "Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy". Developmental Medicine and Child Neurology. 30 (5): 667–72. doi:10.1111/j.1469-8749.1988.tb04806.x. PMID 3229565. S2CID 33989343.
Liang WC, Ohkuma A, Hayashi YK, López LC, Hirano M, Nonaka I, Noguchi S, Chen LH, Jong YJ, Nishino I (Mar 2009). "ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency". Neuromuscular Disorders. 19 (3): 212–6. doi:10.1016/j.nmd.2009.01.008. PMC 10409523. PMID 19249206. S2CID 28328495.