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Similar articles for PubMed (Select 17050691)


Structure of electron transfer flavoprotein-ubiquinone oxidoreductase and electron transfer to the mitochondrial ubiquinone pool.

Zhang J, Frerman FE, Kim JJ.

Proc Natl Acad Sci U S A. 2006 Oct 31;103(44):16212-7. Epub 2006 Oct 18.


The iron-sulfur cluster of electron transfer flavoprotein-ubiquinone oxidoreductase is the electron acceptor for electron transfer flavoprotein.

Swanson MA, Usselman RJ, Frerman FE, Eaton GR, Eaton SS.

Biochemistry. 2008 Aug 26;47(34):8894-901. doi: 10.1021/bi800507p. Epub 2008 Aug 2.


The electron transfer flavoprotein: ubiquinone oxidoreductases.

Watmough NJ, Frerman FE.

Biochim Biophys Acta. 2010 Dec;1797(12):1910-6. doi: 10.1016/j.bbabio.2010.10.007. Epub 2010 Oct 16. Review.


Impact of mutations on the midpoint potential of the [4Fe-4S]+1,+2 cluster and on catalytic activity in electron transfer flavoprotein-ubiquinone oxidoreductase (ETF-QO).

Usselman RJ, Fielding AJ, Frerman FE, Watmough NJ, Eaton GR, Eaton SS.

Biochemistry. 2008 Jan 8;47(1):92-100. Epub 2007 Dec 11.


Electron spin relaxation enhancement measurements of interspin distances in human, porcine, and Rhodobacter electron transfer flavoprotein-ubiquinone oxidoreductase (ETF-QO).

Fielding AJ, Usselman RJ, Watmough N, Simkovic M, Frerman FE, Eaton GR, Eaton SS.

J Magn Reson. 2008 Feb;190(2):222-32. Epub 2007 Nov 6.


Molecular cloning and expression of a cDNA encoding human electron transfer flavoprotein-ubiquinone oxidoreductase.

Goodman SI, Axtell KM, Bindoff LA, Beard SE, Gill RE, Frerman FE.

Eur J Biochem. 1994 Jan 15;219(1-2):277-86.


Computational analysis of a novel mutation in ETFDH gene highlights its long-range effects on the FAD-binding motif.

Er TK, Chen CC, Liu YY, Chang HC, Chien YH, Chang JG, Hwang JK, Jong YJ.

BMC Struct Biol. 2011 Oct 21;11:43. doi: 10.1186/1472-6807-11-43.


Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency.

Cornelius N, Frerman FE, Corydon TJ, Palmfeldt J, Bross P, Gregersen N, Olsen RK.

Hum Mol Genet. 2012 Aug 1;21(15):3435-48. doi: 10.1093/hmg/dds175. Epub 2012 May 18.


Characterization of a mutation that abolishes quinone reduction by electron transfer flavoprotein-ubiquinone oxidoreductase.

Beard SE, Goodman SI, Bemelen K, Frerman FE.

Hum Mol Genet. 1995 Feb;4(2):157-61.


The intraflavin hydrogen bond in human electron transfer flavoprotein modulates redox potentials and may participate in electron transfer.

Dwyer TM, Mortl S, Kemter K, Bacher A, Fauq A, Frerman FE.

Biochemistry. 1999 Jul 27;38(30):9735-45.


Secondary coenzyme Q10 deficiency and oxidative stress in cultured fibroblasts from patients with riboflavin responsive multiple Acyl-CoA dehydrogenation deficiency.

Cornelius N, Byron C, Hargreaves I, Guerra PF, Furdek AK, Land J, Radford WW, Frerman F, Corydon TJ, Gregersen N, Olsen RK.

Hum Mol Genet. 2013 Oct 1;22(19):3819-27. doi: 10.1093/hmg/ddt232. Epub 2013 May 31.


Redox properties of electron-transfer flavoprotein ubiquinone oxidoreductase as determined by EPR-spectroelectrochemistry.

Paulsen KE, Orville AM, Frerman FE, Lipscomb JD, Stankovich MT.

Biochemistry. 1992 Dec 1;31(47):11755-61.


ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.

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.

Brain. 2007 Aug;130(Pt 8):2045-54. Epub 2007 Jun 20.

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