Literature DB >> 8391327

Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain.

R W Taylor1, M A Birch-Machin, K Bartlett, D M Turnbull.   

Abstract

Defects of the respiratory chain are important causes of human disease and one of the most commonly used assays in the investigation of these patients is the measurement of succinate-cytochrome c reductase. However, this assay measures several components of the respiratory chain and the ability to detect a partial defect in one enzyme complex will depend on the amount of control exerted by that enzyme step on overall electron flux. We show that measurement of succinate-cytochrome c reductase activity may fail to detect partial defects of complex III and therefore is of limited diagnostic value in the identification of complex III defects. However, complex II is a major point of control of flux through succinate-cytochrome reductase and it is likely that measurement of the latter will detect defects of complex II.

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Year:  1993        PMID: 8391327     DOI: 10.1016/0925-4439(93)90030-5

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  13 in total

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3.  Evidence for altered structure and impaired mitochondrial electron transport function in selenium deficiency.

Authors:  P Rani; K Lalitha
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4.  The investigation of mitochondrial respiratory chain disease.

Authors:  A A Morris; M J Jackson; L A Bindoff; D M Turnbull
Journal:  J R Soc Med       Date:  1995-04       Impact factor: 5.344

5.  The kinetic basis of threshold effects observed in mitochondrial diseases: a systemic approach.

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6.  A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency.

Authors:  May Christine V Malicdan; Thierry Vilboux; Bruria Ben-Zeev; Jennifer Guo; Aviva Eliyahu; Ben Pode-Shakked; Amir Dori; Sravan Kakani; Settara C Chandrasekharappa; Carlos R Ferreira; Natalia Shelestovich; Dina Marek-Yagel; Hadass Pri-Chen; Ilan Blatt; John E Niederhuber; Langping He; Camilo Toro; Robert W Taylor; John Deeken; Tal Yardeni; Douglas C Wallace; William A Gahl; Yair Anikster
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7.  Evaluation of brain and kidney energy metabolism in an animal model of contrast-induced nephropathy.

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Review 8.  Biochemical diagnosis of mitochondrial disorders.

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9.  Neonatal De Toni-Debré-Fanconi syndrome due to a defect in complex III of the respiratory chain.

Authors:  U Wendel; W Ruitenbeek; H A Bentlage; R C Sengers; J M Trijbels
Journal:  Eur J Pediatr       Date:  1995-11       Impact factor: 3.183

10.  Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chain.

Authors:  A A Morris; R W Taylor; M A Birch-Machin; M J Jackson; M G Coulthard; L A Bindoff; R J Welch; N Howell; D M Turnbull
Journal:  Pediatr Nephrol       Date:  1995-08       Impact factor: 3.714

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