"NADH Dehydrogenase" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A flavoprotein and iron sulfur-containing oxidoreductase that catalyzes the oxidation of NADH to NAD. In eukaryotes the enzyme can be found as a component of mitochondrial electron transport complex I. Under experimental conditions the enzyme can use CYTOCHROME C GROUP as the reducing cofactor. The enzyme was formerly listed as EC 1.6.2.1.
| Descriptor ID |
D009245
|
| MeSH Number(s) |
D08.811.682.608.504.500 D12.776.157.427.374.375.863.500 D12.776.331.887 D12.776.556.579.374.375.140.500
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| Concept/Terms |
NADH Dehydrogenase- NADH Dehydrogenase
- Dehydrogenase, NADH
- NADH Cytochrome c Oxidoreductase
- Diaphorase (NADH Dehydrogenase)
- NADH (Acceptor) Oxidoreductase
- NADH Cytochrome c Reductase
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Below are MeSH descriptors whose meaning is more general than "NADH Dehydrogenase".
Below are MeSH descriptors whose meaning is more specific than "NADH Dehydrogenase".
This graph shows the total number of publications written about "NADH Dehydrogenase" by people in this website by year, and whether "NADH Dehydrogenase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1993 | 0 | 1 | 1 |
| 1997 | 0 | 2 | 2 |
| 2000 | 0 | 1 | 1 |
| 2013 | 0 | 1 | 1 |
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Below are the most recent publications written about "NADH Dehydrogenase" by people in Profiles.
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Ramos PS, Oates JC, Kamen DL, Williams AH, Gaffney PM, Kelly JA, Kaufman KM, Kimberly RP, Niewold TB, Jacob CO, Tsao BP, Alarcón GS, Brown EE, Edberg JC, Petri MA, Ramsey-Goldman R, Reveille JD, Vilá LM, James JA, Guthridge JM, Merrill JT, Boackle SA, Freedman BI, Scofield RH, Stevens AM, Vyse TJ, Criswell LA, Moser KL, Alarcón-Riquelme ME, Langefeld CD, Harley JB, Gilkeson GS. Variable association of reactive intermediate genes with systemic lupus erythematosus in populations with different African ancestry. J Rheumatol. 2013 Jun; 40(6):842-9.
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Sandhir R, Khan M, Singh I. Identification of the pathway of alpha-oxidation of cerebronic acid in peroxisomes. Lipids. 2000 Oct; 35(10):1127-33.
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Gupta M, Dobashi K, Greene EL, Orak JK, Singh I. Studies on hepatic injury and antioxidant enzyme activities in rat subcellular organelles following in vivo ischemia and reperfusion. Mol Cell Biochem. 1997 Nov; 176(1-2):337-47.
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Singh I, Voigt RG, Sheikh FG, Kremser K, Brown FR. Biochemical features of a patient with Zellweger-like syndrome with normal PTS-1 and PTS-2 peroxisomal protein import systems: a new peroxisomal disease. Biochem Mol Med. 1997 Aug; 61(2):198-207.
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Gulati S, Ainol L, Orak J, Singh AK, Singh I. Alterations of peroxisomal function in ischemia-reperfusion injury of rat kidney. Biochim Biophys Acta. 1993 Oct 20; 1182(3):291-8.
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Yoshida Y, Singh I. Effect of clofibrate on peroxisomal lignoceroyl-CoA ligase activity. Biochem Med Metab Biol. 1990 Feb; 43(1):22-9.
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Bright GM, Singh I. Adrenal autoantibodies bind to adrenal subcellular fractions enriched in cytochrome-c reductase and 5'-nucleotidase. J Clin Endocrinol Metab. 1990 Jan; 70(1):95-9.