Dihydrolipoamide Dehydrogenase
"Dihydrolipoamide 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 containing oxidoreductase that catalyzes the reduction of lipoamide by NADH to yield dihydrolipoamide and NAD+. The enzyme is a component of several MULTIENZYME COMPLEXES.
Descriptor ID |
D008058
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MeSH Number(s) |
D05.500.562.452.150 D05.500.562.468.500 D05.500.562.625.500 D08.811.600.391.150 D08.811.600.465.500 D08.811.600.741.525 D08.811.682.657.350.750.500 D08.811.682.667.061 D12.776.331.192
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Concept/Terms |
Dihydrolipoamide Dehydrogenase- Dihydrolipoamide Dehydrogenase
- Dehydrogenase, Dihydrolipoamide
- Dihydrolipoyl Dehydrogenase
- Dehydrogenase, Dihydrolipoyl
- Glycine Decarboxylase Complex L-Protein
- Glycine Decarboxylase Complex L Protein
- NADH Diaphorase
- Diaphorase, NADH
- Lipoamide Dehydrogenase
- Dehydrogenase, Lipoamide
- Lipoic Acid Dehydrogenase
- Dehydrogenase, Lipoic Acid
- Lipoyl Dehydrogenase
- Dehydrogenase, Lipoyl
- NAD Diaphorase
- Diaphorase, NAD
- Diaphorase (Lipoamide Dehydrogenase)
- L-Protein, Glycine Decarboxylase Complex
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Below are MeSH descriptors whose meaning is more general than "Dihydrolipoamide Dehydrogenase".
Below are MeSH descriptors whose meaning is more specific than "Dihydrolipoamide Dehydrogenase".
This graph shows the total number of publications written about "Dihydrolipoamide Dehydrogenase" by people in this website by year, and whether "Dihydrolipoamide Dehydrogenase" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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1997 | 0 | 1 | 1 | 2009 | 0 | 1 | 1 | 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Dihydrolipoamide Dehydrogenase" by people in Profiles.
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Coughlin CR, Swanson MA, Kronquist K, Acquaviva C, Hutchin T, Rodr?guez-Pombo P, V?is?nen ML, Spector E, Creadon-Swindell G, Br?s-Goldberg AM, Rahikkala E, Moilanen JS, Mahieu V, Matthijs G, Bravo-Alonso I, P?rez-Cerd? C, Ugarte M, Vianey-Saban C, Scharer GH, Van Hove JL. The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT. Genet Med. 2017 01; 19(1):104-111.
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Stern JM, Gupta A, Raman JD, Cost N, Lucas S, Lotan Y, Raj GV, Cadeddu JA. Radiofrequency ablation of small renal cortical tumours in healthy adults: renal function preservation and intermediate oncological outcome. BJU Int. 2009 Sep; 104(6):786-9.
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Vasiliou V, Ross D, Nebert DW. Update of the NAD(P)H:quinone oxidoreductase (NQO) gene family. Hum Genomics. 2006 Mar; 2(5):329-35.
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Sauer SW, Okun JG, Schwab MA, Crnic LR, Hoffmann GF, Goodman SI, Koeller DM, K?lker S. Bioenergetics in glutaryl-coenzyme A dehydrogenase deficiency: a role for glutaryl-coenzyme A. J Biol Chem. 2005 Jun 10; 280(23):21830-6.
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Janoff EN, Hayakawa H, Taylor DN, Fasching CE, Kenner JR, Jaimes E, Raij L. Nitric oxide production during Vibrio cholerae infection. Am J Physiol. 1997 11; 273(5):G1160-7.
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Matalon R, Stumpf DA, Michals K, Hart RD, Parks JK, Goodman SI. Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acid. J Pediatr. 1984 Jan; 104(1):65-9.
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