"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
|
| Concept/Terms |
NADH Dehydrogenase- NADH Dehydrogenase
- Dehydrogenase, NADH
- NADH Cytochrome c Oxidoreductase
- Diaphorase (NADH Dehydrogenase)
- NADH (Acceptor) Oxidoreductase
- NADH Cytochrome c Reductase
|
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 |
|---|
| 1999 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2013 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "NADH Dehydrogenase" by people in Profiles.
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Oxyphil cell metaplasia in the parathyroids is characterized by somatic mitochondrial DNA mutations in NADH dehydrogenase genes and cytochrome c oxidase activity-impairing genes. Am J Pathol. 2014 Nov; 184(11):2922-35.
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Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosis. Neurogenetics. 2013 Feb; 14(1):85-7.
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Overexpression of bcl-2 results in reduction of cytochrome c content and inhibition of complex I activity. Biochem Biophys Res Commun. 2001 Feb 02; 280(4):1021-7.
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Detection of respiratory chain defects in cultivated skin fibroblasts and skeletal muscle of patients with Parkinson's disease. Ann N Y Acad Sci. 1999; 893:426-9.
MeSH information
