Oxidoreductases Acting on CH-CH Group Donors
"Oxidoreductases Acting on CH-CH Group Donors" 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 subclass of enzymes which includes all dehydrogenases acting on carbon-carbon bonds. This enzyme group includes all the enzymes that introduce double bonds into substrates by direct dehydrogenation of carbon-carbon single bonds.
Descriptor ID |
D044925
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MeSH Number(s) |
D08.811.682.660
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Oxidoreductases Acting on CH-CH Group Donors".
Below are MeSH descriptors whose meaning is more specific than "Oxidoreductases Acting on CH-CH Group Donors".
This graph shows the total number of publications written about "Oxidoreductases Acting on CH-CH Group Donors" by people in this website by year, and whether "Oxidoreductases Acting on CH-CH Group Donors" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1997 | 1 | 0 | 1 |
1998 | 1 | 0 | 1 |
1999 | 1 | 0 | 1 |
2005 | 0 | 1 | 1 |
2014 | 0 | 1 | 1 |
2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Oxidoreductases Acting on CH-CH Group Donors" by people in Profiles.
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Chandler PD, Tobias DK, Wang L, Smith-Warner SA, Chasman DI, Rose L, Giovannucci EL, Buring JE, Ridker PM, Cook NR, Manson JE, Sesso HD. Association between Vitamin D Genetic Risk Score and Cancer Risk in a Large Cohort of U.S. Women. Nutrients. 2018 Jan 09; 10(1).
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Terczynska-Dyla E, Bibert S, Duong FH, Krol I, J?rgensen S, Collinet E, Kutalik Z, Aubert V, Cerny A, Kaiser L, Malinverni R, Mangia A, Moradpour D, M?llhaupt B, Negro F, Santoro R, Semela D, Semmo N, Heim MH, Bochud PY, Hartmann R. Reduced IFN?4 activity is associated with improved HCV clearance and reduced expression of interferon-stimulated genes. Nat Commun. 2014 Dec 23; 5:5699.
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Tulenko TN, Boeze-Battaglia K, Mason RP, Tint GS, Steiner RD, Connor WE, Labelle EF. A membrane defect in the pathogenesis of the Smith-Lemli-Opitz syndrome. J Lipid Res. 2006 Jan; 47(1):134-43.
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Frank J, McGrath JA, Poh-Fitzpatrick MB, Hawk JL, Christiano AM. Mutations in the translation initiation codon of the protoporphyrinogen oxidase gene underlie variegate porphyria. Clin Exp Dermatol. 1999 Jul; 24(4):296-301.
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Frank J, McGrath J, Lam H, Graham RM, Hawk JL, Christiano AM. Homozygous variegate porphyria: identification of mutations on both alleles of the protoporphyrinogen oxidase gene in a severely affected proband. J Invest Dermatol. 1998 Apr; 110(4):452-5.
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McGrath JA, Hawk JL, Graham RM, Christiano AM. Lack of the R59W South African founder effect mutation in protoporphyrinogen oxidase in a British patient with homozygous variegate porphyria. Br J Dermatol. 1997 Feb; 136(2):292.
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Kahler SG, Sherwood WG, Woolf D, Lawless ST, Zaritsky A, Bonham J, Taylor CJ, Clarke JT, Durie P, Leonard JV. Pancreatitis in patients with organic acidemias. J Pediatr. 1994 Feb; 124(2):239-43.