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1 monstrated to be predominantly attributed to aldehyde oxidase.
2 xamined to predict the likely metabolites of aldehyde oxidase.
3 HNA to HNC, which is likely catalyzed by an aldehyde oxidase.
4 iver expressed kinetically distinct forms of aldehyde oxidase.
5 s protein was shown to belong to a family of aldehyde oxidases.
6 cytosolic FeS enzymes such as aconitase and aldehyde oxidases.
7 uted to aldehyde dehydrogenases but never to aldehyde oxidases.
8 se, expression analysis of UHRF1, ATP7A, and aldehyde oxidase 1 in combination could potentially prov
9 IS-EPOXYCAROTENOID DIOXYGENASE 3 (NCED3) and ALDEHYDE OXIDASE 3 (AAO3) are expressed at much higher l
13 d that 11a was not at risk of metabolism via aldehyde oxidase, an advantage over previously described
17 t, chlorate6 (chl6), have similar defects in aldehyde oxidase (AO) enzyme activity, which is required
18 anthine oxidase (XO) inhibitor oxypurinol or aldehyde oxidase (AO) inhibitor raloxifene significantly
20 lete nucleotide sequence of the first insect aldehyde oxidase (AO) was obtained from the common house
21 at the low exposure was due to metabolism by aldehyde oxidase (AO), so we sought to identify quinazol
23 o be manifested by a metabolite-generated by aldehyde oxidase (AO)-possessing a similar pharmacophore
34 hibitors suggested that xanthine oxidase and aldehyde oxidase are involved in the oxidative metabolis
36 ifferences between male and female rat liver aldehyde oxidases are sensitive to redox manipulation.
38 male rat liver and post-benzamidine-purified aldehyde oxidase differed substantially from each other
39 to Glu-869 in the crystallographically known aldehyde oxidase from Desulfovibrio gigas) and the highe
40 human cytochrome P450 3A4 (CYP3A4) and human aldehyde oxidase (hAOX) for more in-depth data interpret
43 idase (and by inference, the closely related aldehyde oxidases) hydroxylates both aromatic heterocycl
45 roxypyrimidine suggesting the involvement of aldehyde oxidase in the reduction of the sulfoxides.
48 dopterin cofactor, an essential cofactor for aldehyde oxidases, led to resistance to sirtinol, probab
50 iate corresponded to the observed product of aldehyde oxidase metabolism >or=90% for the compounds ex
52 code for Moco-sulfurase, which activates the aldehyde oxidases required for the biosynthesis of the p
55 Here, we show that the AAO4 protein is an aldehyde oxidase that can use several substrates but tha
56 rylated form of MoCo, a cofactor required by aldehyde oxidase that functions in the last step of ABA
58 activity in both organs was associated with aldehyde oxidase, which could be easily separated from d