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1 tween complex II and complex III, presumably coenzyme Q.
2  electron transport, including Vitamin K and Coenzyme Q.
3  which was accompanied by a lower content of coenzyme Q.
4 es electrons from acyl-CoA dehydrogenases to coenzyme Q.
5 diate, as well as the final product (13)C(6)-coenzyme Q.
6 and transferring the energy to mitochondrial coenzyme Q.
7                                              Coenzyme Q(0) (Q(0)), a strong electrophile, is toxic to
8         The purified enzyme had also an NADH-coenzyme Q(0) reductase (NADH: external acceptor (quinon
9 ADH-ferricyanide reductase activity and NADH-coenzyme Q(0) reductase activity of plasma membranes and
10      The enzyme was not NAD(P)(+) dependent; coenzyme Q(0) was the preferred electron acceptor.
11           K(M) values for dihydroorotate and coenzyme Q(0) were similar to wild type.
12                                              Coenzyme Q(1)(0) (1-10 nM), which has been reported to f
13                                              Coenzyme Q(1)(0) (CoQ(1)(0); also called ubiquinone) is
14                             In mitochondria, coenzymes Q(1) and Q(2) did not bond to the 50-kDa prote
15                               The effects of coenzyme Q(10) (CoQ(10)) and alpha-tocopherol on the rat
16                                              Coenzyme Q(10) (CoQ(10)) is a vital lipophilic molecule
17                                              Coenzyme Q(10) (CoQ(10)) is essential for electron trans
18                                              Coenzyme Q(10) (CoQ(10)) is essential for electron trans
19 esponse-attenuating effects of vitamin E and coenzyme Q(10) (CoQ(10)) supplementation.
20 neficial effects of supplementing cells with coenzyme Q(10) (CoQ(10)).
21        Glucose tolerance and skeletal muscle coenzyme Q(10) (Q(10)) content, mitochondrial density, a
22 chondrial antioxidants alpha-lipoic acid and coenzyme Q(10) also suppresses Bak expression in the coc
23 dismutase, catalase, glutathione peroxidase, coenzyme Q(10) and ORAC levels in diabetic rats.
24                                   Defects of coenzyme Q(10) biosynthesis represent one of the few tre
25 wo of 16 candidate genes implicated in human coenzyme Q(10) biosynthesis.
26 ured skin fibroblasts from the patient had a coenzyme Q(10) biosynthetic rate of 11% of normal contro
27          We genotyped a patient with primary coenzyme Q(10) deficiency who presented with neonatal la
28                     In view of the rarity of coenzyme Q(10) deficiency, we hypothesized that the dise
29                                              Coenzyme Q(10) is a mobile lipophilic electron carrier l
30                                   Similarly, coenzyme Q(10) is also effective in animal models and ha
31 ial in animal models of PD include creatine, coenzyme Q(10), Ginkgo biloba, nicotinamide, and acetyl-
32          The method is also able to separate coenzyme Q(10).
33 toxicity was seen with the parent ubiquinone coenzyme Q(10.) Inhibition of cancer cell growth by Mito
34 tidepressants, anticonvulsants (topiramate), coenzyme Q-10, and L-carnitine.
35 n of complex I, complex II, complex III, and coenzyme Q [11-14].
36 he Caenorhabditis elegans clk-1 mutants lack coenzyme Q(9) and instead accumulate the biosynthetic in
37 s indicated that both codon reassignment and coenzyme Q(9) likely had single origins with multiple lo
38                   This pathway also produces coenzyme Q (a component of the respiratory chain), dolic
39 n to 4-hydroxybenzoic acid as a precursor of coenzyme Q, a redox lipid essential to the function of t
40  by increasing concentrations of the reduced coenzyme Q analog decylubiquinol.
41 , alpha tocopherol, ebselen, or idebenone (a coenzyme Q analogue); or the MPT blockers, cyclosporin A
42 s of Complex III, cyanide, oligomycin A, and coenzyme Q analogues decreased 4HPR-induced hydroperoxid
43                                          The coenzyme Q analogues were very effective in this respect
44 bolism and recycling of antioxidants such as coenzyme Q and alpha-tocopherol.
45 nzyme Q but there was no interaction between coenzyme Q and the effect of rosuvastatin.
46  pet mutant C92 was found to be deficient in coenzyme Q and to have low mitochondrial NADH-cytochrome
47  reaction in the biosynthesis of ubiquinone (coenzyme Q) and menaquinone (vitamin K2), essential isop
48 sue concentrations of the essential cofactor coenzyme Q are decreased by statins, and this could be h
49  was exhibited with both NAD(P)H and reduced coenzyme Q as substrate.
50 e of electron leakage is located proximal to coenzyme Q at the electron transfer flavoprotein that sh
51                                 Cytochrome b coenzyme Q binding site mutations were observed in 33% o
52 amino acid changes in one of the ubiquinone (coenzyme Q) binding sites (Qo).
53 est that the np 14459 mutation may alter the coenzyme Q-binding site of complex I.
54 and enables autophosphorylation but inhibits coenzyme Q biosynthesis in vivo, demonstrating functiona
55 atter gene has been shown to be required for coenzyme Q biosynthesis in yeast and bacteria.
56  a nonfermentable carbon source and restored coenzyme Q biosynthesis, although at lower levels than t
57 ntrol of several metabolic processes such as coenzyme Q biosynthesis, assuring an appropriate energy
58 athway, which is necessary for mitochondrial coenzyme Q biosynthesis.
59  role in bacterial ubiquinone (also known as coenzyme Q) biosynthesis or microbial biodegradation of
60 rnesylated analogues of intermediates in the coenzyme Q biosynthetic pathway as substrates showed tha
61  Coq9p may either catalyze a reaction in the coenzyme Q biosynthetic pathway or have a regulatory rol
62 yme Q by the other proteins constituting the coenzyme Q biosynthetic pathway.
63      Here we present physical evidence for a coenzyme Q-biosynthetic polypeptide complex in isolated
64                         Rosuvastatin reduced coenzyme Q but there was no interaction between coenzyme
65                         Rosuvastatin reduced coenzyme Q, but even in patients with a low baseline coe
66 amination and ultimately its conversion into coenzyme Q by the other proteins constituting the coenzy
67                          Patients with lower coenzyme Q concentrations were older and had more advanc
68 y shuttling elections from NADH and FADH2 to coenzyme Q (CoQ) and cytochrome c.
69 d its human homolog ALDH3A1 to mitochondrial coenzyme Q (CoQ) biosynthesis, an essential pathway disr
70 mitochondrial matrix octapeptidase Oct1p and coenzyme Q (CoQ) biosynthesis-a pathway essential for mi
71 gene in Providencia stuartii is required for coenzyme Q (CoQ) biosynthesis.
72 n to knock down expression of enzymes in the Coenzyme Q (CoQ) biosynthetic pathway.
73 t the relative amounts of the ubiquinones or coenzyme Q (CoQ) homologues, CoQ9 and CoQ10, are related
74 6.99.2] functions to maintain membrane-bound coenzyme Q (CoQ) in its reduced antioxidant state, there
75                                              Coenzyme Q (CoQ) is an essential lipid of cells present
76                                              Coenzyme Q (CoQ) is an isoprenylated quinone that is ess
77                                              Coenzyme Q (CoQ) is utilized as the oxidant.
78 erated) have a programmed deficit in cardiac coenzyme Q (CoQ) that was associated with accelerated ca
79 ring flavoprotein that shuttles electrons to coenzyme Q (CoQ).
80 erting lanostane to ergostane triterpenoids, coenzymes Q (COQ) for antroquinonol biosynthesis in myce
81                          The biosynthesis of coenzyme Q from pABA requires a deamination reaction at
82  deletion in COQ7 leading to a deficiency in coenzyme Q had a much more severe thermosensitivity phen
83                                We found that coenzyme Q had no effect on the fatty acid-dependent pro
84 ynthesis of sterols, carotenoids, dolichols, coenzyme Q, heme a and farnesylated proteins.
85                            We measured serum coenzyme Q in 1,191 patients with ischemic systolic hear
86               The isoprenylated benzoquinone coenzyme Q is a redox-active lipid essential for electro
87 rpose of this study was to determine whether coenzyme Q is an independent predictor of prognosis in h
88                             We conclude that coenzyme Q is not a cofactor of UCP-mediated proton tran
89                                              Coenzyme Q is not an independent prognostic variable in
90                                  Ubiquinone (coenzyme Q) is a lipid that transports electrons in the
91                    Ubiquinone (also known as coenzyme Q) is a ubiquitous lipid-soluble redox cofactor
92                                  Ubiquinone (coenzyme Q) is the generic name of a class of lipid-solu
93         Ubiquinone (UQ), also referred to as coenzyme Q, is a widespread lipophilic molecule in both
94 es the electrons one at a time from FMN to a coenzyme Q molecule bound in the vicinity of the junctio
95               We also examined the effect of coenzyme Q on fatty acid-catalyzed proton flux in liposo
96                                  Ubiquinone (coenzyme Q or Q) is a lipid that functions in the electr
97                                  Ubiquinone (coenzyme Q or Q) is a lipophilic metabolite that functio
98                                  Ubiquinone (coenzyme Q or Q) is an essential component of the mitoch
99 siae homologue, is essential for ubiquinone (coenzyme Q or Q) synthesis and therefore respiration.
100    RQ is structurally similar to ubiquinone (coenzyme Q or Q), a polyprenylated benzoquinone used in
101 d in the biosynthetic pathway of ubiquinone (coenzyme Q or UQ).
102 s in the biosynthetic pathway of ubiquinone (coenzyme Q, or Q).
103                                  Ubiquinone (Coenzyme Q) plays an important role in the mitochondrial
104 inates from a depletion of the mitochondrial coenzyme Q pool.
105                                              Coenzyme Q (Q or ubiquinone) is a redox active lipid com
106             Here, we show that withdrawal of coenzyme Q (Q) from the diet of wild-type nematodes exte
107                                              Coenzyme Q (Q) functions in the electron transport chain
108                                              Coenzyme Q (Q) is a lipid that functions as an electron
109                                              Coenzyme Q (Q) is a lipid that functions as an electron
110                                              Coenzyme Q (Q) is a redox active lipid essential for aer
111                                              Coenzyme Q (Q) is an essential component of the mitochon
112  Q, but even in patients with a low baseline coenzyme Q, rosuvastatin treatment was not associated wi
113 tients in the lowest compared to the highest coenzyme Q tertile in a univariate analysis (hazard rati
114         Most of the Coq proteins involved in coenzyme Q (ubiquinone or Q) biosynthesis are interdepen
115                                              Coenzyme Q (ubiquinone or Q) functions in the respirator
116                                              Coenzyme Q (ubiquinone or Q) is a crucial mitochondrial
117                                              Coenzyme Q (ubiquinone or Q) is a redox-active lipid fou
118                                              Coenzyme Q (ubiquinone or Q) is an essential lipid compo
119                                              Coenzyme Q (ubiquinone or Q) plays a well known electron
120 n which the intra-mitochondrial synthesis of coenzyme Q (ubiquinone, Q) and Q levels are profoundly d
121  a triphenylphosphonium-conjugated analog of coenzyme Q, using a rat model.
122 S to a persulfide and transfers electrons to coenzyme Q via a flavin cofactor.
123                                              Coenzyme Q was not an independent predictor of any other
124  such as COQ3, required for the synthesis of coenzyme Q, were reduced in their ability to accumulate

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