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1 re-engineered component of glucometers: PQQ-glucose dehydrogenase.
2 ferentiated fiber cells also contain SDH and glucose dehydrogenase.
3 A (or ugd) that is predicted to encode a UDP-glucose dehydrogenase.
4 , that encodes a homologue of vertebrate UDP-glucose dehydrogenase.
5 ed with high similarity to the family of UDP-glucose dehydrogenases.
6 a series of binary and ternary complexes of glucose dehydrogenase, an MDR enzyme from Haloferax medi
12 second film (F2) contained also added enzyme glucose dehydrogenase and its cofactor beta-nicotinamide
13 ctate with using D-sorbitol dehydrogenase, D-glucose dehydrogenase and L-lactate dehydrogenase respec
14 that sqv-4 encodes a protein similar to UDP-glucose dehydrogenases and showed that the SQV-4 protein
15 arboxylethyl)-l-norvaline dehydrogenase, UDP-glucose dehydrogenase, and 6-phosphogluconate dehydrogen
16 minomethylpyridine)Cl].PF6, an FAD-dependent glucose dehydrogenase, and carbon nanotubes achieve curr
17 sed of three enzymes (alcohol dehydrogenase, glucose dehydrogenase, and glucose oxidase) operating in
20 which encodes a protein with homology to UDP-glucose dehydrogenase, compromise the synthesis of both
22 In this study, a novel fungus FAD dependent glucose dehydrogenase, derived from Aspergillus niger (A
23 he effect of possible contaminating enzymes (glucose dehydrogenase, EC 1.1.1.47; glucose 6-phosphatas
24 n aqueous solution, of the bacterial soluble glucose dehydrogenase enzyme.PQQ.glucose complex and int
25 nascus thermophilus or soluble PQQ-dependent glucose dehydrogenase from Acinetobacter calcoaceticus.
26 the IPUT1 gene together with genes for a UDP-glucose dehydrogenase from Arabidopsis and a human UDP-G
27 flavin adenine dinucleotide (FAD)-dependent glucose dehydrogenase from Glomerella cingulata (GcGDH)
28 s Blue-Reinecke salt, coated with the enzyme glucose dehydrogenase (from Bacillus sp.), and nicotinam
29 imary objectives were to: a) introduce a new glucose dehydrogenase (GD)-based electrochemical biosens
30 ors were developed using the model system of glucose dehydrogenase (GDH) and its nicotinamide adenine
31 a dealloyed nanoporous gold (NPG) supported glucose dehydrogenase (GDH) bioanode, immobilised with t
32 lectrode based on the covalent attachment of glucose dehydrogenase (GDH) enzyme and safranin O to ami
33 es are being explored for efficiently wiring glucose dehydrogenase (GDh) enzymes capable of glucose (
34 s explored in order to covalently immobilize glucose dehydrogenase (GDH) in the CNT-CHIT films using
35 Flavin-adenine dinucleotide (FAD) dependent glucose dehydrogenase (GDH) is a thermostable, oxygen in
36 , which can be concurrently regenerated by a glucose dehydrogenase (GDH) using only 1.2 equiv of gluc
39 PQQ, the prosthetic group of the apo-enzyme glucose dehydrogenase (GDH), are used as the label to pr
40 (PQQ), the prosthetic group of the apoenzyme glucose dehydrogenase (GDH), are used to detect membrane
43 nalyzed nucleotide sequence variation at the Glucose dehydrogenase (Gld) locus from four populations
44 (Adh), Alcohol dehydrogenase related (Adhr), Glucose dehydrogenase (Gld), and rosy (ry) genes (totali
45 ur immunity-related enzymes (phenol oxidase, glucose dehydrogenase, glucose oxidase, and lysozyme) we
46 substrate complex of a similar quinoprotein, glucose dehydrogenase, has recently been reported that s
48 f cps2K, cps2J, or cps2H, which encode a UDP-glucose dehydrogenase necessary for side chain synthesis
49 systems of S. typhimurium; ugd, encoding UDP-glucose dehydrogenase; phoP, indicative that the phoPQ o
50 group 2 dehydrin proteins (pPCB2), a barely glucose dehydrogenase (pPCB6) and the glutathione S-tran
51 cally modified with pyrroloquinoline quinone glucose dehydrogenase (PQQ-GDH) and bilirubin oxidase (B
52 es with redox enzymes, pyroquinoline quinone glucose dehydrogenase (PQQ-GDH) and laccase functioning
53 ogeneous reconstitution of the PQQ-dependent glucose dehydrogenase (PQQ-GDH) through the specific bin
54 hanism of electron transfer in PQQ-dependent glucose dehydrogenase (PQQ-sGDH) anodes has been determi
55 bling pyrroloquinoline quinone (PQQ)-soluble glucose dehydrogenase (PQQ-sGDH) from Acinetobacter calc
56 the anode pyrroloquinoline quinone dependent glucose dehydrogenase ((PQQ)GDH) has been immobilized on
57 ate arose predominantly by the action of UDP-glucose dehydrogenase rather than through the postulated
58 la Sugarless, a uridine 5'-diphosphate (UDP)-glucose dehydrogenase required for heparan sulfate, chon
59 arison of the GMD structure with that of UDP-glucose dehydrogenase reveals the structural basis of su
60 Asd and Acinetobacter calcoaceticus soluble glucose dehydrogenase (sGdh), with major structural diff
61 that Gcd1 encodes a novel NADP(+)-dependent glucose dehydrogenase that acts in a pathway with the Id
62 ort the crystal structure of the apo form of glucose dehydrogenase to a resolution of 1.8 A and a com
64 r dehydrogenase-based biosensing by allowing glucose dehydrogenase to spontaneously adsorb onto the N
66 induces transcription of the Salmonella UDP-glucose dehydrogenase ugd gene in an RcsA- and RcsB-depe
70 n zebrafish revealed a critical role for UDP-glucose dehydrogenase (UGDH) in valve development, so th
74 disrupts the single mouse gene encoding UDP-glucose dehydrogenase (Ugdh), an enzyme required for the
75 have generated a mesenchymal ablation of UDP-glucose dehydrogenase (Ugdh), an essential biosynthetic
76 aphite with glucose oxidase or FAD-dependent glucose dehydrogenase using a range of crosslinkers and
82 ation of glucose by Thermoplasma acidophilum glucose dehydrogenase with the concomitant oxidation of
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