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1 H 7.4 with the addition of 20mM of synthetic glucose solution.
2 resented with a less palatable, yet caloric, glucose solution.
3 re optimized experimentally using a standard glucose solution.
4 s polarization and continuous flow of 5.0 mM glucose solution.
5 s were not adversely affected by infusion of glucose solution.
6  mg/dL) for identifying the concentration of glucose solution.
7 on of preference for the flavour of a paired glucose solution.
8 ver underwent bending when it was exposed to glucose solutions.
9 was not different among sucrose, FruGlu, and glucose solutions.
10 nking tube or intraperitoneal injection of a glucose solution (10%).
11 sucrose (0-10%) and fat (0-10%) contents and glucose solutions (10-160 mmol/L).
12 pH solutions (4, 5, 6, 7, 7.5, 8, and 9) and glucose solutions (2.5%, 5.0%, 10%, 20%, 40%, and 50%) w
13 ), ciprofloxacin (0.3%), mannitol (20%), and glucose solution (20%) were examined, and their permeabi
14               Another group of rats received glucose solution (20%, 5 ml IP) 30 minutes before testin
15 ion; clinical need of fluid therapy with 10% glucose solution; a history of diabetes, diabetic ketoac
16  records for those treatments (high-strength glucose solution and glucagon) commonly given to reverse
17 n was induced in vitro by incubation in high-glucose solutions and in vivo by acetaminophen toxicity.
18 t the consumption or a single injection of a glucose solution at the onset of the feeding cycle simil
19 terization of optical rotatory dispersion of glucose solutions at two-peak and three-peak narrowband
20                  Compared with the reference glucose solution, beer had no significant effect on gluc
21      Supplemental treatment of newborns with glucose solution can be a convenient and efficient metho
22 faster when rinsing their mouths with a 6.4% glucose solution compared with a placebo containing sacc
23                  Specifically, a 10% (wt/wt) glucose solution containing a catalytic amount of Sn-Bet
24 level was maintained by perfusion with 30-mM glucose solution delivered from a surgically implanted o
25 ched exponential dynamics that we fit to the glucose solution experimental data at short times.
26 0-fold in AQP1-null lenses bathed in a 55-mM glucose solution for 18 hours.
27               Tests performed in different D-Glucose solutions have revealed a limit of detection clo
28 or a 4 % glucose solution (Lo-Glu) or a 22 % glucose solution (Hi-Glu) during exercise.
29            Automated amperometric sensing of glucose solutions in microtiter-plate wells used compute
30        Parenteral administration of 2.2 g/kg glucose solution increased the blood glucose concentrati
31      Introducing fructose but not lysine and glucose solutions into the lumen increased by 2- to 10-f
32 nd subsequent prolotherapy with hyperosmolar glucose solution is safe, effective, inexpensive, and vi
33 is reactivity is achieved also when a 45 wt% glucose solution is used.
34 e and ingested either water (Fast), or a 4 % glucose solution (Lo-Glu) or a 22 % glucose solution (Hi
35 Thirteen healthy subjects consumed 50 g oral glucose solution mixed with d-xylose during fixed hyperg
36 n, animals were randomized to receive either glucose solution or saline solution before the induced i
37 e sensor alternately to 0 and 100 mM aqueous glucose solutions (pH approximately 7).
38 let oxygen was also detected in fructose and glucose solutions prepared in phosphate buffer.
39            Five minutes before access to the glucose solution, rats were injected with dose pairs of
40 6 mm3 in the animals that received saline or glucose solution, respectively (p = .005), and reducing
41 he animals that received saline solution and glucose solution, respectively (p = .038).
42                  Compared with the reference glucose solution, the glucose solution with alcohol prod
43  the potential of 0.7 V in steps of adding a glucose solution to a potassium phosphate buffer.
44 includes adding a small drop of concentrated glucose solution to the sample in the NMR tube, mixing,
45 ielded sandwich complex was transferred to a glucose solution to trigger an enzymatic reaction to pro
46 abricated LPG sensor was tested on different glucose solutions to record the transmission spectra on
47 solution with alcohol once and the reference glucose solution twice.
48  growth in the wild, rather than in the high-glucose solutions used in most laboratory studies, they
49                The repeatability for a 4.0mM glucose solution was 1.0%.The method was validated by co
50                                After drying, glucose solution was added to the paper, on the opposite
51  In a third trial (150 min duration), an 18% glucose solution was infused (GI) at a rate that maintai
52 num was also cannulated and a fasting saline-glucose solution was infused overnight at 3 mL/h.
53                             Using an aqueous glucose solution, we now extended the technique to froze
54  1.0, 1.5 and 2.0 uM of starch with 2.5 uM D-glucose solutions were coated over freshly harvested cuc
55                                    Also, all glucose solutions were deleterious to RPE (P < .001) eve
56 5 g available carbohydrate, and the beer and glucose solution with alcohol contained 21 g alcohol.
57  alcohol by volume, nonalcoholic beer, and a glucose solution with alcohol once and the reference glu
58 red with the reference glucose solution, the glucose solution with alcohol produced an 18% higher pos
59 travenous administration of 20% hyperosmotic glucose solution with dialysis and pan-retinal photocoag