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

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