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1 hyperinsulinemic-euglycemic clamp and a 2-h hyperglycemic clamp.
2 n littermates (ZCL rats) before and during a hyperglycemic clamp.
3 (pot) or AIR(max), but requires conduct of a hyperglycemic clamp.
4 ons, after a 30-g oral glucose, and during a hyperglycemic clamp.
5 s (1stIR and 2ndIR) were assessed by using a hyperglycemic clamp.
6 /min) during euglycemia and after 6 hours of hyperglycemic clamp.
7 ynthesis and glucose turnover rates during a hyperglycemic clamp.
8 oral glucose challenge and hyperinsulinemic-hyperglycemic clamps.
9 normal-weight AA versus C peers during a 2-h hyperglycemic clamp (12.5 mmol/L) on two occasions: 1) i
10 sensitivity and insulin clearance and a 2-h hyperglycemic clamp (12.5 mmol/l) to assess first- and s
13 8 micromol x kg(-1) x min(-1)), and during a hyperglycemic clamp, a failure to suppress endogenous gl
16 beta-Cell function was determined with the hyperglycemic clamp and morphometric analysis of pancrea
17 d-phase insulin responses to a 2-h 13 mmol/l hyperglycemic clamp and the insulin response to a subseq
19 se-induced insulin secretion both in vivo in hyperglycemic clamps and ex vivo in isolated islets from
21 ndirect calorimetry), insulin secretion (2-h hyperglycemic clamp), and body composition (dual-energy
22 in the overnight fasting state and during a hyperglycemic clamp ( approximately 150 mg/dl) in 10 rec
25 dogs underwent a hyperinsulinemic (4x basal) hyperglycemic clamp (arterial blood glucose 146 +/- 2 mg
26 ges, glucose tolerance tests, euglycemic and hyperglycemic clamps, as well as isolated islet and peri
28 insulin release in response to i.v. glucose (hyperglycemic clamps at 250 or 350 mg/dl plasma glucose)
29 -cell function was measured with a nine-step hyperglycemic clamp before and 48 h and 14 days after th
31 rst- and second-phase insulin secretion (2-h hyperglycemic clamp), body composition and abdominal adi
32 travenous glucose tolerance test (IVGTT) and hyperglycemic clamp characterized the insulinotropic eff
36 tration curve during the first 12 min of the hyperglycemic clamp (DeltaC-pep[AUC]0-12) was inversely
37 rements, and hyperinsulinemic-euglycemic and hyperglycemic clamp experiments were performed in RLIP76
38 n and two women, BMI 32.6 +/- 0.6) underwent hyperglycemic clamping for 24 h with hourly determinatio
40 travenous glucose tolerance test (IVGTT) and hyperglycemic clamp (HGC) in 17 nondiabetic subjects (14
41 1c [HbA1c] 7.8 +/- 1.1%) or hyperinsulinemic-hyperglycemic clamp (HH) (n = 10; 44 +/- 12 years, 8 fem
42 e reabsorption was measured with the stepped hyperglycemic clamp in 15 subjects with type 2 diabetes
43 by applying mathematical modeling during the hyperglycemic clamp in 60 normal glucose tolerance (NGT)
44 ein for 150 min to create a hyperinsulinemic-hyperglycemic clamp in EX-Basal, EX-Sim, and sedentary d
46 e clearance versus insulin levels during the hyperglycemic clamp in the two small groups showed both
48 ensitivity and secretion were assessed using hyperglycemic clamps in adults and frequently sampled in
49 on GLP-1-stimulated insulin secretion during hyperglycemic clamps in nondiabetic Caucasian individual
51 sma C-peptide concentration curve during the hyperglycemic clamp increased by 22 +/- 4 and 23 +/- 4%
55 -1, we performed a five-step (1-h intervals) hyperglycemic clamp on seven heterozygous members (NM) a
56 Intravenous infusion of indinavir during hyperglycemic clamps on rats significantly suppressed th
57 intravenous glucose challenge followed by a hyperglycemic clamp protocol, during which the plasma-in
58 meostasis by hyperinsulinemic-euglycemic and hyperglycemic clamp studies and energy expenditure by in
60 Dawley rats (n = 28) were subjected to a 4-h hyperglycemic clamp study (approximately 11 mmol/l).
61 rglycemia on incretin receptor expression, a hyperglycemic clamp study was performed for 96 h with re
62 and free fatty acid (FFA) turnover using the hyperglycemic clamp technique in combination with isotop
63 ealthy subjects (HS) was conducted using the hyperglycemic clamp technique together with duodenal nut
68 active such as during fasting, diabetes, and hyperglycemic clamp, the concentration of GR mRNA increa
72 ucose infusion rates during hyperinsulinemic-hyperglycemic clamps were increased with GLUT4 overexpre
74 for hepatic glycogen synthesis and turnover, hyperglycemic clamps were performed with somatostatin [0
75 ulin secretion rates (ISR) measured during a hyperglycemic clamp with either GLP-1 receptor blockade
76 e diet [P-HFF]) underwent a hyperinsulinemic-hyperglycemic clamp with intraportal glucose infusion.
77 ut (Cx36(-/-)) mouse phenotype and performed hyperglycemic clamps with rapid sampling of insulin in C
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