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1 nd hepatic glucose production as assessed by euglycemic hyperinsulinemic clamp.
2 althy, young male subjects was determined by euglycemic hyperinsulinemic clamp.
3 ipid or glycerol (control), rats underwent a euglycemic hyperinsulinemic clamp.
4 zed in vivo using indirect calorimetry and a euglycemic hyperinsulinemic clamp.
5 insulin sensitivity was quantitated with the euglycemic-hyperinsulinemic clamp.
6 travenous glucose tolerance test (IVGTT) and euglycemic-hyperinsulinemic clamp.
7 lucose production is impaired as assessed by euglycemic-hyperinsulinemic clamp.
8 as compared before and during AICAR with the euglycemic-hyperinsulinemic clamp.
9 out (n = 34) a family history of diabetes by euglycemic-hyperinsulinemic clamp.
10 Fifty-eight subjects also received a euglycemic-hyperinsulinemic clamp.
11 o induce insulin resistance in rats during a euglycemic-hyperinsulinemic clamp.
12 atic insulin resistance, as verified using a euglycemic/hyperinsulinemic clamp.
13 alysis with oral glucose tolerance tests and euglycemic-hyperinsulinemic clamps.
14 asured in SU and SU + MET rats by performing euglycemic-hyperinsulinemic clamps.
15 TIMPs]) in aortic tissue of male rats during euglycemic-hyperinsulinemic clamping.
16 lthy nonobese male volunteers using two-step euglycemic-hyperinsulinemic clamps (2 h at 16.6 micro g
18 and the other with insulin (0.03 U/kg) and a euglycemic hyperinsulinemic clamp (40 mU x m(-2) x min(-
19 eride content of the soleus muscle, 2) a 2-h euglycemic-hyperinsulinemic clamp (40 mU.m(-2).min(-1))
20 measurements before and at the end of a 3-h euglycemic-hyperinsulinemic clamp (40 or 240 mU x min(-1
21 of disappearance [G(R)(d)], determined using euglycemic-hyperinsulinemic clamp) 442% (P < 0.01), oral
22 educed insulin resistance, measured with the euglycemic hyperinsulinemic clamp, along with the ratio
24 hin skeletal muscle of an awake rat during a euglycemic-hyperinsulinemic clamp and increased levels o
26 glucose metabolism (insulin tolerance test, euglycemic-hyperinsulinemic clamp, and hepatic expressio
27 the basal state and during 240 pmol/m(2)/min euglycemic-hyperinsulinemic clamp, and liver (LF) subcut
28 ripheral insulin sensitivity was analyzed by euglycemic-hyperinsulinemic clamp, and molecular tools w
29 gated the association of genetic scores with euglycemic-hyperinsulinemic clamp- and oral glucose tole
30 ese, and type 2 subjects before and after an euglycemic-hyperinsulinemic clamp as well as pre-and pos
31 ; P = 0.21), or glucose disposal rates under euglycemic hyperinsulinemic clamp conditions (SMD: 0.00;
33 is of glucose homeostasis was assessed using euglycemic-hyperinsulinemic clamp coupled with tracer ra
34 er, insulin stimulation during a 100-140-min euglycemic/hyperinsulinemic clamp did not result in any
36 ere studied before and 1 month after RYGB by euglycemic hyperinsulinemic clamp (EHC), by intravenous
39 nges in glucose-6-phosphate (G-6-P) during a euglycemic-hyperinsulinemic clamp in awake Zucker fatty
40 was investigated in normal volunteers during euglycemic-hyperinsulinemic clamping in which plasma fre
41 se transport in muscle biopsies taken during euglycemic-hyperinsulinemic clamps in nondiabetic, obese
43 nsulin clamp method: subjects received a 7-h euglycemic-hyperinsulinemic clamp (insulin infusion rate
44 emulsion (liposyn) infusion during a 120-min euglycemic-hyperinsulinemic clamp led to significant red
47 Thirty patients at risk for CIM underwent euglycemic-hyperinsulinemic clamp, muscle microdialysis
48 s with infusion of saline alone (n = 16) and euglycemic-hyperinsulinemic clamps (n = 10, serum insuli
49 ct of physiological hyperinsulinemia (during euglycemic-hyperinsulinemic clamping) on free fatty acid
50 and 4 h after lowering of plasma FFAs (with euglycemic-hyperinsulinemic clamping) or after increasin
52 skeletal muscle, and adipose tissue (with a euglycemic-hyperinsulinemic clamp procedure and isotope-
54 Stable isotope tracer techniques and the euglycemic-hyperinsulinemic clamp procedure were used to
55 10 with normal glucose tolerance) using the euglycemic-hyperinsulinemic clamp procedure, before preg
56 trates that infusion of glucosamine during a euglycemic-hyperinsulinemic clamp results in marked accu
58 nondiabetic patients, 135 of whom underwent euglycemic-hyperinsulinemic clamps, showed that subjects
59 by isotope dilution, insulin sensitivity by euglycemic-hyperinsulinemic clamp (steady-state glucose
60 in vivo hepatic insulin action, we performed euglycemic hyperinsulinemic clamp studies in conscious L
70 edly enhanced glucose uptake measured during euglycemic-hyperinsulinemic clamps, suggesting a role of
71 nt measurement of insulin sensitivity by the euglycemic hyperinsulinemic clamp technique (soluble ins
74 In vivo insulin action was measured by the euglycemic-hyperinsulinemic clamp technique at a submaxi
75 was measured in 26 healthy adults using the euglycemic-hyperinsulinemic clamp technique to achieve a
76 ects for insulin sensitivity (measured using euglycemic-hyperinsulinemic clamp technique with [3-3H]g
77 dy insulin sensitivity, as determined by the euglycemic-hyperinsulinemic clamp technique, was signifi
78 onfirmed in both males and females using the euglycemic-hyperinsulinemic clamp technique; glucose dis
82 lin-stimulated glucose uptake as measured by euglycemic-hyperinsulinemic clamps throughout the course
83 of pancreas transplants, we devised a staged euglycemic hyperinsulinemic clamp to measure hepatic glu
84 entions, we conducted a meal challenge and a euglycemic-hyperinsulinemic clamp to evaluate insulin se
86 extensor digitorum longus muscle during the euglycemic-hyperinsulinemic clamp was increased in lean
87 when plasma FFA levels were elevated during euglycemic-hyperinsulinemic clamping was associated with
88 tion (a measure of NO bioavailability) after euglycemic-hyperinsulinemic clamp were blunted in the ao
89 etabolism was measured by real-time PCR, and euglycemic-hyperinsulinemic clamps were used for insulin
90 3.6 years) pre- and 3 months post-RYGB, and euglycemic-hyperinsulinemic clamps were used to assess i
92 ty in liver, muscle, and adipose tissue by a euglycemic hyperinsulinemic clamp with 3-(3)H-glucose.
93 , whole-body and muscle insulin sensitivity (euglycemic-hyperinsulinemic clamp with 2-deoxyglucose) a
94 on insulin sensitivity, as measured by using euglycemic-hyperinsulinemic clamps with infusion of [6,6
96 in-resistant subjects (n = 10 each) received euglycemic-hyperinsulinemic clamps with muscle biopsies
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