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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
17            Here we show that initiation of a euglycemic-hyperinsulinemic clamp 4 h after single-legge
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
23               The OG-CLAMP method combines a euglycemic, hyperinsulinemic clamp and an oral glucose t
24 hin skeletal muscle of an awake rat during a euglycemic-hyperinsulinemic clamp and increased levels o
25                                            A euglycemic-hyperinsulinemic clamp and skeletal muscle bi
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;
32                                        Under euglycemic- hyperinsulinemic clamp conditions, indinavir
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
35                        SI was measured using euglycemic-hyperinsulinemic clamp (EGC), before (week 0
36 ere studied before and 1 month after RYGB by euglycemic hyperinsulinemic clamp (EHC), by intravenous
37                                              Euglycemic-hyperinsulinemic clamp (EHC) was preformed to
38                                              Euglycemic-hyperinsulinemic-clamp experiments further de
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
42                                              Euglycemic, hyperinsulinemic clamp (insulin clamp, n=8)
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
45                         This study using the euglycemic-hyperinsulinemic clamp method was performed i
46                                            A euglycemic-hyperinsulinemic clamp, muscle biopsy specime
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
51                Subjects were also studied by euglycemic-hyperinsulinemic clamps performed at rest and
52  skeletal muscle, and adipose tissue (with a euglycemic-hyperinsulinemic clamp procedure and isotope-
53                                            A euglycemic-hyperinsulinemic clamp procedure and stable i
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
57                  Fetuin KO mice subjected to euglycemic-hyperinsulinemic clamp show augmented sensiti
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
61                                              Euglycemic hyperinsulinemic clamp studies were performed
62                                              Euglycemic, hyperinsulinemic clamp studies indicated RYG
63 stered for 30, 60, 90, or 120 min during 2-h euglycemic, hyperinsulinemic clamp studies.
64                                              Euglycemic-hyperinsulinemic clamp studies (12 mU x kg(-1
65                                              Euglycemic-hyperinsulinemic clamp studies confirmed the
66                                              Euglycemic-hyperinsulinemic clamp studies demonstrate th
67 re assessed before (basal period) and during euglycemic-hyperinsulinemic clamp studies.
68 n PAI-1(-/-) mice on an HF diet, as shown by euglycemic-hyperinsulinemic clamp studies.
69 ications (EDC) Study and was validated using euglycemic-hyperinsulinemic clamp studies.
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
72 seline and 2 weeks after treatment using the euglycemic hyperinsulinemic clamp technique.
73 insulin action were assessed by means of the euglycemic hyperinsulinemic clamp technique.
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
79                               The next day a euglycemic hyperinsulinemic clamp test was administered.
80              Insulin sensitivity measured by euglycemic hyperinsulinemic clamp testing; subcutaneous
81                                       During euglycemic-hyperinsulinemic clamp, there is no suppressi
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
85                             In this study, a euglycemic hyperinsulinemic clamp was performed on obese
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
91                                   During the euglycemic hyperinsulinemic clamp, whole body glucose di
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
95                                    Four-hour euglycemic-hyperinsulinemic clamps with infusion of sali
96 in-resistant subjects (n = 10 each) received euglycemic-hyperinsulinemic clamps with muscle biopsies

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