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1 , a lipocalin superfamily member, is a novel insulin sensitizer.
2 SH2B1 is an endogenous insulin sensitizer.
3 ns for all causes did not differ with either insulin sensitizer.
4 bolic parameters showed that R-1 and S-1 are insulin sensitizers.
5 ption factors to dial out adverse effects of insulin sensitizers.
6 ma-dependent effects transcend their role as insulin sensitizers.
7 etagogues, and thiazolidinediones, which are insulin sensitizers.
8 g a TZD and 4,700 (65.8%) were not receiving insulin sensitizers.
9 o PTP1B can act as both insulin mimetics and insulin sensitizers.
10 per se and are influenced by the actions of insulin sensitizers.
11 rget of the thiazolidinedione (TZD) class of insulin sensitizers.
12 ng adipose-derived factor that, unlike other insulin sensitizers, acts directly on the insulin recept
13 olidinediones (TZDs), a widely used class of insulin sensitizers, acutely and specifically inhibit mi
16 amma (PPAR-gamma) agonist, rosiglitazone, an insulin sensitizer and mitochondrial activator, improves
17 as thiazolidinediones (TZDs), are effective insulin sensitizers and anti-inflammatory agents, but th
18 NIDDM) and obesity, RXR agonists function as insulin sensitizers and can decrease hyperglycaemia, hyp
19 able by reduction of insulin resistance with insulin sensitizers and stringent control of hyperglycem
20 ds (thiazolidinediones (TZDs)) are important insulin sensitizers and were recently shown to indirectl
21 new class of oral antidiabetic agents, are "insulin sensitizers" and exert direct effects on the mec
23 festyle modification, lipid-lowering agents, insulin sensitizers, and treatments to reverse endocrine
26 igned to determine whether they (or similar "insulin sensitizers") decrease cardiovascular events in
27 Ertiprotafib belongs to a novel class of insulin sensitizers developed for treatment of type 2 di
29 the impaired glucose-tolerant subjects with insulin sensitizers for 10 weeks, pioglitazone (but not
30 sm and is the molecular target of a class of insulin sensitizers, genetic variants that alter Pparg g
32 t RXR-selective agonists (e.g., 3 and 4) are insulin sensitizers in rodent models of non-insulin-depe
33 compounds that serve as insulin mimetics or insulin sensitizers in skeletal muscle may be effective
34 cological PPAR-gamma ligands, widely used as insulin sensitizers in the treatment of type-2 diabetes
36 ifestyle changes (weight loss and exercise), insulin sensitizers (metformin, troglitazone), angiotens
37 d to determine the effects of treatment with insulin sensitizers on lipolysis, we measured palmitate
39 ed with decreased insulin sensitivity and if insulin sensitizers play a role in prolonging islet graf
40 ARgamma), the molecular target of a class of insulin sensitizers, regulates adipocyte differentiation
43 on in 3T3-L1 adipocytes is stimulated by the insulin sensitizer rosiglitazone and inhibited by the in
44 atherosclerosis, whereas treatment with the insulin sensitizer rosiglitazone attenuated both metabol
48 atment of insulin-resistant animals with the insulin sensitizer rosiglitazone restores vessel wall CR
52 adiponectin as an important adipose-derived insulin sensitizer that enhances fatty acid oxidation an
53 Our results demonstrate that MTZ acts as an insulin sensitizer that suppresses hepatic glucose produ
56 After a prolonged fast, FGF21 acts as an insulin sensitizer to overcome the peripheral insulin re
57 t that FGF21 functions physiologically as an insulin sensitizer under conditions of acute refeeding a
59 tin is an adipose tissue-secreted endogenous insulin sensitizer, which plays a key role as a mediator
61 rn regulate SREBP processing and thus couple insulin sensitizers with the regulation of lipid homeost
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