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1 ed apoptosis induced by 15d-PGJ2, but not by ciglitazone.
2 vent B cell apoptosis induced by 15d-PGJ2 or ciglitazone.
3 lization by 15-deoxy-Delta(12,14)-PGJ(2) and ciglitazone.
4 porter gene response even in the presence of ciglitazone.
5 atment with 15-deoxy-Delta(12, 14)-PGJ(2) or ciglitazone.
6 5-deoxy-Delta(12,14)-PGJ(2) (15d-PGJ(2)) and ciglitazone.
7 by the PPARgamma agonists, troglitazone and ciglitazone.
8 4 mRNA is only expressed in cells exposed to ciglitazone.
11 lls, PPAR-gamma activation by 15d-PGJ(2) and ciglitazone (a synthetic ligand) leads to reduction in b
12 ed to dexamethasone and the PPARgamma ligand ciglitazone (a thiazolidinedione) resulted in expression
15 eatment of cultured human keratinocytes with ciglitazone, a PPAR-gamma activator, increases involucri
18 in vitro and in vivo antimelanoma effects of ciglitazone, a synthetic ligand-activating PPARgamma.
19 characterize the novel relationship between ciglitazone, a thiazolidinedione class of PPARgamma liga
20 l burdens were significantly lower following ciglitazone administration, which could be explained, in
24 troglitazone, two other thiazolidinediones, ciglitazone and englitazone, exhibited similar inhibitor
25 bone marrow B cells with PPARgamma agonists (ciglitazone and GW347845X) resulted in rapid apoptosis.
27 The induction of RAR beta expression by the ciglitazone and SR11237 combination was diminished by a
29 ll-trans-retinoic acid or the combination of ciglitazone and SR11237 was able to induce RAR beta in a
30 ncreased expression of PPARgamma, as well as ciglitazone and sulindac sulfide induced expression of E
31 RXRalpha agonist plus the PPARgamma agonist ciglitazone and the inhibition of 9-cis-RA-induced coact
32 xamined the effects of the PPAR gamma ligand ciglitazone and the RXR ligand SR11237 on growth and ind
34 hat various PPARalpha (nafenopin) and gamma (ciglitazone and troglitazone) agonists rapidly induced e
35 4-PGJ2 (15d-PGJ2) and synthetic ligands like ciglitazone and troglitazone, all induce apoptosis in no
37 ha (WY14643), PPARdelta (GW1514), PPARgamma (ciglitazone), and LXR (22(R)-cholesterol or TO901317) or
39 bited ABCA1 expression (while rosiglitazone, ciglitazone, and pioglitazone had little effect) and cho
40 Rgamma agonists 15-deoxy-prostaglandin-J(2), ciglitazone, and pioglitazone reduced intimal expansion,
41 PAR-gamma (including the TZDs rosiglitazone, ciglitazone, and pioglitazone, as well as the cyclopenta
42 s that the apoptotic effect of troglitazone, ciglitazone, and their PPARgamma-inactive analogues 5-[4
43 r kappaB protein kinase activity afforded by ciglitazone appeared to be a consequence of a physical i
44 activated receptor gamma (PPARgamma) agonist ciglitazone at high doses was able to mediate PPARgamma-
47 In reporter gene assays, RXR ligands and ciglitazone, but not the PPAR gamma ligand 15d-PGJ(2), c
48 ARgamma-inactive analogs of troglitazone and ciglitazone [Delta2TG (5-[4-(6-hydroxy-2,5,7,8-tetrameth
49 the specific PPARgamma agonists LY17883 and ciglitazone, demonstrate that the PPRE element confers p
50 oliferator-activated receptor gamma-inactive ciglitazone derivative, exhibits 1- and 3-order of magni
52 port here that troglitazone and another TZD, ciglitazone, dramatically inhibited mitogen-induced cell
53 d be explained, in part, by the finding that ciglitazone enhanced S. aureus phagocytosis by microglia
54 PARgamma) agonists, such as troglitazone and ciglitazone, exhibit antitumor effects; however, the und
56 effect on other cells of the immune system, ciglitazone has an enhancing effect on both iTregs and n
57 irst, the novel function of troglitazone and ciglitazone in targeting energy restriction provides a m
58 Treatment of cultured 3T3-L1 adipocytes with ciglitazone increased apoE mRNA levels by 2-4-fold in a
59 )-PGJ(2) and the synthetic PPARgamma agonist ciglitazone induced activation of caspase 3 and caspase
60 apacitative calcium entry by 2-APB prevented ciglitazone-induced EGFR transactivation and Erk activat
61 ation; here, Src activation by both TZDs and ciglitazone-induced EGFR transactivation were prevented
62 12,14)-prostaglandin J(2), troglitazone, and ciglitazone inhibited 17beta-estradiol-stimulated cell p
64 PPARgamma agonists such as rosiglitazone and ciglitazone, is coactivated by 9 cis-retinoic acid and i
65 mation and accelerate abscess encapsulation, ciglitazone may effectively sequester brain abscesses an
66 PAR gamma, 15d-PGJ2 and a thiazolidinedione, ciglitazone, mediate significant inhibition of prolifera
68 totic mechanism, the effects of 15d-PGJ2 and ciglitazone on reactive oxygen species were investigated
69 tor-activated receptor (PPAR) gamma agonists ciglitazone or 15-deoxy-Delta 12,14-prostaglandin J2 res
72 l cells with the PPAR gamma-specific agonist ciglitazone or azPC augmented cyclooxygenase-2 expressio
73 ver, topical treatment of hairless mice with ciglitazone or troglitazone increases loricrin, involucr
75 ons from intracellular stores; however, only ciglitazone produced a secondary calcium influx in the p
79 ost disease, the immunotherapeutic effect of ciglitazone requires the presence of nTregs that express
82 eatment with 9-hydroxyoctadecanoic acids and ciglitazone significantly rescued lal-/- pulmonary infla
83 lective thiazolidinedione PPARgamma agonist, ciglitazone, significantly reduced neuronal death in res
84 staglandin J2 (15d-PGJ2) or troglitazone and ciglitazone suppressed TGF-beta1-mediated alpha-smooth m
85 d Delta2CG, a PPARgamma-inactive analogue of ciglitazone, to conduct lead optimization to develop a n
87 ctivated receptor gamma (PPARgamma) ligands (ciglitazone, troglitazone, and 15-deoxy-Delta(12,14) pro
88 This neuroprotective effect of 15d-PGJ2 and ciglitazone was linked to increased PPARgamma DNA bindin
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