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