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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.
9 one (2), as had been previously reported for ciglitazone (1).
10  and every hour thereafter, animals received ciglitazone (10 mg/kg) or vehicle intraperitoneally.
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
13                    Both sulindac sulfide and ciglitazone, a defined peroxisome proliferator-activated
14                                              Ciglitazone, a peroxisome proliferator-activated recepto
15 eatment of cultured human keratinocytes with ciglitazone, a PPAR-gamma activator, increases involucri
16                                              Ciglitazone, a PPAR-gamma agonist with anti-inflammatory
17                                              Ciglitazone, a PPARgamma ligand, consistently decreased
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
21                                Unexpectedly, ciglitazone also accelerated brain abscess encapsulation
22                                              Ciglitazone also suppressed HIV-1 mRNA levels as measure
23                                              Ciglitazone ameliorates the inflammatory response and ma
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.
26              The thiazolidinedione moiety of ciglitazone and its analogues can be replaced by an alph
27  The induction of RAR beta expression by the ciglitazone and SR11237 combination was diminished by a
28                Our results demonstrated that ciglitazone and SR11237 cooperatively inhibited the grow
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
33                          In this study, both ciglitazone and troglitazone increased Src activation.
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
36      Our laboratory has shown that two TZDs, ciglitazone and troglitazone, rapidly induce calcium-dep
37 ha (WY14643), PPARdelta (GW1514), PPARgamma (ciglitazone), and LXR (22(R)-cholesterol or TO901317) or
38           The combination of low-dose MK886, ciglitazone, and 13-cis-retinoic acid interacted at leas
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-
45                                 In addition, ciglitazone attenuated the expression of select inflamma
46                                              Ciglitazone, but not 15d-PGJ(2), strongly induced RAR be
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
51 t of human monocyte-derived macrophages with ciglitazone did not regulate expression of apoE.
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
55 liferator-activated receptor-gamma activator ciglitazone had only a moderate effect.
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
63                        The PPARgamma agonist ciglitazone inhibited HIV-1 replication in a dose-depend
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
67               We investigated the effects of ciglitazone on lung inflammation after severe hemorrhage
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
70                       In vivo treatment with ciglitazone or 15d-PGJ(2) ameliorated hypotension and su
71                  Furthermore, treatment with ciglitazone or 15d-PGJ(2) up-regulated the expression of
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
74                            15d-PGJ2, but not ciglitazone, potently induced reactive oxygen species in
75 ons from intracellular stores; however, only ciglitazone produced a secondary calcium influx in the p
76                                              Ciglitazone rapidly activates extracellular signal-regul
77                        In addition, cyPG and ciglitazone reduced HIV replication in latently infected
78              In addition, 15d-PGJ(2) but not ciglitazone reduces expression of CD69 in human NK cells
79 ost disease, the immunotherapeutic effect of ciglitazone requires the presence of nTregs that express
80                                    In vitro, ciglitazone significantly enhances generation of iTregs
81                               Treatment with ciglitazone significantly reduced inhibitor kappaB prote
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
86                                              Ciglitazone treatment ameliorated mean arterial pressure
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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