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1 pha-Tocopherol is both an antioxidant and an antiinflammatory agent.
2 irin is the most commonly used analgesic and antiinflammatory agent.
3 ivated protein C, a potent anticoagulant and antiinflammatory agent.
4 se of this nonpsychoactive cannabinoid as an antiinflammatory agent.
5 nts and that these effects were inhibited by antiinflammatory agents.
6 may do so more strongly in combination with antiinflammatory agents.
7 n and for some cancers that are sensitive to antiinflammatory agents.
8 e characterization of novel, mucosal sparing antiinflammatory agents.
9 ions of CpG-ODNs and downstream molecules as antiinflammatory agents.
10 Thus, n-3 PUFAs are potentially potent antiinflammatory agents.
11 y acting muscarinic cholinergic enhancers as antiinflammatory agents.
12 ors, and nitric oxide releasing nonsteroidal antiinflammatory agents.
13 ro and in vivo evidence regarding statins as antiinflammatory agents.
14 e antagonists might be useful as GI specific antiinflammatory agents.
15 rculosis in humans to evaluate the effect of antiinflammatory agents.
16 stimulus of ICAM-1 up-regulation, are potent antiinflammatory agents.
17 s or pain syndromes requiring treatment with antiinflammatory agents.
18 for the use of selective Hdac inhibitors as antiinflammatory agents.
19 tion and fibrosis, may have potential as new antiinflammatory agents.
20 ir action could be useful therapeutically as antiinflammatory agents.
21 5-position were generally quite effective as antiinflammatory agents.
22 hat the 1,2-diarylpyrroles are orally active antiinflammatory agents.
23 bitory properties, may have potential as new antiinflammatory agents.
24 have generated much interest as targets for antiinflammatory agents.
26 An enantioselective synthesis of the potent antiinflammatory agent (-)-acanthoic acid (1) is describ
28 The conjugate G5-FA-MTX acted as a potent antiinflammatory agent and reduced arthritis-induced par
29 a (Camellia sinensis) polyphenols are potent antiinflammatory agents and have been shown to inhibit N
30 al injury related to the use of nonsteroidal antiinflammatory agents and may be an important alternat
31 continued on a daily regimen of nonsteroidal antiinflammatory agents and prednisone, with a weekly su
32 Our data indicate that TIMP-4 is a potent antiinflammatory agent, and that its antiarthritis funct
33 d significantly less medication (analgesics, antiinflammatory agents, and muscle relaxants) (P< 0.001
36 ER-mediated gene expression, but is a potent antiinflammatory agent, as demonstrated in the HLA-B27 t
37 nstrate that SLPI also functions as a potent antiinflammatory agent by interfering with the signal tr
39 Leflunomide is a novel immunosuppressive and antiinflammatory agent currently being tested for treatm
41 in similar but nonidentical fashions by the antiinflammatory agents dexamethasone and sodium salicyl
43 iomarker in interventions (particularly with antiinflammatory agents) directed at slowing or halting
47 lthough Helicobacter pylori and nonsteroidal antiinflammatory agents have been identified as key pro-
49 isease, such as probiotics, antibiotics, and antiinflammatory agents, have been suggested as possible
50 ce among bacteria and the adverse effects of antiinflammatory agents highlight the need for alternati
52 this relationship prospectively, we studied antiinflammatory agents in models employing differing do
54 and act as stable, orally available powerful antiinflammatory agents in vivo with doses of 1 mg/kg.
56 One of the mechanisms by which nonsteroidal antiinflammatory agents inhibit colon carcinogenesis is
58 active protein, raising the possibility that antiinflammatory agents may have clinical benefits in pr
60 tory effects of other potent and widely used antiinflammatory agents, methotrexate and sulfasalazine,
61 We therefore determined the effect of the antiinflammatory agents montelukast (ML) and fluticasone
64 ing inflammatory pain is to use nonsteroidal antiinflammatory agents (NSAIDs) that reduce prostanoid
65 comparing aspirin, nonselective nonsteroidal antiinflammatory agents (NSAIDs), and cyclooxygenase (CO
66 nteraction between antidepressant agents and antiinflammatory agents on antidepressant-induced behavi
68 ur study provides a rationale for the use of antiinflammatory agents or NO-mimetics in the treatment
71 dietary omega-3 fatty acids and nonsteroidal antiinflammatory agents such as Celecoxib suppress colon
73 ng animals given placebo or doxycycline plus antiinflammatory agents than among those given doxycycli
74 tudies thus identify vinpocetine as a unique antiinflammatory agent that may be repositioned for the
75 and apoA-I mimetic peptides such as D-4F are antiinflammatory agents that may have therapeutic potent
76 arefully balance the therapeutic benefits of antiinflammatory agents versus the potentially negative
77 transgenic HDL to function as an antioxidant/antiinflammatory agent was associated with a decreased c
79 analysis of the clinical trials showed that antiinflammatory agents were also significantly more eff
80 n all the benefits of classical nonsteroidal antiinflammatory agents while avoiding the major side ef
82 having therapeutic potential as nonsteroidal antiinflammatory agents with an enhanced gastric safety
84 e for the combination of peripherally active antiinflammatory agents with drugs that counteract chron
85 X-2) inhibitors have been shown to be potent antiinflammatory agents with fewer side effects than cur
86 6) are particularly interesting as potential antiinflammatory agents with reduced side-effect profile
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