ライフサイエンスコーパス: aminosalicylic acid

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1 tment with infliximab (0.36; P = .0005) or 5-aminosalicylic acid (0.44; P < .0001) were associated wi

2 The 5-aminosalicylic acid (5-ASA) agents and oral steroids rem

3 We recently reported that 5-aminosalicylic acid (5-ASA) inhibits TNFalpha-regulated

4 L-1-mediated COX-2 gene expression whereas 5-aminosalicylic acid (5-ASA) or indomethacin had no effec

5 AIDs) 4-aminophenylacetic acid (4-APAA) or 5-aminosalicylic acid (5-ASA) with peptides, including an

6 nd its metabolites, sulfapyridine (SP) and 5-aminosalicylic acid (5-ASA), on components of angiogenes

7 ory drugs (OR, 0.1; 95% CI: 0.03-0.5), and 5-aminosalicylic acid agents (OR, 0.4; 95% CI: 0.2-0.9), a

8 sulfasalazine (SSZ) with its two moieties, 5-aminosalicylic acid (ASA) and sulfapyridine (SP), in pat

9 , and smoking and drug history (mesalamine 5-aminosalicylic acid, azathioprine, and folate).

10 , ofloxacin, moxifloxacin, ethionamide, para-aminosalicylic acid, cycloserine, and linezolid.

11 Corticosteroids, 5-aminosalicylic acid derivatives, immunomodulators, and m

12 Treatments for ulcerative colitis include 5-aminosalicylic acid drugs, steroids, and immunosuppressa

13 Two lanthanide complexes, namely 5-aminosalicylic acid ethylenediaminetetraacetate europium

14 aacetate europium(III) (5As-EDTA-Eu3+) and 4-aminosalicylic acid ethylenediaminetetraacetate terbium(

15 Streptomycin and para-aminosalicylic acid had just been discovered; the discov

16 nventional therapy, once daily therapy for 5-aminosalicylic acid is generally sufficient.

17 , ofloxacin, moxifloxacin, ethionamide, para-aminosalicylic acid, linezolid, and cycloserine and comp

18 Furthermore, a new 5-aminosalicylic acid (mesalamine MMX) has been released t

19 Derivatives of 5-aminosalicylic acid (mesalamine) represent a mainstay in

20 eatment with a regimen based on capreomycin, aminosalicylic acid, or both).

21 quency of dosing for standard 4-g doses of p-aminosalicylic acid (PAS) granules.

22 para-Aminosalicylic acid (PAS) is one of the antimycobacteria

23 ti-infective target, and the antifolate para-aminosalicylic acid (PAS) was one of the first anti-infe

24 synthase (DHPS), such as sulfonamides and p-aminosalicylic acid (PAS), we hypothesized that bacteria

25 use of second-line antibiotics such as para-aminosalicylic acid (PAS).

26 ification; and use of sulfasalazine, other 5-aminosalicylic acid preparations, prednisone, cyclospori

27 Surveillance colonoscopy and 5-aminosalicylic acid therapy may mitigate cancer risk, bu

28 wed by acylation with N-hydroxysuccinimide p-aminosalicylic acid to form the final product, i.e., 5-[

29 sensitization of Eu3+ is accomplished with 5-aminosalicylic acid, which provides energy transfer for

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