ライフサイエンスコーパス: antimutagenic

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1 tituting for holE when it is assayed for its antimutagenic action on the proofreading-impaired dnaQ49

2 dant activity and moderate antibacterial and antimutagenic action.

3 its antioxidant capacity contributes to its antimutagenic action.

4 The antibacterial and antimutagenic activities exhibited by zerumbone and its

5 termine bioactive compounds, antioxidant and antimutagenic activities of copaiba pulp.

6 y was designed to evaluate the mutagenic and antimutagenic activities of luteolin derivatives (luteol

7 entrifugation and tested for antioxidant and antimutagenic activities.

8 azerumbone 2 showed better antibacterial and antimutagenic activity than azazerumbone 1.

9 They exhibited significantly higher antimutagenic activity than zerumbone against Salmonella

10 y processed red-grape sample has the highest antimutagenic activity toward S. typhimurium TA98 and TA

11 The dose which showed antimutagenic activity was 100 mg kg(-1).

12 Antimutagenic activity was determined at the hypoxanthin

13 by the hole plate and MIC techniques and the antimutagenic activity was evaluated by the Ames test.

14 Chlorophyllin (CHL), an antimutagenic and anticarcinogenic water-soluble derivat

15 e compounds and to evaluate the antioxidant, antimutagenic and antimicrobial activities of the major

16 In the present study the antimutagenic and antioxidant effects of a powder of gra

17 y (RP-HPLC) and each fraction was tested for antimutagenic and antiproliferative activities.

18 The present focused on the study of the antimutagenic and antiproliferative potential of pulp Ja

19 he inhibition of NHEJ is consistent with the antimutagenic and other biological properties of vanilli

20 t time that DMT and PM can contribute to the antimutagenic and the antioxidative property of Allium v

21 onation of the active extracts produced both antimutagenic and/or antiproliferative fractions.

22 d spectrum of antioxidant, anticarcinogenic, antimutagenic, and anti-inflammatory properties makes it

23 properties that include strong antioxidant, antimutagenic, anti-inflammatory and antiarthritic effec

24 -inflammatory, antimicrobial, antiparasitic, antimutagenic, chemopreventive and chemotherapeutic acti

25 ndicating a heretofore unknown and redundant antimutagenic effect of these repair polymerases.

26 tion of IM and an antioxidant exerted better antimutagenic effect than an antioxidant alone.

27 ty assays, these luteolin derivatives showed antimutagenic effects in deletion and intrachromosomal r

28 acity, the highest dose of copaiba showed no antimutagenic effects in the in vivo study.

29 tinoside and luteolin 7-O-glucuronide showed antimutagenic effects on TA1537 and TA1535 strains.

30 ant, antiinflammatory, anticarcinogenic, and antimutagenic effects.

31 these tests, all compounds were shown to be antimutagenic in more than one strain and various mechan

32 DNA mismatch repair is a conserved antimutagenic pathway that maintains genomic stability t

33 se IV (Pol IV), encoded by dinB; most of the antimutagenic phenotype of the ppk mutant disappears in

34 study, we aimed to examine the mutagenic and antimutagenic potencies of three luteolin derivatives (l

35 The clarification of differences in antimutagenic potency of these luteolin derivatives base

36 hat these luteolin derivatives have stronger antimutagenic properties against ethyl methanesulfonate

37 Our findings showed that the antimutagenic properties of luteolin derivatives on TA15

38 Here, we show that the antimutagenic property of nm23-H2 in E. coli is independ

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