ライフサイエンスコーパス: enzyme test

コーパス検索結果 (１語後でソート)

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1 E(2) in 100 mM NaCl at all concentrations of enzyme tested.

2 meaningful or sustained improvement in liver enzyme testing.

3 -fold selectivity vs. a range of kinases and enzymes tested.

4 yed sub-100 nM activity against all HIV-1 RT enzymes tested.

5 nded more efficiently than 8-oxo-dGTP by all enzymes tested.

6 teins for all of the tryptophan biosynthetic enzymes tested.

7 tive blood cultures and all 14 carbapenemase enzymes tested.

8 lities in the activity of four additional KP enzymes tested.

9 Reactivation rates are equivalent for all enzymes tested (1 x 10(-)(4) s(-)(1)), indicating hydrol

10 ings may help in the interpretation of liver-enzyme tests and provide candidate genes for liver disea

11 Plasma liver-enzyme tests are widely used in the clinic for the diagn

12 was inactive against two other DNA-modifying enzymes tested as a counterscreen.

13 The rapid protocol included serum enzyme testing at 0, 3, 6 and 9h, serial electrocardiogr

14 DM-INDO bound to all enzymes tested, but only inhibited wt mCOX-2 and the V34

15 less than 5% received all recommended liver enzyme tests by the third month of continuous use.

16 values were considered, the results of liver enzyme testing could reduce the probability of an IDU ha

17 Among the different commercial enzymes tested for extraction, Celluclast 10% (36 degree

18 A polymerase was found to be the best of the enzymes tested for this purpose.

19 consists of 4 carbohydrate and 14 preformed enzyme tests, for the identification of 98 clinical isol

20 of the fraction of active molecules for each enzyme tested from both the Fpg/Nei family and HhH-GPD N

21 To date, all known fungal enzymes tested have great difficulty degrading highly cr

22 owed moderate inhibitory activity toward the enzymes tested (IC50 10-100 microM), the more complex fl

23 s more slippage in vitro than the retroviral enzymes tested including that from HIV.

24 atio of M1-1 among the human GSH transferase enzymes tested is consistent with other work in which GS

25 For each of two target enzymes tested, lipoamide dehydrogenase and mycobacteria

26 Among the enzymes tested, Nmnat1 had the strongest protective effe

27 No human microsomal cytochrome P450 enzyme tested, other than CYP3A5, supported these reacti

28 e (WT) C57BL/6 mice, as evaluated by a liver enzyme test, quantitative histology, mononuclear cell (M

29 one orientation, react more rapidly with the enzymes tested than one symmetrical parent but not both.

30 l mode of molecular recognition in which the enzyme tests the suitability of aromatic substrates befo

31 from Toxoplasma gondii (tg) were the target enzymes tested; these organisms are responsible for fata

32 For each enzyme tested, we could determine the kinetic constant f

33 Several of the enzymes tested were capable of inhibiting virus binding

34 The enzymes tested were Escherichia coli topo IV and yeast t

35 Other enzymes tested were inactivated only with severalfold hi

36 By contrast, GH3.6 and the other five enzymes tested were inactive on halogenated auxins, and

37 mited influence on the Ki values for all the enzymes tested, with the values for p. pepsin remaining

38 Among the three enzymes tested (yeast Sir2, human SIRT1, and human SIRT2

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