ライフサイエンスコーパス: pelleted

1 luble fraction with retention of much of the pelleted activity concomitant with extensive protein deg

2 The cells were pelleted and lysed, and the levels of lipid peroxidation

3 Partially inhibited enzyme could be rapidly pelleted and resuspended in NENMBA-free buffer and inhib

4 The cells were pelleted, and ribonucleic acid (RNA) was extracted by us

5 the rightward displacement seen in morphine-pelleted animals.

6 of a P15 fraction (the cell fraction that is pelleted at 15,000 x g) from cells infected with recombi

7 The nebulin aggregates were pelleted by centrifugation at 5200 x g, whereas the acti

8 4-ml aliquot was removed, and the cells were pelleted by centrifugation.

9 inal cleavage fragment of Glycogag which was pelleted by high-speed centrifugation and sedimented in

10 To establish DS, rats were inoculated with pelleted Candida albicans, which resulted in sustained c

11 gm, there was no difference between morphine-pelleted (dependent) and placebo-pelleted (non-dependent

12 to conventional rats fed a basic PRM diet (a pelleted diet containing cereal meals, soybean meals, wh

13 mosquitoes in the laboratory, including two pelleted diets, Dr.

14 Fourier-transform IR (FT-IR) spectra of pelleted exfoliated cervical cells from patients with ce

15 tivation in the soluble fraction than in the pelleted fraction.

16 HIV type 1 virions are pelleted from up to 1 ml of plasma, gently lysed with a

17 was increased relative to respective control pelleted islet grafts.

18 sed in matrigel was also better than that of pelleted islets (5/8 islet-matrigel implanted mice vs. 1

19 mplanted mice vs. 1/7 mice transplanted with pelleted islets cured by one month).

20 After one month 1/6 mice transplanted with pelleted islets cured compared to 5/6 mice transplanted

21 ained near normal morphology, in contrast to pelleted islets, where individual islets fused to form l

22 nzamide], a delta agonist, in the naltrexone-pelleted KI animals resulted in a dose-dependent inducti

23 The two methods using pelleted material from positive culture bottles performe

24 creasing the intestinal motility in morphine-pelleted mice (ED(50) = 0.03 mg/kg).

25 effect of acute morphine compared to placebo-pelleted mice in the tail immersion test.

26 The morphine-pelleted mice showed a 5.5-fold tolerance to the antinoc

27 also conducted to determine whether morphine-pelleted mice were physically dependent when pre-treated

28 /mouse; a dose tested to be inert in placebo-pelleted mice) enhanced the level of morphine antinocice

29 (PAG) from morphine-pelleted versus placebo-pelleted mice, 72-h after pellet implantation.

30 antinociceptive tolerance in 3-day morphine-pelleted mice.

31 en morphine-pelleted (dependent) and placebo-pelleted (non-dependent) rats in place preference at any

32 id not change response thresholds in placebo-pelleted rats but blocked opioid-induced pain.

33 lter the intrathecal morphine DRC in placebo-pelleted rats but blocked the rightward displacement see

34 Placebo-pelleted rats did not show enhanced preference after re-

35 However, these same morphine-pelleted rats expressed significantly increased preferen

36 nhanced evoked release of CGRP from morphine-pelleted rats was blocked by dynorphin antiserum or by p

37 eptive dose-response curve (DRC) in morphine-pelleted rats was displaced to the right of that in plac

38 ous morphine antinociceptive DRC in morphine-pelleted rats was displaced to the right of that in plac

39 as displaced to the right of that in placebo-pelleted rats, indicating antinociceptive "tolerance." R

40 In placebo-pelleted rats, the toxin injection did not alter behavio

41 itization of dorsal horn neurons in morphine-pelleted rats, we injected morphine-tolerant and control

42 as displaced to the right of that in placebo-pelleted rats; this right shift was blocked by RVM lidoc

43 The membranes were pelleted, supernatant with unbound antibody was removed,

44 Contact angle of water on esters' pelleted surface increased as the hydrophobicity increas

45 Previous studies on the drug content of pelleted tubulin polymers suggest that peloruside A bind

46 riaqueductal gray matter (PAG) from morphine-pelleted versus placebo-pelleted mice, 72-h after pellet

47 elopes was demonstrated by immunoblotting of pelleted virions and their specific attachment to Kit re

48 While drug-naive mice pelleted with a 75 mg morphine pellet for 3 days develop

49 The aggregate formed rapidly and pelleted with low speed centrifugation.

50 In binding assays, some calmodulin pelleted with Myo1c heavy chain when actin was present,

51 nts showed that gastric ezrin selectively co-pelleted with the beta-actin isoform and only very poorl

52 In ATP a smaller proportion of calmodulin pelleted with the heavy chain, suggesting that Myo1c und