ライフサイエンスコーパス: were normalized by

1 contents were increased following trauma-hemorrhage, which were normalized by 17beta-estradiol.

2 oreover, the reciprocal changes in iNOS and eNOS expression were normalized by 1D11.

3 nts were also decreased in OFC of ketamine-treated rats and were normalized by activation of alpha4beta2 nAChRs.

4 sceromotor responses to colorectal distention in STZ-D rats were normalized by administration of MAPK inhibitor U0126.

5 induced increases in neostriatal DOPAC/DA and HVA/DA ratios were normalized by age/food-deprivation while that of 3MT/DA

6 airment in diastolic function in diabetic rat hearts, which were normalized by all three treatments.

7 blood pressure of Ang II-infused rats and plasma Hcy level were normalized by BT consumption.

8 cumbens associated with stimulus cue-induced heroin seeking were normalized by CBD treatment.

9 re upregulated in MRL/lpr mice compared with MRL/+ mice and were normalized by Crry-Ig treatment, suggesting that the pro

10 rent arterioles from diabetic rats (delta = 63+/-5 nM), but were normalized by decreasing bath glucose concentration from

11 rves of three patients, and all the excitability parameters were normalized by depolarization.

12 The results were normalized by different combinations of 7 control microR

13 ADC values were normalized by dividing ADC values of tumors by those of

14 Hospital margin data were normalized by dividing by a constant such that the highe

15 These abnormalities were normalized by exogenously acidifying the SC, suggesting

16 n myocardial gene and protein expression altered by MI that were normalized by GGF2 treatment, many of which are involved

17 Although elevated plasma levels of corticosterone were normalized by i.v. leptin infusion at a dose that raises

18 All were normalized by IL-10.

19 acrophage content, were reversed when plasma insulin levels were normalized by insulin supplementation.

20 o decrease corticotropin-releasing hormone (CRH) expression were normalized by insulin treatment, whereas the expression

21 nhanced cell death and sensitivity to Abeta toxicity, which were normalized by interfering with the InsP(3)R-CAMKIV-CREB

22 ione transferase genes and elevated total glutathione level were normalized by KD.

23 r at least 1 year of hyperglycemia, and these abnormalities were normalized by multi-antioxidant therapy.

24 Gene expression in tumor cells that were normalized by neighboring nontransformed cells was used

25 Tonotopicity and frequency-response selectivity were normalized by perceptual training.

26 y rats and patients with advanced diabetic nephropathy, and were normalized by pharmacological inhibition of the renin-an

27 (Px) hyperglycemic rats, with recovery when glucose levels were normalized by phlorizin.

28 ptor and cytokine gene expression in the spinal cord, which were normalized by postnatal colonization with microbiota fro

29 s and decreased marrow B220(+) (B-lymphocytic) cells, which were normalized by PTH.

30 When all biomes were normalized by rainfall, shrublands however, were most ef

31 The properties of the ileal mucus of CF mice were normalized by secretion into a high concentration sodium

32 tinence have different synaptic expression mechanisms, they were normalized by stimulation of D1DRs.

33 nduced regulatory changes in CSAD, CDO, and GOT1 expression were normalized by taurine supplementation, indicating that c

34 %), or Rp-cAMP (competitive inhibitor of cAMP; -56 +/- 4%); were normalized by tempol; but were unaffected by ICI-118,551

35 vities resulted from abnormal myogenin-Jun-D complexes, and were normalized by the addition of Jun-D, dithiothreitol or R

36 om t-PA-null mice were hyporesponsive to EFS (P<0.0001) but were normalized by the addition of rt-PA.

37 All of these amygdala disruptions were normalized by the additional deletion of the p21 protein

38 Patients' exaggerated anxiety responses to pentagastrin were normalized by the intervention.

39 Registered DNP images were normalized by the mean to estimate perfusion redistribut

40 Isomerization rate constants were normalized by the number of accessible protons, measured

41 When the EC QCM biosensor Deltaf shift values were normalized by the number of ECs found firmly attached to

42 proliferation were increased in podocan-deficient SMCs and were normalized by transfection with the wild-type podocan ge

43 dATP levels were normalized by treatment with either carbobenzoxy-Val-Ala

44 and virus-induced cell death was enhanced; these conditions were normalized by treatment with interferon alfa-2b or after

45 model for routine chest and abdominopelvic examinations and were normalized by volume CT dose index (CTDI(vol)).