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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 airment in diastolic function in diabetic rat hearts, which were normalized by all three treatments.
6 ood pressure (BP) were also higher in Snx1(-/-) mice, which were normalized by apocynin, a drug that prevents NOX assembl
7 brosis markers (sirius red, hydroxyproline, and collagen-1) were normalized by both modes of CVC administration.
8  blood pressure of Ang II-infused rats and plasma Hcy level were normalized by BT consumption.
9 cumbens associated with stimulus cue-induced heroin seeking were normalized by CBD treatment.
10 branched-chain amino acids (BCAAs), whereas both parameters were normalized by chronic treatment with metformin (Met).
11 type (WT) mice, including an increase in Bacteroides, which were normalized by CR.
12 re upregulated in MRL/lpr mice compared with MRL/+ mice and were normalized by Crry-Ig treatment, suggesting that the pro
13 rves of three patients, and all the excitability parameters were normalized by depolarization.
14                                                 The results were normalized by different combinations of 7 control microR
15                                                  ADC values were normalized by dividing ADC values of tumors by those of
16                                        Hospital margin data were normalized by dividing by a constant such that the highe
17                                         These abnormalities were normalized by exogenously acidifying the SC, suggesting
18 n myocardial gene and protein expression altered by MI that were normalized by GGF2 treatment, many of which are involved
19           Although elevated plasma levels of corticosterone were normalized by i.v. leptin infusion at a dose that raises
20                                                         All were normalized by IL-10.
21 acrophage content, were reversed when plasma insulin levels were normalized by insulin supplementation.
22 o decrease corticotropin-releasing hormone (CRH) expression were normalized by insulin treatment, whereas the expression
23 nhanced cell death and sensitivity to Abeta toxicity, which were normalized by interfering with the InsP(3)R-CAMKIV-CREB
24 ione transferase genes and elevated total glutathione level were normalized by KD.
25 r at least 1 year of hyperglycemia, and these abnormalities were normalized by multi-antioxidant therapy.
26                         Gene expression in tumor cells that were normalized by neighboring nontransformed cells was used
27 MP production and decrease in Na(+) transport, effects that were normalized by over-expression of SNX1.
28             Tonotopicity and frequency-response selectivity were normalized by perceptual training.
29 y rats and patients with advanced diabetic nephropathy, and were normalized by pharmacological inhibition of the renin-an
30  (Px) hyperglycemic rats, with recovery when glucose levels were normalized by phlorizin.
31 ptor and cytokine gene expression in the spinal cord, which were normalized by postnatal colonization with microbiota fro
32 s and decreased marrow B220(+) (B-lymphocytic) cells, which were normalized by PTH.
33                                             When all biomes were normalized by rainfall, shrublands however, were most ef
34                The properties of the ileal mucus of CF mice were normalized by secretion into a high concentration sodium
35 tinence have different synaptic expression mechanisms, they were normalized by stimulation of D1DRs.
36 ns are elevated compared with controls, and PPG projections were normalized by targeted rescue of leptin receptors in Lep
37 nduced regulatory changes in CSAD, CDO, and GOT1 expression were normalized by taurine supplementation, indicating that c
38 %), or Rp-cAMP (competitive inhibitor of cAMP; -56 +/- 4%); were normalized by tempol; but were unaffected by ICI-118,551
39 om t-PA-null mice were hyporesponsive to EFS (P<0.0001) but were normalized by the addition of rt-PA.
40                           All of these amygdala disruptions were normalized by the additional deletion of the p21 protein
41 in the hippocampus and shifts in the microbiota composition were normalized by the enriched diet.
42     Patients' exaggerated anxiety responses to pentagastrin were normalized by the intervention.
43                                       Registered DNP images were normalized by the mean to estimate perfusion redistribut
44                                Isomerization rate constants were normalized by the number of accessible protons, measured
45               When the EC QCM biosensor Deltaf shift values were normalized by the number of ECs found firmly attached to
46  proliferation were increased in podocan-deficient SMCs and were normalized by transfection with the wild-type podocan ge
47                                                 dATP levels were normalized by treatment with either carbobenzoxy-Val-Ala
48 and virus-induced cell death was enhanced; these conditions were normalized by treatment with interferon alfa-2b or after
49                                        These graph measures were normalized by values obtained in equivalent random netwo
50 model for routine chest and abdominopelvic examinations and were normalized by volume CT dose index (CTDI(vol)).