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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.
10 branched-chain amino acids (BCAAs), whereas both parameters were normalized by chronic treatment with metformin (Met).
12 re upregulated in MRL/lpr mice compared with MRL/+ mice and were normalized by Crry-Ig treatment, suggesting that the pro
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
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
25 r at least 1 year of hyperglycemia, and these abnormalities were normalized by multi-antioxidant therapy.
27 MP production and decrease in Na(+) transport, effects that were normalized by over-expression of SNX1.
29 y rats and patients with advanced diabetic nephropathy, and were normalized by pharmacological inhibition of the renin-an
31 ptor and cytokine gene expression in the spinal cord, which were normalized by postnatal colonization with microbiota fro
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.
41 in the hippocampus and shifts in the microbiota composition were normalized by the enriched diet.
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
48 and virus-induced cell death was enhanced; these conditions were normalized by treatment with interferon alfa-2b or after
50 model for routine chest and abdominopelvic examinations and were normalized by volume CT dose index (CTDI(vol)).