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1                                         While the DeltaF508 mice had a normal immune cell repertoire, unchanged serum imm
2 ) analyses showed that 100% of male and female Erk5 (fl/fl) mice had a severely deformed curved thoracic spine, with an a
3 HR), OVA allergen-challenged Ormdl3(Delta2-3/Delta2-3)/CC10 mice had a significant increase in AHR compared with wild-typ
4                               We showed that JNK1-deficient mice had a significantly higher survival rate than wild-type
5                          The bone marrow cells of Dnmt3a+/- mice had a subtle but statistically significant DNA hypomethy
6 d on the brain cytokine levels, MAV-1-infected Unc93b1(-/-) mice had a very different inflammatory profile from infected
7                                                   Notch2HCS mice had an increase in CD21/35(high)CD23(-) splenic MZ B cel
8                                  Nod2-deficient (Nod2(-/-)) mice had an inherently altered skin microbiome compared with
9                                            Septic fabpi-TAg mice had an unexpected increase in villus proliferation compa
10                                     Biochemically, Rrh(-/-) mice had approximately 2-fold higher vitamin A (all-trans-ret
11                                                         SEC mice had decreased lipogenesis mediated by hepatic cholestero
12                          M. tuberculosis-infected IL-21R KO mice had enhanced bacterial burden and reduced infiltration o
13 e with maternal separation and from Sox9(flox/flox)-vil-cre mice had evidence for intestinal dysbiosis of the microbiota,
14  Compared with wild-type controls, HAT-L4-deficient newborn mice had greater body fluid loss and higher mortality in a tr
15                                                      SC-Dep mice had >93% depletion of satellite cells compared to SC-WT
16                                              On chow, JAK2L mice had hepatic steatosis and severe whole-body and hepatic
17           At early but not at later stages of infection, WT mice had higher circulatory proinflammatory cytokines and low
18                               Lgr5(Creert2)/Met(fl/fl)/LacZ mice had impaired regeneration of MET-deficient ISCs.
19                               In addition, fasted Tgr5(-/-) mice had increased activation of hepatic growth hormone-signa
20                                       At 24 hours, Darc(E2) mice had increased airway hyperresponsiveness; however, at 7
21              Hyperplastic livers and tumors from YAP(S127A) mice had increased CIN25 and CIN70 gene expression patterns,
22                               Aortic tissue from Micu2(-/-) mice had increased expression of extracellular matrix remodel
23                                                       KERKO mice had increased LH pulse frequency, indicating loss of neg
24    Uterine neoplasms, myometria and jaw bones of Cdc73(+/-) mice had increased proliferation rates that were 2-fold highe
25                                                Hdc(-/-) HFD mice had increased steatosis compared with WT HFD mice.
26 n/+) mice, resulting from the cross of V33 with Apc (Min/+) mice, had increased intestinal tumor burden compared with lit
27 ior to the onset of photoreceptor degeneration, Mertk (-/-) mice had less accumulation of retinyl esters and dysregulatio
28 d for normal platelet exocytosis or hemostasis, VAMP-3(-/-) mice had less platelet-associated Fg, indicating a defect in
29 ional studies showed that, on a high-salt diet, Tmem27(Y/-) mice had lower renal blood flow, higher abundance of renal so
30                                            Folate deficient mice had lower serum folate (-60%).
31                   In contrast to C3(-/-) mice, C5-deficient mice had no apparent defect in platelet activation in vitro,
32 itional knockout of MYPT1 or the knock-in mutation T853A in mice had no effect on muscarinic force responses in isolated
33                                          Although Il18(-/-) mice had normal levels of inflammatory monocytes, their NK ce
34                          Bone marrow cells from CLP-treated mice had normal OC precursor frequency, but formed significan
35                           By contrast, Ilk(fl/+) ;Pkhd1-Cre mice had normal renal morphology and function and survived >1
36                                        At two years, CalpTG mice had preserved kidney tissue, less vascular remodelling a
37                          Moreover, Th17 cells from 13R(-/-) mice had reduced ability to convert to Th1 cells and displaye
38                                    Intestines of Atp7b(-/-) mice had reduced Cu storage pools in intestine, Cu depletion,
39 eloid cells in the colon of DSS-treated LysM-Cre; Egfr(f/f) mice had reduced expression of interleukin 6 (IL6), and epith
40                                       Finally, CysLT1R(-/-) mice had reduced lung eosinophils and ILC2 responses after ex
41                                                      CalpTG mice had reduced macrophage infiltration with aging and CalpT
42                       In response to Ang-II, TLR4 deficient mice had reduced renal resistive index and increased renal co
43                                         Remarkably, SIRT5KO mice had reduced survival upon TAC compared with wild-type mi
44                                    Behaviorally, the mutant mice had reduced voluntary locomotion and exploration, increa
45                                        The stressor-exposed mice had significant differences in microbial community compo
46        The large polyps from the Slco2a1 (-/-) /Apc (716/+) mice had significant reductions in microvascular density, con
47 ndens stent peritonitis surgery, we observed that wild type mice had significantly elevated proinflammatory cytokine leve
48 rs in Cdc73(+/-), Cdc73(+/L)/PTH-Cre and Cdc73(L/L)/PTH-Cre mice had significantly increased proliferation, with rates >f
49                   Our data revealed that male WD-fed FXR KO mice had the most severe steatosis and highest hepatic and se
50                              At 12 months of age, P2X7-null mice had thickening of Bruchs membrane and retinal pigment ep

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