ライフサイエンスコーパス: compared to WT

1 ey were smaller in size and have markedly reduced bone mass compared to WT.

2 d diffusion of TCE from transgenic stems was reduced by 90% compared to WT.

3 vels of IL1beta and TNFalpha were reduced in PDE3B(-/-)mice compared to WT.

4 c conductivity of four week-old Arabidopsis thaliana plants compared to WT.

5 -2-deficient mice developed anastomotic leakage (P = 0.003) compared to WT.

6 ere independently found to be downregulated in Q175 KI mice compared to WT (5.2e-7 < P < 0.04).

7 ential binding of Abeta42 with the A2V and A2T hexapeptides compared to WT Abeta6.

8 stinct differences in metabolites in the livers of KO mice, compared to WT and Het mice.

9 consumption ratio (OCR) and higher VDAC protein levels when compared to WT and Myd88(-/-) cells.

10 ing sleep apnea, M94I resulted in 37% reduction in peak INa compared to WT and the combination of VCL-M94I and pH 7.0 dec

11 Plasmodium berghei ANKA had significantly delayed mortality compared to WT animals (P < 0.0001), despite higher parasite

12 ffects were significantly attenuated and shorter-lasting as compared to WT animals.

13 pansion of splenic CXCR2(+) neutrophils in chGRKO arthritic compared to WT arthritic mice.

14 mbination of VCL-M94I and pH 7.0 decreased peak INa by 56% compared to WT at pH 7.4.

15 40 in MyD88(-/-)bone marrow-derived dendritic cells (BMDCs) compared to WT BMDCs, although costimulatory molecules were u

16 to BSA and dextran and reduced transendothelial resistance compared to WT cells.

17 HDAC11 deletion had no effect on health or development, and compared to WT controls, Foxp3+ Tregs lacking HDAC11 showed i

18 infected mice were significantly reduced in MyD88(-/-)mice compared to WT controls, suggesting that in vitro and in vivo

19 diets induced severe hepatic steatosis in the LTKO mice as compared to WT controls.

20 ory and pro-fibrotic genes and collagen deposition after MI compared to WT counterparts.

21 days of differentiation VIM -/- EBs had altered morphology compared to WT EBs, with a rippled outer surface and a smalle

22 preCGG hippocampal neurons is chronically elevated, 3-fold compared to Wt; elevated ROS and abnormal glutamatergic respo

23 reduced proteasome activity and diminished FOXO4 expression compared to WT-iPSC-derived neurons.

24 Compared to WT leukocytes, CtsB(-/-) leukocytes accumulated i

25 show that the pKas are more clustered in the mutant channel compared to WT M2.

26 ease in the incidence of lung metastases in Tg mice (33.3%) compared to WT mice (62.5%).

27 ulminating in prostate cancer, is reduced in SFM of ESR1 KO compared to WT mice (P </= 0.0007).

28 educed significantly (by approximately 20%) in EHD4-KO mice compared to WT mice in baseline conditions, suggesting an imp

29 Finally, TANGO1(+/-) mice displayed less hepatic fibrosis compared to WT mice in two separate murine models: CCl4 and b

30 bited significantly prolonged times to occlusive thrombosis compared to WT mice indicating a protective effect of miR-223

31 ed Ca(2+) signals during normal network activity in FHM1 as compared to WT mice may explain impaired neurovascular respon

32 neal water load was significantly increased in EHD4-KO mice compared to WT mice, and although EHD4-KO mice concentrated t

33 of Cx36-KO mice displayed lower levels of spikelet activity compared to WT mice, indicating reduced gap junction coupling

34 Compared to WT mice, the B2-deficient lungs exhibited inducti

35 howed a significant reduction in hepatic cholesterol output compared to WT mice, they still formed gallstones.

36 moreceptor stimulation and noxious stimulation were blunted compared to WT mice.

37 ving higher differentiation potential and being more active compared to WT mice.

38 owever leukocyte attachment was reduced in pcsk9 (-/-) mice compared to WT mice.

39 similar phenotype resulting in enhanced airway eosinophilia compared to WT mice.

40 gnificantly better survival of endophilin B2-deficient mice compared to WT mice.

41 ced by no loss in body weight and reduced lung viral titers compared to WT mice.

42 TES were significantly increased in infected MyD88(-/-)mice compared to WT mice.

43 rk5 expression in cultures generated from Erk5 (fl/fl) mice compared to WT mice.

44 ted against age-related insulin resistance under ND and HFD compared to WT mice.

45 When compared to WT offspring, systolic (SBP), diastolic (DBP) and

46 lotting time of human blood (115.0 +/- 16.1 min, p < 0.001) compared to WT PAEC (34.0 +/- 8.2 min).

47 affinity by 114-fold and increased Mg(2+) affinity 28-fold compared to WT-Parv.

48 Likewise, compared to WT recipients, conditional deletion of HDAC11 wit

49 aling with ethylene and jasmonate sensing/signaling in RNAi compared to WT roots.

50 caused 30% decrease in peak sodium current (INa) amplitude compared to WT; under acidotic conditions (pH 7.0) typically