ライフサイエンスコーパス: compared to WT

1 nd presented differential expression of endothelial markers compared to WT.

2 itrosoglutathione concentrations were higher in mutant mice compared to WT.

3 py, significantly decreased DKO and Mdr2(-/-) ERC viability compared to WT.

4 oryzae strains lacking NDK1 through targeted gene deletion, compared to WT.

5 in central waves (II-IV) that in some cases disappear when compared to WT.

6 te early (MIE) enhancer results in inefficient reactivation compared to WT.

7 in Src-1/-2 double-deficient (Src-1/-2(d/d) ) fetal lungs, compared to WT.

8 yoblasts demonstrated delayed and reduced fusion efficiency compared to WT.

9 lm, T2DM hearts exhibited improved contractility/relaxation compared to WT, accompanied by extensive metabolic remodellin

10 ce lung neutrophil myeloperoxidase levels in PLD2(-/-) mice compared to WT and PLD1(-/-) mice, confirming a novel role of

11 ncreased bacterial dissemination, and pulmonary dysfunction compared to WT animals.

12 animals exhibit enhanced spontaneous and evoked exocytosis compared to WT animals.

13 sed calcium deposition, phenotypic change and sEV secretion compared to WT CASMCs, which was associated with reduced lyso

14 ly increased oxidative phosphorylation and basal glycolysis compared to WT cells and correlated with motor dysfunction.

15 /6(-/-) pmLF and ROCE was similar in STIM1/2-deficient pmLF compared to Wt cells.

16 iminished expression of IFNbeta and IFNbeta target genes as compared to WT cells.

17 sion of Nrf2, ALP and wnt5a in cultured primary osteoblasts compared to WT control.

18 in the brains of J20-hAPP mice were substantially enhanced compared to WT controls, but this effect disappeared under no

19 eater slopes at all layers of interest for AD mouse retinas compared to WT controls.

20 iated oligodendrocytes in the healthy or remyelinating CNS, compared to WT controls.

21 icant thinning of the nerve fiber layer in AD mouse retinas compared to WT controls.

22 nd variance in nerve fiber layer light scattering intensity compared to WT controls.

23 d MBOAT in the stomach, and lower levels of circulating Ghr compared to WT-controls.

24 d a significantly depressed activation-induced zinc release compared to WT eggs.

25 Compared to WT, fat-1 mice exhibited a markedly plastic trans

26 We found changes of the SNO-proteome in the mutant compared to WT in both ages.

27 but S411A Kunjin infection resulted in increased mortality compared to WT Kunjin infection.

28 ination and saliva positivity rates in surviving mosquitoes compared to WT Kunjin infection.

29 Nhe6 knockout (KO) mice showed significant hearing loss compared to WT littermates.

30 vels were significantly elevated in the SG of Nhe6 KO mice, compared to WT littermates.

31 mpanied by an increase in blood pH and a decrease in pCO(2) compared to WT littermates.

32 ntly lower Rab7, and higher Rab11 levels in the Nhe6 KO OC, compared to WT littermates.

33 tin administration during the active phase (nighttime) when compared to WT mice and treatment during the inactive phase (

34 CF mice also exhibit depression-like behaviors compared to WT mice in an age dependent manner.

35 Compared to WT mice, RdRP mice had significantly reduced sple

36 educed synaptic vesicle pool and impaired neurotransmission compared to WT mice, while nCLCa-only mice had increased syna

37 ology we find feedforward excitatory drive is reduced in HD compared to WT mice, while recurrent inhibition also shows ph

38 seline, 5xFAD mice presented significant alveolar bone loss compared to WT mice.

39 l cells were decreased in Alt Ext challenged Esr1(-/-) mice compared to WT mice.

40 Dys(-/-) mice showed significant increased b-wave in ERG, compared to WT mice.

41 ity (Apom, Pgc1alpha) and immune modulation (Apelin, Icam1) compared to WT mice.

42 antly increased in HDM sensitized/challenged Pag1(-/-) mice compared to WT mice.

43 score were also significantly decreased in TSLPR(-/-) mice compared to WT mice.

44 -5 and IL-13 production, BAL eosinophils, and IL-33 release compared to WT mice.

45 ILC2 expressing IL-5 and IL-13 following Alt-Ext-challenge compared to WT mice.

46 ing showed axon loss in the cochlear nerves of Nhe6 KO mice compared to WT mice.

47 acterial killing by Ly6B.2(+) myeloid cells and macrophages compared to WT neonates.

48 in system (RAS) upregulated in the kidney of KS-tg/OVE mice compared to WT/OVE mice, suggesting a disturbed balance betwe

49 Compared to WT, p.P888L SAP97 significantly increased the cha

50 ffects (approximately 2- to 93-fold improvements) of Mut268 compared to WT using targeted deep-sequencing analyses.