ライフサイエンスコーパス: we induced

1 We induced a genetic neuronal lesion in mice for 25 d and fou

2 c signals and metabolic pathways can be readily elucidated, we induced a glycolytic tumor in the Drosophila wing imaginal

3 Here, we induced a hippocampal lesion in mice for 25 d via neuronal

4 We induced a sustained hyperfibrinolytic state in mice by hyd

5 We induced acute pancreatitis by repeated caerulein injection

6 We induced anti-MPO GN by immunizing mice with MPO and a low

7 We induced atherosclerotic plaque formation in hypercholester

8 We induced autonomous expression of diphtheria toxin to kill

9 We induced bleb formation by disruption of the cortex and fou

10 al agency over the VB movements, we conducted a study where we induced body ownership using visuotactile (VT) synchrony r

11 We induced C-type inactivation in BK channels and studied the

12 Here we induced chloroplast and mitochondrial development in rice

13 een the N terminus and loop2 in full-length Orai1 channels, we induced close proximity of the N terminus and loop2 via cy

14 Using a Pavlovian learning task, we induced conditioned hallucinations in four groups of peopl

15 role for PTEN in pre-B acute lymphoblastic leukemia (ALL), we induced Cre-mediated deletion of Pten in mouse models of p

16 We induced dissociation and auto-inhibition of the V1 and VO

17 We induced either pleasant or unpleasant affect in participan

18 By genetic sex reversal of a specific gut region, we induced female-like aging pathologies in males, associated

19 and the molecular mechanisms underlying these observations, we induced glomerular proteinuria in two animal models.

20 ere not the consequence of the actions of gonadal hormones, we induced gonadal sex reversal to alter the hormonal environ

21 Using 3F3A as a reporter, we induced Gp78 S538 phosphorylation by serum starvation and

22 on rather than one involving a specific GPP130 determinant, we induced homo-oligomerization of two unrelated Golgi-target

23 To identify the receptors involved, we induced latent sensitization in mice and rats by injecting

24 To study the role of Stat1 in a lupus model, we induced lupus-like chronic graft-versus-host disease (cGVH

25 e the metabolic requirements for productive KSHV infection, we induced lytic replication in the presence of inhibitors of

26 We induced mast cell degranulation by local subconjunctival i

27 In this study, we induced MetS in C57BL/6 mice by feeding them high-fat diet

28 he role of CCR2 activation on Nf1(+/-) neointima formation, we induced neointima formation by carotid artery ligation in

29 Here, we induced neuronal excitation by anodal transcranial direct

30 We induced palindrome formation by passaging cells lacking an

31 tS in C57BL/6 mice by feeding them high-fat diet (HFD), and we induced periodontitis by periodontal injection of Aggregat

32 To test this possibility, we induced persistent hypertension in three mouse models of t

33 toxin-initiated OM inflammation on the olfactory bulb (OB), we induced persistent rhinitis in mice and analyzed the spati

34 ity lipoprotein receptor-deficient mouse (LDLR(-/-)) model, we induced plasma APN levels using a recombinant adenovirus e

35 We induced prehepatic PH by partial portal vein ligation (PPV

36 We induced pressure overload by transthoracic aortic constric

37 the droplet monolayer with nanolitre injections of buffer, we induced quantifiable DHB tension, which could be related t

38 Thus, we induced renal failure in mice with targeted deletion of Kl

39 To decipher ribosome kinetics at stall sites, we induced ribosome stalling at specific codons by starving t

40 We induced RPE injury pharmacologically and genetically in tr

41 To address this issue, we induced SD in murine hippocampal slices by focal KCl micro

42 UBJECTS:: Male wild type and transgenic miceINTERVENTIONS:: We induced sepsis in mice using the colon ascendens stent per

43 We induced small bowel injury in rats using high- (15 mg/kg),

44 2 (hAgo2) and Cryptosporidium single-stranded RNA (ssRNA), we induced specific slicing in Cryptosporidium RNA targets.

45 Twenty-four hours later, we induced stress in half of the participants and assessed su

46 Here, we induced switching in the absence of CheY-P by introducing

47 CMV Armstrong strain, but the more rapidly replicating LCMV-WE induced T cell exhaustion and viral persistence.

48 To address this hypothesis, we induced the differentiation of spheres and purified the my

49 We induced the self-photosensitization of a nonphotosynthetic

50 To test this hypothesis, we induced transient, forebrain-specific, CRH overexpression