ライフサイエンスコーパス: continuous expression

1 efine safe and effective levels of FVIIa for continuous expression.

2 bitor p16 is reversible and dependent on its continuous expression.

3 ststem cell/predifferentiation step, and its continuous expression caused a precocious phenotype unli

4 rine vestibular and cochlea hair cells, with continuous expression in hair cells and postnatal expres

5 ost reliable lymphatic marker because of its continuous expression in lymphatic endothelium.

6 nsmitter receptors, adhesion molecules) with continuous expression in MNs.

7 demonstration of the hemostatic efficacy of continuous expression, in the presence or absence of inh

8 Continuous expression is in contrast to many other toxin

9 of cytoskeletal actin filaments and high and continuous expression levels of beta-catenin indicating

10 es at the single-cell level can be on (and a continuous expression measure is recorded) or dichotomou

11 uman cancers have recently demonstrated that continuous expression of a dominantly acting oncogene (f

12 Continuous expression of activated factor VII (FVIIa) vi

13 We hypothesized that continuous expression of an anti-CTLA-4 antibody localiz

14 g, and their viability is dependent upon the continuous expression of antiapoptotic proteins, we hypo

15 ed early adaptive immune responses, only the continuous expression of bacterial PAMPs on transgenic T

16 in 32Dcl3 cells expressing bcrabl, there was continuous expression of Bcl-2 at a level greater than o

17 Continuous expression of bcl-XS, at levels approximately

18 These data suggest that continuous expression of BDNF, unlike intravitreous inje

19 m bp -650 to -453 may be responsible for the continuous expression of bFGF that leads to the uncontro

20 Confocal microscopy demonstrated continuous expression of both occludin and JAM-1, each c

21 These results demonstrate that continuous expression of both the E6 and the E7 protein

22 This continuous expression of Cbfa1 in nonhypertrophic chondr

23 In contrast, continuous expression of cooperating oncogenes in immort

24 The RPE is a quiescent epithelium, and continuous expression of Cre could affect its function.

25 approach for the treatment of hemophilia, as continuous expression of donated clotting factor VIII (F

26 Continuous expression of DUB-1 from a steroid-inducible

27 HPV-16 E7 in an inducible manner require the continuous expression of E7 for their maintenance.

28 l tumors, indicating that they depend on the continuous expression of E7 for their persistence.

29 tigated whether cervical cancers rely on the continuous expression of E7 in the context of constituti

30 presence of constitutively expressed E6, the continuous expression of E7 is required for the maintena

31 Supporting this idea, continuous expression of each TTP/TIS11 protein at physi

32 Simulations suggest that endogenous, continuous expression of eCD4Ig at levels greater than 1

33 hough Ewing cells are crucially dependent on continuous expression of EWS-FLI1, its regulation of tur

34 al hyperplasia in Upk2-HRAS* mice depends on continuous expression of Foxa1 and activated HRAS, and t

35 na fide epigenetic mark because they require continuous expression of H3K36M to be inherited.

36 Continuous expression of HER2(YVMA) is essential for tum

37 pathogenic T cells in I-E+ donors, and that continuous expression of I-E on hemopoietically derived

38 We found that continuous expression of mFVIIa at levels at or below 1.

39 show here that either exogenous addition or continuous expression of MGSA/GROalpha in immortalized m

40 ion of SCA1 pathogenesis is dependent on the continuous expression of mutant ataxin-1.

41 Growth under continuous expression of mutant p53 proteins for 16-17 p

42 This correlated with continuous expression of p16 protein in these cells.

43 PAMPs, we demonstrate a requirement for the continuous expression of PAMPs for optimal anti-pathogen

44 increased RUNX1 expression, indicating that continuous expression of physiological levels of RUNX3 i

45 To obtain constitutive and continuous expression of RNase L cDNA, Jurkat cells were

46 Continuous expression of Smad1 from day 2 of EB culture

47 Continuous expression of Sox1 and Sox2 in transgenic emb

48 rtebrate embryogenesis appear to require the continuous expression of spatial regulators such as the

49 Stable knock-down can be achieved by continuous expression of synthetic short hairpin RNAs, t

50 Here we show that continuous expression of the chemokine receptor CXCR4 in

51 We have observed that continuous expression of the Cre recombinase in cultured

52 wever, the bacteria do not appear to require continuous expression of the DotA protein to maintain a

53 This occurs despite continuous expression of the entire epitope-bearing P29

54 Continuous expression of the latency-to-lytic switch pro

55 ture but, once established, does not require continuous expression of the polymerase beta variant pro

56 ubpopulations and/or of episodic rather than continuous expression of the SM-MHC gene.

57 regulatory T (T(reg)) cells is dependent on continuous expression of the transcription factor Foxp3.

58 Continuous expression of VAB-8L in the ALM mechanosensor

59 adult stages examined, UNC-3 is required for continuous expression of various protein classes (e.g. r

60 this study was to investigate the effects of continuous expression of VEGF in myocardium by use of my

61 In this model, unregulated continuous expression of VEGF is associated with (1) a h

62 stence of functional therapeutic T cells and continuous expression of WT1 and HLA-A2 by the patient's

63 rtantly, alpha-DB but not dystrophins showed continuous expression throughout development in BBB mode

64 CD34+ hematopoietic progenitors revealed its continuous expression throughout human development with

65 and mouse genes, excess RA causes either (1) continuous expression throughout the preotic hindbrain (

66 ofile of Cas9 circumvents its requirement of continuous expression within the cell for targeting DMD