ライフサイエンスコーパス: expression levels of

1 mediated repression of the SHH pathway, as shown by altered expression levels of several target genes.

2 Na(+) levels were not increased, and expression levels of Ca(2+)- or Na(+)-handling proteins were

3 In comparing expression levels of genes between the mouse tumor and non-tu

4 s and classic M1 proinflammatory macrophages) and decreased expression levels of proinflammatory and profibrotic markers

5 ch of those panels contains a series of X-Y plots depicting expression levels of subsystems of that panel, e.g. subsystem

6 he purpose of this study was to determine whether the early expression levels of any of these 16 genes are predictive for

7 In addition to IL-27, gene expression levels of the specific IL-27 receptor (IL27RA) in

8 RNA was isolated from the paraffin material, and gene expression levels of IL-32 alpha, beta, and gamma isoforms, I

9 Higher expression levels of IL1R1, IL1RAP, and IL4R were associated

10 This effect is accompanied by higher expression levels of the gibberellic acid (GA) catabolic enzy

11 ind that early replication is a requirement for the highest expression levels of certain genes.

12 y, consisting of vigorous increase in number and changes in expression levels of inflammation-related genes, monitored by

13 Both groups demonstrated increased expression levels of fibroblast growth factor-2, transforming

14 Consistently, clinical HLRCC tissues showed increased expression levels of both FOXM1 and its proliferation-associa

15 reast cancer (BC) imaging is limited mainly by insufficient expression levels of facilitative glucose transporter (GLUT)1

16 dy (MAb) inhibited HHV-8 infection of iDDC, as shown by low expression levels of viral proteins and DNA.

17 Using reverse-phase protein arrays, we measured expression levels of approximately 230 key cancer-related pro

18 yme activities are correlated with protein amounts and mRNA expression levels of five major human sulfotransferase (SULT)

19 om a macrophage/monocyte clade, as supported by higher mRNA expression levels of several dendritic cell-associated genes,

20 The mRNA expression levels of some genes related to neurotransmission

21 TIMBD inhibited gp120-induced RNA and protein expression levels of IL6 and IL8, but not that of CCL5 in SVG

22 The mRNA and protein expression levels of proinflammatory cytokines IL6, IL8 and C

23 As protein expression levels of AROM, estrogen and androgen receptors di

24 lthough all SERPINA1 mRNAs encode exactly the same protein, expression levels of the individual mRNAs vary substantially

25 reased intracellular TNFalpha immunoreactivity, and reduced expression levels of macrophage factors that are associated w

26 Seattle, WA), a molecular signature measuring the relative expression levels of four host messenger RNAs, was developed

27 Interestingly, the relative expression levels of Tau isoforms containing either 3 (3R-Tau

28 der different ambient temperatures correlated with relative expression levels of the BARLEY MADS-box genes VERNALIZATION1

29 Messenger RNA expression levels of nuclear factor kappa-light-chain-enhance

30 Messenger RNA expression levels of p38 mitogen activated protein kinase and

31 a stochastic minimization process, which causes the scaled expression levels of all transcript isoforms to follow the sa

32 pecify regulatory proteins controlling the context-specific expression levels of genes.

33 The expression levels of Adipoq and fatty acid synthesis-related

34 The expression levels of FXR1 (fragile X mental retardation autos

35 The expression levels of some markers for AML subtypes and c-MYC

36 The expression levels of tau and TDP-43 were inverse in the front

37 The expression levels of the immature-like neutrophil signature i

38 We revealed that DC3000 significantly alters the expression levels of 71% effector targets and their downstrea

39 portrayed a strong and significant correlation between the expression levels of FOXM1 and AURKA.

40 The strong correlation between the expression levels of these known marker genes and the express

41 The silencing of SALL4 in cancer cells decreased the expression levels of Glut1 and inhibited glycolysis in cancer

42 e found that the PHD inhibitors significantly increased the expression levels of genes involved in gluconeogenesis in the

43 Interestingly, the expression levels of CIITA and MHC-II significantly increased

44 sequencing, and suitable for computational inference of the expression levels of 81% of non-measured transcripts.

45 The accessions were selected based on the expression levels of ANNEXIN1, a drought-related marker.

46 nthesis of MG secretions, we analyzed by means of qPCR, the expression levels of six of the CYP450 genes most abundantly

47 ese two strains, nor did we observe that ZnO NPs reduce the expression levels of CT mRNA and protein.

48 In addition, we verified miR-449b could regulate the expression levels of CDK6, c-MYC, HDAC1 and BCL-2.

49 In this study, we showed that the expression levels of LDHA mRNA and protein were significantly

50 We show that the expression levels of SOX5, SOX6, and SOX21 (SOX5/6/21) transc