ライフサイエンスコーパス: enhanced transcription of

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1 I, respectively, but infection with wt virus enhanced transcription of 5S rRNA by RNAPIII.

2 influences E2F-1 protein stability, and the enhanced transcription of a variety of downstream target

3 ddition to the C1/P1 DNA-binding sites for R-enhanced transcription of a1.

4 ed Ang-2 protein synthesis and secretion via enhanced transcription of Ang-2.

5 (NRF2) is orchestrated and amplified through enhanced transcription of antioxidant and antiinflammato

6 licited by activation of TRPM3 channels with enhanced transcription of AP-1-regulated genes.

7 the unfolded protein response, manifested by enhanced transcription of ATF4 and C/EBP homologous prot

8 egions (-8.2 to -7.5 kb and -7.5 to -7.0 kb) enhanced transcription of both A-chain and heterologous

9 ely dependent on YvrI and is correlated with enhanced transcription of both the yvrI-yvrHa and the ox

10 nc finger transcription factor GKLF-mediated enhanced transcription of c-myc.

11 That the G488A mutation indeed enhanced transcription of ccl1-2 was demonstrated by the

12 G1 cyclins and CDKs and the other involving enhanced transcription of CDIs by the activated receptor

13 RBP2-/- mouse cells displayed enhanced transcription of certain cytokine genes, which,

14 epithelial cells with PMA is associated with enhanced transcription of Cox-2 and increased production

15 t cellular transformation is associated with enhanced transcription of Cox-2 and increased production

16 of transcription factor, NF-kappaB; and (iv) enhanced transcription of cytochrome oxidase Vb (COX Vb)

17 the mouse dor promoter was required for the enhanced transcription of dor gene in phytohemagglutinin

18 lation induced by DNA damage correlates with enhanced transcription of downstream p53 target genes.

19 res despite the fact that neither polyphenol enhanced transcription of elastin mRNA or cellular proli

20 tion of AI-2 increased cell motility through enhanced transcription of five motility genes, we propos

21 f lamprey blood cells with rIL-17D.1 protein enhanced transcription of genes expressed by the B-like

22 e acetylation, chromatin reorganization, and enhanced transcription of genes, such as ET-1, enhancing

23 active Smo and does not necessarily involve enhanced transcription of Gli1.

24 ives HIF-1alpha protein accumulation through enhanced transcription of HIF-1alpha mRNA, a process tha

25 ylated form of nuclear MLC(20), resulting in enhanced transcription of ICAM-1.

26 ich causes nuclear accumulation of TRX-1 and enhanced transcription of inflammatory mediators through

27 ed the inflammatory response, as measured by enhanced transcription of interleukin-6 and tumor necros

28 ng to an altered chromatin landscape and the enhanced transcription of low-expressed genes.

29 increased C-Jun transcriptional activity and enhanced transcription of matrix metalloproteinase 10 (M

30 Stimulation of memory cells revealed enhanced transcription of "memory-primed" genes compared

31 It was found that OSM induced/enhanced transcription of MMP-1 (interstitial collagenas

32 d through an induction process that requires enhanced transcription of mtrCDE when gonococci are grow

33 of NOXA at the protein level was preceded by enhanced transcription of NOXA mRNA.

34 lycosaminoglycan binding was associated with enhanced transcription of peptidoglycan recognition prot

35 that recognizes the inducers and signals the enhanced transcription of phase 2 genes does so by virtu

36 ERH1 results in salicylic acid accumulation, enhanced transcription of RPW8 and RPW8-dependent sponta

37 We discovered that csrR mutants have enhanced transcription of sagA, a gene associated with s

38 pendent interactions are required to achieve enhanced transcription of specific estrogen-receptor tar

39 ere with beta-catenin turnover, resulting in enhanced transcription of target genes through the incre

40 Jun, resulting in diminished degradation and enhanced transcription of the Bcl-2 homology 3 domain-on

41 tigen and beta-catenin in colon cancer cells enhanced transcription of the c-myc promoter, the downst

42 NtSLT1 enhanced transcription of the CaN-dependent ENA1 gene pr

43 ncrease in Egr-1 protein and mRNA levels and enhanced transcription of the Egr-1 gene via serum respo

44 The mechanisms contributing to enhanced transcription of the gene coding for PKCbetaII,

45 stasis by insulin is mediated in part by the enhanced transcription of the gene encoding SREBP-1c (st

46 stasis by insulin is mediated in part by the enhanced transcription of the gene encoding sterol regul

47 and the overexpression of COX-2 is caused by enhanced transcription of the gene.

48 hese, is amplification of the SERCA gene and enhanced transcription of the gene.

49 This increase in enzyme activity reflects E6-enhanced transcription of the human telomerase reverse t

50 dence that these mutations in SRC-3 promoted enhanced transcription of the IGFBP3 gene and globally i

51 we present evidence that anguibactin itself enhanced transcription of the iron-transport genes fatA

52 the activation of nuclear factor kappaB and enhanced transcription of the KC gene with equal potency

53 the leukotoxin gene operon which results in enhanced transcription of the leukotoxin.

54 the short half-lives of the P2Y(1) mRNAs, it enhanced transcription of the P2Y(1) gene.

55 This latter property resulted from enhanced transcription of the streptolysin S biogenesis

56 Moreover, Myd88(MYEL) mice showed enhanced transcription of the Tnfa gene and an excessive

57 ases in RPE cells occurred primarily through enhanced transcription of the VEGF gene and via the IGF-

58 secreted protein levels in RPE cells through enhanced transcription of the VEGF gene.

59 rd4 with growth factor-responsive genes, and enhanced transcription of these genes that could be atte

60 PR55alpha-PP2A also enhanced transcription of these genes, without affecting

61 ription factors, and that is associated with enhanced transcription of this gene and increased enzyme

62 ha (HIF-1alpha) and HIF-2alpha, resulting in enhanced transcription of transforming growth factor-alp

63 Reduced expression of NME2 led to enhanced transcription of vinculin.

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