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

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

2 Enz-resistant CRPC cells and associated with enhanced transcription of a subset of tumor promoting ge

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

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

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

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

7 Genetic disruption of NELF in macrophages enhanced transcription of AP-1-encoding Fos and Jun and,

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

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

10 n the planktonic form of growth resulting in enhanced transcription of biofilm-specific genes.

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

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

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

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

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

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

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

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

19 We found enhanced transcription of cyclooxygenase (COX)-2 and pro

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

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

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

23 nally triggered CDNs lead to the CDNs-guided enhanced transcription of either the DFHBI aptamer or th

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

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

26 on of both ERalpha and FOXM1, it also led to enhanced transcription of FOXM1.

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

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

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

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

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

32 p 3 innate lymphoid cells and Th17 cells and enhanced transcription of IL-22, Ab-mediated neutralizat

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

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

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

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

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

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

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

40 ions are coupled with reduced phytotoxicity, enhanced transcription of MYB72 in roots, and a positive

41 regions and insulator sites associated with enhanced transcription of nearby genes.

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

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

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

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

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

47 increased G4 accumulation is associated with enhanced transcription of signalling pathways previously

48 FKBP5-deficiency enhanced transcription of Slc8a1 (encoding NCX1) via tra

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

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

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

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

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

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

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

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

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

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

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

60 Transcriptomic analyses reveal enhanced transcription of the HERVs in patients; meanwhi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

75 he DON biosynthesis gene cluster, leading to enhanced transcription of TRI6.

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