ライフサイエンスコーパス: were upregulated

1 ron-stimulated genes (eg, OAS1, ISG15, Mx1; each P < .0001) were upregulated in CD4+ T cells as demonstrated by RNA seque

2 Among the miRNAs differently expressed, 2 were upregulated and 14 were downregulated in children with a

3 Other 45 were upregulated throughout the symbiotic interaction, from r

4 ntially expressed genes between the two groups, of which 62 were upregulated and 98 downregulated in control vs. Trpc3-de

5 By contrast, cathepsin B3 protein and activity were upregulated by ERFVIIs independent of transcript.

6 rticular, pyruvate kinase M2 (PKM2) expression and activity were upregulated.

7 % of the transcriptome and that 95.4% of the genes affected were upregulated.

8 implantation, proteins involved in regulating calcification were upregulated in the neointima of drug-eluting stents.

9 Several CAZymes were upregulated at all studied stages of the interaction.

10 Mast cells were upregulated in painful human IVD tissue and induced an i

11 Here, we showed that CXCL12 and CXCR4 were upregulated in the dorsal root ganglion (DRG) after chro

12 In PVR vitreous, 29 cytokines were upregulated compared to controls.

13 Most of the complement-activating factors were upregulated, whereas the complement regulator CD55 was s

14 s showed that genes and proteins inducing fusion or fission were upregulated and downregulated, respectively, in mTBI, bu

15 e expression time course revealed that VE-cadherin and FLK1 were upregulated in a dynamically similar manner as integrin

16 ALS3, which are also involved in fungal biofilm formation, were upregulated in the presence of S. mutans.

17 matory cytokines including IL-10 and IL-11 as well as FOXP3 were upregulated in the colon by ETO-curcumin.

18 h of stimulation with ligands, 87, 138, 1013, and 22 genes were upregulated for LTA, LPS, Poly(dT), and Poly(I:C), and 1

19 .5-fold change), 670 genes were downregulated and 296 genes were upregulated.

20 expressed by over two-fold and p < 0.05, of which 46 genes were upregulated and 200 genes were downregulated in the fibr

21 With H2/CO2, flavodoxin and histidine biosynthesis genes were upregulated.

22 involved in immune processes and epididymis-specific genes were upregulated in the testes.

23 cell differentiation, particularly astrocyte lineage genes, were upregulated in KO cells.

24 Several cytokines relevant to healing were upregulated during storage.

25 Different hydrophobins were upregulated upon early root adhesion, in mycorrhizas or

26 the expression of inhibitor of DNA binding protein 1 (ID1) were upregulated in HCV-infected cells or viral core gene-tra

27 cMNPV), the transcript levels of most SNARE genes initially were upregulated.

28 Significantly, VprBP protein levels were upregulated in high-grade serous ovarian patient tumors,

29 In the optic nerve, pro-inflammatory markers were upregulated within 6 hours following injury.

30 oxidative stress, cellular repair and protective mechanisms were upregulated in E. coli PI-7.

31 We found that all three family members were upregulated during postnatal development coinciding with

32 s revealed that WNT5A and matrix metalloproteinase-7 (MMP7) were upregulated by FOXC1 in TNBC cells.

33 Microarray analysis revealed that 214 mRNAs were upregulated and 149 were downregulated >3-fold by IL-4 i

34 box1, 2, 5, 7, Meis2 and Sall4; and (2) twice as many mRNAs were upregulated than downregulated, suggesting that Setd1b a

35 A total of 29 genes from the IL-6/STAT3 pathway were upregulated on PgPE stimulation.

36 We found that SNCA, SIAH2, UBB, HSPA1A, TUBB2A, and PINK1 were upregulated (fold-increases, >/=2.6), whereas UBD and PS

37 Forty-two genes probes were upregulated (>2-fold) in nonsmoking patients with severe

38 Ileal genes controlling extracellular matrix production were upregulated at diagnosis, and this gene signature was as

39 Gene expression of ET-1 and ETA but not ETB receptors were upregulated in the PVN and RVLM of E2 treated animals.

40 A subset of Ras GTPase genes linked to membrane remodeling were upregulated in cells infected with the hyperfusogenic mu

41 We show that MAIT cell cytotoxic responses were upregulated by a combination of both time-dependent anti

42 ction factors (IFIT1, -2, -3, and -5, OASL, CD74, and RTP4) were upregulated.

43 o arginine/histidine permease genes (SSA_1568 and SSA_1569) were upregulated in DeltaciaR.

44 , expression analysis revealed that both SNHG6-003 and TAK1 were upregulated in human cancers, exhibiting a co-expression

45 In addition, we identified transcription factors that were upregulated during drought conditions and that may act a

46 n-seq were analyzed by targeted proteomics, and 70% of them were upregulated by H2O2.

47 were the complement-3 components C3b, iC3b, and C3d, which were upregulated in LTBI and markedly decreased upon stimulat

48 and replicated 3 differentially expressed microRNAs, which were upregulated in patients with IS compared with both healt

49 pneumoniae pneumonia contained 4127 DE mRNAs, 36% of which were upregulated at least 2-fold.

50 t of APOBEC3G anti-viral restriction factors, both of which were upregulated.