ライフサイエンスコーパス: were upregulated in

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

2 necrosis factor alpha, gamma interferon, and interleukin-10 were upregulated in infected mice.

3 Protein and mRNA levels of NDPK-C were upregulated in end-stage human HF, in rats after long-te

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

5 f cytokine and chemokine receptor genes, most notably CCR8, were upregulated in tumor-resident Treg cells in comparison t

6 MIF, CD74, and CD44 were upregulated in the glomeruli of patients and mice with p

7 tation to and priming of alphabetaT cells, HLA-DR and CD86, were upregulated in monocytes and inflammatory CD16 myeloid D

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

9 Additionally, COL1A1 and COL1A2 were upregulated in Mkx-overexpressing human PDL fibroblasts,

10 hich have not been previously associated with skin SCC CSC, were upregulated in late CSC and promoted tumor growth and me

11 alpha (TNF-alpha), IL-10, and IL-6 and the chemokine CXCL1 were upregulated in cocultured HT-29 cells at 4 h compared to

12 mokine ligands (CXCL1-4, CXCL6, CXCL10, CXCL11, and CXCL13) were upregulated in human quiescent CD34(+)Hoescht(-)Pyronin

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

14 dentified to be responsible for protocatechuate degradation were upregulated in the presence of BPA.

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 In previous studies, the t-bet and granulysin genes were upregulated in peripheral blood before and after intesti

19 s after transplant, IFN-inducible and damage-response genes were upregulated in monocytes at CGVHD onset and declined upo

20 Interferon signature genes were upregulated in SMS individuals' blood and dental cells.

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

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

23 Finally, GLI1 and GLI2 were upregulated in the kidneys of patients with high-grade f

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

25 nes, including IFNA, IFNG, MX1, IFITM1, IFITM3, and IFITM5, were upregulated in response to infection.

26 CAIX, GLUT1, and Ki67 were upregulated in the tumor edge, consistent with an acid-p

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

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

29 DCs) compared to WT BMDCs, although costimulatory molecules were upregulated in both types of BMDCs.

30 none were present at levels near ANXA5 in bundles and none were upregulated in stereocilia of Anxa5(-/-) mice.

31 DNA methylation-related genes including OsMET1b and OsCMT3a were upregulated in the 2x4 cross (pollinating a diploid "mot

32 Several mRNA targets of the NMD pathway were upregulated in IMT samples, indicating that the UPF1 mut

33 The Hedgehog (Hh) and PI3K/AKT pathways were upregulated in the RR population, which was further conf

34 1beta, IL6 and SPP1 (osteopontin, a key biomarker for PCa), were upregulated in NFATc1-induced PCa, establishing a tumori

35 C-CMs, we found that phosphodiesterases (PDEs) 2A and PDE3A were upregulated in DCM iPSC-CMs and that PDE2A was also upre

36 We found YAP protein expression and phosphorylation were upregulated in diabetic mouse renal proximal tubule epit

37 itates activation of the fibrin-degrading protease plasmin, were upregulated in Chd4 mutant LYVE1+ cells, and plasmin act

38 thology of L. pneumophila TNFAIP2 messenger RNA and protein were upregulated in response to L. pneumophila infection of h

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 The mRNA expression levels of RUNX2 were upregulated in calcified valves and associated with eQTL

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

43 vant for facilitating interactions with microbial symbionts were upregulated in wood-feeding larvae compared to larvae fe

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

45 Of the 6 genes that were upregulated in both hemogenic mesoderm and hemogenic end

46 rs for hypertrophy and extracellular matrix remodeling that were upregulated in HF, promoted beneficial remodeling, and i

47 at circles, although APOBEC3G, TRIM5alpha, BST2, and TRIM22 were upregulated in the IFN group.

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

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

50 Additionally, NPY and Y5R were upregulated in a BDNF-independent manner in NB cells und