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1                                          NLRP3 and IL-1beta were upregulated in the G, CP, and AgP groups compared with g
2                     The cytokines IL-36alpha and IL-36gamma were upregulated in HI skin, whereas the innate immune inhibi
3 nes was seen in the HSV-1-infected type 3 ILCs, whereas 414 were upregulated in the infected type 1 ILCs and 128 in the i
4                           We found that miR-17 and miR-548b were upregulated in alveolar epithelial cells after CI/EVR, w
5                                     MIR182-5p and MIR20a-5p were upregulated in human thyroid cancer and thyroid cancer e
6            Both L3MBTL1 and SET domain-containing protein 8 were upregulated in the central nervous systems of mouse mode
7                                Antimicrobial peptides (AMP) were upregulated in vaginal delivery compared to CS with or w
8 t modifications during most of the grain filling period and were upregulated in response to S deficiency.
9 els of the NLRP3-related proteins NLRP3, ASC, and pro-casp1 were upregulated in BD patients, followed by an increase in c
10                            Type I collagen, VEGF, and Cbfa1 were upregulated in the scaffold-treated defects by day 7.
11 al production of OEA and expression of both GPR119 and CD36 were upregulated in wild-type mice after VSG.
12 ow indicated that progenitor bone marrow cells MPP2 and CMP were upregulated in GT3-Nano-treated mice.
13 ansporters, and NODULE INCEPTION-like transcription factors were upregulated in rice roots within 24 h of JGTA-S1 treatme
14 ns and enzymes relating to heme and mitochondrial functions were upregulated in human NSCLC tissues relative to normal ti
15 mor necrosis factor-alpha) and IFN-gamma (interferon-gamma) were upregulated in the DC ACT renal CD8(+) T cells but not C
16  of Igf2 (+41%) and placental lactogen (Prl3b1: +59%) genes were upregulated in female, but not male fetuses.
17 ession of p53 and most endothelial lineage commitment genes were upregulated in MEndoT-derived cells; however, the furthe
18                           On the other hand, immunity genes were upregulated in MG with a predominance of defensins and l
19 ng developmental progression, but more beta-oxidation genes were upregulated in early C5s compared to late C5s and adults
20                                  All immunity-related genes were upregulated in the bumblebees inoculated with N. ceranae
21 throughout the plant; and (iii) a number of S1 and S2 genes were upregulated in leucaena under iron-deficiency condition
22                             Importantly, these target genes were upregulated in Rspo2-depleted explants.
23 nal domain (CTD) family proteins, including the gingipains, were upregulated in 33277 relative to 381.
24 he intestinal environment, TWIST1, TWIST2, HDAC1, and HDAC3 were upregulated in human intestinal relative to peripheral m
25                                       Notch4, Wnt and Hippo were upregulated in circulating T(reg) cells of individuals w
26  Nos2) were downregulated, whereas iNKT markers (Il4, Il15) were upregulated in ileum of CS-delivered mice.
27 h primarily hepatic IR, while genes related to inflammation were upregulated in individuals with primarily muscle IR.
28 t-infection; however, duIL-17A and IL-17F expression levels were upregulated in both spleens of RA-infected ducks and spl
29                  Interleukin-1b and interferon-gamma levels were upregulated in skin of allogeneic limbs.
30                                  We report that NO66 levels were upregulated in advanced primary prostate tumors compared
31                                Moreover, Myt(MYT)-TF levels were upregulated in mouse and human beta cells during metabol
32                       The lincRNAs, LINC00960 and LINC01140 were upregulated in IPF fibroblasts.
33 rthologs of genes expressed by the transitional macrophages were upregulated in samples from patients with idiopathic pul
34                         Mesenchymal markers snail and MMP14 were upregulated in cancer cells maintained in 3D (P < 0.001)
35 led that the majority of affected proteins in murine models were upregulated in patients.
36                              Mucins Clca1 (Gob5) and Muc5ac were upregulated in eosinophilic and even more in neutrophili
37                       Moreover, we show that TRPV3 and PAR2 were upregulated in skin biopsies from patients and mice with
38                           Multiple proinflammatory pathways were upregulated in the cavity wall, whereas a downregulation
39 ere likely downregulated, while the same signaling pathways were upregulated in the CTSS group.
40 in-like proteases, and other antimicrobial defense proteins were upregulated in low-acylsugar-producing accessions.
41                        mRNA and protein expression of PTPN6 were upregulated in smokers, but were not associated with emp
42                   Genes related to extracellular remodeling were upregulated in individuals with primarily hepatic IR, wh
43    Accordingly, a set of endogenous retroviral element RNAs were upregulated in metastatic cells and detected extracellul
44          Furthermore, genes involved in NF-kappaB signaling were upregulated in BETi-resistant cells, and the transcripti
45 lutathione-ascorbate cycle, and various antioxidant systems were upregulated in the mutants, suggesting cascading respons
46 L-6, IL-18, and MIG, as well as anti-inflammatory IL-2 that were upregulated in a correlated fashion.
47 entified five MYB and three bHLH transcription factors that were upregulated in the inner pericarp.
48 Display (PD) technology to identify candidate proteins that were upregulated in saliva of OSCC by selecting ligands to sa
49 us and intermediate expression profiles of transcripts that were upregulated in cTCMR.
50                         We found that both VEGFC and VEGFR3 were upregulated in human nonmetastatic colorectal cancer, wi