戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 ( left1)

通し番号をクリックするとPubMedの該当ページを表示します
1                                          NLRP3 and IL-1beta were upregulated in the G, CP, and AgP groups compared with g
2                  Of 410 differentially expressed genes, 286 were upregulated and 124 downregulated by mCD40L versus sCD40
3                     The cytokines IL-36alpha and IL-36gamma were upregulated in HI skin, whereas the innate immune inhibi
4                                             PD-1 and CTLA-4 were upregulated on tumor-infiltrating CD4(+) and CD8(+) T ce
5 namide adenine dinucleotide phosphatase] oxidase subunit 4) were upregulated.
6                           We found that miR-17 and miR-548b were upregulated in alveolar epithelial cells after CI/EVR, w
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 bited, while genes involved in fatty acid (FA) biosynthesis were upregulated.
10                                C5a and its receptor (C5aR1) were upregulated early in the disease process and prior to ma
11                                              C1, C7, and C8 were upregulated for cellular and mitochondrial translation,
12                            Type I collagen, VEGF, and Cbfa1 were upregulated in the scaffold-treated defects by day 7.
13 al production of OEA and expression of both GPR119 and CD36 were upregulated in wild-type mice after VSG.
14                 Cell cycle regulators, most notably Cdkn2a, were upregulated by p53 inactivation in gastric premalignancy
15 s of p53-induced mRNAs upon DNA damage, only a few circRNAs were upregulated from p53-induced genes.
16 ow indicated that progenitor bone marrow cells MPP2 and CMP were upregulated in GT3-Nano-treated mice.
17 ansporters, and NODULE INCEPTION-like transcription factors were upregulated in rice roots within 24 h of JGTA-S1 treatme
18  all genes coding for members of the cytochrome P450 family were upregulated.
19                                  All immunity-related genes were upregulated in the bumblebees inoculated with N. ceranae
20 munity were downregulated, while inflammation-related genes were upregulated.
21 throughout the plant; and (iii) a number of S1 and S2 genes were upregulated in leucaena under iron-deficiency condition
22  to IFN-beta stimulation, whereas other IFN signature genes were upregulated by both IFN-gamma and IFN-beta.
23                             Importantly, these target genes were upregulated in Rspo2-depleted explants.
24                      However, nitrate ABC transporter genes were upregulated under UV and FR light indicating increased n
25                                       Notch4, Wnt and Hippo were upregulated in circulating T(reg) cells of individuals w
26 , tumor necrosis factor alpha (TNF-alpha), and IL-12 levels were upregulated.
27                  Interleukin-1b and interferon-gamma levels were upregulated in skin of allogeneic limbs.
28                                Moreover, Myt(MYT)-TF levels were upregulated in mouse and human beta cells during metabol
29 steine protease, serine carboxypeptidase, and lipoxygenase2 were upregulated at the proteome level, corroborating previou
30 ansporters and genes involved in sulfate and Met metabolism were upregulated, suggesting regulation of the pool of free a
31                         Mesenchymal markers snail and MMP14 were upregulated in cancer cells maintained in 3D (P < 0.001)
32 led that the majority of affected proteins in murine models were upregulated in patients.
33                       Moreover, we show that TRPV3 and PAR2 were upregulated in skin biopsies from patients and mice with
34 structural components and fatty acid beta-oxidation pathway were upregulated.
35 ere likely downregulated, while the same signaling pathways were upregulated in the CTSS group.
36           Three virulence genes including ply (pneumolysin) were upregulated >20-fold in the lung compared with the nasop
37                             Muscle wasting pathway proteins were upregulated while those that promote growth decreased as
38 m schizophrenic subjects, even though both D(2)R and A(2A)R were upregulated.
39    Accordingly, a set of endogenous retroviral element RNAs were upregulated in metastatic cells and detected extracellul
40 esponse to EtOH, while defense responses and PPAR signaling were upregulated.
41 d that several genes involved in de novo ceramide synthesis were upregulated and that ceramide (C16, C20, C20:1, and C24)
42 lutathione-ascorbate cycle, and various antioxidant systems were upregulated in the mutants, suggesting cascading respons
43 hesis of precursors for indirect defence-related terpenoids were upregulated while those involved in the biosynthesis of
44 L-6, IL-18, and MIG, as well as anti-inflammatory IL-2 that were upregulated in a correlated fashion.
45   Using RNA-seq, we identify B. thetaiotaomicron genes that were upregulated during Salmonella-induced gut inflammation a
46 us and intermediate expression profiles of transcripts that were upregulated in cTCMR.
47 sing machinery component gene transcription and translation were upregulated, consequently resulting in increased major h
48 on transporters, such as copper, iron and zinc transporters were upregulated and transferase-encoding genes, for example
49                         The SLCO2A1 and CYP1A1 genes, which were upregulated at the forearm of nonhealers, were mainly ex
50 acetylase (HDAC) inhibition; three (H1F0, IRGM, and WIPI49) were upregulated, and two (PHF15 and PRDM10) were downregulat