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1  that the catalytic activity of the Ser/Thr kinase Aurora A was inhibited by the oxidation of a conserved cysteine residu
2 y of MRP3 promoter (ABCC3pr) revealed that ABCC3pr activity was inhibited by SOX17 expression and SOX2/SOX9 silencing.
3 ted in simulated gastric fluid and their enzymatic activity was inhibited upon heat treatment.
4                                         Kallikrein activity was inhibited while the renin-angiotensin system (RAS) upregu
5 rylated on IQGAP1 when phosphotyrosine phosphatase activity was inhibited in cells.
6 atocytes using the developed protocol could be observed and was inhibited by ribavirin.
7 infection was promoted in ATG5- or ATG7-silenced plants and was inhibited in GAPC-silenced plants where autophagy was act
8 reover, DSBs were not detected after therapy when apoptosis was inhibited, supporting a framework in which DSBs are not d
9 ge, where both Arp2/3 and Mena/VASP-based filament assembly was inhibited.
10               Subsequently, the STAT3 pathway in astrocytes was inhibited with WP1066 to determine the role of STAT3-medi
11 '-sulfate ligated to an inert polymer scaffold, and binding was inhibited by competing dextran sulfate.
12 ed BMDCs exacerbate a live challenge with RSV infection but was inhibited when BMDCs were treated with GSK J4 prior to se
13                         Leukocyte infiltration into the CNS was inhibited in cortactin-deficient mice, and lack of cortac
14                                Surprisingly, THIK-1 current was inhibited when IBMX was applied from the extracellular si
15                           The HPK1-mediated AXL degradation was inhibited by the endocytic pathway inhibitors leupeptin,
16                                    When protein degradation was inhibited, we observed a coordinate dramatic reduction in
17  changes in exRNA population when enzymatic RNA degradation was inhibited.
18 ies, while exposure of CD4-induced (CD4i) non-bNAb epitopes was inhibited.
19         Moreover, when endosome translocation or exocytosis was inhibited by depletion of Protrudin or Synaptotagmin VII,
20 levels were decreased in Deltapa2072, and biofilm formation was inhibited, compared to wild type.
21                                           However, when GBA was inhibited, TJP1 levels remained stable, suggesting that B
22                                      Neurons in which GCase was inhibited by conduritol beta-epoxide did not increase the
23                                                  Glycolysis was inhibited in cells and mice by administration of a small
24                                            Coliforms growth was inhibited at pH 2 even at the absence of ultrasonic treat
25 le administration of (67)Cu-CuSarTATE (5 MBq), tumor growth was inhibited by 75% compared with vehicle control.
26                                    Binding to CHX ImmunoCAP was inhibited by ALX in 1/32 sera, and binding to PHMB was bl
27 d from transient to sustained when receptor internalization was inhibited with drugs or mutations, or when cells expresse
28                                Tumor cell migration to LECs was inhibited by blocking CXCL11 whereas recombinant CXCL11 s
29                                              When lipolysis was inhibited, the stress-induced insulin resistance and hype
30 r, TNFalpha release induced by 12(S)-HETE-lysophospholipids was inhibited by the TNFalpha converting enzyme inhibitor TAP
31                  In contrast, HO-1-mediated heme metabolism was inhibited at subsaturating POR.
32 A tumors subcutaneously implanted into immunodeficient mice was inhibited by 5-fluorouracil.
33        In critically ill patients, we showed that mitophagy was inhibited in blood monocytes of patients with sepsis as c
34  (Nox5 inhibitor) and Nox5 siRNA, while p53 phosphorylation was inhibited by NoxA1ds (Nox1 inhibitor).
35                                    C2C12 cell proliferation was inhibited in a dose-dependent manner following 48 h 3-MPA
36                                    Lymphocyte proliferation was inhibited after 2 h of noradrenaline infusion, and both c
37 , Chikungunya, or eastern equine encephalitis pseudoviruses was inhibited with greater efficiency by the liposomes contai
38 pp71 is not protein S-nitrosylated, host antiviral response was inhibited.
39                               Phosphatase activity of Siw14 was inhibited by oxidation that was reversible.
40  increased sensitivity to hydrogen peroxide-induced stress, was inhibited in its ability to form biofilm and had reduced
41                                 However, when LOS synthesis was inhibited during Chlamydia trachomatis infection, HeLa ce
42 retch evoked a rapid increase in transmembrane current that was inhibited by antagonists of the mechanogated channel Piez
43 regate with F nucleatum subspecies in vitro; an effect that was inhibited by blocking or mutating the adhesin RadD on Fus
44 ivo in monocytes from healthy volunteers, a phenomenon that was inhibited by platelet P-selectin neutralization or integr
45 differentiated into ASC in response to Ag in vivo, but this was inhibited in the presence of NP-specific IgG.
46  the transfer-messenger RNA system, even when transcription was inhibited.
47 mdx macrophages revealed functional activity of Cx43, which was inhibited by administration of Gap19 peptide mimetic, a C
48 a1 caused an increase in [Ca(2+)](i) and PS exposure, which was inhibited by its antagonist Dooku1 and the PIEZO1 inhibit
49  In contrast, amino-cSS supported protein expression, which was inhibited upon photoisomerization to amino-tSS.
50 ctor-alpha, when cultured under hyperglycemic stress, which was inhibited by heparin.