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1 6 exerts many of its effects via the soluble interleukin-6 receptor.
2 embles cytokine receptors, which include the interleukin-6 receptor.
3 either express low or no detectable surface interleukin-6 receptor.
4 iation with ErbB-2, the EGF-receptor, or the interleukin-6 receptor.
5 GF-alpha, cell adhesion receptor L-selectin, interleukin 6 receptor alpha subunit, beta-amyloid precu
6 ult from a transcriptional downregulation of interleukin-6 receptor alpha (IL-6Ralpha) with IL-6Rbeta
7 te that the proportion of CD5(+) relative to interleukin-6 receptor alpha (IL-6Ralpha)-expressing B c
9 The efficacy and safety of tocilizumab, an interleukin 6 receptor-alpha inhibitor, was assessed in
10 cient T cells showed decreased expression of interleukin-6 receptor-alpha and other Tfh cell-related
11 sGAP, AP-2, p53BP-2 (p53-binding protein-2), interleukin-6 receptor-alpha, chloride channel CLCN5, an
12 duction of interleukin-6), and serum soluble interleukin-6 receptor (an enhancer of myeloma cell resp
14 7), adaptive immune response (interleukin32, interleukin 6 receptor), and reactive oxygen species (ne
16 atory drugs and glucocorticoids) to the anti-interleukin-6 receptor antibody tocilizumab (at a dose o
21 cacy and safety of strategies initiating the interleukin-6 receptor-blocking monoclonal antibody toci
22 sly identified gene-protein associations for interleukin-6 receptor, chemokine CC-4, angiotensin-conv
23 cluding T cell factor-1, Ikaros, AP-1, CK-2, interleukin-6 receptor E (IL-6RE), ISRE, GAS, NF-kappaB,
26 s was paralleled by a down-regulation of the interleukin 6 receptor (IL-6R) on naive CD4(+) T cells o
28 es of CD341 cells, simultaneous reduction of interleukin-6 receptor (IL-6R) expression on myeloid pro
29 es to map integratively the epitope of human interleukin-6 receptor (IL-6R) for two adnectins with di
31 lin-like growth factor receptor (IGF-1R) and interleukin-6 receptor (IL-6R) signaling (eg, IKK/NF-kap
32 /or the clinical monoclonal antibody against interleukin-6 receptor (IL-6R), tocilizumab, prevented M
33 itors prevent shedding of both TNFR1 and the interleukin-6 receptor (IL-6Ralpha), we hypothesized tha
34 though neither Toll-like receptor (TLR)2 nor interleukin 6 receptor (IL6R) signaling is involved, a r
35 pecifically cleaved by RHBDL2, including the interleukin-6 receptor (IL6R), cell surface protease inh
36 s in the levels of interleukin-6 and soluble interleukin-6 receptor in acute meningococcal septicemia
37 s in the levels of interleukin-6 and soluble interleukin-6 receptor in acute meningococcemia may affe
38 ly that alterations in the levels of soluble interleukin-6 receptor in septic shock could affect the
39 ia is associated with a reduction in soluble interleukin-6 receptor levels in proportion to disease s
41 ls are elevated in patients with MM; soluble interleukin-6 receptor may amplify circulating interleuk
42 petuation has led to the use of an antihuman interleukin-6 receptor monoclonal antibody, tocilizumab.
45 protein gene, the apolipoprotein E gene, the interleukin-6 receptor protein gene, or the CRP gene its
47 rotein S[rs6123] in the schizophrenia group; Interleukin-6 receptor[rs7553796] in both the control an
49 s shows that caveolin-1 is co-localized with interleukin-6 receptor signal transducing chain gp130 an
50 ocyte receptor (GLM-R), with homology to the interleukin-6 receptor signal transducing chain, gp130,
53 tivation-regulated chemokine (TARC), soluble interleukin 6 receptor (sIL-6R), and soluble tumor necro
55 ow PC labeling indices, higher serum soluble interleukin-6 receptor (sIL-6R) levels, and a higher pro
57 active protein [CRP], interleukin 6, soluble interleukin 6 receptor [sIL-6R], soluble gp130, tumor ne
58 thway, including janus kinase-1, gp 130, the interleukin-6 receptor, STAT1, and STAT3, were examined
60 r's laboratory reveals that the gp130-linked interleukin-6 receptor, which usually activates STAT3 pr
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