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1 DL) cells have been shown to express several integrins (alphav, alpha5, beta1, beta3) that use RGD (a
4 ed a direct physical interaction of MBD with integrins alphav and beta1, caveolin-1, and transferrin
6 In addition, a cross-talk between EMP2 and integrins alphaV and beta3 was shown in the regulation o
8 a tumor vasculature-specific antiangiogenic integrin alphav antagonist and tumor-specific antibody-i
9 urthermore, simultaneous treatments with the integrin alphav antagonist and tumor-specific antibody-I
10 monotherapies with either an antiangiogenic integrin alphav antagonist or antibody-IL-2 fusion prote
11 Systemic administration of neutralizing anti-integrin alphaV antibody or a genetic deficiency of inte
14 of mouse mAb LM609 that is directed to human integrin alphav beta3 and has potential applicability in
15 We have shown that osteopontin binding to integrin alphav beta3 in osteoclasts stimulates gelsolin
16 NA plasmids encoding the individual complete integrin alphaV, beta3, and beta6 subunits were used to
18 ine osteoclast precursors bind matrix is the integrin alphav beta5 and that granulocyte-macrophage co
20 We report here the expression of soluble integrin alphav beta5, which retains the ability to reco
21 conclude that deletion or inhibition of the integrin alphav beta6 did not protect animals from P. ae
24 s revealed that PKCalpha was up-regulated by integrin alphav in a three-dimensional microenvironment-
26 on and blocked the signaling transduction by integrin alphaV, inhibited migration signaling pathways
31 alpha constitutes a crucial component of the integrin alphav-mediated pathway(s) that promote p53 rel
33 raction with integrin alphaV is required for integrin alphaV-mediated Src activation, and the subsequ
36 ectin and vitronectin, by down-regulation of integrin alphav, or by a peptide corresponding to 13 aa
37 to macrophages and, considering that Mer and integrin alphaV promote phagocytosis of apoptotic cells,
38 zation of sOPN and blockade of its receptor, integrin alphav, significantly inhibited CD4(+) T cell m
40 neration of Tregs required expression of the integrin alphav subunit by DCs; mice that lacked alphav
42 TSRI265) selected for its ability to bind to integrin alphav(v)beta3 and block alpha(v)beta3 interact
45 microenvironments requires the expression of integrin alphav, which acts to suppress p53 activity.
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