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1 -Me-NB1 enables imaging of GluN1/GluN2B NMDA receptor cross talk.
2 ptor activation, suggesting the existence of receptor cross talk.
3 eta-arrestins and reveal their novel role in receptor cross-talk.
4 to study events such as desensitization and receptor cross-talk.
5 a novel mechanism of signal transduction and receptor cross-talk.
6 rc homology phosphatase-1 in Ly49A/chemokine receptor cross-talk.
7 y tool to study the underlying mechanisms of receptor cross-talk.
8 molecular mechanism responsible for cytokine receptor cross-talk.
9 lso discuss recent advances in understanding receptor cross talk and how the activities of guidance c
11 asing interest for potentially circumventing receptor cross-talk and c-MET-mediated acquired resistan
12 s what we believe to be a novel mechanism of receptor cross-talk and highlights the potential importa
13 s provides a novel mechanism that may govern receptor cross-talk and the hierarchy of xenobiotic and
14 tolerance, we propose that G-protein coupled receptor cross-talk and the level of protein kinase C ac
15 ylinositol-3 kinase and Akt, perhaps through receptor cross talk, and that ligand-induced internaliza
17 These results identify a novel system of receptor cross-talk between CD40 and BCR and indicate th
18 findings suggest that Src mediates the inter-receptor cross-talk between Na(+)/K(+)-ATPase and the EG
19 tain tolerance through a mechanism involving receptor cross-talk between the BCR, TLR4, and the IL-6R
20 d heterotrimeric GTP-binding protein-coupled receptor cross talk by which D1 receptors can shift effe
21 n monomer may promote receptor clustering or receptor cross-talking for regulation of the cytoskeleto
22 n of multiple receptors has been ascribed to receptor cross talk; however, the specific molecules tha
25 eserved, indicating that membrane-to-nuclear receptor cross-talk in vivo is modest in the uterus.
26 mic analysis and subsequent investigation of receptor cross-talk indicate that growth signaling betwe
29 receptor-mediated gene transcription through receptor cross-talk, possibly involving competition for
31 and an enhancement of integrin-growth factor receptor cross-talk, specifically in unanchored cell sta
33 ignaling specifically phosphorylates TF in a receptor cross-talk that distinguishes upstream from dow
34 n cytoskeleton is a point of integration for receptor cross talk through modulation of protein dynami
36 resses chemokine receptor function, and such receptor cross-talk was based on the simple mechanism of
38 it between LAMA and LABA as a consequence of receptor cross-talk, which in turn could modify beta-2 r
39 sical association of CD4 and CCR5 results in receptor cross-talk with allosteric CD4-dependent regula
41 s increasing evidence that G-protein-coupled receptors cross-talk with growth factor receptor-mediate
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