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1 hages, demonstrating a key role for IL-1beta autocrine secretion in Nod2-mediated responses.
2  in isolated myocytes, suggesting continuous autocrine secretion of A2 into a restricted diffusion co
3 nes where they are transmurally regulated by autocrine secretion of A2 into the T-system lumen and ac
4                                              Autocrine secretion of cytokines by metastatic colorecta
5                              We propose that autocrine secretion of exosomes powerfully promotes dire
6 t costimulation of ErbB2 and TGFbeta induces autocrine secretion of factors that are sufficient to in
7                                              Autocrine secretion of FAS ligand and upregulated FAS ex
8  molecular mechanisms that lead to sustained autocrine secretion of growth factors, permanent T-cell
9      FcepsilonRI stimulation of MCs promotes autocrine secretion of HK-1, which signals through NK1R
10 n and that this response can be sustained by autocrine secretion of IFN-alpha.
11 t Ang II's actions were not mediated via the autocrine secretion of IGF I.
12 c cells appear to be mediated mainly through autocrine secretion of IL-10 and subsequent activation o
13 ted with the ability of LMP2A to inhibit the autocrine secretion of IL-6 from carcinoma cell lines.
14 oted migration of a2Neu was dependent on the autocrine secretion of IL-8 from a2Neu.
15 t not for IL-6, revealing a critical role of autocrine secretion of LIF in TNF-alpha-induced STAT3 ac
16 n of the ERK/MAP kinase pathway promoted the autocrine secretion of megakaryocytic lineage determinat
17                                          The autocrine secretion of OPN appears to play an important
18     This basal phosphorylation was linked to autocrine secretion of TGF-beta in eosinophils.
19  of Ras(V12) are not the result of increased autocrine secretion of VEGF.
20     Because the critical effects of IL-1beta autocrine secretion on MAPK activation are observed as e

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