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1 in, laminin, leukemia-inhibitory factor, and fibroblast growth factor 4.
2 ior expression of Sonic hedgehog, HoxD13 and fibroblast growth factor-4.
3 atase, FIN13, whose expression is induced by fibroblast growth factor 4 and serum in late G1 phase.
4 ate, including Oct3/4, alkaline phosphatase, fibroblast growth factor 4, and Nanog.
5 em (TS) cells proliferate in the presence of fibroblast growth factor 4, but in its absence, they dif
6  the known autocrine differentiation inducer fibroblast growth factor 4, but, remarkably, it can be p
7 retion of several protumor cytokines such as fibroblast growth factor-4, CX3CL1/fractalkine, neurotro
8 an in vitro spatial and temporal analysis of fibroblast growth factor 4-dependent trophoblast stem ce
9 blocker) derived from the signal sequence of fibroblast growth factor 4 exhibits broad-spectrum antiv
10        Mechanisms, including ras activation, fibroblast growth factor 4 expression, and human DNA met
11 y described the independent isolation of the fibroblast growth factor 4 (FGF-4) gene by NIH3T3 transf
12                We have previously shown that fibroblast growth factor 4 (FGF-4) gene expression in em
13                         Transcription of the fibroblast growth factor-4 (FGF-4) gene during early dev
14 this study, we show that the promoter of the fibroblast growth factor-4 (FGF-4) gene is strongly acti
15                                              Fibroblast growth factor-4 (FGF-4), a highly mitogenic p
16  nm23, DNA methyltransferase, activated ras, fibroblast growth factor-4 (FGF-4), or epidermal growth
17 cluding stromal-derived factor-1 (SDF-1) and fibroblast growth factor-4 (FGF-4), restored thrombopoie
18 retory transforming gene (hst) which encodes fibroblast growth factor-4 (FGF-4).
19 elineate the role of autocrine production of fibroblast growth factor 4 (Fgf4) and associated activat
20 the affected growth factors, the addition of fibroblast growth factor 4 (FGF4) and neutralizing antib
21                        It first appears when fibroblast growth factor 4 (FGF4) deprivation induces di
22  self-renewing conditions in the presence of fibroblast growth factor 4 (FGF4) display increased expr
23 on of a recently acquired retrogene encoding fibroblast growth factor 4 (fgf4) is strongly associated
24                                              Fibroblast growth factor 4 (FGF4) is the key signal driv
25 al genes, including Sonic Hedgehog (Shh) and Fibroblast Growth Factor 4 (Fgf4), was found in Dorking
26 layer of rat embryonic fibroblasts (REFs) in fibroblast growth factor-4 (FGF4) and heparin supplement
27 ifferentiation program, a modified transient fibroblast growth factor-4 (FGF4) promoter-enhancer repo
28 st differentiation into TGCs is regulated by fibroblast growth factor-4 (FGF4), and that geminin is r
29  components such as Sonic hedgehog (Shh) and fibroblast growth factor-4 (Fgf4), but little is known a
30 that the trophoblast lineage, which requires fibroblast growth factor-4 (FGF4), is specified but fail
31 g with advanced stage abundantly express the fibroblast growth factor-4 (FGF4).
32                                              Fibroblast growth factor 4 has been implicated in stimul
33                                    Recently, fibroblast growth factor-4 has been identified as a cruc
34 otein A-II and cortisol levels in plasma and fibroblast growth factor 4, heart-type fatty acid bindin
35 Protein-2) and apical ectodermal ridge (e.g. Fibroblast Growth Factor-4) in response to Sonic hedgeho
36 ls: mouse mammary Mm5MT cells overexpressing fibroblast growth factor 4 (Mm5MT-FGF4) and NGP human ne

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