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1 n-activated protein kinase and overexpressed fibroblast growth factor receptor 1.
2 elial growth factor receptor 2 (VEGFR-2) and fibroblast growth factor receptor 1.
3 asic fibroblast growth factor for binding to fibroblast growth factor receptor 1.
4 lar endothelial growth factor receptor-2 and fibroblast growth factor receptor-1.
5 volves fibroblast growth factor-2 as well as fibroblast growth factor receptor-1.
6 the second half of Ig-like domain 3 (D3) of fibroblast growth factor receptors 1-3 (FGFR1 to -3) gen
8 s of hypertrophy, including type X collagen, fibroblast growth factor receptors 1-3, parathyroid horm
9 vitro, this differentiation was inhibited by fibroblast growth factor receptor-1 Ab, demonstrating a
11 llagen and fibronectin and the expression of fibroblast growth factor receptor-1 and suppressed the c
13 lar endothelial growth factor, cysteine-rich fibroblast growth factor receptor-1, and platelet-derive
14 usion is inhibited using a dominant-negative fibroblast growth factor receptor-1 construct, whereas t
16 FK506-binding protein (F36V) fused with the fibroblast growth factor receptor-1 cytoplasmic domain.
18 as inhibited the mitogenic activity of both fibroblast growth factor receptor 1-expressing BaF3 cell
19 ellular matrix protein production, increased fibroblast growth factor receptor-1 expression, and redu
22 owever, DNA synthesis and phosphorylation of fibroblast growth factor receptor-1 (FGFR-1) induced by
24 of basic fibroblast growth factor (bFGF) and fibroblast growth factor receptor-1 (FGFR-1) messenger R
25 alters inclusion of the alpha exon in human fibroblast growth factor receptor-1 (FGFR-1) mRNA transc
27 As coding for dominant-negative forms of the fibroblast growth factor receptors 1 (FGFR-1) and 2 (FGF
28 rrelations of diseases caused by variants in Fibroblast Growth Factor Receptor 1 ( FGFR1) and report
29 revious studies have individually implicated fibroblast growth factor receptor 1 (FGFR1) and canonica
31 this class inhibited the kinase activity of fibroblast growth factor receptor 1 (FGFR1) and showed d
33 infection, and that AAV also requires human fibroblast growth factor receptor 1 (FGFR1) as a co-rece
35 post-implantation lethality associated with fibroblast growth factor receptor 1 (FGFR1) deficiency,
36 L in cell motility control via regulation of fibroblast growth factor receptor 1 (FGFR1) endocytosis.
39 on and differentiation via expression of the fibroblast growth factor receptor 1 (FGFR1) gene is posi
40 atively spliced alpha-exon of the endogenous fibroblast growth factor receptor 1 (FGFR1) gene, which
53 lpha-exon by alternative RNA splicing of the fibroblast growth factor receptor 1 (FGFR1) primary tran
55 d growth factor receptor alpha (PDGFRA), and fibroblast growth factor receptor 1 (FGFR1) to cell prol
57 expression of alphaA- and betaB2-crystallin, fibroblast growth factor receptor 1 (FGFR1), and major i
59 tivated with other tyrosine kinases, such as fibroblast growth factor receptor 1 (FGFR1), concomitant
60 rosine residues to the signaling capacity of fibroblast growth factor receptor 1 (FGFR1), stably tran
61 nescence resonance energy transfer analysis, fibroblast growth factor receptor 1 (FGFR1)-5-hydroxytry
64 contrast, hypoxic mice carrying a disrupted fibroblast growth factor receptor-1 (Fgfr1) gene in GFAP
67 which the ZNF198 was fused to exon 9 of the fibroblast growth factor receptor-1 (FGFR1), a gene know
68 zed ES lines carrying targeted mutations for fibroblast growth factor receptor-1 (fgfr1), a receptor
69 on-cleavage screen, including Hsp70, Notch1, fibroblast growth factor receptor-1 (FGFR1), poly-A-bind
70 ell-surface proteins cytokeratin-7 (CK7) and fibroblast growth factor receptor-1 (FGFR1), which are t
72 l structure of the tyrosine kinase domain of fibroblast growth factor receptor 1 (FGFR1K) has been de
73 s translocation results in the fusion of the fibroblast growth factor receptor 1 gene (FGFR1), a memb
75 hypothalamic amenorrhea: two variants in the fibroblast growth factor receptor 1 gene FGFR1 (G260E an
76 13q11-q12, was recently shown to fuse to the fibroblast growth factor receptor 1 gene in the t(8;13)(
77 mal growth factor receptor (HEGFR) and human fibroblast growth factor receptor 1 (HFGFR1) mRNAs in th
78 , we discovered that activation of inducible fibroblast growth factor receptor-1 (iFGFR1) in the mamm
80 the production of the high affinity form of fibroblast growth factor receptor-1 in glioblastomas.
81 r-1 Ab, demonstrating a role of the CD56 and fibroblast growth factor receptor-1 interaction in this
82 old of CSK is most similar to c-Src, Hck and fibroblast growth factor receptor 1 kinase (FGFR1K) and
83 et-derived growth factor receptor beta and a fibroblast growth factor receptor 1 kinase inhibitor) an
84 cible transcript-3.0 (wit3.0), also known as fibroblast growth factor receptor 1 oncogene partner 2 (
85 ss in self-renewal occurs via alterations in fibroblast growth factor receptor-1, p38alpha and p38bet
88 lar endothelial growth factor receptor-2 and fibroblast growth factor receptor-1 that are two key gro
89 thelial growth factor receptors 1, 2, and 3, fibroblast growth factor receptors 1 through 4, platelet
91 d that cellular transfectants expressing the fibroblast growth factor receptor 1 variant are mitogeni
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