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1 lar endothelial growth factor-A (VEGF-A) and pigment epithelium-derived factor.
2 Inhibitor, Clade F) gene which encodes PEDF (pigment epithelium-derived factor), a potent inhibitor o
3 antichymotrypsin), a neuroprotective factor (pigment epithelium-derived factor), an antiangiogenesis
4 high glucose while increasing the levels of pigment epithelium-derived factor, an endogenous inhibit
5 The bioactivity of signaling activated by pigment epithelium-derived factor and DHA uncovered syne
7 three agents, combretastatin A-4 phosphate, pigment epithelium-derived factor, and angiopoietin-2.
9 -angiogenic activity of thrombospondin-1 and pigment epithelium-derived factor both in vitro and in v
11 at two such inhibitors, thrombospondin-1 and pigment epithelium-derived factor, derive specificity fo
12 elial growth factor while increasing that of pigment epithelium-derived factor in diabetic retinas.
14 re, we show that neurotrophins, particularly pigment epithelium-derived factor, induce NPD1 synthesis
15 tor receptor-Erk1/2 signaling pathway by the pigment epithelium-derived factor is sufficient to maint
16 rly population doubling level cDNA-1/retinal pigmented epithelium-derived factor) is a single-copy, q
19 ial growth factor (VEGF) and anti-angiogenic pigment epithelium derived factor (PEDF) may cause choro
20 lial growth factor (VEGF) and antiangiogenic pigment epithelium derived factor (PEDF) may cause choro
21 R), and VEGFR3 (FLT4); and the gene encoding pigment epithelium-derived factor (PEDF) (SERPINF1) was
22 te cyclase (GUC2D), beta-arrestin 2 (ARRB2), pigment epithelium-derived factor (PEDF) and recoverin (
23 rain-derived neurotrophic factor (BDNF), and pigment epithelium-derived factor (PEDF) and significant
24 Here, we identify the angiogenesis inhibitor pigment epithelium-derived factor (PEDF) as a key inhibi
26 ransmembrane (IFITM)-like protein (BRIL) and pigment epithelium-derived factor (PEDF) defects cause t
28 ferative diabetic retinopathy, we found that pigment epithelium-derived factor (PEDF) effectively aba
29 ors tested the effect of adenoviral vectored pigment epithelium-derived factor (PEDF) gene transfer o
32 F) and up-regulates an angiogenic inhibitor, pigment epithelium-derived factor (PEDF) in a dose-depen
33 tudy, we tested the effect of treatment with pigment epithelium-derived factor (PEDF) in combination
35 duction of a secreted protein, expression of pigment epithelium-derived factor (PEDF) in mice harbori
36 er AAV-mediated intraocular gene transfer of pigment epithelium-derived factor (PEDF) inhibits the de
53 a1 transcription factor and are dependent on pigment epithelium-derived factor (PEDF) on the outer su
54 ral (rAAV) serotype-2-mediated expression of pigment epithelium-derived factor (PEDF) or Kringle doma
55 ation of the known neuroprotective molecule, pigment epithelium-derived factor (PEDF) plus docosahexa
57 ascular endothelial growth factor (VEGF) and pigment epithelium-derived factor (PEDF) protein, and mR
59 vIII induces the expression and secretion of pigment epithelium-derived factor (PEDF) via activation
61 eptors (VEGFR-1, VEGFR-2, Npn-1, Npn-2), and pigment epithelium-derived factor (PEDF) were also exami
62 asminogen activator inhibitor-1 (PAI-1), and pigment epithelium-derived factor (PEDF) were measured b
64 identify proteolytic activities that cleave pigment epithelium-derived factor (PEDF), a member of th
65 tified a novel inhibitor of the Wnt pathway, pigment epithelium-derived factor (PEDF), a multifunctio
69 f these ocular compartments is identified as pigment epithelium-derived factor (PEDF), a protein prev
72 n difference, we have measured the levels of pigment epithelium-derived factor (PEDF), an angiogenic
73 ociated transcription factor (MITF) acts via pigment epithelium-derived factor (PEDF), an antiangioge
75 ng endostatin, thrombospondin-1 (TSP-1), and pigment epithelium-derived factor (PEDF), as well as by
79 or 26 weeks, was analyzed by immunoassay for pigment epithelium-derived factor (PEDF), vascular endot
86 corneas were harvested for ELISA (VEGFR3 and pigment epithelium-derived factor [PEDF]) and for quanti
87 l, revealed that they constitutively secrete pigment epithelium-derived factor, PEDF, which is known
88 ults further indicate that activation of the pigment epithelium-derived factor receptor-Erk1/2 signal
90 ing alpha-1 microglobulin/bikunin precursor, pigment epithelium-derived factor, surfactant protein B,
92 th increased levels of type III collagen and pigment epithelium-derived factor, which accumulate in t
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