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1 ranscriptional upregulation and secretion of vascular endothelial growth factor A.
2 important for tumor angiogenesis induced by vascular endothelial growth factor A.
3 wo layers of collagen and in the presence of vascular endothelial growth factor-A.
4 egion via upregulation of the ER target gene vascular endothelial growth factor-a.
5 ia as efficiently as a 21-nt siRNA targeting vascular endothelial growth factor-A.
6 a similar proportion was observed to secrete vascular endothelial growth factor-A.
7 is with comparable magnitude as observed for vascular endothelial growth factor-A.
8 athway, activating HIF-target genes, notably vascular endothelial growth factor-A.
9 mpanied by increased plasma concentration of vascular endothelial growth factor-A.
10 f a novel alginate-based delivery system for vascular endothelial growth factor-A(165) (VEGF) that ex
11 wound beds, fibroblasts are rich sources of vascular endothelial growth factor A, a cytokine necessa
12 h factor AA and BB; placental growth factor; vascular endothelial growth factor A and D; vascular end
14 abundance of the proangiogenic growth factor vascular endothelial growth factor A and promoted the pr
15 crovascular endothelial cells in response to vascular endothelial growth factor A and showed less int
16 tration from E6.5, which increases placental vascular endothelial growth factor A and, thus, vascular
18 try identified significant overexpression of vascular endothelial growth factor-A and C as well as p-
19 poptosis, with significant decreases of both vascular endothelial growth factor-A and nephrin protein
20 ucible factor-1alpha-dependent expression of vascular endothelial growth factor-A and platelet-derive
21 Leishmania major increases the expression of vascular endothelial growth factor-A and vascular endoth
22 neoangiogenesis and increased expression of vascular endothelial growth factor-a and vascular endoth
23 x and examined whether these are modified by vascular endothelial growth factors A and C (VEGFA and V
24 e of BM-mononuclear cells in the presence of vascular endothelial growth factors A and C and endothel
25 ncreased IL-1R antagonist, downregulation of vascular endothelial growth factor A, and glomerular and
26 epression of IL-1alpha and beta, IL-1R1, and vascular endothelial growth factor A, and upregulation o
27 et genes, such as matrix metalloproteinases, vascular endothelial growth factor-A, and chemokine (C-C
28 g against CD31 (vascular endothelial cells), vascular endothelial growth factor-A, and D2-40 (lymphat
29 ced angiogenesis and decreases expression of vascular endothelial growth factor A, angiopoietin 1, an
30 thelial sprouting and vascular leak, such as vascular endothelial growth factor A, are well described
31 rkers and the angiogenesis-related proteins: vascular endothelial growth factor-A, Arginase-1, and CC
32 lase, methylthioadenosine phosphorylase, and vascular endothelial growth factor-A as potential therap
33 ctivated PlexinD1 enhanced the expression of vascular endothelial growth factor-A, but not of inflamm
34 o, ramipril was associated with increases in vascular endothelial growth factor-A by 38% (95% confide
35 rs of proliferation and angiogenesis (Ki-67, vascular endothelial growth factors A/C, vascular endoth
36 growth factor beta 1, alpha 2 macroglobulin, vascular endothelial growth factor A, connective tissue
38 at significantly decreased the expression of vascular endothelial growth factor, a down target of HIF
42 a biomarkers of angiogenesis/arteriogenesis (vascular endothelial growth factor-A, fibroblast growth
43 r zinc finger transcription activator of the vascular endothelial growth factor A gene-has recently e
44 progenitor cell differentiation factor, and vascular endothelial growth factor, a growth factor impo
45 Bevacizumab, a monoclonal antibody against vascular endothelial growth factor A, has shown clinical
46 ody Fab that neutralizes all active forms of vascular endothelial growth factor A--has been evaluated
48 atation of dermal microvessels stimulated by vascular endothelial growth factor A, histamine, and thr
49 oxide synthase-2 and decreased expression of vascular endothelial growth factor A in the OB, striatum
50 responses to fibroblast growth factor-2 and vascular endothelial growth factor-A in "motheaten viabl
51 nesis is associated with lower expression of vascular endothelial growth factor-A in integrin beta5-d
52 esis by releasing extracellular matrix-bound vascular endothelial growth factor A, increasing its bio
55 oxidative stress-induced ROS generation and vascular endothelial growth factor A induction, thus pre
57 mab, a humanized monoclonal antibody against vascular endothelial growth factor A, is currently appro
58 cription polymerase chain reaction; and with vascular endothelial growth factor A isoforms using enzy
60 r resulted in reduced tumor growth, although vascular endothelial growth factor-A levels and vascular
61 trate that FGF upregulated the production of vascular endothelial growth factor A mainly by increasin
62 us also inhibited Akt and p38 stimulation by vascular endothelial growth factor, a major driver of an
63 tes Flt1, a naturally occurring inhibitor of vascular endothelial growth factor-A-mediated angiogenes
65 that the RBP HuR (a.k.a. Elavl1) stabilizes vascular endothelial growth factor-A mRNA, a potent angi
66 the actions of vascular permeability factor/vascular endothelial growth factor-A on both tumor endot
67 urther increased when HemECs were exposed to vascular endothelial growth factor-A or tumor necrosis f
69 increased expression of functionally active vascular endothelial growth factor, a potent vascular pe
70 ptors present in dermal fibroblasts restores vascular endothelial growth factor A production by these
72 ally impaired and produce reduced amounts of vascular endothelial growth factor A, resulting in defic
73 d phosphatidylinositol 3-kinase and inhibits vascular endothelial growth factor A secretion by tumor
74 Maintenance of LSEC differentiation requires vascular endothelial growth factor-A stimulation of nitr
75 -1alpha axis in CLL-BMSCs with production of vascular endothelial growth factor, a survival factor fo
78 The two most abundant secreted isoforms of vascular endothelial growth factor A (VEGF(165) and VEGF
80 er target the proangiogenesis growth factor, vascular endothelial growth factor A (VEGF) by preventin
83 rk was designed to determine the role of the vascular endothelial growth factor A (VEGF) isoforms dur
85 vo and the action of alcohol, glutamate, and vascular endothelial growth factor A (VEGF) on activity,
86 tor tyrosine kinase VEGFR2 after binding the vascular endothelial growth factor A (VEGF) to enhance a
87 are associated with increased expression of vascular endothelial growth factor A (VEGF), a potent en
94 planation for such diversity at the level of vascular endothelial growth factor A (VEGF-A) and other
95 he balance between corneal concentrations of vascular endothelial growth factor A (VEGF-A) and the so
98 ct of hypoxia on VV infection, we found that vascular endothelial growth factor A (VEGF-A) augments o
99 BMP4 expression was negatively regulated by vascular endothelial growth factor A (VEGF-A) by way of
103 epithelial phenotype was enhanced following vascular endothelial growth factor A (VEGF-A) exposure.
105 use of reduced B-cell lymphoma 2 (BCL-2) and vascular endothelial growth factor A (VEGF-A) expression
106 chain of Myosin IIA, resulting in augmented vascular endothelial growth factor A (VEGF-A) expression
108 transporter (xCT), interleukin 6 (IL-6), and vascular endothelial growth factor A (VEGF-A) genes.
112 angioma-derived stem cells for expression of vascular endothelial growth factor A (VEGF-A) in vitro a
120 l vision, and although the angiogenic factor vascular endothelial growth factor A (VEGF-A) is present
121 The transcript of the angiogenic factor vascular endothelial growth factor A (VEGF-A) is subject
122 ies suggest that circulating levels of short vascular endothelial growth factor A (VEGF-A) isoforms,
124 atment, there was a rapid increase in plasma vascular endothelial growth factor A (VEGF-A) levels and
127 kade was more effective at reducing CNV than vascular endothelial growth factor A (VEGF-A) neutraliza
130 e to evaluate retrograde axonal transport of vascular endothelial growth factor A (VEGF-A) protein to
132 KEY POINTS: Progressive depletion of all vascular endothelial growth factor A (VEGF-A) splice iso
133 helial cell migration, and tube formation in vascular endothelial growth factor A (VEGF-A) stimulated
134 lated SMAD1/5/8 (phospho-SMAD), osterix, and vascular endothelial growth factor A (VEGF-A) was carrie
135 occurs despite higher circulating levels of vascular endothelial growth factor A (VEGF-A), a key reg
136 oproteinases-1 (TIMP1), beta2-Microglobulin, Vascular Endothelial Growth Factor A (VEGF-A), and clust
137 f two principal effectors of vasculogenesis, vascular endothelial growth factor A (VEGF-A), and plate
141 e and bind to the Flk-1/KDR receptor for the vascular endothelial growth factor A (VEGF-A), which is
142 it reduced hematopoietic potential caused by vascular endothelial growth factor A (Vegf-a)-dependent
153 Following acute exercise, protein levels of vascular endothelial growth factor-A (VEGF), endostatin
156 omeruli, the proendothelial survival factors vascular endothelial growth factor-A (VEGF-A) and angiop
157 on, tube formation, and increased release of vascular endothelial growth factor-A (VEGF-A) and basic
158 t tamoxifen decreased the mRNA expression of vascular endothelial growth factor-A (VEGF-A) and increa
160 ed retinal function and an imbalance between vascular endothelial growth factor-A (VEGF-A) and pigmen
161 is, collagen quantity, and the expression of vascular endothelial growth factor-A (VEGF-A) and VEGF-C
162 bservation that therapeutic agents targeting vascular endothelial growth factor-A (VEGF-A) associate
168 ed tumor angiogenesis through the release of vascular endothelial growth factor-A (VEGF-A) from cance
170 ut not GLI1, binds to and enhances the human vascular endothelial growth factor-A (VEGF-A) gene promo
172 tes mRNA and protein expression of epidermal vascular endothelial growth factor-A (VEGF-A) in normal
178 implicate a mechanism wherein tumor-derived vascular endothelial growth factor-A (VEGF-A) promotes t
179 nthetic modified RNA (modRNA) encoding human vascular endothelial growth factor-A (VEGF-A) results in
183 tion resolution by suppressing expression of vascular endothelial growth factor-A (VEGF-A), a macroph
184 r-2 (FGF-2), hepatocyte growth factor (HGF), vascular endothelial growth factor-A (VEGF-A), and vascu
185 ene) to increase the beta cell production of vascular endothelial growth factor-A (VEGF-A), angiopoie
186 M had significantly higher concentrations of vascular endothelial growth factor-A (VEGF-A), brain-der
187 action with one of its main natural ligands, vascular endothelial growth factor-A (VEGF-A), contribut
188 binant humanized monoclonal antibody against vascular endothelial growth factor-A (VEGF-A), has clini
190 n derived neurotrophic growth factor (BDNF), vascular endothelial growth factor-A (VEGF-A), insulin-l
191 Prespecified biomarkers included plasma vascular endothelial growth factor-A (VEGF-A), protein e
192 -angiogenic factors and molecules, including vascular endothelial growth factor-A (VEGF-A), SRY-box c
194 he role of a novel antiangiogenic isoform of vascular endothelial growth factor-A (VEGF-A), VEGF-A165
195 define the mechanisms by which PTK7 promotes vascular endothelial growth factor-A (VEGF-A)-induced an
201 network is illustrated by the actions of the vascular endothelial growth factor-A (VEGF-A)/VEGF recep
203 (rAAV) (5 x 10(12) viral particles encoding vascular endothelial growth factor-A [VEGF-A] or thymosi
204 a 4-fold elevation in proangiogenic factors (vascular endothelial growth factor-A [VEGF-A], stromal c
207 d new blood vessel sprouts is coordinated by vascular endothelial growth factor A (VEGFA) and Delta-l
210 a-induced factor 1a (Hif1a) and secretion of vascular endothelial growth factor A (Vegfa) by starved
212 proper through epithelial cell expression of vascular endothelial growth factor A (VEGFA) dependent u
213 ecent evidence indicates a specific role for vascular endothelial growth factor a (Vegfa) during arte
215 d by breaching Bruch's membrane and inducing vascular endothelial growth factor A (VEGFa) expression
217 sease progression through adipocyte-mediated vascular endothelial growth factor A (VEGFA) expression
219 of hypoxia inducible factor (HIF)-1alpha and vascular endothelial growth factor A (VEGFA) in MDA-231
220 at miR-1/206 directly regulate the levels of Vascular endothelial growth factor A (VegfA) in muscle,
221 egulation of angiogenic mediators, including vascular endothelial growth factor A (VEGFA) in OIR.
229 dr expression to enable the DH to respond to vascular endothelial growth factor A (VEGFA) ligand from
230 tes and glomerular endothelial cells through vascular endothelial growth factor A (VEGFA) maintains a
235 in- or rapamycin-evoked mitophagy, increased vascular endothelial growth factor A (VEGFA) production,
236 deletion of hypoxia-response element in the vascular endothelial growth factor A (VEGFA) promoter sh
237 ty of efferocytosis and subsequently blunted vascular endothelial growth factor A (VEGFA) release.
238 oxia-inducible factor 1alpha (Hif1alpha) and vascular endothelial growth factor A (Vegfa) transcripts
239 y of the genes assayed, but up-regulation of vascular endothelial growth factor A (VEGFA) was observe
242 Glucose deprivation induced the secretion of vascular endothelial growth factor A (VEGFA), basic fibr
243 luding those for interleukin-6 (IL-6), IL-8, vascular endothelial growth factor A (VEGFA), cyclin D,
245 sms of Src-PLD1-PKCgamma-cPLA2 activation by vascular endothelial growth factor A (VEGFA), we studied
249 (P </= 0.003) of rs3736265 with a variant in vascular endothelial growth factor A (VEGFA, rs3025033),
251 s of small interfering RNA (siRNA) targeting vascular endothelial growth factor-A (VEGFA) or its rece
254 d; angiogenic and vessel maturation factors (vascular endothelial growth factor a [VEGFa], angiopoiet
255 w that L. major infection initiates enhanced vascular endothelial growth factor-A/VEGFR-2 signaling a
258 ible factor-1alpha protein and expression of vascular endothelial growth factor-A were increased in e
259 rstitial cells (mesenchymal cells), requires vascular endothelial growth factor A, which stimulates m
260 essel formation in endothelial cells through vascular endothelial growth factor-A, which was up-regul
261 ody Fab that neutralizes all active forms of vascular endothelial growth factor A--with photodynamic
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