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1 ic rings and neoangiogenesis in chick embryo chorioallantoic membrane.
2 U human prostate cancer cells growing on the chorioallantoic membrane.
3 al growth factor-induced angiogenesis on the chorioallantoic membrane.
4 h factor-induced angiogenesis in the chicken chorioallantoic membrane.
5 hen applied to the rabbit cornea and chicken chorioallantoic membrane.
6 ctor-induced neovascularization of the chick chorioallantoic membrane.
7 sed avascular zones when placed on the chick chorioallantoic membrane.
8 ort hairpin RNAs from cells that invaded the chorioallantoic membrane.
9 d genes and tested for invasion of the chick chorioallantoic membrane.
10 mbly and opposes angiogenesis in the chicken chorioallantoic membrane.
11 esis assays, the frog embryo and the chicken chorioallantoic membrane.
12 ase 2 activation and angiogenesis on chicken chorioallantoic membranes.
13 vement of Na+ in either direction across the chorioallantoic membrane according to the changing deman
14 mation, and suppresses angiogenesis in chick chorioallantoic membrane, after subcutaneous implantatio
15 orphogenesis, and blood vessel growth in the chorioallantoic membrane and in Matrigel plug assays.
18 ntagonists inhibit angiogenesis in the chick chorioallantoic membrane and neovascularization of mouse
20 peptide were demonstrated by using the chick chorioallantoic membrane and rat corneal micropocket ass
21 ood vessels in vivo as assessed by the chick chorioallantoic membrane and the matrigel plug assays.
22 r endothelial growth factor-stimulated chick chorioallantoic membranes and basic fibroblast growth fa
23 nists specifically inhibited angiogenesis in chorioallantoic membranes and in the retina and suppress
27 icantly impaired retinal neovascularization, chorioallantoic membrane angiogenesis, and xenograft tum
28 endothelial growth factor-dependent chicken chorioallantoic membrane angiogenic assay recapitulated
30 nd high electric field, was first applied to chorioallantoic membrane as a model system and then to r
31 rring was explored in HDFs, zebrafish, chick chorioallantoic membrane assay (CAM), and a porcine skin
32 GRO-alpha enhanced angiogenesis in the chick chorioallantoic membrane assay 2.2-fold, providing direc
33 bited angiogenesis, as analyzed by a chicken chorioallantoic membrane assay and a human umbilical vei
34 imately 3-fold decrease in tumor growth on a chorioallantoic membrane assay and approximately 2-fold
36 oblast growth factor FGF2 (97%) in a chicken chorioallantoic membrane assay at 270 nM, and peptide 40
37 inhibit angiogenesis in vivo using the chick chorioallantoic membrane assay by the inhibition of capi
38 tion potential in vivo in the chicken embryo chorioallantoic membrane assay for blood vessel penetrat
40 Angiogenesis induced by FGF2 in the chick chorioallantoic membrane assay was also inhibited by SCH
41 nhibited angiogenesis in vivo in the chicken chorioallantoic membrane assay, and in the Lewis lung sy
42 lary formation on Matrigel, and chick embryo chorioallantoic membrane assay, bortezomib induced a dos
43 l AngsFvs elicited angiogenesis in the chick chorioallantoic membrane assay, demonstrating that Ang i
44 binant Del1 was evaluated in an in ovo chick chorioallantoic membrane assay, it was found to have pot
45 sculitis disrupted blood flow in the chicken chorioallantoic membrane assay, suggesting an antiangiog
49 ected in vivo angiogenesis assay and a chick chorioallantoic membrane assay, we show that Nodal promo
51 s was observed with GW654652 using the chick chorioallantoic membrane assay, whereas GW654652 produce
52 (rat aortic ring assay), and in vivo (chick chorioallantoic membrane assay, zebrafish, murine wild-t
71 ells induced angiogenesis in "in vivo" chick chorioallantoic membrane assays that could be reversed w
74 giogenin-induced angiogenesis in the chicken chorioallantoic membrane at a dose as low as 20 ng per e
76 sing recombinant fragments of the protein on chorioallantoic membrane (CAM) angiogenesis and endothel
77 released from a polymeric implant in a chick chorioallantoic membrane (CAM) assay and laser-induced e
80 ls (HUVEC) differentiation assay and chicken chorioallantoic membrane (CAM) assay we document that st
81 is: the endothelial cell culture system, the chorioallantoic membrane (CAM) assay, and the laser-indu
82 epG2 tumor growth in a modified chick embryo chorioallantoic membrane (CAM) assay, associated with a
86 says using human vascular endothelial cells, chorioallantoic membrane (CAM) assays and xenograft tumo
88 tested the hypothesis that the chick embryo chorioallantoic membrane (CAM) can be used as a bioreact
89 collagen onplants placed on the chick embryo chorioallantoic membrane (CAM) has been used in this stu
94 lied topically on embryonic day (E) 7 to the chorioallantoic membrane (CAM) of quail embryos cultured
95 nic growth factors in onplants placed on the chorioallantoic membrane (CAM) of the chick embryos is c
96 nal, Myr-P3k, can induce angiogenesis in the chorioallantoic membrane (CAM) of the chicken embryo.
97 MD on the production of blood vessels in the chorioallantoic membrane (CAM) of the developing chicken
98 tracers, but the growth of tumors on chicken chorioallantoic membrane (CAM) provides a more rapid, lo
99 also used in vivo tumor growth on the chick chorioallantoic membrane (CAM) to observe the disseminat
100 s (HUVECs) and neovascularization in chicken chorioallantoic membrane (CAM) was examined by MTT assay
101 d in developing blood vessels of the chicken chorioallantoic membrane (CAM), a highly vascular embryo
102 injected intravenously into the chick embryo chorioallantoic membrane (CAM), and mRNA levels in the m
103 fibroblast growth factor (bFGF) on the chick chorioallantoic membrane (CAM), endothelial cell mitogen
107 vessels, and eventually observed inside the chorioallantoic membrane capillaries, thus reflecting ea
110 the central cell-binding domain to the chick chorioallantoic membrane enhanced angiogenesis in an int
112 itazone suppresses angiogenesis in the chick chorioallantoic membrane, in the avascular cornea, and i
113 nt fibroblasts explanted atop the live chick chorioallantoic membrane lack tissue-invasive potential
114 avasation of tumor cells in an in vivo chick chorioallantoic membrane model of metastasis as well as
118 inhibits angiogenesis in Matrigel and chick chorioallantoic membrane models and also inhibits metast
120 y and migration assays) and in vivo (chicken chorioallantoic membrane) models and were found to exhib
121 Xenograft Panx1-KD cells grown within the chorioallantoic membrane of avian embryos developed tumo
122 cells from the two HT-1080 variants onto the chorioallantoic membrane of chick embryos and measured l
124 y until an assay of ectodermal pocks of the chorioallantoic membrane of chicken embryos was introduc
125 of endothelial cells; (c) when placed on the chorioallantoic membrane of chicken embryos, these cells
127 ox, LoVo and SW-480 tumor transplants on the chorioallantoic membrane of embryonated hen eggs showed
128 x 3c also disrupted the blood vessels in the chorioallantoic membrane of fertilized chicken eggs.
129 d in two in vivo models of angiogenesis: the chorioallantoic membrane of the chick assay and the mous
131 products in collagen onplants grafted on the chorioallantoic membrane of the chicken embryo, we demon
132 It also blocked the growth of tumors on the chorioallantoic membranes of 10-day chicken embryos.
133 in could inhibit the growth of tumors on the chorioallantoic membranes of chicken embryos and in syng
134 e xenografts in a novel system that employed chorioallantoic membranes of fertilized chicken eggs as
135 rthermore, when grown in vivo in the chicken chorioallantoic membrane, primary tumors derived from Cx
136 lginate-g-pyrrole hydrogel system on chicken chorioallantoic membranes resulted in the formation of b
137 ed expression of Hox D3 in vivo on the chick chorioallantoic membrane retained EC in this invasive st
138 ure of newborn condylar cartilage on a chick chorioallantoic membrane showed that after 5 d the cells
140 neovascularization in an experimental quail chorioallantoic membrane system and Matrigel plug format
142 constitutively expressed Hox B3 in the chick chorioallantoic membrane using avian retroviruses that r
143 ls of tumor cell intravasation in the distal chorioallantoic membrane using quantitative human-specif
144 he primary tumor (i.e., intravasate into the chorioallantoic membrane vasculature and metastasize to
146 g of human HT-1080 fibrosarcoma cells on the chorioallantoic membrane was used in conjunction with qu
147 antiangiogenic activity of HKa in the chick chorioallantoic membrane, was inhibited completely by an
149 ation and inhibits angiogenesis in the chick chorioallantoic membrane, whereas a fragment of TSP1 con
150 mediated Ras and c-Raf activity on the chick chorioallantoic membrane, whereas blockade of FAK or int
151 s on the primitive vascular bed of the chick chorioallantoic membrane, which has striking similaritie
152 T-1080 fibrosarcoma cells grafted onto chick chorioallantoic membranes, which was similar to cisplati
153 of zebrafish or local treatment of the chick chorioallantoic membrane with ScA resulted in dose-depen
154 wth factor-induced angiogenesis on the chick chorioallantoic membrane, with an IC50 of 10 microM.
155 etion reduced tumor development in a chicken chorioallantoic membrane xenograft model of human breast
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