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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  of xenografted MKL-1 and WaGa tumors on the chorioallantoic membrane.
9 ort hairpin RNAs from cells that invaded the chorioallantoic membrane.
10 d genes and tested for invasion of the chick chorioallantoic membrane.
11 mbly and opposes angiogenesis in the chicken chorioallantoic membrane.
12 esis assays, the frog embryo and the chicken chorioallantoic membrane.
13 ase 2 activation and angiogenesis on chicken chorioallantoic membranes.
14 vement of Na+ in either direction across the chorioallantoic membrane according to the changing deman
15 mation, and suppresses angiogenesis in chick chorioallantoic membrane, after subcutaneous implantatio
16 orphogenesis, and blood vessel growth in the chorioallantoic membrane and in Matrigel plug assays.
17 ood vessels in vivo as assessed by the chick chorioallantoic membrane and Matrigel plug assays.
18 elial growth factor (VEGF) function in chick chorioallantoic membrane and matrigel plug assays.
19 ntagonists inhibit angiogenesis in the chick chorioallantoic membrane and neovascularization of mouse
20 n, microtubule formation and angiogenesis in chorioallantoic membrane and nude mice models.
21 peptide were demonstrated by using the chick chorioallantoic membrane and rat corneal micropocket ass
22 ood vessels in vivo as assessed by the chick chorioallantoic membrane and the matrigel plug assays.
23 ogenic activity by two in vivo models, chick chorioallantoic membrane and zebrafish embryos.
24 r endothelial growth factor-stimulated chick chorioallantoic membranes and basic fibroblast growth fa
25 nists specifically inhibited angiogenesis in chorioallantoic membranes and in the retina and suppress
26       Breast cancer cells implanted on chick chorioallantoic membranes and treated with CoCl(2), to m
27 scularized 3D tumors grown on chicken-embryo chorioallantoic membranes, and a syngeneic PC mouse mode
28                      Finally, in the chicken chorioallantoic membrane angiogenesis assay, FGF-BP1 syn
29 is more potent in blocking C16-induced chick chorioallantoic membrane angiogenesis than C16S.
30 icantly impaired retinal neovascularization, chorioallantoic membrane angiogenesis, and xenograft tum
31  endothelial growth factor-dependent chicken chorioallantoic membrane angiogenic assay recapitulated
32                                              Chorioallantoic membrane application of follistatin (1 m
33 nd high electric field, was first applied to chorioallantoic membrane as a model system and then to r
34 ts on vascularisation was examined using the chorioallantoic membrane assay (CAM) model and compared
35 rring was explored in HDFs, zebrafish, chick chorioallantoic membrane assay (CAM), and a porcine skin
36 GRO-alpha enhanced angiogenesis in the chick chorioallantoic membrane assay 2.2-fold, providing direc
37 bited angiogenesis, as analyzed by a chicken chorioallantoic membrane assay and a human umbilical vei
38 imately 3-fold decrease in tumor growth on a chorioallantoic membrane assay and approximately 2-fold
39                                Using chicken chorioallantoic membrane assay and vascular endothelial
40 oblast growth factor FGF2 (97%) in a chicken chorioallantoic membrane assay at 270 nM, and peptide 40
41 inhibit angiogenesis in vivo using the chick chorioallantoic membrane assay by the inhibition of capi
42 tion potential in vivo in the chicken embryo chorioallantoic membrane assay for blood vessel penetrat
43 togenesis, and blood vessel formation in the chorioallantoic membrane assay have been found.
44 so had an angiogenic activity in vivo in the chorioallantoic membrane assay system.
45    Angiogenesis induced by FGF2 in the chick chorioallantoic membrane assay was also inhibited by SCH
46                                 In the chick chorioallantoic membrane assay, 6AF treatment profoundly
47 nhibited angiogenesis in vivo in the chicken chorioallantoic membrane assay, and in the Lewis lung sy
48 lary formation on Matrigel, and chick embryo chorioallantoic membrane assay, bortezomib induced a dos
49 l AngsFvs elicited angiogenesis in the chick chorioallantoic membrane assay, demonstrating that Ang i
50 binant Del1 was evaluated in an in ovo chick chorioallantoic membrane assay, it was found to have pot
51 sculitis disrupted blood flow in the chicken chorioallantoic membrane assay, suggesting an antiangiog
52                         In the in vivo chick chorioallantoic membrane assay, the mouse and the trunca
53                          In an in vivo chick chorioallantoic membrane assay, the PAK peptide specific
54                           By using the chick chorioallantoic membrane assay, we show that HCV-infecte
55 ected in vivo angiogenesis assay and a chick chorioallantoic membrane assay, we show that Nodal promo
56                       Using an ex vivo chick chorioallantoic membrane assay, we show that opticin inh
57 s was observed with GW654652 using the chick chorioallantoic membrane assay, whereas GW654652 produce
58 outing assay and become more invasive in the Chorioallantoic Membrane assay, which assesses cell pene
59  (rat aortic ring assay), and in vivo (chick chorioallantoic membrane assay, zebrafish, murine wild-t
60  of HT C6 was confirmed in vivo in the chick chorioallantoic membrane assay.
61 cytotrophoblast-derived factors in the chick chorioallantoic membrane assay.
62 ophil elastase, inhibits angiogenesis in the chorioallantoic membrane assay.
63 in vitro and neovascularization in the chick chorioallantoic membrane assay.
64 okine, like vMIP-I and vMIP-II, in the chick chorioallantoic membrane assay.
65 ntial both in vitro and in vivo in the chick chorioallantoic membrane assay.
66 al growth factor-induced angiogenesis in the chorioallantoic membrane assay.
67 om aorta rings and angiogenesis in the chick chorioallantoic membrane assay.
68 AM-1 also mediates angiogenesis in the chick chorioallantoic membrane assay.
69 cells and is angiogenic in vivo in the chick chorioallantoic membrane assay.
70  their effects on vessel formation using the chorioallantoic membrane assay.
71 biocompatibility following evaluation on the chorioallantoic membrane assay.
72 and neuroblastoma tumour growth in the chick chorioallantoic membrane assay.
73 dently induced vessel formation in the chick chorioallantoic membrane assay.
74  the mouse Matrigel plug assay and the chick chorioallantoic membrane assay.
75 ive in the low-pH environment of the chicken chorioallantoic membrane assay.
76 vivo angiogenesis as revealed by chicken egg chorioallantoic membrane assay.
77 and the transformed cells are tumorigenic in chorioallantoic membrane assay.
78 as H2O2-dependent as assessed by the chicken chorioallantoic membrane assay.
79 development of new veins and arteries in the chorioallantoic membrane assay.
80 ells induced angiogenesis in "in vivo" chick chorioallantoic membrane assays that could be reversed w
81 iserum in both endothelial proliferation and chorioallantoic membrane assays.
82 V-ERV infected newly formed blood vessels in chorioallantoic membrane assays.
83 giogenin-induced angiogenesis in the chicken chorioallantoic membrane at a dose as low as 20 ng per e
84       It is angiogenically potent on chicken chorioallantoic membrane, but less so than angiogenin.
85 sing recombinant fragments of the protein on chorioallantoic membrane (CAM) angiogenesis and endothel
86 released from a polymeric implant in a chick chorioallantoic membrane (CAM) assay and laser-induced e
87                     We used the chick embryo chorioallantoic membrane (CAM) assay to test the hypothe
88                                 In the chick chorioallantoic membrane (CAM) assay used to measure ang
89                                   An in vivo chorioallantoic membrane (CAM) assay was performed using
90 ls (HUVEC) differentiation assay and chicken chorioallantoic membrane (CAM) assay we document that st
91 is: the endothelial cell culture system, the chorioallantoic membrane (CAM) assay, and the laser-indu
92 epG2 tumor growth in a modified chick embryo chorioallantoic membrane (CAM) assay, associated with a
93                                 In the chick chorioallantoic membrane (CAM) assay, SsnB caused signif
94 ocomputed tomography; MicroCT) and using the chorioallantoic membrane (CAM) assay, we present and val
95 asis in both in vivo mouse models and in the chorioallantoic membrane (CAM) assay.
96 icant antitumor activity and low toxicity in chorioallantoic membrane (CAM) assay.
97 stimulated developmental angiogenesis in the chorioallantoic membrane (CAM) assay.
98 neovascularization in the chick embryo chick chorioallantoic membrane (CAM) assay.
99 says using human vascular endothelial cells, chorioallantoic membrane (CAM) assays and xenograft tumo
100                                              Chorioallantoic membrane (CAM) assays utilizing Japanese
101 tro and to stimulate angiogenesis ex vivo in chorioallantoic membrane (CAM) assays.
102  tested the hypothesis that the chick embryo chorioallantoic membrane (CAM) can be used as a bioreact
103 scaffold and incubated on the chicken embryo chorioallantoic membrane (CAM) for 7 days.
104 collagen onplants placed on the chick embryo chorioallantoic membrane (CAM) has been used in this stu
105                                   In a Chick Chorioallantoic Membrane (CAM) in vivo model, lincNMR-de
106                          We used the chicken chorioallantoic membrane (CAM) model to determine whethe
107 ly expressed in MNA(+) NB and, using a chick chorioallantoic membrane (CAM) model, as a crucial regul
108                              Using a chicken chorioallantoic membrane (CAM) model, we demonstrated th
109 own for (SiFA)SeFe-rhTATE2 using the chicken chorioallantoic membrane (CAM) model.
110 C ES-2 cell tumor growth and metastasis in a chorioallantoic membrane (CAM) model.
111  to deliver a therapeutic agent by using the chorioallantoic membrane (CAM) model.
112 lied topically on embryonic day (E) 7 to the chorioallantoic membrane (CAM) of quail embryos cultured
113 nic growth factors in onplants placed on the chorioallantoic membrane (CAM) of the chick embryos is c
114 nal, Myr-P3k, can induce angiogenesis in the chorioallantoic membrane (CAM) of the chicken embryo.
115 MD on the production of blood vessels in the chorioallantoic membrane (CAM) of the developing chicken
116 tracers, but the growth of tumors on chicken chorioallantoic membrane (CAM) provides a more rapid, lo
117  also used in vivo tumor growth on the chick chorioallantoic membrane (CAM) to observe the disseminat
118 s (HUVECs) and neovascularization in chicken chorioallantoic membrane (CAM) was examined by MTT assay
119 d in developing blood vessels of the chicken chorioallantoic membrane (CAM), a highly vascular embryo
120 injected intravenously into the chick embryo chorioallantoic membrane (CAM), and mRNA levels in the m
121 fibroblast growth factor (bFGF) on the chick chorioallantoic membrane (CAM), endothelial cell mitogen
122 eveloped using human trabecular bone and the chorioallantoic membrane (CAM), to form a functioning va
123  and stimulated vascular growth in the chick chorioallantoic membrane (CAM).
124 12 dose-dependently enhanced angiogenesis in chorioallantoic membranes (CAMs) and HUVECs.
125 astatic tumors within 2 wk of inoculation on chorioallantoic membranes (CAMs) of chick embryos.
126  vessels, and eventually observed inside the chorioallantoic membrane capillaries, thus reflecting ea
127                            The properties of chorioallantoic membrane derived from Large White Landra
128                                           In chorioallantoic membrane, electron avalanche transfectio
129 e containing hydrogel films applied to chick chorioallantoic membranes encourages neovascularization,
130 the central cell-binding domain to the chick chorioallantoic membrane enhanced angiogenesis in an int
131 cular endothelial growth factor in the chick chorioallantoic membrane in vivo.
132 itazone suppresses angiogenesis in the chick chorioallantoic membrane, in the avascular cornea, and i
133 nt fibroblasts explanted atop the live chick chorioallantoic membrane lack tissue-invasive potential
134 avasation of tumor cells in an in vivo chick chorioallantoic membrane model of metastasis as well as
135              Furthermore, in an in ovo chick chorioallantoic membrane model, overexpression of EMILIN
136 wth factor-induced angiogenesis in the chick chorioallantoic membrane model.
137 r 221*2-mediated angiogenesis in the chicken chorioallantoic membrane model.
138  angiogenesis have been studied in the chick chorioallantoic membrane model.
139  inhibits angiogenesis in Matrigel and chick chorioallantoic membrane models and also inhibits metast
140 lpha7-nAChR was confirmed in vivo by chicken chorioallantoic membrane models.
141 y and migration assays) and in vivo (chicken chorioallantoic membrane) models and were found to exhib
142    Xenograft Panx1-KD cells grown within the chorioallantoic membrane of avian embryos developed tumo
143 cells from the two HT-1080 variants onto the chorioallantoic membrane of chick embryos and measured l
144 and BE(2)C cell lines, when engrafted on the chorioallantoic membrane of chick embryos, we observed a
145 ed on grafting of collagen onplants onto the chorioallantoic membrane of chick embryos.
146 ascular pattern formation was studied in the chorioallantoic membrane of chicken embryos (CAM assay).
147  y until an assay of ectodermal pocks of the chorioallantoic membrane of chicken embryos was introduc
148 ted in flow channel phantom data, and in the chorioallantoic membrane of chicken embryos with optical
149 of endothelial cells; (c) when placed on the chorioallantoic membrane of chicken embryos, these cells
150 s and promoted blood vessel formation in the chorioallantoic membrane of chicken embryos.
151  cell carcinoma xenograft model grown in the chorioallantoic membrane of chicken embryos.
152 ox, LoVo and SW-480 tumor transplants on the chorioallantoic membrane of embryonated hen eggs showed
153 x 3c also disrupted the blood vessels in the chorioallantoic membrane of fertilized chicken eggs.
154 d in two in vivo models of angiogenesis: the chorioallantoic membrane of the chick assay and the mous
155                    They induce tumors in the chorioallantoic membrane of the chicken embryo and cause
156 products in collagen onplants grafted on the chorioallantoic membrane of the chicken embryo, we demon
157  It also blocked the growth of tumors on the chorioallantoic membranes of 10-day chicken embryos.
158 in could inhibit the growth of tumors on the chorioallantoic membranes of chicken embryos and in syng
159 e xenografts in a novel system that employed chorioallantoic membranes of fertilized chicken eggs as
160 rthermore, when grown in vivo in the chicken chorioallantoic membrane, primary tumors derived from Cx
161 lginate-g-pyrrole hydrogel system on chicken chorioallantoic membranes resulted in the formation of b
162 ed expression of Hox D3 in vivo on the chick chorioallantoic membrane retained EC in this invasive st
163 ure of newborn condylar cartilage on a chick chorioallantoic membrane showed that after 5 d the cells
164            Tumor growth studies on the chick chorioallantoic membrane showed that C16Y reduces breast
165  neovascularization in an experimental quail chorioallantoic membrane system and Matrigel plug format
166                                       On the chorioallantoic membrane the 9E3 protein is chemotactic
167           After transplantation to the chick chorioallantoic membrane, the network reorganizes into a
168 constitutively expressed Hox B3 in the chick chorioallantoic membrane using avian retroviruses that r
169 ls of tumor cell intravasation in the distal chorioallantoic membrane using quantitative human-specif
170 he primary tumor (i.e., intravasate into the chorioallantoic membrane vasculature and metastasize to
171 cular permeability was assessed in the chick chorioallantoic membrane vasculature following minibeam
172 revented in vitro tube formation and in vivo chorioallantoic membrane vessel development.
173 g of human HT-1080 fibrosarcoma cells on the chorioallantoic membrane was used in conjunction with qu
174  antiangiogenic activity of HKa in the chick chorioallantoic membrane, was inhibited completely by an
175       PEX blocks MMP-2 activity on the chick chorioallantoic membrane where it disrupts angiogenesis
176 ation and inhibits angiogenesis in the chick chorioallantoic membrane, whereas a fragment of TSP1 con
177 mediated Ras and c-Raf activity on the chick chorioallantoic membrane, whereas blockade of FAK or int
178 s on the primitive vascular bed of the chick chorioallantoic membrane, which has striking similaritie
179 T-1080 fibrosarcoma cells grafted onto chick chorioallantoic membranes, which was similar to cisplati
180 of zebrafish or local treatment of the chick chorioallantoic membrane with ScA resulted in dose-depen
181 wth factor-induced angiogenesis on the chick chorioallantoic membrane, with an IC50 of 10 microM.
182 etion reduced tumor development in a chicken chorioallantoic membrane xenograft model of human breast

 
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