ライフサイエンスコーパス: vascular endothelial cell

1 pression of Slco2a1 in the tumour-associated vascular endothelial cells.

2 l-intrinsic and were not obviously involving vascular endothelial cells.

3 ing events between neuroepithelial cells and vascular endothelial cells.

4 expressed in bronchial epithelial cells and vascular endothelial cells.

5 ression between circulating erythrocytes and vascular endothelial cells.

6 novel polyomavirus that may have tropism for vascular endothelial cells.

7 oncentration and transcriptional activity in vascular endothelial cells.

8 critical for coronary heart disease in human vascular endothelial cells.

9 CD144/VE-cadherin, and CD106/Endoglin, from vascular endothelial cells.

10 mRNAs, and suppressed sprouting behavior of vascular endothelial cells.

11 s the flow-induced Ca(2+) increase in native vascular endothelial cells.

12 stimulating adhesion molecule expression in vascular endothelial cells.

13 repulsion are conserved between neurons and vascular endothelial cells.

14 ignant cells, as well as by immune cells and vascular endothelial cells.

15 olecules that specify the differentiation of vascular endothelial cells.

16 in/+) mice with loss of insulin receptors in vascular endothelial cells.

17 is involved in the induction of apoptosis in vascular endothelial cells.

18 little ability to roll or adhere to inflamed vascular endothelial cells.

19 uced CD31 staining and specific apoptosis of vascular endothelial cells.

20 l types, including microglia, astrocytes and vascular endothelial cells.

21 ation is a commonplace activity of embryonic vascular endothelial cells.

22 ly reduced VEGFR2 phosphorylation in retinal vascular endothelial cells.

23 ing transmembrane glycoprotein identified in vascular endothelial cells.

24 ial cells and corneal keratocytes as well as vascular endothelial cells.

25 icroRNAs (HRMs) that are strongly induced in vascular endothelial cells.

26 ing role of AS in the citrulline-NO cycle of vascular endothelial cells.

27 tain a reduced number of resident intraislet vascular endothelial cells.

28 imigratory effects of 3MC in human umbilical vascular endothelial cells.

29 to stimulate in vitro angiogenesis of human vascular endothelial cells.

30 king the chromatin-remodeling enzyme Chd4 in vascular endothelial cells.

31 n cyclic AMP-modulated signaling pathways in vascular endothelial cells.

32 mor blood vessel-associated pericytes and/or vascular endothelial cells.

33 a-associated herpesvirus (KSHV) infection of vascular endothelial cells.

34 og which is expressed in endocardial but not vascular endothelial cells.

35 measure PTK7 expression in several types of vascular endothelial cells.

36 atopoietic precursors arise from a subset of vascular endothelial cells.

37 a(3) integrin, endoglin, and VEGFR2 on tumor vascular endothelial cells.

38 in exhibit a potent antiangiogenic action on vascular endothelial cells.

39 ession was largely confined to proliferating vascular endothelial cells.

40 tudied canonical interactions identified for vascular endothelial cells.

41 rs, and beta-catenin-dependent signalling in vascular endothelial cells.

42 r pericytes, enwrapping and associating with vascular endothelial cells.

43 ates independent of the production system in vascular endothelial cells.

44 increased ferritin immunolabeling in retinal vascular endothelial cells.

45 ay limit iron transport into the retina from vascular endothelial cells.

46 ensibly all epicardial cells and in coronary vascular endothelial cells.

47 the establishment of apicobasal polarity of vascular endothelial cells.

48 entiated cardiac myocytes, smooth muscle and vascular endothelial cells.

49 vascular development with a special focus on vascular endothelial cells.

50 hrough the regulation of AKT and PKCalpha in vascular endothelial cells.

51 IL-1beta, TNF-alpha, and IL-10 secretion in vascular endothelial cells.

52 mprise an on-demand storage organelle within vascular endothelial cells.

53 tive contribution of mTORC1 versus mTORC2 in vascular endothelial cells.

54 derived from the effect of this compound on vascular endothelial cells.

55 lls can in addition infect and destroy tumor vascular endothelial cells.

56 critical role in controlling the survival of vascular endothelial cells.

57 These cells include vascular endothelial cells, a host of immune cells, and

58 othelin-1(8-12)] on astrocytes, neurons, and vascular endothelial cells after induction of cerebral i

59 protein A that binds to laminin receptor on vascular endothelial cells and binding of phosphorylchol

60 ed cysLTs that activated CysLT1 expressed in vascular endothelial cells and bronchial smooth muscle c

61 g its nuclear receptor in cardiomyocytes and vascular endothelial cells and by regulating the renin-a

62 hese cells are induced to differentiate into vascular endothelial cells and cardiomyocytes possibly b

63 on of galectin-3 with unknown receptor(s) on vascular endothelial cells and causes endothelial secret

64 onclude that the expression of PD-L1 in both vascular endothelial cells and corneal epithelial cells

65 s expressed in several cell types, including vascular endothelial cells and duct epithelial cells.

66 romotes the angiogenesis and the invasion of vascular endothelial cells and fibroblasts by enhancing

67 ular myoid cells, interstitial Leydig cells, vascular endothelial cells and germ cells, while absent

68 enesis dynamics as scored in human umbilical vascular endothelial cells and human MCF-7 breast tumor

69 ire a molecular identity distinct from other vascular endothelial cells and initiate expression of sp

70 tional adhesion molecule, expressed on human vascular endothelial cells and involved in the control o

71 Inflammasome in vascular endothelial cells and its causal relationship w

72 sic shear stress responses commonly in blood vascular endothelial cells and LECs.

73 Candidate cellular targets of aPC include vascular endothelial cells and leukocytes.

74 om dermal blood and lymphatic vessels (blood vascular endothelial cells and lymphatic endothelial cel

75 acellular accumulation of mutant collagen in vascular endothelial cells and pericytes was a key trigg

76 Vs in the cell-to-cell communication between vascular endothelial cells and pericytes/vSMCs.

77 fected animals was triggered by infection of vascular endothelial cells and the hematogenous spread o

78 e expressed by primary murine lung and heart vascular endothelial cells and the miscrovascular endoth

79 covering the point of contact between donor vascular endothelial cells and the recipient's immune ce

80 ysfunction, which includes the activation of vascular endothelial cells, and circulating leucocytes a

81 ) somata and axons, protoplasmic astrocytes, vascular endothelial cells, and ER-mitochondrial contact

82 uced release of shedding type E-EVs from the vascular endothelial cells, and flow cytometry showed th

83 Adrx is constitutively expressed in human vascular endothelial cells, and significantly induced by

84 ate gene expression and protein synthesis in vascular endothelial cells, and this regulation is invol

85 inhibits the cancer-stroma communication and vascular endothelial cells' angiogenic activities.

86 is study, we investigated this process using vascular endothelial cells, APCs that possess a unique a

87 Vascular endothelial cells are both key mediators and ta

88 Because vascular endothelial cells are both stretch sensitive an

89 ranscription factor A (MRTF-A) and MRTF-B in vascular endothelial cells are not completely understood

90 exus endothelial cells, as compared to other vascular endothelial cells, are more dependent upon peri

91 CL-12 is highly expressed in umbilical cord vascular endothelial cells as a transmembrane receptor a

92 epressed in KSHV-transformed human umbilical vascular endothelial cells as well as in KSHV-associated

93 Leukocytes attach to vascular endothelial cells at the site of inflammation v

94 diated targeting of activated neutrophils on vascular endothelial cells at the site of injury may be

95 Infection of blood vascular endothelial cells (BEC) by KSHV reactivates an

96 ear to reflect impaired TGFbeta signaling in vascular endothelial cells because retinal deletion of I

97 T)-1 expression in blood-brain barrier (BBB) vascular endothelial cells (BECs) and reduces brain gluc

98 intestinal mouse lymphatic (LECs) and blood vascular endothelial cells (BECs).

99 eoglycans, present at the plasma membrane of vascular endothelial cells, bind to the angiogenic growt

100 biquitination, and TJ trafficking in retinal vascular endothelial cells both in vitro and in vivo and

101 neurite outgrowth, lymphoid trafficking, and vascular endothelial cell branching is linked to integri

102 MMP upregulated the expression of MT1-MMP in vascular endothelial cells, but did not affect MT1-MMP e

103 TGFbetas) and defective TGFbeta signaling in vascular endothelial cells, but not astrocytes.

104 channels are also thought to be expressed in vascular endothelial cells, but their presence and funct

105 inhibits the proliferation and migration of vascular endothelial cells by activating eukaryotic elon

106 that invades pulmonary epithelial cells and vascular endothelial cells by inducing its own endocytos

107 hus plays a critical role in the behavior of vascular endothelial cells by inhibiting migration.

108 sed in endothelial cells using a promoter of vascular endothelial cell cadherin.

109 reduces ICAM-1-stimulated phosphorylation of vascular endothelial-cell cadherin (VE-cadherin).

110 sed no obvious changes, specific deletion in vascular endothelial cells caused CNV and a phenotype si

111 including tube formation assays using human vascular endothelial cells, chorioallantoic membrane (CA

112 We investigated whether vascular endothelial cells circumvent anti-VEGF therapie

113 ge cells, which include bone marrow (BM) and vascular endothelial cells, compared with control litter

114 for cis-regulatory elements, particularly in vascular endothelial cells, consistent with a primary ro

115 Vascular endothelial cells contain unique rod-shaped sec

116 On this basis, we suggest that vascular endothelial cells contribute to tumor dissemina

117 ioglitazone cytoprotection in mouse cerebral vascular endothelial cell cultures after oxygen-glucose

118 ulting in endothelial protection in cerebral vascular endothelial cell cultures and cerebral microvas

119 and regulated its function in mouse cerebral vascular endothelial cell cultures.

120 oxygen-glucose deprivation-induced cerebral vascular endothelial cell death and middle cerebral arte

121 ly lack ET-1 in hematopoietic stem cells and vascular endothelial cells, did not produce ET-1 even wh

122 normoxic glioma cells, hypoxic glioma cells, vascular endothelial cells, diffusible angiogenic factor

123 ed in vivo and in vitro effects of Nogo-A on vascular endothelial cells during angiogenesis of the ea

124 Vascular endothelial cell dysfunction mediated by antiph

125 polipoprotein CIII links hyperlipidemia with vascular endothelial cell dysfunction.

126 ace-relevant irradiation induces a sustained vascular endothelial cell dysfunction.

127 Vascular endothelial cell (EC) barrier integrity is crit

128 However, whether NO directly regulates vascular endothelial cell (EC) insulin uptake and its tr

129 lular tensions in subconfluent and confluent vascular endothelial cell (EC) monolayers under static a

130 The effects and potential mechanisms of the vascular endothelial cell (EC)-enriched microRNA-15a (mi

131 ew blood vessel formation, we have generated vascular endothelial cell (EC)-specific Cdc42 knockout m

132 We show here that vascular endothelial cell (EC)-specific reduction in Rec

133 are upregulated on cultured human and mouse vascular endothelial cells (EC) and cell lines by proinf

134 Vascular endothelial cells (EC) are an exposed tissue wi

135 teraction between pancreatic islet cells and vascular endothelial cells (EC) in which EC-derived sign

136 functions ascribed in its interactions with vascular endothelial cells (EC), including migration and

137 , an orphan nuclear transcription factor, in vascular endothelial cells (EC).

138 t study, we investigated the role of LXRs in vascular endothelial cells (ECs) and discovered that LXR

139 tion factor HIF2alpha is highly expressed in vascular endothelial cells (ECs) and may regulate endoth

140 The communication between vascular endothelial cells (ECs) and pericytes in the mi

141 Vascular endothelial cells (ECs) and several cancer cell

142 Vascular endothelial cells (ECs) are constantly exposed

143 Vascular endothelial cells (ECs) are exposed to differen

144 elial NO synthase (eNOS) expression in human vascular endothelial cells (ECs) because of the key role

145 BCECs and bovine vascular endothelial cells (ECs) derived from aorta, cor

146 nner, for the proliferation and migration of vascular endothelial cells (ECs) during retinal angiogen

147 Vascular endothelial cells (ECs) express and release pro

148 Vascular endothelial cells (ECs) express erbB receptors

149 encing cell-to-cell interactions between the vascular endothelial cells (ECs) in post-capillary venul

150 that activated EPOR was localized to retinal vascular endothelial cells (ECs) in retinas at postnatal

151 Adhesion of circulating monocytes to vascular endothelial cells (ECs) is a critical event lea

152 Insulin signaling in vascular endothelial cells (ECs) is critical to maintain

153 Vascular endothelial cells (ECs) link hemostasis, thromb

154 ed lymphocytes interact with CD44(-/-) brain vascular endothelial cells (ECs) than with WT ECs.

155 Transplanting vascular endothelial cells (ECs) to support metabolism a

156 se BRB disintegration, it sensitizes retinal vascular endothelial cells (ECs) to VEGF-A, leading to u

157 The average age of cardiomyocytes, vascular endothelial cells (ECs), and fibroblasts and th

158 Infantile hemangiomas are benign tumors of vascular endothelial cells (ECs), characterized by three

159 ogenes (SpCas9) is used to deplete VEGFR2 in vascular endothelial cells (ECs), whereby the expression

160 sic pathway of apoptosis is a key feature of vascular endothelial cells (ECs).

161 ized by excessive proliferation of pulmonary vascular endothelial cells (ECs).

162 We were surprised to observe GFP(+) vascular endothelial cells (ECs).

163 deletion of IFN-alpha/betaR in Tie2-positive vascular endothelial cells eliminated most of the antitu

164 . 106.4 +/- 6.8 pg/mg; P < 0.05), but not in vascular endothelial cell endothelin-1 knockout (VEET KO

165 ss II expression, or from a pig with "local" vascular endothelial cell expression of an immunosuppres

166 meostasis and repair, and instead maintain a vascular endothelial cell fate.

167 ble and directly recognized pericytes and/or vascular endothelial cells flow-sorted from tumor tissue

168 ithelial cells, macrophages, fibroblasts and vascular endothelial cells formed the majority of cells

169 Lymphatic and blood vascular endothelial cells from mouse intestine were iso

170 s indicated that the mechanosensory cilia of vascular endothelial cells from the Adamts16(mutant) rat

171 therosclerotic effects through modulation of vascular endothelial cell function.

172 vitational loading could dramatically affect vascular endothelial cell function.

173 , GSC also transdifferentiate into bona fide vascular endothelial cells (GEC), which inherit mutation

174 Vascular endothelial cell growth factor (VEGF) can promo

175 Hepatocyte growth factor (HGF) and vascular endothelial cell growth factor (VEGF) regulate

176 signal-related kinases 1 and 2 (ERK1/2), and vascular endothelial cell growth factor (VEGF).

177 Vascular endothelial cell growth factor A (VEGF) is a bi

178 ortion of this inhibitory activity is due to vascular endothelial cell growth factor A (VEGF-A).

179 In primary cultures of endothelial cells, vascular endothelial cell growth factor and basic fibrob

180 We found that vascular endothelial cell growth factor induced the kina

181 Vascular endothelial cell growth factor plays a pivotal

182 s unknown whether there is crosstalk between vascular endothelial cell growth factor signaling and XB

183 e previously implicated in the regulation of vascular endothelial cell growth factor signaling, offer

184 endothelial cell proliferation but abrogated vascular endothelial cell growth factor-induced and basi

185 duced activation of ERK1/2 but inhibited the vascular endothelial cell growth factor-induced and basi

186 atrix metalloproteinases (MMP-2 and -9), and vascular endothelial cell growth factor.

187 ial cells (HCAEC) toward the chemoattractant vascular endothelial cell growth factor.

188 The receptors for hepatocyte and vascular endothelial cell growth factors (MET and VEGFR2

189 Recently, cross-talk between GSC and vascular endothelial cells has been shown to significant

190 imizes binding to receptors present on brain vascular endothelial cells has enabled them to cross thr

191 on of IL-25R and VEGF mRNA in cultured human vascular endothelial cells (HUVEC), and a cell prolifera

192 vation of VEGFR2 and MMP2 in human umbilical vascular endothelial cells (HUVEC).

193 and wound-healing activity of PGE2 in human vascular endothelial cells (HUVECs) although the amount

194 ytotoxicity test of the Mg extract via human vascular endothelial cells (HUVECs) indicates that the c

195 min synthesis) when in co-culture with human vascular endothelial cells (HUVECs), thus demonstrating

196 n in breast cancer cells and human umbilical vascular endothelial cells (HUVECs).

197 In cultured vascular endothelial cells, IgG antibodies from patients

198 luding cancer-associated fibroblasts (CAFs), vascular endothelial cells, immune cells, and cancer cel

199 STA4-4 gene was constructed and delivered to vascular endothelial cells in an in vivo rabbit carotid

200 ironment, and activation of tumor-associated vascular endothelial cells in association with elevated

201 cytotoxic T cells, is generally expressed in vascular endothelial cells in healthy human tissues.

202 ted increased adhesion of monocytes to human vascular endothelial cells in HIV-infected individuals.

203 CSF, beta-galactosidase) in tumor-associated vascular endothelial cells in humans.

204 ian lectin galectin-1 is highly expressed by vascular endothelial cells in inflamed tissue and has be

205 ntribute to our understanding of the role of vascular endothelial cells in metabolism.

206 mRNA levels and density of FABP4-expressing vascular endothelial cells in mouse airways with VEGF ov

207 cells, suggesting that HGF might target the vascular endothelial cells in resistant tumors.

208 Vascular endothelial cells in the central nervous system

209 tor cells first arise from a subset of blood vascular endothelial cells in the dorsolateral aspects o

210 s the expression of proinflammatory genes in vascular endothelial cells in vitro and the persistent i

211 Short-term deletion of Vegfr3 in blood vascular endothelial cells increased baseline leakage in

212 Endothelin 1 (ET-1), mainly produced from vascular endothelial cells, induces vasoconstriction in

213 ory diseases result from the interactions of vascular endothelial cells, inflammatory cells, and plat

214 lmark of all thrombotic microangiopathies is vascular endothelial cell injury of various origins, res

215 ar margination of monocytes and neutrophils, vascular endothelial cell injury, and intense vasculocen

216 In human vascular endothelial cells, interferon-gamma activation

217 a2-p11 heterotetrameric protein, can mediate vascular endothelial cell invasion.

218 covers that the response to hyperglycemia in vascular endothelial cells involves the H3K4 methyltrans

219 Nitric oxide (NO) produced by vascular endothelial cells is a potent vasodilator and a

220 (PK), the proenzyme of plasma kallikrein, on vascular endothelial cells is not fully defined.

221 form of Sema3A, the ligand of Nrp1, by adult vascular endothelial cells, is regulated during the ovar

222 S) interaction, which occurs specifically in vascular endothelial cells, is responsible for the multi

223 specify pluripotent stem cells into induced vascular endothelial cells (iVECs).

224 reatly hindered by barriers presented by the vascular endothelial cell layer and by the aberrant natu

225 from sickle erythrocytes can deliver heme to vascular endothelial cells, leading to their activation

226 mpJX-594 initially infected tumor vascular endothelial cells, leading to vascular pruning

227 The vascular endothelial cells line the inner surface of blo

228 mice lacking NRP1 in the sympathetic versus vascular endothelial cell lineages, we demonstrate that

229 to the pathogenesis of AMD and suggest that vascular endothelial cell loss occurs in association wit

230 oxylin-eosin staining) and immunostaining of vascular endothelial cell marker CD31 and VEGFR2.

231 in the retinal pigmented epithelium and the vascular endothelial cell marker CD34.

232 Sirtuin 1 (SIRT1) depletion in vascular endothelial cells mediates endothelial dysfunct

233 S is an actin-binding protein that modulates vascular endothelial cell migration and cytoskeleton sig

234 IL-6 increases vascular endothelial cell monolayer permeability in vitr

235 measure traction forces exerted by confluent vascular endothelial cell monolayers under slow shear fl

236 to the abluminal side of the outer plexiform vascular endothelial cells, Muller glia cells, and the b

237 ell types, including photoreceptors, retinal vascular endothelial cells, Muller glia, and retinal pig

238 r 1 (RUNX1) as a gene upregulated in CD31(+) vascular endothelial cells obtained from human PDR fibro

239 On vascular endothelial cells of heart and spleen, only typ

240 inished expression of p110gamma in pulmonary vascular endothelial cells of patients with acute respir

241 istry revealed that SOX7 is expressed in the vascular endothelial cells of the developing diaphragm a

242 adhesion molecule-1 (MAdCAM-1) expressed by vascular endothelial cells of the intestine, further med

243 notype, GL-3 inclusions were not detected in vascular endothelial cells or cardiomyocytes.

244 Mechanistic investigations in cultured blood vascular endothelial cells or transgenic mice revealed t

245 s TIE2 activation, is upregulated in hypoxic vascular endothelial cells, particularly in retinal NV.

246 diated immediate hypersensitivity reactions, vascular endothelial cells permeabilize in response to m

247 Determine whether reporters of vascular endothelial cell perturbation correlate with ai

248 Vascular endothelial cell products have not been explore

249 t the cellular level, a notable reduction in vascular endothelial cell proliferation exists in the re

250 Insulin treatment of vascular endothelial cells promoted the dose- and time-d

251 MDBA after acute ascorbic acid infusion, and vascular endothelial cell protein expression of NADPH ox

252 Vascular endothelial cells provide essential support to

253 mniotic cells (ACs) can be reprogrammed into vascular endothelial cells (rAC-VECs) without transition

254 gene expression are regulated by glucose in vascular endothelial cells remain to be fully defined.

255 Conditional deletion of Brg1 from vascular endothelial cells resulted in downregulated COU

256 g, selective (PPARgamma) genetic deletion in vascular endothelial cells resulted in increased cerebro

257 p(a)) elicits cytoskeletal rearrangements in vascular endothelial cells, resulting in increased cellu

258 lood flow because of the disruption of tumor vascular endothelial cells, resulting in tumor necrosis.

259 hat SIEH is produced by an effect of ET-1 on vascular endothelial cells, sensitizing its release of A

260 unction and suggest that nesprin-3 regulates vascular endothelial cell shape, perinuclear cytoskeleta

261 c elements in the etv2 locus responsible for vascular endothelial cell specification.

262 f pro-angiogenic functions for annexin A1 in vascular endothelial cell sprouting, wound healing, tumo

263 re cocultured with primary cultures of brain vascular endothelial cells, stabilization of HIF-1alpha

264 ained in other tissue-invasive cells such as vascular endothelial cells, suggesting a novel mechanism

265 kine (C-X-C motif) ligand 9 (CXCL9) in brain vascular endothelial cells that attract T cells to the b

266 l survival, and tumor cell interactions with vascular endothelial cells that facilitate metastasis to

267 distance interactions, we find that in human vascular endothelial cells the enhancer interval contain

268 It is stored in secretory granules of vascular endothelial cells, the Weibel-Palade bodies (WP

269 y activity in quiescent and angiogenic blood vascular endothelial cells, thereby preventing excessive

270 tective and cytotoxic signaling responses in vascular endothelial cells through cleavage of the recep

271 uring ECM by induction of apoptosis of brain vascular endothelial cells through STAT3 and its target

272 oxidant that induces oxidative stress on the vascular endothelial cells, thus mediating progression o

273 y wound healing or infection activates local vascular endothelial cells to mediate leukocyte rolling,

274 tion revealed enhanced adhesion to activated vascular endothelial cells under flow conditions in vitr

275 We recently demonstrated that vascular endothelial cells unexpectedly express ferlins,

276 d -3, which function to recruit monocytes to vascular endothelial cells upon inflammation.

277 immunohistochemistry staining against CD31 (vascular endothelial cells), vascular endothelial growth

278 BRG1 is required for vascular endothelial cell (VEC) development and embryoni

279 ng effects are mediated specifically through vascular endothelial cell (VEC) PECAM-1.

280 eding Cx40-deficient mice (Cx40(-/-)) with a vascular endothelial cell (VEC)-specific Cx43-deficient

281 ligand) and enhanced expression of VCAM-1 by vascular endothelial cells (VEC) were observed in the TM

282 nt/beta-catenin pathway target genes, but in vascular endothelial cells (VEC), expression of these ge

283 g human monocytes, cultured fibroblasts, and vascular endothelial cells (VEC); (2) gene expression by

284 Conditional deletion of the Crim1 gene in vascular endothelial cells (VECs) causes delayed vessel

285 T cells were either cocultured with vascular endothelial cells (VECs) to assess VEC prolifer

286 Upon their activation and firm adhesion to vascular endothelial cells (VECs), leukocytes preferenti

287 BLB, there were numerous vesicles within the vascular endothelial cells (VECs), with increased number

288 lation via PD-1, CD8 T cells killed infected vascular endothelial cells via perforin-mediated cytolys

289 e to form the NLRP3 inflammasome scaffold in vascular endothelial cells via sterol regulatory element

290 (fli1:egfp) that stably express eGFP within vascular endothelial cells, we have developed and optimi

291 oxLDL-induced signaling events in human vascular endothelial cells were abolished by knockdown o

292 Human umbilical vascular endothelial cells were exposed to 1-gravity env

293 When human vascular endothelial cells were exposed to tumor necrosi

294 By contrast, the epicardial cells and vascular endothelial cells were not affected by blocking

295 VECs, mouse B16LS9 melanoma cells, and mouse vascular endothelial cells were separately cultured or c

296 Disturbed blood flow induces apoptosis of vascular endothelial cells, which causes atherosclerosis

297 ighboring cancer cells, adjacent stroma, and vascular endothelial cells, which induces metabolic repr

298 alpha) and also confer tumor cells and tumor vascular endothelial cells with enhanced prosurvival pat

299 in the normal human utricular stroma showed vascular endothelial cells with few pinocytotic vesicles

300 Similarly, vascular endothelial cells with the Ala/Ala genotype had