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

1 ocytes, macrophages, CD4+ T cells, and micro-vascular endothelial cells).

2 tudied canonical interactions identified for vascular endothelial cells.

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

4 yx is a layer coating the luminal surface of vascular endothelial cells.

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

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

7 increased ferritin immunolabeling in retinal vascular endothelial cells.

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

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

10 the establishment of apicobasal polarity of vascular endothelial cells.

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

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

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

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

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

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

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

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

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

20 ing events between neuroepithelial cells and vascular endothelial cells.

21 expressed in bronchial epithelial cells and vascular endothelial cells.

22 ression between circulating erythrocytes and vascular endothelial cells.

23 nical models through localized insult to the vascular endothelial cells.

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

25 oncentration and transcriptional activity in vascular endothelial cells.

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

27 id droplets by increasing autophagic flux in vascular endothelial cells.

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

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

30 stimulating adhesion molecule expression in vascular endothelial cells.

31 repulsion are conserved between neurons and vascular endothelial cells.

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

33 olecules that specify the differentiation of vascular endothelial cells.

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

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

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

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

38 ly reduced VEGFR2 phosphorylation in retinal vascular endothelial cells.

39 ing transmembrane glycoprotein identified in vascular endothelial cells.

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

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

42 SS transcripts inhibits monocyte adhesion to vascular endothelial cells.

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

44 preferential T-cell homing via modulation of vascular endothelial cells.

45 ytes and lymphatic endothelial cells but not vascular endothelial cells.

46 ycan-bound chemokines on the luminal side of vascular endothelial cells.

47 orneal keratocytes, lens fibers, and retinal vascular endothelial cells.

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

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

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

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

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

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

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

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

56 istent increased vascular resistance damages vascular endothelial cells-a marker of which is increase

57 ular endothelial growth factor receptor 2 in vascular endothelial cells abolished injury-induced HA a

58 In both retina and brain, vascular endothelial cells activate a previously dormant

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

60 Using primary human retinal vascular endothelial cells and an established human endo

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

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

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

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

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

66 consisting of patient-derived tumour cells, vascular endothelial cells and decellularized extracellu

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

68 y expressed unconventional myosin in retinal vascular endothelial cells and expression levels increas

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

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

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

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

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

74 Inflammasome in vascular endothelial cells and its causal relationship w

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

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

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

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

79 vents that govern hemogenic specification of vascular endothelial cells and the generation of multili

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

81 unb-malate MS mitigated the proliferation of vascular endothelial cells and the recruitment of mural

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

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

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

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

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

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

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

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

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

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

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

96 Blood vascular endothelial cells (BECs) control the immune res

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

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

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

100 ch is expressed on the surface of angiogenic vascular endothelial cells, but is absent in quiescent e

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

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

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

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

105 timulation of non-excitable cells, including vascular endothelial cells, calcium (Ca(2+)) shuttling b

106 monocytogenes infection among primary human vascular endothelial cells can be attributed entirely to

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

108 nal and non-neuronal (astrocytes, microglia, vascular endothelial cells) cells of cortical (medial pr

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

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

111 of nonhealers, were mainly expressed by the vascular endothelial cell cluster almost exclusively in

112 nificant apoptosis in the retina and retinal vascular endothelial cells compared to control groups (p

113 r cells, tumor-infiltrating lymphocytes, and vascular endothelial cells compete for oxygen and nutrie

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 In vascular endothelial cells, cysteine metabolism by the c

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

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

123 indicate that Adora2a-mediated signaling in vascular endothelial cells disrupts the BBB in dietary o

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

125 efining the molecular signatures of coronary vascular endothelial cells during these complex processe

126 Vascular endothelial cell dysfunction mediated by antiph

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

128 Vascular endothelial cell (EC) barrier integrity is crit

129 Vascular endothelial cell (EC) dysfunction plays a key r

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

131 y depend on circulating tumor cell (CTC) and vascular endothelial cell (EC) interactions by incomplet

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

133 oteins in beta-catenin signaling, we studied vascular endothelial cell (EC)-specific knockout of Dlg1

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

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

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

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

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

143 Vascular endothelial cells (ECs) derived from the centra

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

145 Vascular endothelial cells (ECs) express and release pro

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

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

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

149 Vascular endothelial cells (ECs) link hemostasis, thromb

150 the activation of the gene transcriptions in vascular endothelial cells (ECs) plays an essential role

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

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

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

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

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

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

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

158 of early postnatal inactivation of Kif11 in vascular endothelial cells (ECs).

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

160 se that is driven, in part, by activation of vascular endothelial cells (ECs).

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

162 . 106.4 +/- 6.8 pg/mg; P < 0.05), but not in vascular endothelial cell endothelin-1 knockout (VEET KO

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

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

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

166 els were elevated in human keratinocytes and vascular endothelial cells following IL-26 stimulation.

167 requirement of mitochondrial respiration in vascular endothelial cells for neoangiogenesis during de

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 A (VEGF) is a bi

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

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

177 Vascular endothelial cell growth factor plays a pivotal

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

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

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

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

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

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

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

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

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

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

188 n C5a receptor 1 [C5aR1]) on human umbilical vascular endothelial cells (HUVECs) and examined how C3a

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

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

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

192 In cultured vascular endothelial cells, IgG antibodies from patients

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

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

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

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

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

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

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

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

201 Our findings highlight the role of vascular endothelial cells in regulating cognitive funct

202 al up-regulation of Pfn1 in tumor-associated vascular endothelial cells in the clinical specimens of

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

204 mab-induced interactions between T cells and vascular endothelial cells in vitro and in patients.

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

206 momab-induced T-cell rolling and adhesion to vascular endothelial cells in vitro, and (v) the ability

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

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

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

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

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

212 amined the influence of SLURP1 on neutrophil-vascular endothelial cell interactions using human umbil

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

214 retina, and electron microscopy demonstrated vascular endothelial cell irregularity with narrowing of

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

216 lating lymphocyte function via activation of vascular endothelial cells is unknown.

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

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

219 Here, we generated induced vascular endothelial cells (iVECs) and smooth muscle cel

220 gs are nitrated, (6) cytoplasmic vesicles in vascular endothelial cells known to stain for NADPH diap

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

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

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

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

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

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

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

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

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

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

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

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

233 naling via the S1P receptor 1 (S1PR1) in the vascular endothelial cells of lung and kidney.

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

235 Meanwhile, mesenteric arteries and lung vascular endothelial cells of tamoxifen-inducible endoth

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

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

238 ion induced ectopic podoplanin expression in vascular endothelial cells or macrophages, which may als

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

240 ptional and spatial gradients-emanating from vascular endothelial cells outwards-in fibroblasts.

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

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

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

244 Rickettsia conorii infects vascular endothelial cells producing disseminated plasma

245 Vascular endothelial cell products have not been explore

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

247 od-borne transport of miR-210 into pulmonary vascular endothelial cells promotes PH, offering fundame

248 livery of extracellular miR-210 to pulmonary vascular endothelial cells promotes PH.

249 Furthermore, IL-26 acted directly on vascular endothelial cells, promoting proliferation and

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

251 straints of bioprinted scaffolds-the 'reset' vascular endothelial cells (R-VECs) self-assemble into s

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

253 Vascular endothelial cells respond to blood flow-induced

254 Vascular endothelial cells respond to proangiogenic cues

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

259 isms that drive angiogenesis and organotypic vascular endothelial cell specialization are poorly unde

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

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

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

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

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

265 romoting adhesion of neutrophils to coronary vascular endothelial cells through a TLR4/TRIF/type I IF

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

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

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

269 ss requires the specification of a subset of vascular endothelial cells to become blood-forming, or h

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

271 In turn, dopamine acts directly on hyaloid vascular endothelial cells to suppress the activity of v

272 C cells and in soluble Pfn1's involvement in vascular endothelial cell tumor cell cross-talk.

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

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

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

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

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

278 m of trigeminal ganglion sensory neurons and vascular endothelial cells (VEC) and found that neurons

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

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

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

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

283 tionally deleted a floxed allele of Podxl in vascular endothelial cells (vECs) using Tie2Cre mice (Po

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

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

286 ric acid induced the phenotype transition of vascular endothelial cells via induction of oxidative st

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

288 on of CD31, which indicates presence of more vascular endothelial cells, was associated with signific

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

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

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

292 When human vascular endothelial cells were exposed to tumor necrosi

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

294 he crosstalk between EphA4-Tie2 signaling in vascular endothelial cells, which is mediated through p-

295 Vascular endothelial cells, which line the lumen of bloo

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

297 Incubation of vascular endothelial cells with saturated fatty acid (SF

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

299 ure of islets on 3D-ECM promoted recovery of vascular endothelial cells within the islets and restore

300 s demonstrated, involving mainly stromal and vascular endothelial cells within the tissue.