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1 ing in increased monocyte recruitment to the vascular endothelium.
2 or systemic activation of coagulation or the vascular endothelium.
3 a characteristic of pathologically activated vascular endothelium.
4 ne kidney grafts may depend on expression in vascular endothelium.
5 ; however, A/H antigens were not detected in vascular endothelium.
6 posed to nitric oxide (NO) released from the vascular endothelium.
7  expression also decreases with age in human vascular endothelium.
8 uggesting a direct or indirect effect on the vascular endothelium.
9 dant specific binding sites at the pulmonary vascular endothelium.
10 ly associated with better functioning of the vascular endothelium.
11  especially as nitric oxide precursor in the vascular endothelium.
12 derm to specify somites instead of posterior vascular endothelium.
13 stitutive or inducible deletion of Epn1/2 in vascular endothelium.
14 more than 20 years as a prototype marker for vascular endothelium.
15 dium, atrioventricular cushions and coronary vascular endothelium.
16 sential in regulating the development of the vascular endothelium.
17 aggerated inflammatory response in pulmonary vascular endothelium.
18 tonella henselae in the chronically infected vascular endothelium.
19 s of caveolae at the luminal surface of lung vascular endothelium.
20 tate of chronic inflammation and damages the vascular endothelium.
21 itor populations that establish the coronary vascular endothelium.
22 sponsive/HIF target genes, especially in the vascular endothelium.
23 ransmigration using an in vitro model of the vascular endothelium.
24 roteins, mediates homophilic adhesion in the vascular endothelium.
25 Ab to non-BM-derived cells such as pulmonary vascular endothelium.
26 est fatty streaks, DCs are found next to the vascular endothelium.
27 eactive oxygen species that damage pulmonary vascular endothelium.
28 human primary monocyte adhesion to activated vascular endothelium.
29 on layer forms on the luminal surface of the vascular endothelium.
30 utrophils interacted, promoting anchoring to vascular endothelium.
31 n assembly and directed cell movement in the vascular endothelium.
32 nflammatory and anti-atherogenic molecule in vascular endothelium.
33 mediating interaction of leukocytes with the vascular endothelium.
34 exclusion properties found in the vertebrate vascular endothelium.
35 podoplanin as specific markers for lymphatic vascular endothelium.
36 ated versican fragment uniquely localized to vascular endothelium.
37 n sph/sph mice, suggesting activation of the vascular endothelium.
38 dditional receptors in the immune system and vascular endothelium.
39 e therefore studied Bmx signaling within the vascular endothelium.
40 studies show that monocytes may give rise to vascular endothelium.
41 ecifically and exclusively to the developing vascular endothelium.
42 the major end product of cyclooxygenase-2 in vascular endothelium.
43 tribute to the radiation response within the vascular endothelium.
44 ESL mediates adhesion of T cells to inflamed vascular endothelium.
45 itors are thought to derive from a subset of vascular endothelium.
46 paB alpha (I-kappaB alpha mt) selectively on vascular endothelium.
47 sition in a continuous linear pattern on the vascular endothelium.
48 duction of the vasodilator nitric oxide from vascular endothelium.
49 ligand for VLA-4), and leukocyte adhesion to vascular endothelium.
50 and injury with functional impairment of the vascular endothelium.
51 es themselves as well as with the underlying vascular endothelium.
52 ss does not depend on a breech in the limbal vascular endothelium.
53 nner in several cell types, most prominently vascular endothelium.
54 in increased expression of ICAM-1 protein in vascular endothelium.
55 X-2 expression and prostanoid homeostasis in vascular endothelium.
56 restricted to the endocardial, lymphatic and vascular endothelium.
57 sition of globotriaosylceramide (Gb3) in the vascular endothelium.
58  enhance the effect of ionizing radiation on vascular endothelium.
59 cal vein endothelial cells (HUVEC) and tumor vascular endothelium.
60 lar basis for a novel AP-1/GR-Notch4 axis in vascular endothelium.
61 ntaining KATP channels are indeed present in vascular endothelium.
62          Estrogen exerts many effects on the vascular endothelium.
63 onses, and activation of coagulation and the vascular endothelium.
64 , patrol blood vessels by crawling along the vascular endothelium.
65 the retinal pigment epithelium (RPE), or the vascular endothelium.
66 r hyaluronan (HA) with CD44, its receptor in vascular endothelium.
67 reflect inflammatory processes affecting the vascular endothelium.
68 mmune system and a transplanted graft is the vascular endothelium.
69 ovel roles of MRTF-A/B in the homeostasis of vascular endothelium.
70 form of thrombomodulin that is shed from the vascular endothelium.
71  multidomain receptor primarily expressed by vascular endothelium.
72 ences expression of protein kinase N3 in the vascular endothelium.
73 localized at low nanomolar concentrations on vascular endothelium.
74 ha (TNFalpha) to increase recruitment to the vascular endothelium.
75 g to vessels and CNS infiltration at the CNS vascular endothelium.
76 egy of leukocytes to adhere and traverse the vascular endothelium.
77 however, is known concerning its role in the vascular endothelium, a major regulator of blood pressur
78                                              Vascular endothelium activation and lymphocyte attractio
79  adhesion is triggered by the interaction of vascular endothelium adhesion molecules, such as ICAM-1,
80 not nontargeted counterparts, accumulated in vascular endothelium after intravenous injection, locali
81 or activity and suggest that statins protect vascular endothelium against the adverse effect of ox-LD
82               JAM3 is known to be present in vascular endothelium, although its roles in cerebral vas
83 stopathology suggest that AECAs activate the vascular endothelium, amplifying the alloimmune response
84 tain basal barrier properties in the retinal vascular endothelium and activation of the EPAC-Rap1 pat
85 operative versican proteolysis by ADAMTS9 in vascular endothelium and by ADAMTS20 in palate mesenchym
86 ents that include transmigration through the vascular endothelium and chemotaxis through the vicinal
87 hemistry demonstrated CD31/34 positivity for vascular endothelium and D2-40 negativity for lymphatic
88 kappaB signaling and leukocyte influx in the vascular endothelium and decreased lung injury and morta
89 ARdelta activity and induce TF expression in vascular endothelium and elevate circulating TF activity
90 rs; (iii) P-glycoprotein is expressed on the vascular endothelium and end-feet of vascular glia (form
91 f a factor promoting COUP-TFII expression in vascular endothelium and highlights a novel role for chr
92  adhesion molecule C (JAM-C) is expressed by vascular endothelium and human but not mouse B lymphocyt
93 tumor suppressor that is highly expressed in vascular endothelium and inflamed tissues, yet its role
94      Blood cell aggregation and adherence to vascular endothelium and inflammation play a central rol
95 revents patrolling monocyte migration on the vascular endothelium and interrupts MCMV dissemination t
96 tide that is synthesized and released by the vascular endothelium and is a marker of endothelial func
97 Tie-2 is expressed almost exclusively in the vascular endothelium and is required for developmental a
98  demonstrate the nonthrombotic nature of the vascular endothelium and its transition to a prothrombot
99 telets that expressed P-selectin attached to vascular endothelium and macrophages.
100 tion of chemotherapeutic drugs with both the vascular endothelium and monocytes.
101             A-Tg mice expressed A-antigen on vascular endothelium and other cells including erythrocy
102  they also exhibit enhanced cytoadherence to vascular endothelium and other healthy and infected RBCs
103  synthase uncoupling and oxidative stress in vascular endothelium and peripheral nerve.
104          We detected ELA expression in human vascular endothelium and plasma.
105 t hypoxia, complement/antibody deposition on vascular endothelium and promoted vascular perfusion by
106 vitro that mediates Th17 cell rolling on the vascular endothelium and recruitment in vivo.
107           Notch4 is selectively expressed in vascular endothelium and regulates vascular remodeling.
108 megalovirus (CMV) infection directly targets vascular endothelium and smooth muscle and at older ages
109 n on human platelets that is also present on vascular endothelium and smooth muscle.
110 e selectively recovered from atherosclerotic vascular endothelium and subjacent tissues.
111 f p66shc expression that is operative in the vascular endothelium and suggest that this mechanism is
112 t sections demonstrated C3 deposition on the vascular endothelium and surrounding myocytes.
113 monstrates that DDAH1 is highly expressed in vascular endothelium and that endothelial DDAH1 plays an
114 found that these ligands directly target the vascular endothelium and that the CNS uses the canonical
115 e of activation of the cytokine network, the vascular endothelium and the coagulation system, with th
116 integrins and their ligands expressed on the vascular endothelium and the extracellular matrix.
117 AM15 in prostate tumor cell interaction with vascular endothelium and the metastatic progression of h
118 denosine receptor disrupted scl(+) hemogenic vascular endothelium and the subsequent EHT process.
119 contrast material-enhanced ultrasound on the vascular endothelium and to determine the parameters and
120 ular parameters for schizont adhesion to the vascular endothelium and to predict bond dynamics in the
121 he more adhesive SS2 cells interact with the vascular endothelium and trap ISC cells, resulting in va
122 --to the lining of the circulatory system or vascular endothelium and unchecked neutrophil transmigra
123 eolar lavage macrophages, airway epithelium, vascular endothelium, and airway smooth muscle.
124 uding pain), regulation of renal blood flow, vascular endothelium, and inflammatory responses.
125 phron, kidney interstitial cell populations, vascular endothelium, and macrophages/monocytes.
126  vascular and airway smooth muscle, proximal vascular endothelium, and pericyte-like cells.
127 lateral line, osteoblast, dermal fibroblast, vascular endothelium, and resident blood.
128 re, we report expression of delta-catenin in vascular endothelium, and show that deletion of only one
129 e of activation of the cytokine network, the vascular endothelium, and the coagulation system in pati
130 ns in hemodynamic shear stress acting on the vascular endothelium are critical for adaptive arterial
131         Monocyte recruitment and adhesion to vascular endothelium are key early events in atheroscler
132 essive mechanical forces experienced by lung vascular endothelium are known to lead to increased vasc
133                 Microtubule (MT) dynamics in vascular endothelium are modulated by vasoactive mediato
134                    Critical functions of the vascular endothelium are regulated by changes in intrace
135         Thus, physical interactions with the vascular endothelium are required for OPC migration.
136  inflammatory response, thus pointing at the vascular endothelium as a therapeutic target for the man
137                     The deposition of C4d on vascular endothelium as well as the coincident presence
138 39 transgene expression was localized to the vascular endothelium at baseline and did not affect tota
139 e adenosine receptor A2b is expressed in the vascular endothelium before HSPC emergence.
140 serum IgG indicating that in addition to the vascular endothelium, bone marrow-derived phagocytic cel
141 ng proepicardial cells give rise to coronary vascular endothelium both in vivo and in vitro.
142 tions between the coagulation system and the vascular endothelium, brain tissue, inflammatory mechani
143   CD146 is fairly homogeneously expressed on vascular endothelium but not on viable CECs or progenito
144 t impaired rolling or sticking to lymph node vascular endothelium but rather decreased migration acro
145 esults suggest that SHS not only affects the vascular endothelium, but also the function of EPCs.
146 lls emerge from Drosha-deficient and control vascular endothelium, but Drosha (cKO)-derived hematopoi
147                     OSA directly affects the vascular endothelium by promoting inflammation and oxida
148  13 were identified in human placenta and in vascular endothelium by ribonuclease protection assay (R
149 tor of downstream NF-kappaB signaling in the vascular endothelium by targeting importin-alpha3, a pro
150 ith microRNA (miRNA) sequences controlled by vascular endothelium cadherin (VE-cad) to study the spec
151 antibody directed at an epitope of monomeric vascular endothelium cadherin that is expressed in tumor
152 l and physiopathologic evidences showed that vascular endothelium can be a target of GvHD in the earl
153 thelium demonstrates for the first time that vascular endothelium can be an important site to activel
154        Here we show that the permeability of vascular endothelium can be increased using an external
155 idly adheres to and penetrates the zebrafish vascular endothelium causing a dose- and time-dependent
156 m and progenitor cells (CD34(+)/CD31(-)) and vascular endothelium (CD34(+)/CD31(+)).
157 90 fibroblast line; and human umbilical vein vascular endothelium cells.
158 ecular determinant of Gata2 transcription in vascular endothelium, composed of a core enhancer module
159                                          The vascular endothelium continually senses and responds to
160               Enhancement of EPC adhesion to vascular endothelium could improve cell retention within
161 of this study was to determine whether human vascular endothelium could produce C4 in response to sti
162 ype of cells, the strong DDAH1 expression in vascular endothelium demonstrates for the first time tha
163                   Among 11 DHHCs detected in vascular endothelium, DHHC21 is required for barrier res
164 e 7 (HDAC7) is specifically expressed in the vascular endothelium during early embryogenesis, where i
165 rmeability and inflammatory responses of the vascular endothelium during endotoxemia.
166 attachment of circulating tumor cells to the vascular endothelium during metastasis.
167               We found Sdc1 expressed in the vascular endothelium during microvessel outgrowth from a
168  hyperbaric (pressurized) oxygen (HBO) alter vascular endothelium dysfunction and modulate the host i
169 lveolar macrophages and was also detected in vascular endothelium (eg, lymphatics) and pleural mesoth
170 titutive exposure to disruptive strains, the vascular endothelium exhibits robust barrier function.
171  observed that NF-kappaB can be activated in vascular endothelium exposed to laminar shear stress in
172                              Although normal vascular endothelium expresses low levels of CXCR7, mark
173 paring the transcriptional profiles of blood vascular endothelium from human invasive bladder cancer
174               Collagen XIII is absent in the vascular endothelium from normal renal cortex and abunda
175 efense and protects the developing pulmonary vascular endothelium from ongoing inflammatory injury.
176                                       In the vascular endothelium, group IV phospholipase A(2)alpha (
177 size vessels can become occluded during anti-vascular endothelium growth factor (anti-VEGF) therapy,
178 gering expression of the angiogenic cytokine vascular endothelium growth factor (VEGF).
179                               The Lama2(-/-) vascular endothelium had significant abnormalities, incl
180         However, it is not clear whether the vascular endothelium has a role in contributing osteopro
181 t studies of control pathways regulating the vascular endothelium have illuminated how this single ce
182 e we show that in addition to activating the vascular endothelium, hemoglobin and heme excess alters
183 ating memory CD8(+) T cells that express the vascular endothelium-homing receptor CX3CR1 (fractalkine
184  and the lymphatic markers LYVE-1 (lymphatic vascular endothelium hyaluronate receptor) and podoplani
185 minitis, thrombocytopenia, and injury to the vascular endothelium, illustrating challenges yet to ove
186 ta strongly support an important role of the vascular endothelium in determining whole-organ glucose
187 esponsible for the phenotypic changes to the vascular endothelium in inflammation, which allows fluid
188 herapy in endothelial cells as well as tumor vascular endothelium in lung cancer tumors in mice.
189 expressing beta(S) hemoglobin have activated vascular endothelium in multiple organs that exhibits en
190  tumor cells at the periphery and to CD31(+) vascular endothelium in the core.
191 equire these substrates, a major role of the vascular endothelium in the regulation of tissue metabol
192 ur evolving understanding of the role of the vascular endothelium in this process.
193 both SS RBC and murine leukocyte adhesion to vascular endothelium in vivo.
194                  These data suggest that the vascular endothelium, in addition to the hematopoietic s
195 cadherin, which localizes adiponectin to the vascular endothelium, in the revascularization response
196 ate angiogenesis and contribute to repair of vascular endothelium, increase during pregnancy.
197 pe I extracellular membrane protein on brain vascular endothelium inducing platelet aggregation via t
198  Furthermore, overexpression of Bcl-2 in the vascular endothelium inhibited the diabetes-induced dege
199 d minimal hepatocyte, biliary epithelium and vascular endothelium injury during preservation and post
200          Adherens junctions are required for vascular endothelium integrity.
201 vels of reactive oxygen species (ROS) in the vascular endothelium is a common pathogenic pathway in m
202                  Cancer cell adhesion to the vascular endothelium is a critical step of tumour metast
203                                          The vascular endothelium is a highly dynamic structure, and
204 phocytes across central nervous system (CNS) vascular endothelium is a key step in inflammatory demye
205 sion of indoleamine-2,3-dioxygenase (IDO) by vascular endothelium is a newly identified vasomotor-reg
206                                          The vascular endothelium is a particularly important target
207                                          The vascular endothelium is best known for its role in oxyge
208                                          The vascular endothelium is critical for induction of approp
209                                        Tumor vascular endothelium is rather resistant to the cytotoxi
210 ouse brain, pericyte investment of the tumor vascular endothelium is reduced, causing deficiencies in
211 tumour immune response and its expression on vascular endothelium is responsible for life threatening
212                                          The vascular endothelium is the continuous single-cell linin
213 context of cardiovascular disease (CVD), the vascular endothelium is the layer of initiation for the
214  expressed in nonphagocytic cells, including vascular endothelium, is localized to the endoplasmic re
215 nent, where neutrophil interactions with the vascular endothelium lead to barrier dysfunction and inc
216 duction in BMDACs enhances their adhesion to vascular endothelium, leading to synergistic effects of
217 sruption of the function and/or integrity of vascular endothelium leads to an increased risk for thro
218                  Gremlin 1 released from the vascular endothelium may inhibit endogenous bone morphog
219 hat previously overlooked involvement of the vascular endothelium may provide a more complete picture
220                       Selectins on activated vascular endothelium mediate inflammation by binding to
221  infected erythrocytes (IE) to adhere to the vascular endothelium, mediated by P. falciparum erythroc
222 ate arrest of circulating tumor cells at the vascular endothelium, melanoma cell attachment to endoth
223  and add to the perturbation of the maternal vascular endothelium, normally attributed to non-membran
224 y arterial hypertension and in the pulmonary vascular endothelium of 3 rat models of pulmonary hypert
225 d expression of E-selectin and VCAM-1 in the vascular endothelium of Ad(-/-) mice.
226  we conditionally deleted this receptor from vascular endothelium of adult mice, generating CXCR7(Del
227 nce CPATAERPC) that selectively binds to the vascular endothelium of brown adipose tissue, but not of
228  hypothesized that antibody targeting of the vascular endothelium of glioblastoma with cytotoxic shor
229 , we show that it is highly expressed in the vascular endothelium of human cancers and in a banded pa
230 asite-infected red blood cells (irbc) to the vascular endothelium of organs plays a key role in the p
231 human B-domain deleted FVIII (hFVIII) in the vascular endothelium of otherwise FVIII-deficient mice r
232 nction and inflammation occur in vivo in the vascular endothelium of patients with OSA.
233                                          The vascular endothelium of proliferating intrarenal vessels
234 alcium (Ca(2+)) signals ("sparklets") in the vascular endothelium of resistance arteries that represe
235 , but not C4, is expressed in the stroma and vascular endothelium of several human malignant tumours.
236         In addition to its expression in the vascular endothelium of several organs, we found FcRn to
237 nduced astrocyte loss and at the fenestrated vascular endothelium of the area postrema.
238 nism by which they initiate contact with the vascular endothelium of the blood brain barrier (BBB) is
239 thy is mediated by leukocyte adhesion to the vascular endothelium of the diabetic retina, which resul
240 tic stem and progenitor cells arise from the vascular endothelium of the dorsal aorta and subsequentl
241 rogenitor cells are generated first from the vascular endothelium of the dorsal aorta and then the fe
242 that impairment of TGF-beta signaling in the vascular endothelium of the eye is sufficient to trigger
243 ormal adhesion of circulating blood cells to vascular endothelium of the microcirculation.
244                                              Vascular endothelium offers a variety of therapeutic tar
245            The synthetic endothelial ECM and vascular endothelium on it may help us enter in a new ph
246 oreactor to culture pulmonary epithelium and vascular endothelium on the acellular lung matrix.
247                                          The vascular endothelium operates in a highly polarized envi
248 ese circulating cells as engrafting cells in vascular endothelium or as promoters of tumor growth.
249 eptor with counter-adhesion molecules on the vascular endothelium or extracellular matrix and lead to
250 e adhesion of infected erythrocytes (IEs) to vascular endothelium or placenta is the key event in the
251 ecessarily exerting its effect solely in the vascular endothelium, or might this "endothelial enzyme"
252                            Activation of the vascular endothelium (plasma von Willebrand levels) and
253                                          The vascular endothelium plays a central role in the regulat
254                                          The vascular endothelium plays a critical role in the respon
255                                          The vascular endothelium plays a critical role in vascular h
256 R1 expressed on aortic and limb arterial pig vascular endothelium plays a role in binding and phagocy
257                          Cell rolling on the vascular endothelium plays an important role in traffick
258                                          The vascular endothelium presents a major transport barrier
259      The surface proteins in the bone marrow vascular endothelium provide docking sites for targeted
260                                              Vascular endothelium provides a selective barrier betwee
261 how that Galpha(i) signaling pathways in the vascular endothelium regulate a critical step required f
262  Fluid shear stress due to blood flow on the vascular endothelium regulates blood vessel development,
263 tro models of physiological and pathological vascular endothelium remains a fundamental challenge in
264 sduction in several cell types including the vascular endothelium, renal tubular cells and erythrocyt
265      Inhibition of leukocyte adhesion to the vascular endothelium represents a novel and important ap
266                                          The vascular endothelium responds to damage through activati
267           Dengue virus causes leakage of the vascular endothelium, resulting in dengue hemorrhagic fe
268  Specific and effective silencing of GIPC in vascular endothelium results in inhibition of NRP-1-medi
269 ndothelium; the hematopoietic system and the vascular endothelium share a common embryonic origin; in
270                          Here we report that vascular endothelium-specific deletion of mouse Drosha (
271 e 1 (DNMT1) and a global hypermethylation in vascular endothelium subjected to disturbed flow.
272 gene signatures of mesoderm, trophoblast and vascular endothelium, suggesting correspondence to gastr
273  the expression of adhesion molecules on the vascular endothelium that bind to ligands on circulating
274            Although our study focuses on the vascular endothelium, the findings are likely to be broa
275 e facts: atherosclerosis is a disease of the vascular endothelium; the hematopoietic system and the v
276  Plasmodium falciparum (iRBCs) adhere to the vascular endothelium through adhesive protrusions called
277 is known to exert pleiotropic effects on the vascular endothelium through mitogen-activated protein (
278 nical Wnt pathway at two different levels in vascular endothelium: through transcriptional regulation
279 across the blood-brain barrier and the gut's vascular endothelium thus compromising immune surveillan
280 gnaling in both types of mice stimulates the vascular endothelium to contribute osteoprogenitor cells
281 function and that LPC impacts on the retinal vascular endothelium to induce vasopermeability via VEGF
282      These data indicate that on exposure of vascular endothelium to ionizing radiation, activation o
283  by which rapamycin modulates the ability of vascular endothelium to mediate inflammation and identif
284 fluence leukocyte recruitment, it primes the vascular endothelium to mount a more intense response wh
285 gated the ability of overexpressing Bcl-2 in vascular endothelium to protect against early stages of
286 AT1 activation in innate immune responses of vascular endothelium to R. conorii infection.
287      LSTc was instead found on microglia and vascular endothelium, to which virus bound abundantly.
288 ributing to the proinflammatory responses of vascular endothelium under OSS.
289  Adiponectin colocalized within the cerebral vascular endothelium under transient ischemic conditions
290 nal antioxidant intervention targeted to the vascular endothelium using PEG-liposomes loaded with EUK
291                                           In vascular endothelium VEGF signals through two receptor-t
292  tissues was linked to the activation of the vascular endothelium via one or more Galpha(i)-coupled r
293 e hypothesis for this study was that retinal vascular endothelium was a cell population of unique mol
294 y concurrent discovery in the 1980s that the vascular endothelium was a key site of vasomotor control
295                 Likewise, CD59 expression on vascular endothelium was significantly higher in atheror
296     It also has antiproliferative effects on vascular endothelium when used to coat coronary artery s
297 d receptor gamma (PPARgamma) is expressed in vascular endothelium where it exerts anti-inflammatory a
298 trate that NPP4 is present on the surface of vascular endothelium, where it hydrolyzes Ap3A into AMP
299 expressed in prostate cancer cells and tumor vascular endothelium, whereas the siRNA portion targets
300 ced IP is associated with injury to the lung vascular endothelium, with decreased TJ and PPAR-gamma e

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