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1 fect CD4-negative cells such as rhesus brain capillary endothelial cells.
2 pression of the VEGF receptor KDR in retinal capillary endothelial cells.
3 EPCR staining was usually negative on capillary endothelial cells.
4 inding protein 1 (GPIHBP1) on the surface of capillary endothelial cells.
5 the series was assessed using bovine retinal capillary endothelial cells.
6 in the luminal membranes of brain and testes capillary endothelial cells.
7 glycoprotein (P-gp) at the membrane of brain capillary endothelial cells.
8 g that mouse Abcg4 is expressed in the brain capillary endothelial cells.
9 rotubules following laser severing in bovine capillary endothelial cells.
10 hosphatase histochemistry to demonstrate the capillary endothelial cells.
11 signal" to the cell-cycle machinery in human capillary endothelial cells.
12 and increased adherence to cultured retinal capillary endothelial cells.
13 , survival and migration of adrenal cortical capillary endothelial cells.
14 he CD39L2 message is expressed in muscle and capillary endothelial cells.
15 Here, we show that cyclically stretching capillary endothelial cells adherent to flexible extrace
16 ght junction morphology and abnormalities in capillary endothelial cell adhesion to the basement memb
17 P1 is responsible for trafficking LPL across capillary endothelial cells and anchors LPL to the capil
18 red isozyme expressed on plasma membranes of capillary endothelial cells and certain epithelial cells
19 ly expressed on the luminal surface of brain capillary endothelial cells and contributes to the BBB.
20 ound to block in vitro tube formation by rat capillary endothelial cells and cytokine-induced rat cor
21 ated with decreased deltaPKC accumulation in capillary endothelial cells and in the endfeet of capill
22 tions revealed GL-3 deposits in interstitial capillary endothelial cells and large, laminated inclusi
23 lular matrix regulate cell fate switching in capillary endothelial cells and megakaryocytes in vitro,
26 n the OIR rat retina and in cultured retinal capillary endothelial cells and retinal pigment epitheli
27 indicate that brain injury causes a loss of capillary endothelial cells and tight junction proteins,
28 ptosis/necrosis in intestinal epithelial and capillary endothelial cells, and improved graft tissue b
29 helial (RPE) cells, H-ras-transfected murine capillary endothelial cells, and nuclear factor-kappaB (
32 yte foot processes, swollen and degenerating capillary endothelial cells, astrocytes and motor neuron
33 of characteristic herpesviral inclusions in capillary endothelial cells at several sites was consist
34 ain parenchyma by efflux of xenobiotics from capillary endothelial cells at the blood-brain barrier (
35 resisted the adsorption of protein]; bovine capillary endothelial cells attached only on the regions
36 nfected erythrocytes (IRBCs) to bovine brain capillary endothelial cells (BBEC) in vitro were isolate
38 211 MuLV infection in the brain is the brain capillary endothelial cell (BCEC), which is resistant to
39 h allowed it to efficiently infect rat brain capillary endothelial cells (BCEC) in vivo and in vitro.
40 selective syncytium induction (SI) of brain capillary endothelial cells (BCEC), intracerebral hemorr
48 al vein endothelial cells and bovine retinal capillary endothelial cells (BRCECs) while promoting pro
50 antigens have been demonstrated in pulmonary capillary endothelial cells, but the mechanisms causing
52 was previously shown that tropism for brain capillary endothelial cells (CEC) was a determinant of t
53 feration in vitro, inhibited bFGF-stimulated capillary endothelial cell chemotaxis in vitro, and caus
54 NA uptake by 2.1-fold in bEnd.3 murine brain capillary endothelial cells compared to the unmodified d
55 ier (BRB) consists of tightly interconnected capillary endothelial cells covered with pericytes and g
57 least 20% of embryonic coronary arterial and capillary endothelial cells derive from the ST/PE compar
58 in the angiogenic response was determined in capillary endothelial cells derived from coronary microv
59 he formation of membrane discontinuities) in capillary endothelial cells derived from endocrine gland
60 ls and on putative progenitors of glomerular capillary endothelial cells early in their recruitment t
61 ogenous MMP inhibitor that uniquely inhibits capillary endothelial cell (EC) proliferation as well as
62 e then screened for their ability to inhibit capillary endothelial cell (EC) proliferation in vitro.
63 pecific angiogenesis assays such as enhanced capillary endothelial cells (EC) sprouting and by increa
64 ved in angiogenesis, presumably by mediating capillary (endothelial cell [EC]) stability, its involve
65 a collagen-cross-linking enzyme, in retinal capillary endothelial cells (ECs) enhances subendothelia
66 te targeted to the ADAMTS9 locus showed that capillary endothelial cells (ECs) in embryonic and adult
69 al F-MuLV, PVC-211 MuLV can infect rat brain capillary endothelial cells efficiently and that it has
72 proteolytic cascade used by tumor cells and capillary endothelial cells for basement membrane invasi
73 nt of leukocyte adhesion to cultured retinal capillary endothelial cells for diabetic patients but no
75 In this study, cultures of astrocytes and capillary endothelial cells from the blood-brain barrier
76 ster (NMMA) increased TGF-beta in glomerular capillary endothelial cells (GCECs) and stimulated colla
78 nduces inflammation in primary human retinal capillary endothelial cells (HRCEC) and human umbilical
80 ol pericytes are capable of growth-arresting capillary endothelial cells in a cell contact-dependent
81 to severe loss of fenestration of glomerular capillary endothelial cells in both eNOS-deficient and w
82 CCR2 was not detected in myogenic cells or capillary endothelial cells in injured muscle to suggest
84 r type I and type II cells, fibroblasts, and capillary endothelial cells in strain B6C3 mice was achi
85 resumably exerts its effects, while bound to capillary endothelial cells in the liver, adrenal gland,
86 receptor-mediated nanoparticle targeting to capillary endothelial cells in the retina after i.v. app
88 and adhesion of human leukocytes to retinal capillary endothelial cells, in a dose-dependent manner,
90 sion of Mrp4 in the choroid plexus and brain capillary endothelial cells indicate that Mrp4 has a dua
91 f MP observed within clefts between adjacent capillary endothelial cells indicate that some endotheli
92 Captopril acted directly and specifically on capillary endothelial cells, inhibiting their chemotaxis
93 byproduct of neural activity-which activates capillary endothelial cell inward-rectifier K(+) (KIR2.1
94 chemical theory of the surface glycocalyx on capillary endothelial cells is presented that models the
95 the SVCT2 is induced by culture of cortical capillary endothelial cells, its absence in vivo remains
96 uman endothelial cell types (the human brain capillary endothelial cell line hCMEC/D3 and human umbil
99 ociated with more glomerular and peritubular capillary endothelial cell loss in association with an i
101 phenotype, as measured by the inhibition of capillary endothelial cell migration and of corneal neov
102 f the CXC chemokine family can induce bovine capillary endothelial cell migration in vitro and cornea
103 e, for a period of 1-2 h, destabilizes brain capillary endothelial cell monolayer and introduces the
105 ), E-selectin, and P-selectin on human brain capillary endothelial cell monolayers exposed to VEGF wa
106 is reorganized when DCs migrate across brain capillary endothelial cell monolayers without causing si
109 sitive method allows the detection of Pgp in capillary endothelial cells of normal brain in conventio
110 on of human MDR1 P-glycoprotein (Pgp) in the capillary endothelial cells of the central nervous syste
114 t repetitive lung injury activates pulmonary capillary endothelial cells (PCECs) and perivascular mac
117 lised RBE4 cell line, derived from rat brain capillary endothelial cells, preserves many features of
118 P < 0.05), a twofold increase in peritubular capillary endothelial cell proliferation (1.60 +/- 0.30
119 of TIMP-2 and, in particular, Loop 6 inhibit capillary endothelial cell proliferation and angiogenesi
120 ascular endothelial growth factor-stimulated capillary endothelial cell proliferation in vitro, inhib
122 Use of an anti-VEGF antibody blocked the capillary endothelial cell proliferation induced by the
123 nsulin-conditioned RPE cell media stimulated capillary endothelial cell proliferation, an effect that
127 e blood-brain barrier (BBB), formed by brain capillary endothelial cells, protects the brain from exp
129 rmeability were measured in cultured retinal capillary endothelial cells (RCECs) and in db/db mice tr
130 Here we show that targeted ablation of lung capillary endothelial cells recapitulates the cellular e
131 Cs) but could be modulated in bovine retinal capillary endothelial cells (RECs) by cell confluency, h
132 osylphosphatidylinositol-anchored protein of capillary endothelial cells, shuttles lipoprotein lipase
133 creases in iron export from cultured retinal capillary endothelial cells suggest that the retina may
134 This ability of the cytoskeleton to control capillary endothelial cell survival may be important for
135 is a glycolipid-anchored membrane protein of capillary endothelial cells that binds lipoprotein lipas
136 , we report intact CD31(+) corneal lymphatic capillary endothelial cells that do not express LYVE-1.
137 f substrates and are highly expressed in the capillary endothelial cells that form part of the blood-
138 ces a sustained paracellular permeability in capillary endothelial cells that is mediated by activati
139 essive extracellular edema in neural tissue, capillary endothelial cell tight junctions appeared to r
141 esent study, the transport of insulin across capillary endothelial cells was investigated in vivo.
142 VEGF on cultured bovine retinal and adrenal capillary endothelial cells were examined in the presenc
143 estigate viral entry into the CNS, rat brain capillary endothelial cells were exposed to human lympho
146 rteries was usually less than in surrounding capillary endothelial cells, whereas it was usually of c
147 al amino acid transporter (LAT) at the brain capillary endothelial cell, which forms the blood-brain
148 rmed by resident macrophages and peritubular capillary endothelial cells, which monitors the transpor
149 stituted peptides inhibited the migration of capillary endothelial cells with an ED50 of 8.5 nM for t
150 increase the selectivity of PDT in damaging capillary endothelial cells with less damage to RPE cell
151 plexus epithelium but not on the fenestrated capillary endothelial cells within the choroid plexus.
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