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1 lyceride-rich lipoproteins on the surface of capillary endothelial cells.
2 he CD39L2 message is expressed in muscle and capillary endothelial cells.
3 fect CD4-negative cells such as rhesus brain capillary endothelial cells.
4 pression of the VEGF receptor KDR in retinal capillary endothelial cells.
5 g that mouse Abcg4 is expressed in the brain capillary endothelial cells.
6        EPCR staining was usually negative on capillary endothelial cells.
7 the series was assessed using bovine retinal capillary endothelial cells.
8  YAP/TAZ activity in ACKR1+ venous and TrkB+ capillary endothelial cells.
9 echanical forces triggered Ca(2+) signals in capillary endothelial cells.
10 ates TJ disruption and barrier loss in human capillary endothelial cells.
11 inding protein 1 (GPIHBP1) on the surface of capillary endothelial cells.
12 in the luminal membranes of brain and testes capillary endothelial cells.
13 glycoprotein (P-gp) at the membrane of brain capillary endothelial cells.
14 rotubules following laser severing in bovine capillary endothelial cells.
15 hosphatase histochemistry to demonstrate the capillary endothelial cells.
16 signal" to the cell-cycle machinery in human capillary endothelial cells.
17  and increased adherence to cultured retinal capillary endothelial cells.
18 , survival and migration of adrenal cortical capillary endothelial cells.
19     Here, we show that cyclically stretching capillary endothelial cells adherent to flexible extrace
20 ght junction morphology and abnormalities in capillary endothelial cell adhesion to the basement memb
21 P1 is responsible for trafficking LPL across capillary endothelial cells and anchors LPL to the capil
22 red isozyme expressed on plasma membranes of capillary endothelial cells and certain epithelial cells
23 ly expressed on the luminal surface of brain capillary endothelial cells and contributes to the BBB.
24 ound to block in vitro tube formation by rat capillary endothelial cells and cytokine-induced rat cor
25 ated with decreased deltaPKC accumulation in capillary endothelial cells and in the endfeet of capill
26 tions revealed GL-3 deposits in interstitial capillary endothelial cells and large, laminated inclusi
27 lular matrix regulate cell fate switching in capillary endothelial cells and megakaryocytes in vitro,
28                               Bovine retinal capillary endothelial cells and microvascular pericytes
29 -LDL) decreases survival of cultured retinal capillary endothelial cells and pericytes.
30 n the OIR rat retina and in cultured retinal capillary endothelial cells and retinal pigment epitheli
31  indicate that brain injury causes a loss of capillary endothelial cells and tight junction proteins,
32 ptosis/necrosis in intestinal epithelial and capillary endothelial cells, and improved graft tissue b
33 helial (RPE) cells, H-ras-transfected murine capillary endothelial cells, and nuclear factor-kappaB (
34 al complexes in both alveolar epithelial and capillary endothelial cells, and that one or both barrie
35                                     In brain capillaries, endothelial cells are connected closely wit
36                                     Alveolar capillary endothelial cells are critical in maintaining
37  transcriptomic network analyses, we predict capillary endothelial cells are inflamed in COPD, partic
38 acellular trafficking of riboflavin in brain capillary endothelial cells are poorly understood.
39       We hypothesized that TRPA1 channels in capillary endothelial cells are stimulated by neuronal a
40 yte foot processes, swollen and degenerating capillary endothelial cells, astrocytes and motor neuron
41       Pericytes are positioned between brain capillary endothelial cells, astrocytes and neurons.
42  of characteristic herpesviral inclusions in capillary endothelial cells at several sites was consist
43 ain parenchyma by efflux of xenobiotics from capillary endothelial cells at the blood-brain barrier (
44  resisted the adsorption of protein]; bovine capillary endothelial cells attached only on the regions
45 nfected erythrocytes (IRBCs) to bovine brain capillary endothelial cells (BBEC) in vitro were isolate
46 eversed the binding of IRBCs to bovine brain capillary endothelial cells (BBECs).
47 211 MuLV infection in the brain is the brain capillary endothelial cell (BCEC), which is resistant to
48 h allowed it to efficiently infect rat brain capillary endothelial cells (BCEC) in vivo and in vitro.
49  selective syncytium induction (SI) of brain capillary endothelial cells (BCEC), intracerebral hemorr
50 ctly to in vivo syncytium formation of brain capillary endothelial cells (BCEC).
51 hat allow it to efficiently infect rat brain capillary endothelial cells (BCEC).
52 e development of extensive syncytia in brain capillary endothelial cells (BCEC).
53 s cell-specific syncytium formation of brain capillary endothelial cells (BCEC).
54                                        Brain capillary endothelial cells (BCECs) are targets of CD4-i
55                                        Brain capillary endothelial cells (BCECs) express IL-25.
56  of brain microvessels, likely through brain capillary endothelial cells (BCECs).
57 rebral endothelium monolayer formed by brain capillary endothelial cells (bEnd.3 cells).
58           GPIHBP1, a GPI-anchored protein of capillary endothelial cells, binds lipoprotein lipase (L
59 s reduced form is not transported across the capillary endothelial cell blood-brain barrier.
60 lent manganese ions within the microvascular capillary endothelial cells (BMVECs) that constitute the
61 al vein endothelial cells and bovine retinal capillary endothelial cells (BRCECs) while promoting pro
62                Rosiglitazone inhibits bovine capillary endothelial cell but not tumor cell proliferat
63 antigens have been demonstrated in pulmonary capillary endothelial cells, but the mechanisms causing
64                                              Capillary endothelial cells can be switched between grow
65                                        Renal capillary endothelial cells can undergo EndMT in associa
66                We have previously shown that capillary endothelial cell (cEC) inwardly rectifying K(+
67                   We recently identified two capillary endothelial cell (cEC)-based mechanisms that c
68  was previously shown that tropism for brain capillary endothelial cells (CEC) was a determinant of t
69 The dense network of capillaries composed of capillary endothelial cells (cECs) and pericytes lies in
70     Genetic deletion of AIBP expanded CXCR4+ capillary endothelial cells (CECs) with stemlike and pro
71 feration in vitro, inhibited bFGF-stimulated capillary endothelial cell chemotaxis in vitro, and caus
72 NA uptake by 2.1-fold in bEnd.3 murine brain capillary endothelial cells compared to the unmodified d
73 g in anesthetized mice, we reveal that brain capillary endothelial cells control blood flow through a
74 ier (BRB) consists of tightly interconnected capillary endothelial cells covered with pericytes and g
75                                    A retinal capillary endothelial cell culture system was used to as
76 least 20% of embryonic coronary arterial and capillary endothelial cells derive from the ST/PE compar
77 in the angiogenic response was determined in capillary endothelial cells derived from coronary microv
78 he formation of membrane discontinuities) in capillary endothelial cells derived from endocrine gland
79 ls and on putative progenitors of glomerular capillary endothelial cells early in their recruitment t
80 ogenous MMP inhibitor that uniquely inhibits capillary endothelial cell (EC) proliferation as well as
81 e then screened for their ability to inhibit capillary endothelial cell (EC) proliferation in vitro.
82 ellular protein, is upregulated in pulmonary capillary endothelial cells (EC) during influenza-induce
83 arrested cancer cells occurred when adjacent capillary endothelial cells (EC) entered into a distinct
84 pecific angiogenesis assays such as enhanced capillary endothelial cells (EC) sprouting and by increa
85 ved in angiogenesis, presumably by mediating capillary (endothelial cell [EC]) stability, its involve
86        In many organs, small openings across capillary endothelial cells (ECs) allow the diffusion of
87 ression of PPARgamma and its target genes in capillary endothelial cells (ECs) and pericytes, which t
88  a collagen-cross-linking enzyme, in retinal capillary endothelial cells (ECs) enhances subendothelia
89 te targeted to the ADAMTS9 locus showed that capillary endothelial cells (ECs) in embryonic and adult
90    However, specific information about heart capillary endothelial cells (ECs) is lacking.
91                                              Capillary endothelial cells (ECs) maintain a semi-permea
92 ecently identified reduced nuclear TDP-43 in capillary endothelial cells (ECs) of donors with ALS-FTD
93               When a brain region is active, capillary endothelial cells (ECs) sense neuron-derived m
94   Shortly after coronary development begins, capillary endothelial cells (ECs) transcriptionally segr
95 blood-brain barrier (BBB) is formed by brain capillary endothelial cells (ECs).
96 al F-MuLV, PVC-211 MuLV can infect rat brain capillary endothelial cells efficiently and that it has
97              Conversely, in cultured retinal capillary endothelial cells, exogenous Hepc decreased bo
98                                      Retinal capillary endothelial cells, experiencing the same gluco
99  proteolytic cascade used by tumor cells and capillary endothelial cells for basement membrane invasi
100 nt of leukocyte adhesion to cultured retinal capillary endothelial cells for diabetic patients but no
101                                     Cerebral capillary endothelial cells form the BBB that surrounds
102    In this study, cultures of astrocytes and capillary endothelial cells from the blood-brain barrier
103  We further demonstrate that fibroblasts and capillary endothelial cells function as central communic
104 ster (NMMA) increased TGF-beta in glomerular capillary endothelial cells (GCECs) and stimulated colla
105                               Cultured human capillary endothelial cells (HCEC) contain a large inwar
106 nduces inflammation in primary human retinal capillary endothelial cells (HRCEC) and human umbilical
107                               VEGF increased capillary endothelial cell ICAM-1 levels in a dose- and
108 ng subtype of Ptx3-positive dermal lymphatic capillary endothelial cells (iLECs) that recruit pro-lym
109 ol pericytes are capable of growth-arresting capillary endothelial cells in a cell contact-dependent
110 to severe loss of fenestration of glomerular capillary endothelial cells in both eNOS-deficient and w
111   CCR2 was not detected in myogenic cells or capillary endothelial cells in injured muscle to suggest
112       Here we demonstrate a central role for capillary endothelial cells in sensing neural activity a
113 r type I and type II cells, fibroblasts, and capillary endothelial cells in strain B6C3 mice was achi
114 resumably exerts its effects, while bound to capillary endothelial cells in the liver, adrenal gland,
115  receptor-mediated nanoparticle targeting to capillary endothelial cells in the retina after i.v. app
116 rotein inhibited the proliferation of bovine capillary endothelial cells in vitro.
117  and adhesion of human leukocytes to retinal capillary endothelial cells, in a dose-dependent manner,
118                Bromodeoxyuridine labeling of capillary endothelial cells increased during the first 2
119 sion of Mrp4 in the choroid plexus and brain capillary endothelial cells indicate that Mrp4 has a dua
120 f MP observed within clefts between adjacent capillary endothelial cells indicate that some endotheli
121 Captopril acted directly and specifically on capillary endothelial cells, inhibiting their chemotaxis
122 byproduct of neural activity-which activates capillary endothelial cell inward-rectifier K(+) (KIR2.1
123 yperemia) through diminished activity of the capillary endothelial cell inward-rectifier potassium ch
124 chemical theory of the surface glycocalyx on capillary endothelial cells is presented that models the
125  the SVCT2 is induced by culture of cortical capillary endothelial cells, its absence in vivo remains
126 linositol 4,5 bisphosphate (PIP(2)) in brain capillary endothelial cells, leading to the loss of inwa
127 uman endothelial cell types (the human brain capillary endothelial cell line hCMEC/D3 and human umbil
128 tion in a conditionally immortalized retinal capillary endothelial cell line, Tr-iBRB.
129 ial cells and to cells from human and rodent capillary endothelial cell lines.
130 ociated with more glomerular and peritubular capillary endothelial cell loss in association with an i
131                                    The brain capillary endothelial cells maintain the structure and f
132  phenotype, as measured by the inhibition of capillary endothelial cell migration and of corneal neov
133 f the CXC chemokine family can induce bovine capillary endothelial cell migration in vitro and cornea
134 e, for a period of 1-2 h, destabilizes brain capillary endothelial cell monolayer and introduces the
135                      Incubation of the brain capillary endothelial cell monolayer with 0.3-0.6 mumol/
136 ), E-selectin, and P-selectin on human brain capillary endothelial cell monolayers exposed to VEGF wa
137 is reorganized when DCs migrate across brain capillary endothelial cell monolayers without causing si
138                     Confluent bovine retinal capillary endothelial cells (n = 13) and pericytes (n =
139 e, and caused lack of ESAM expression in the capillary endothelial cells of damaged brain.
140                                              Capillary endothelial cells of neovasculature in 137 mal
141 sitive method allows the detection of Pgp in capillary endothelial cells of normal brain in conventio
142 on of human MDR1 P-glycoprotein (Pgp) in the capillary endothelial cells of the central nervous syste
143                                              Capillary endothelial cells of the human blood-brain bar
144                    Binding to primary bovine capillary endothelial cells or a human endothelial cell
145          Tie2 was demonstrated on glomerular capillary endothelial cells, particularly on the ablumin
146 er (BBB) consisting of primary porcine brain capillary endothelial cells (pBCEC).
147 t repetitive lung injury activates pulmonary capillary endothelial cells (PCECs) and perivascular mac
148        We show that PNX stimulates pulmonary capillary endothelial cells (PCECs) to produce angiocrin
149                          In cultured retinal capillary endothelial cells, PEDF significantly decrease
150 he electrically connected cells that include capillary endothelial cells, pericytes, and vascular smo
151 lised RBE4 cell line, derived from rat brain capillary endothelial cells, preserves many features of
152 P < 0.05), a twofold increase in peritubular capillary endothelial cell proliferation (1.60 +/- 0.30
153 of TIMP-2 and, in particular, Loop 6 inhibit capillary endothelial cell proliferation and angiogenesi
154 d vascular remodelling through inhibition of capillary endothelial cell proliferation and VEGF expres
155 ascular endothelial growth factor-stimulated capillary endothelial cell proliferation in vitro, inhib
156 pressing endostatin or angiostatin inhibited capillary endothelial cell proliferation in vitro.
157     Use of an anti-VEGF antibody blocked the capillary endothelial cell proliferation induced by the
158 nsulin-conditioned RPE cell media stimulated capillary endothelial cell proliferation, an effect that
159  RPE cells were assayed for VEGF protein and capillary endothelial cell proliferation.
160 n levels in conditioned media and stimulated capillary endothelial cell proliferation.
161 ombined kringle structures of angiostatin on capillary endothelial cell proliferation.
162 e blood-brain barrier (BBB), formed by brain capillary endothelial cells, protects the brain from exp
163 tion of riboflavin in immortalized rat brain capillary endothelial cells (RBE4).
164 rmeability were measured in cultured retinal capillary endothelial cells (RCECs) and in db/db mice tr
165  Here we show that targeted ablation of lung capillary endothelial cells recapitulates the cellular e
166 Cs) but could be modulated in bovine retinal capillary endothelial cells (RECs) by cell confluency, h
167 osylphosphatidylinositol-anchored protein of capillary endothelial cells, shuttles lipoprotein lipase
168                                          The capillary endothelial cell strong inward-rectifier K(+)
169 creases in iron export from cultured retinal capillary endothelial cells suggest that the retina may
170  This ability of the cytoskeleton to control capillary endothelial cell survival may be important for
171 is a glycolipid-anchored membrane protein of capillary endothelial cells that binds lipoprotein lipas
172 , we report intact CD31(+) corneal lymphatic capillary endothelial cells that do not express LYVE-1.
173 f substrates and are highly expressed in the capillary endothelial cells that form part of the blood-
174 ces a sustained paracellular permeability in capillary endothelial cells that is mediated by activati
175 essive extracellular edema in neural tissue, capillary endothelial cell tight junctions appeared to r
176                           The shape of human capillary endothelial cells was controlled by culturing
177 esent study, the transport of insulin across capillary endothelial cells was investigated in vivo.
178  VEGF on cultured bovine retinal and adrenal capillary endothelial cells were examined in the presenc
179 estigate viral entry into the CNS, rat brain capillary endothelial cells were exposed to human lympho
180                             Human and bovine capillary endothelial cells were switched from growth to
181                                      Retinal capillary endothelial cells were visualized by transmiss
182 rteries was usually less than in surrounding capillary endothelial cells, whereas it was usually of c
183 al amino acid transporter (LAT) at the brain capillary endothelial cell, which forms the blood-brain
184 rmed by resident macrophages and peritubular capillary endothelial cells, which monitors the transpor
185 stituted peptides inhibited the migration of capillary endothelial cells with an ED50 of 8.5 nM for t
186  increase the selectivity of PDT in damaging capillary endothelial cells with less damage to RPE cell
187 plexus epithelium but not on the fenestrated capillary endothelial cells within the choroid plexus.

 
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