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1 s is the postsynaptic density 95/discs large/zonula occludens 1 (PDZ) domain, involved in scaffolding
2 and an integrated component of the occludin/zonula occludens 1 (ZO-1) adhesion complex at the BTB, s
3 se cells express the tight junction proteins zonula occludens 1 (ZO-1) and occludin and form a barrie
6 udin-18 to interact with a scaffold protein, zonula occludens 1 (ZO-1), demonstrating that one claudi
7 relationship between neuronal Connexins and Zonula Occludens 1 (ZO1), an intracellular scaffolding p
9 2 mechanisms: it maintained localization of zonula occludens 1 and occludin at apical tight junction
11 nolocalization of the tight junction protein zonula occludens 1 and of the junction-associated actin
13 he GCD had a small decrease in expression of zonula occludens 1 in SB mucosa and significant decrease
14 n claudin-1 protein level, relocation of the zonula occludens 1 protein (ZO-1) to the TJ, and redistr
15 so shown by the disengagement of the protein zonula occludens 1 protein from the tight junctional com
19 nd eosin), apoptosis (M30), tight junctions (zonula occludens 1), and neutrophil influx (myeloperoxid
20 ssion of the tight junction scaffold protein zonula occludens 1, and disrupted junctional localizatio
22 smoplakin, plakoglobin, claudin-4, occludin, zonula occludens 1, and tricellulin were decreased at ce
23 creased, transient disruption of claudin-18, zonula occludens 1, and zonula occludens 2 localization
24 a and significant decreases in expression of zonula occludens 1, claudin-1, and occludin in rectosigm
25 sion of endothelial tight junction proteins (zonula occludens 1, claudin-5, and occludin), astrocyte
26 nce of Ca2+ as revealed by the relocation of zonula occludens 1, the establishment of transepithelial
31 second post-synaptic density-95/discs large/zonula occludens-1 (PDZ) domain of the human protein tyr
32 the post synaptic density, discs large, and zonula occludens-1 (PDZ) domain protein SAP97 is a compo
33 ffolding postsynaptic density-95/disks large/zonula occludens-1 (PDZ) domain-containing protein melan
35 ontaining postsynaptic density 95/disc large/zonula occludens-1 (PDZ) domains have been shown to play
36 three postsynaptic density 95, discs large, zonula occludens-1 (PDZ) domains to engage the transport
37 postsynaptic density protein 95/disks large/zonula occludens-1 (PDZ)-domain proteins and A-kinase an
38 te pore above the tight junctions defined by zonula occludens-1 (ZO-1) and also immediately below the
40 lantation, we investigated the expression of zonula occludens-1 (ZO-1) and E-cadherin, two molecules
42 3 with retention of Cx43 scaffolding protein Zonula Occludens-1 (ZO-1) at cell surfaces, suggesting t
43 ning the steady-state levels of occludin and zonula occludens-1 (ZO-1) at the BTB site via the p38 MA
44 cing the steady-state levels of occludin and zonula occludens-1 (ZO-1) at the BTB via the p38 mitogen
45 protection against IL-1beta-induced loss of zonula occludens-1 (ZO-1) at the tight junctions and alt
48 10 reduced podocyte tight junctional protein zonula occludens-1 (ZO-1) but did not affect its mRNA le
49 nction (TJ)-associated proteins occludin and zonula occludens-1 (ZO-1) following stimulation of brain
50 s serine and threonine residues, we screened zonula occludens-1 (ZO-1) immunoprecipitates for the exi
51 ding G proteins) have been co-localized with zonula occludens-1 (ZO-1) in the tight junction of epith
52 lar, c-Src can disrupt the connexin43 (Cx43)-zonula occludens-1 (ZO-1) interaction, leading to down-r
53 a hallmark of polarized epithelial cells and zonula occludens-1 (ZO-1) is a known key regulator of ti
55 calcium levels, the tight junctional protein Zonula Occludens-1 (ZO-1) is distributed intracellularly
56 s also a marked decrease in beta-catenin and zonula occludens-1 (ZO-1) localization to the intercalat
57 c-Src binds to the Cx43 scaffolding protein zonula occludens-1 (ZO-1) with a higher affinity than do
59 TJ complex with established interaction with zonula occludens-1 (ZO-1), and was building homophilic c
60 used to assay for the presence of occludin, zonula occludens-1 (ZO-1), cadherin-5, and beta-catenin.
62 ial cell-cell contacts in close proximity to zonula occludens-1 (ZO-1), oxLDL treatment induced a dis
64 o activate tight-junction-associated protein Zonula Occludens-1 (ZO-1), which in turn plays a critica
75 inal fatty-acid binding protein [I-FABP] and zonula occludens-1 [ZO-1]) and microbial translocation (
77 the dexamethasone-stimulated localization of zonula occludens-1 and beta-catenin to sites of cell-cel
80 served alterations in the adherens junctions zonula occludens-1 and partitioning defective 3, reduced
81 striking upregulation of dermal N-cadherin, Zonula Occludens-1 and the gap junction protein Connexin
82 ed its composition, with concomitant loss of zonula occludens-1 and upregulation of VE-Cadherin expre
83 sed paracellular flux, and redistribution of zonula occludens-1 and VE-cadherin but failed to induce
84 to the postsynaptic density-95, discs large, zonula occludens-1 binding motif in the C terminus of KV
85 d in large gap junction plaques, had reduced zonula occludens-1 binding, and displayed increased stab
88 ression of epithelial markers E-cadherin and Zonula occludens-1 decreased while expression of mesench
89 calization with both endogenous occludin and zonula occludens-1 demonstrating that exogenous occludin
90 uated cytokine-induced hyperpermeability and zonula occludens-1 downregulation in NS-398-treated C2BB
94 al PDZ (postsynaptic density-95/discs-large /zonula occludens-1 homology) motif SSAV, and yeast Sacch
95 correlated with an increase in claudin-5 and zonula occludens-1 immunofluorescence at cell-cell contr
96 Mechanistically, human breast milk reduces Zonula occludens-1 levels, suggesting a regulatory role
97 t was associated with a potent protection of zonula occludens-1 linear border pattern in endothelial
99 ein, drosophila disc large tumor suppressor, zonula occludens-1 protein (PDZ) consensus binding motif
100 osophila disc large tumor suppressor (Dlg1), zonula occludens-1 protein (zo-1) (PDZ) domain proteins.
101 phosphorylation regulates the known role of zonula occludens-1 protein (ZO-1) in gap junction (GJ) f
102 n addition, immunofluorescent assessments of zonula occludens-1 tight junction protein cellular distr
105 ing PDZ (postsynaptic density 95/discs large/zonula occludens-1) domains are believed to provide rela
106 PDZ (post-synaptic density-95/discs large/zonula occludens-1) domains are small, protein-protein b
107 PDZ (Post-Synaptic Density-95, Discs Large, Zonula Occludens-1) domains followed by a short carboxyl
109 gulated by several PDZ (PSD-95, discs large, zonula occludens-1) proteins, which mediate protein-prot
110 (connexin 43), Cx45 (connexin 45), and ZO-1 (zonula occludens-1) were identified as novel mRNA target
112 Knockdown of Cx43 and N-cadherin, but not Zonula Occludens-1, accelerated cell migration in a scra
113 ecreased levels of alanine aminotransferase, zonula occludens-1, and interleukin-1beta compared with
114 lit diaphragm-associated protein P-cadherin, zonula occludens-1, and nephrin, a change consistent wit
115 ychaetoid (pyd), the Drosophila homologue of Zonula Occludens-1, are characterized by two phenotypes
116 ted proteins, including occludin, claudin-5, zonula occludens-1, junctional adhesion molecule-A, and
117 In vivo, in addition to loss of nephrin and zonula occludens-1, mesenchymal markers such as desmin,
118 nic epithelial cells such as cytokeratin 18, zonula occludens-1, mucins-1 and -2, antigen A33, and di
119 ed expression of the tight junction proteins zonula occludens-1, occludin, and claudin-1 in the ileum
121 representative tight junction proteins (ie, zonula occludens-1, Occludin, Claudin-1) that critically
122 and tracer permeability, junctional protein zonula occludens-1, occludin, claudins and E-cadherin ex
123 with the postsynaptic density-95/discs large/zonula occludens-1-and WW domain-containing scaffold pro
124 binding post-synaptic density-95/discs large/zonula occludens-1-domain-containing (PDZ) proteins and
131 R and its target genes FGF19 and TJ proteins zonula, occludens-1, occludin, and claudin-1, along with
132 d suppression of TJ transcripts, claudin-11, zonula-occludens-1 (ZO-1) and tricellulin in human SC en
134 ption of claudin-18, zonula occludens 1, and zonula occludens 2 localization to lung tight junctions
137 omplete dissolution of some tight junctions (zonula occludens) and zonula adherens without loss of de
138 unohistochemistry showed that E-cadherin and Zonula occludens are down-regulated in MCF-7/CXCR4-Delta
140 e protein, Crumbs, and two PSD95/discs large/zonula occludens domain proteins, protein associated wit
142 g PDZ (postsynaptic density-95, discs large, zonula occludens) domains play a general role in recruit
143 enous GRHL2 and the junction proteins (e.g., zonula occludens, E-cadherin, claudins, and occludin).
148 lial antigen 2), blood-retinal barrier [anti-zonula occludens protein 1 (ZO-1) and anti-occludin], an
149 llagen-IV, laminin, claudin-5, occludin, and zonula occludens protein 1 was also better preserved in
150 s no obvious change of claudin-1, claudin-4, zonula occludens protein 1, and zonula occludens protein
151 , claudin-4, zonula occludens protein 1, and zonula occludens protein 2 expressions was observed.
152 rotein) PDZ (postsynaptic density/disc large/zonula occludens) protein binding assays, that these sol
156 and mechanical tension: the tight junction (zonula occludens), the zonula adherens (ZA), and the mac
157 MDCKII cells, this complex localizes to the zonula occludens (tight junctions) and appears to regula
163 The tissues were also fixed, exposed to zonula occludens toxin, and processed for fluorescence m
164 elial cells is regulated by tight junctions (zonula occludens), we wished to determine whether they a
165 e structural and functional integrity of the zonula occludens (ZA) induced by ATP depletion of renal
167 ability of this barrier are dependent on the zonula occludens (ZO) membrane-associated guanylate kina
171 ility of these junctions is dependent on the zonula occludens (ZO) proteins, members of the membrane-
177 l tight junction proteins, namely, occludin, zonula occludens (ZO)-1, and ZO-2 in the caveolar fracti
178 xpression of occludin, claudin-1, claudin-5, zonula occludens (ZO)-1, and ZO-2, and a TJ accessory pr
179 nucleotide exchange factor (GEF) 2, but not zonula occludens (ZO)-1, in epithelial cells, and these
180 nges in the distribution of the TJ proteins, zonula occludens (ZO)-1, ZO-2, and cingulin, examination
183 ignificant disruption of actin filaments and zonula occludens (ZO-1), and a decrease in transepitheli