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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
8 nolocalization of the tight junction protein zonula occludens 1 and of the junction-associated actin
10 he GCD had a small decrease in expression of zonula occludens 1 in SB mucosa and significant decrease
11 n claudin-1 protein level, relocation of the zonula occludens 1 protein (ZO-1) to the TJ, and redistr
12 so shown by the disengagement of the protein zonula occludens 1 protein from the tight junctional com
16 nd eosin), apoptosis (M30), tight junctions (zonula occludens 1), and neutrophil influx (myeloperoxid
17 ssion of the tight junction scaffold protein zonula occludens 1, and disrupted junctional localizatio
19 smoplakin, plakoglobin, claudin-4, occludin, zonula occludens 1, and tricellulin were decreased at ce
20 creased, transient disruption of claudin-18, zonula occludens 1, and zonula occludens 2 localization
21 a and significant decreases in expression of zonula occludens 1, claudin-1, and occludin in rectosigm
22 sion of endothelial tight junction proteins (zonula occludens 1, claudin-5, and occludin), astrocyte
23 nce of Ca2+ as revealed by the relocation of zonula occludens 1, the establishment of transepithelial
28 second post-synaptic density-95/discs large/zonula occludens-1 (PDZ) domain of the human protein tyr
29 the post synaptic density, discs large, and zonula occludens-1 (PDZ) domain protein SAP97 is a compo
30 ffolding postsynaptic density-95/disks large/zonula occludens-1 (PDZ) domain-containing protein melan
32 ontaining postsynaptic density 95/disc large/zonula occludens-1 (PDZ) domains have been shown to play
33 three postsynaptic density 95, discs large, zonula occludens-1 (PDZ) domains to engage the transport
34 postsynaptic density protein 95/disks large/zonula occludens-1 (PDZ)-domain proteins and A-kinase an
36 lantation, we investigated the expression of zonula occludens-1 (ZO-1) and E-cadherin, two molecules
38 3 with retention of Cx43 scaffolding protein Zonula Occludens-1 (ZO-1) at cell surfaces, suggesting t
39 ning the steady-state levels of occludin and zonula occludens-1 (ZO-1) at the BTB site via the p38 MA
40 cing the steady-state levels of occludin and zonula occludens-1 (ZO-1) at the BTB via the p38 mitogen
41 protection against IL-1beta-induced loss of zonula occludens-1 (ZO-1) at the tight junctions and alt
43 nction (TJ)-associated proteins occludin and zonula occludens-1 (ZO-1) following stimulation of brain
44 s serine and threonine residues, we screened zonula occludens-1 (ZO-1) immunoprecipitates for the exi
45 ding G proteins) have been co-localized with zonula occludens-1 (ZO-1) in the tight junction of epith
46 lar, c-Src can disrupt the connexin43 (Cx43)-zonula occludens-1 (ZO-1) interaction, leading to down-r
47 a hallmark of polarized epithelial cells and zonula occludens-1 (ZO-1) is a known key regulator of ti
49 calcium levels, the tight junctional protein Zonula Occludens-1 (ZO-1) is distributed intracellularly
50 s also a marked decrease in beta-catenin and zonula occludens-1 (ZO-1) localization to the intercalat
51 c-Src binds to the Cx43 scaffolding protein zonula occludens-1 (ZO-1) with a higher affinity than do
53 used to assay for the presence of occludin, zonula occludens-1 (ZO-1), cadherin-5, and beta-catenin.
55 ial cell-cell contacts in close proximity to zonula occludens-1 (ZO-1), oxLDL treatment induced a dis
56 o activate tight-junction-associated protein Zonula Occludens-1 (ZO-1), which in turn plays a critica
64 the dexamethasone-stimulated localization of zonula occludens-1 and beta-catenin to sites of cell-cel
67 striking upregulation of dermal N-cadherin, Zonula Occludens-1 and the gap junction protein Connexin
68 sed paracellular flux, and redistribution of zonula occludens-1 and VE-cadherin but failed to induce
69 to the postsynaptic density-95, discs large, zonula occludens-1 binding motif in the C terminus of KV
70 d in large gap junction plaques, had reduced zonula occludens-1 binding, and displayed increased stab
73 ression of epithelial markers E-cadherin and Zonula occludens-1 decreased while expression of mesench
74 calization with both endogenous occludin and zonula occludens-1 demonstrating that exogenous occludin
75 uated cytokine-induced hyperpermeability and zonula occludens-1 downregulation in NS-398-treated C2BB
79 correlated with an increase in claudin-5 and zonula occludens-1 immunofluorescence at cell-cell contr
80 t was associated with a potent protection of zonula occludens-1 linear border pattern in endothelial
82 osophila disc large tumor suppressor (Dlg1), zonula occludens-1 protein (zo-1) (PDZ) domain proteins.
83 phosphorylation regulates the known role of zonula occludens-1 protein (ZO-1) in gap junction (GJ) f
84 n addition, immunofluorescent assessments of zonula occludens-1 tight junction protein cellular distr
86 ing PDZ (postsynaptic density 95/discs large/zonula occludens-1) domains are believed to provide rela
87 PDZ (post-synaptic density-95/discs large/zonula occludens-1) domains are small, protein-protein b
88 PDZ (Post-Synaptic Density-95, Discs Large, Zonula Occludens-1) domains followed by a short carboxyl
90 gulated by several PDZ (PSD-95, discs large, zonula occludens-1) proteins, which mediate protein-prot
91 (connexin 43), Cx45 (connexin 45), and ZO-1 (zonula occludens-1) were identified as novel mRNA target
93 Knockdown of Cx43 and N-cadherin, but not Zonula Occludens-1, accelerated cell migration in a scra
94 ecreased levels of alanine aminotransferase, zonula occludens-1, and interleukin-1beta compared with
95 lit diaphragm-associated protein P-cadherin, zonula occludens-1, and nephrin, a change consistent wit
96 ychaetoid (pyd), the Drosophila homologue of Zonula Occludens-1, are characterized by two phenotypes
97 ted proteins, including occludin, claudin-5, zonula occludens-1, junctional adhesion molecule-A, and
98 In vivo, in addition to loss of nephrin and zonula occludens-1, mesenchymal markers such as desmin,
99 nic epithelial cells such as cytokeratin 18, zonula occludens-1, mucins-1 and -2, antigen A33, and di
100 ed expression of the tight junction proteins zonula occludens-1, occludin, and claudin-1 in the ileum
102 representative tight junction proteins (ie, zonula occludens-1, Occludin, Claudin-1) that critically
103 and tracer permeability, junctional protein zonula occludens-1, occludin, claudins and E-cadherin ex
104 binding post-synaptic density-95/discs large/zonula occludens-1-domain-containing (PDZ) proteins and
111 d suppression of TJ transcripts, claudin-11, zonula-occludens-1 (ZO-1) and tricellulin in human SC en
113 ption of claudin-18, zonula occludens 1, and zonula occludens 2 localization to lung tight junctions
115 omplete dissolution of some tight junctions (zonula occludens) and zonula adherens without loss of de
116 unohistochemistry showed that E-cadherin and Zonula occludens are down-regulated in MCF-7/CXCR4-Delta
118 e protein, Crumbs, and two PSD95/discs large/zonula occludens domain proteins, protein associated wit
120 g PDZ (postsynaptic density-95, discs large, zonula occludens) domains play a general role in recruit
125 lial antigen 2), blood-retinal barrier [anti-zonula occludens protein 1 (ZO-1) and anti-occludin], an
126 llagen-IV, laminin, claudin-5, occludin, and zonula occludens protein 1 was also better preserved in
127 s no obvious change of claudin-1, claudin-4, zonula occludens protein 1, and zonula occludens protein
128 , claudin-4, zonula occludens protein 1, and zonula occludens protein 2 expressions was observed.
129 rotein) PDZ (postsynaptic density/disc large/zonula occludens) protein binding assays, that these sol
133 MDCKII cells, this complex localizes to the zonula occludens (tight junctions) and appears to regula
139 The tissues were also fixed, exposed to zonula occludens toxin, and processed for fluorescence m
140 elial cells is regulated by tight junctions (zonula occludens), we wished to determine whether they a
141 e structural and functional integrity of the zonula occludens (ZA) induced by ATP depletion of renal
143 ability of this barrier are dependent on the zonula occludens (ZO) membrane-associated guanylate kina
147 ility of these junctions is dependent on the zonula occludens (ZO) proteins, members of the membrane-
153 l tight junction proteins, namely, occludin, zonula occludens (ZO)-1, and ZO-2 in the caveolar fracti
154 xpression of occludin, claudin-1, claudin-5, zonula occludens (ZO)-1, and ZO-2, and a TJ accessory pr
155 nucleotide exchange factor (GEF) 2, but not zonula occludens (ZO)-1, in epithelial cells, and these
156 nges in the distribution of the TJ proteins, zonula occludens (ZO)-1, ZO-2, and cingulin, examination
159 ignificant disruption of actin filaments and zonula occludens (ZO-1), and a decrease in transepitheli
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