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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
4 s of the tight junctional complex, including zonula occludens 1 (ZO-1) and occludin.
5           We previously found that depleting zonula occludens 1 (ZO-1) family proteins in MDCK cells
6 udin-18 to interact with a scaffold protein, zonula occludens 1 (ZO-1), demonstrating that one claudi
7 e 2), and the outer limiting membrane (OLM) (zonula occludens 1 and occludin).
8 nolocalization of the tight junction protein zonula occludens 1 and of the junction-associated actin
9                                      Reduced zonula occludens 1 expression was observed after HbG tra
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
13                                              Zonula occludens 1 protein redistribution after bacteria
14                                 In contrast, zonula occludens 1 was well preserved along intercellula
15  including MUPP1 (multi-PDZ protein-1), ZO1 (zonula occludens 1), and Af6.
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
18            Upon calcium repletion, occludin, zonula occludens 1, and E-cadherin failed to redistribut
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
24 al effects on the cytoplasmic plaque protein zonula occludens 1.
25 pool of ROCK with the tight junction protein zonula occludens 1.
26  expression of the TJ molecules occludin and zonula occludens 1.
27 ly restored the expression of E-cadherin and zonula occludens 1.
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
31  single post-synaptic density-95/discs large/zonula occludens-1 (PDZ) domain.
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
35 ctomyosin ring (PAMR), and redistribution of zonula occludens-1 (ZO-1) and cadherins.
36 lantation, we investigated the expression of zonula occludens-1 (ZO-1) and E-cadherin, two molecules
37 nal barrier using the tight junction markers zonula occludens-1 (ZO-1) and occludin.
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
42                                              Zonula occludens-1 (ZO-1) binds the carboxy terminus of
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
48                                              Zonula occludens-1 (ZO-1) is a submembrane scaffolding p
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
52 sed expression of TTF-1, aquaporin-5 (AQP5), zonula occludens-1 (ZO-1), and cytokeratins.
53  used to assay for the presence of occludin, zonula occludens-1 (ZO-1), cadherin-5, and beta-catenin.
54 MP22 and known junctional proteins including zonula occludens-1 (ZO-1), occludin, and claudin-5.
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
57 ion of another element of the E-cad complex, zonula occludens-1 (ZO-1).
58 ght junction membrane proteins, occludin and zonula occludens-1 (ZO-1).
59 n E-cadherin and tight junction (TJ) protein Zonula Occludens-1 (ZO-1).
60 tight junction proteins such as occludin and zonula occludens-1 (ZO-1).
61 d with the tight junction-associated protein zonula occludens-1 (ZO-1).
62 ion of tight junction proteins, occludin and zonula occludens-1 (ZO-1).
63                      The junctional proteins zonula occludens-1 and beta-catenin stained positively i
64 the dexamethasone-stimulated localization of zonula occludens-1 and beta-catenin to sites of cell-cel
65 n levels of tight junction proteins, such as zonula occludens-1 and Occludin.
66 actin and tight-junction-associated proteins zonula occludens-1 and occludin.
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
71                                 In addition, zonula occludens-1 co-localized with Muller cells within
72 ell adhesion via its effects on the occludin-zonula occludens-1 complex.
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
76  of Id1 suppressed epithelial E-cadherin and zonula occludens-1 expression.
77 ed FD4 permeability and reduced occludin and zonula occludens-1 expression.
78 with HDM-induced AR, with lower occludin and zonula occludens-1 expression.
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
81                                              Zonula occludens-1 molecules are also highly dynamic in
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
85 e PDZ (postsynaptic density 95, discs large, zonula occludens-1) domains and other regions.
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
89 creased tight junction protein (occludin and zonula occludens-1) expression.
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
92 e synthetase, expressed by Muller cells, and zonula occludens-1, a tight-junction protein.
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
101 e expression of junctional proteins, such as zonula occludens-1, occludin, and claudin-4.
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
105 ce staining of the TJ molecules occludin and zonula occludens-1.
106 foil factor 3, Toll-interacting protein, and zonula occludens-1.
107  protein kinase and increasing expression of zonula occludens-1.
108  protein kinase and increasing expression of zonula occludens-1.
109 audin-1, junctional adhesion molecule-A, and zonula occludens-1.
110                                              Zonula occludens-1/NF-kappaB/CXCL8: a new regulatory axi
111 d suppression of TJ transcripts, claudin-11, zonula-occludens-1 (ZO-1) and tricellulin in human SC en
112                         The scaffold protein zonula-occludens-1 (ZO-1), a member of the MAGUK family
113 ption of claudin-18, zonula occludens 1, and zonula occludens 2 localization to lung tight junctions
114 specifically interact with the protein ZO-2 (zonula occludens-2).
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
117                             Staining for the zonula occludens complex (ZO-1) and adherens complex (al
118 e protein, Crumbs, and two PSD95/discs large/zonula occludens domain proteins, protein associated wit
119       The His-ZO-1-PDZ1 (first PDZ domain of zonula occludens) domain that binds Neph1-CD was also an
120 g PDZ (postsynaptic density-95, discs large, zonula occludens) domains play a general role in recruit
121                 The scaffold proteins of the zonula occludens family are required for the correct loc
122                       The tight junction, or zonula occludens, is a specialized cell-cell junction th
123 nction is accomplished in vertebrates by the zonula occludens, or tight junction.
124 ial cells, because the presence of an intact zonula occludens prevented passage.
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
130 audins binds to the N-terminal PDZ domain of zonula occludens proteins (PDZ1).
131                                              Zonula occludens proteins are multidomain proteins usual
132 n of occludin but no change in expression of zonula occludens proteins ZO-1 and -2.
133  MDCKII cells, this complex localizes to the zonula occludens (tight junctions) and appears to regula
134                                              Zonula occludens toxin (Zot) is an enterotoxin elaborate
135 ed that these structures can be modulated by Zonula occludens toxin (Zot).
136          The intestinal secretion induced by zonula occludens toxin follows the opening of tight junc
137                                              Zonula occludens toxin induced a time- and dose-dependen
138                                              Zonula occludens toxin is a novel toxin elaborated by Vi
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
142                  We have determined that the zonula occludens (ZO) family of TJ plaque proteins seque
143 ability of this barrier are dependent on the zonula occludens (ZO) membrane-associated guanylate kina
144                                          The zonula occludens (ZO) protein-1 is a membrane-associated
145                 Thus the manner in which the zonula occludens (ZO) proteins multimerize has implicati
146                Specific TJ proteins, such as zonula occludens (ZO) proteins, localize not only at the
147 ility of these junctions is dependent on the zonula occludens (ZO) proteins, members of the membrane-
148                                          The zonula occludens (ZO) subfamily of membrane-associated g
149                                          The zonula occludens (ZO)-1 and -2 proteins have context-dep
150                                              Zonula occludens (ZO)-1 is a member of the MAGUK (membra
151              The tight junction (TJ) protein zonula occludens (ZO)-1 links the intracellular domain o
152                           Here, we show that zonula occludens (ZO)-1 localizes preferentially to the
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
157 l adhesion molecule-A (JAM)-A, occludin, and zonula occludens (ZO)-1.
158                              In cell culture zonula occludens (ZO)-family proteins are important for
159 ignificant disruption of actin filaments and zonula occludens (ZO-1), and a decrease in transepitheli

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