戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 umor cell adhesion and directly binds to the alpha3beta1 integrin.
2 4SF proteins may link PI 4-K activity to the alpha3beta1 integrin.
3 t their interactions are mediated in part by alpha3beta1 integrin.
4 ot for the association between KAI1/CD82 and alpha3beta1 integrin.
5 -5 and adhere to exogenous laminin-5 through alpha3beta1 integrin.
6 t alpha3 and beta1 integrins, and by soluble alpha3beta1 integrin.
7 t alpha3 and beta1 integrins, and by soluble alpha3beta1 integrin.
8 ectin also enhanced TSP1 binding to purified alpha3beta1 integrin.
9 ance the ability of TSP1 to be recognized by alpha3beta1 integrin.
10 a TSP1 substrate, which was also mediated by alpha3beta1 integrin.
11 o depends on interactions between Reelin and alpha3beta1 integrin.
12 everal signals that regulate activity of the alpha3beta1 integrin.
13 s, including the gB-specific alphaVbeta3 and alpha3beta1 integrins.
14  binding of alpha3(IV)NC1 to alphaVbeta3 and alpha3beta1 integrins.
15  prostate cancer metastasis via depletion of alpha3beta1 integrin, a correlation observed in a signif
16           In this study, we demonstrate that alpha3beta1 integrin, a major laminin receptor involved
17 tional cell-surface proteins associated with alpha3beta1 integrin, a monoclonal antibody selection pr
18              Antibodies directed against the alpha3beta1 integrin also reduce the size and number of
19 PP interacted with alpha3beta1 integrin, and alpha3beta1 integrin altered APP trafficking and process
20 AK-negative mouse DU3 cells suggest that the alpha3beta1 integrin and FAK play roles in the HHV-8 med
21 romote normal cortical lamination by binding alpha3beta1 integrin and modulating integrin-mediated ce
22 s with cell surface heparan sulfate (HS) and alpha3beta1 integrin and plays roles in the initial bind
23 poprotein E receptor 2 (ApoER2; refs 9-11 ), alpha3beta1 integrin and protocadherins.
24 This enhancement of adhesion was mediated by alpha3beta1 integrin and required that the alpha3beta1 i
25 ant role in post-translation modification of alpha3beta1 integrin and strongly suggest that changes i
26           On the basis of these results, the alpha3beta1 integrin and sulfated glycolipids cooperate
27          These findings implicate a role for alpha3beta1 integrin and the associated signaling pathwa
28      Here we describe an association between alpha3beta1 integrin and transmembrane-4 superfamily (TM
29 ements for the interaction of CD151 with the alpha3beta1 integrin and with other tetraspanins.
30 ced glomerular epithelial cell expression of alpha3beta1 integrins and impaired adhesion to type IV c
31        We confirmed that APP interacted with alpha3beta1 integrin, and alpha3beta1 integrin altered A
32                               Addition of an alpha3beta1 integrin antibody prevented APP and Reelin-i
33                              We suggest that alpha3beta1-integrins are important for immature and tra
34 data therefore indicate that the function of alpha3beta1 integrin as a mediator of keratinocyte migra
35                       We have now identified alpha3beta1 integrin as an additional receptor for TSP1
36 ell surface heparan sulfate and utilizes the alpha3beta1 integrin as one of its entry receptors.
37                               HHV-8 utilizes alpha3beta1 integrin as one of the receptors for its ent
38 s bound by the alpha1beta1, alpha2beta1, and alpha3beta1 integrins, as well as cell surface proteogly
39                                 In contrast, alpha3beta1 integrin association of TF is constitutive i
40                    CD151 silencing disrupted alpha3beta1 integrin association with tetraspanin-enrich
41 y alpha3beta1 integrin and required that the alpha3beta1 integrin be in an active state.
42 F-beta receptor signaling complex containing alpha3beta1 integrins, beta-catenin, TGF-beta receptor I
43               Moreover, both alphavbeta3 and alpha3beta1 integrin bind with high affinity to G(919-12
44 ible signal transduction pathways induced by alpha3beta1 integrin binding have been evaluated.
45 e of a peptide (alpha325) that disrupts uPAR/alpha3beta1 integrin binding prevented uPA induction.
46 s a signaling platform; migration depends on alpha3beta1 integrin binding to laminin 332 (LN332; also
47 that was much more pronounced in the case of alpha3beta1 integrin binding.
48                                  TSP1 and an alpha3beta1 integrin-binding peptide from TSP1 also inhi
49                   Recognition of TSP1 and an alpha3beta1 integrin-binding peptide from TSP1 by normal
50        In solution, both intact TSP1 and the alpha3beta1 integrin-binding peptide from TSP1 inhibit p
51 column indicated that D-Hep-III binds to the alpha3beta1 integrin but not to the alpha2 or alpha6 int
52 panins CD9 and CD81 physically link EWI-2 to alpha3beta1 integrin, but not to other integrins.
53 ored the hypothesis that lateral ligation of alpha3beta1 integrin by uPAR contributes to uPA regulati
54 nd raised the question of how the tumor cell alpha3beta1 integrin contacts its best-defined ligand, l
55 retraction and both the alpha6 integrins and alpha3beta1 integrin contribute to lamellae formation.
56                   These results suggest that alpha3beta1 integrin deficiency impairs distinct pattern
57                     Previously we found that alpha3beta1 integrin-deficient neonatal mice develop mic
58 raspanin association were both important for alpha3beta1 integrin-dependent initial adhesion and rapi
59 in alpha3beta1; however, unlike alphavbeta3, alpha3beta1 integrin did not mediate cell adhesion to im
60             The upregulation of keratinocyte alpha3beta1 integrin during reepithelialization suggests
61 s with cell surface heparan sulfate (HS) and alpha3beta1 integrin during the early stages of infectio
62 s 8 (KSHV/HHV-8) interacts with cell surface alpha3beta1 integrin early during in vitro infection of
63 monstrate that the fragment acts through the alpha3beta1-integrin/extracellular matrix metalloprotein
64                                          The alpha3beta1 integrin forms complexes with other cell-sur
65 ly displace the receptor tyrosine kinase and alpha3beta1 integrin from the syndecan with an IC50 of 1
66 ortical neurons occurs following the loss of alpha3beta1 integrin function.
67 reepithelialization but suggest instead that alpha3beta1 integrin has a major new in vivo role as an
68                                  Because the alpha3beta1 integrin has been shown to mediate neurite o
69  cell morphological responses that depend on alpha3beta1-integrin have not been defined.
70 high affinity ligand for the alphavbeta3 and alpha3beta1 integrin heterodimers and that these integri
71    In this paper, we define a novel role for alpha3beta1 integrin in association with the tetraspanin
72 ing Schwann cells, and specifically with the alpha3beta1 integrin in some cells, we tested whether th
73               The interaction of TIMP-2 with alpha3beta1 integrin in the cerebral cortex suggests tha
74 trate the involvement of both galectin-3 and alpha3beta1 integrin in the EC response to NG2 and show
75                Here, we examined the role of alpha3beta1-integrin in ErbB2-dependent proliferation of
76 sion and functional interaction of CD151 and alpha3beta1-integrin in geminin-overexpressing cells.
77 HHV-8 gB-neutralizing antibodies and soluble alpha3beta1 integrin inhibited the virus-induced signali
78 lustrated in models with altered function of alpha3beta1 integrin, integrin-linked kinase, laminin-52
79 , slowing cell locomotion, whereas laminin-5-alpha3beta1 integrin interaction inhibits RhoA and activ
80 alpha1(IV)382-393 but right in the middle of alpha3beta1 integrin interaction with alpha1(IV)531-543.
81 ecific guidance mechanisms, such as netrin-1-alpha3beta1 integrin interactions, modulate distinct rou
82  vitro and in vivo findings demonstrate that alpha3beta1 integrin is critical for alpha3(IV)NC1-media
83 a indicate that a complex comprising LN5 and alpha3beta1 integrin is multifunctional and contributes
84                           Here, we show that alpha3beta1 integrin is necessary for neuron-glial recog
85                 TSP1 binding activity of the alpha3beta1 integrin is not stimulated by CD47-binding p
86                                      Loss of alpha3beta1 integrin leads to increased CD151 homodimer
87     We show that binding of alpha3(IV)NC1 to alpha3beta1 integrin leads to inhibition of COX-2-mediat
88                       However, on laminin-5 (alpha3beta1 integrin ligand), A431 cell reaggregation an
89 3 or beta1 integrin subunits, and by soluble alpha3beta1 integrin ligands.
90            Here, we show that the tumor cell alpha3beta1 integrin makes an important contribution to
91 tatic tumor, and the decreased expression of alpha3beta1 integrin may contribute to its virulence.
92 herefore, recognition of immobilized TSP1 by alpha3beta1 integrin may stimulate endothelial cell prol
93 ry structure) can directly influence several alpha3beta1 integrin-mediated signal transduction events
94 e IV collagen, alpha1(IV)531-543, can induce alpha3beta1 integrin-mediated signal transduction in mel
95 ial cells do not spread on a TSP1 substrate, alpha3beta1 integrin mediates efficient spreading on TSP
96            These results suggest first, that alpha3beta1 integrin mediates homotypic adhesion of SCLC
97 endent of proliferation, but ligation of the alpha3beta1 integrin modulates endothelial cell prolifer
98 ssion levels of the terminal sialic acids of alpha3beta1 integrin N-glycans play an important role in
99     In vivo analysis of interneuron-specific alpha3beta1 integrin, netrin-1-deficient mice (alpha3(lo
100 on, tumor organoid formation, and growth via alpha3beta1 integrin on cancer cells, associated with tu
101  studies revealed that TIMP2 interacted with alpha3beta1 integrin on ECs, inhibiting Src activation-d
102 sed by an antibody that specifically engages alpha3beta1 integrins, P1B5.
103 < 20 nM) and binding was blocked by a 17-mer alpha3beta1 integrin peptide (alpha325) homologous to th
104 ch are binding sites for the alpha2beta1 and alpha3beta1 integrins, respectively.
105  tumor immunity, implicating Col1 homotrimer-alpha3beta1 integrin signaling axis as a cancer-specific
106 2.35 cells express relatively high levels of alpha3beta1-integrins, similar to that previously shown
107 on of SCLC cells, and second, that unengaged alpha3beta1 integrin suppresses the growth of disaggrega
108   Because uPAR is redistributed to clustered alpha3beta1 integrins, the requirement for uPAR/alpha3be
109 e beta1-chain-derived fragment interacts via alpha3beta1-integrins, thereby triggering the down-regul
110 rcinoma cells have been shown to utilize the alpha3beta1 integrin to bind to models of the alpha1(IV)
111 ed by GABAergic interneurons, interacts with alpha3beta1 integrin to promote interneuronal migration.
112 erface as well as impaired relocalization of alpha3beta1 integrin to the basement membrane zone.
113 signaling induces a shift in TF-binding from alpha3beta1-integrin to alpha6beta4 and dictates FAK rec
114  interactions with host receptors, including alpha3beta1 integrin, trigger localized actin rearrangem
115           Because multivalent aggregation of alpha3beta1 integrin up-regulates uPA and induces a dram
116                HHV-8 also interacts with the alpha3beta1 integrin via its glycoprotein gB, and virus
117 alpha3 integrin null eggs, we found that the alpha3beta1 integrin was not essential for sperm-egg bin
118  by alpha3(IV)NC1 in endothelial cells, only alpha3beta1 integrin was sufficient to regulate COX-2 in
119 F did not induce increased expression of the alpha3beta1 integrin, which also has been implicated in
120                                          The alpha3beta1 integrin, which is responsible for the motil
121 g N-linked oligosaccharides, most notably on alpha3beta1 integrin, which is the predominant integrin
122 Recombinant and native Reelin associate with alpha3beta1 integrin, which regulates neuron-glia intera
123 pulmonary vasculature through interaction of alpha3beta1 integrin with LN-5 in exposed BM provides bo

 
Page Top