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1 sion of integrin alpha5/beta1, the principal fibronectin receptor.
2 lpha(5) and beta(1) integrin subunits of the fibronectin receptor.
3 l contacts, particularly those involving the fibronectin receptor.
4 s the ligand binding activity of alpha5beta1 fibronectin receptors.
5 ase-dependent manner following engagement of fibronectin receptors.
6 transfected mammalian cells expressing human fibronectin receptors.
7 ransfected CHO cells expressing alpha4/beta1 fibronectin receptors.
8 d requires alphavbeta3/5 integrins as backup fibronectin receptors.
9 ge adherent area normally when bound through fibronectin receptors.
10 v)beta(3) remains within focal contacts, the fibronectin receptor alpha(5)beta(1) translocates from f
11 s of alpha(IIb) and the alpha subunit of the fibronectin receptor alpha(5)beta(1) were constructed.
12                                          The fibronectin receptors alpha(5)beta(1) integrin and synde
13                              The role of the fibronectin receptor, alpha(5)beta(1)-integrin, as an ad
14               In addition, cells missing the fibronectin receptor alpha5beta1 exhibit defective activ
15 e to enhanced function of the VLA-5 integrin fibronectin receptor and not to increased surface expres
16 inase (Erk) following engagement of integrin/fibronectin receptors and that Raf is the critical targe
17 ning alpha-V (vitronectin receptor), alpha5 (fibronectin receptor), and alpha3 (collagen/laminin rece
18 gh a process that requires engagement of the fibronectin receptor, and promotes attachment and spread
19 cuing the healing defects of animals lacking fibronectin receptors, and can be blocked by pharmacolog
20                                    Thus, the fibronectin receptor appears to be one of the components
21 ctin particle binding through alpha 5 beta 1 fibronectin receptors are independent of IAP expression.
22  in paxillin levels required ligation of the fibronectin receptor, as it was not induced when the cel
23 gh ligand screening that embigin is a direct fibronectin receptor, binding to the N-terminal fibronec
24 in was also found to play a critical role in fibronectin receptor biology ex vivo since cultured paxi
25            Concordantly, the alpha5 integrin fibronectin receptor, but not alpha2 or alpha3, is overe
26 ciated with upregulation of alpha5 integrin (fibronectin receptor component), the antibody-mediated b
27 aSMA, fibronectin, and alpha5beta1 integrin (fibronectin receptor components) in FHL 124 cells and hu
28                 Integrin a(5)B(1) is a major fibronectin receptor critical for cell migration.
29 lin is a critical transducer of signals from fibronectin receptors during early development.
30                              The alpha5beta1 fibronectin receptors exhibited increased clustering on
31  adhesion and migration by downregulation of fibronectin receptor expression.
32  adhesions and expressed more of the classic fibronectin receptor (FNR) alpha5beta1 per cell.
33 es by the application of mechanical force to fibronectin receptors from inside or outside the cell, a
34 in causing loss of the alpha5beta1 integrin (fibronectin receptor) from HGF.
35              The alpha 5 alpha 1 integrin, a fibronectin receptor, has been implicated in the control
36 s expressed alpha 4 beta 1 integrin (another fibronectin receptor); however, addition of anti-human i
37 ular regulated kinase 2 (Erk2) activation by fibronectin receptors in Cos7 cells.
38 roles of alpha(5)beta(1) and alpha(4)beta(1) fibronectin receptors in regulating matrix metalloprotei
39 v integrins, which are the major endothelial fibronectin receptors, in developmental angiogenesis.
40                   Among other receptors, the fibronectin receptor integrin a5B1 plays a pivotal role
41                                              Fibronectin receptor integrin-mediated cell adhesion tri
42                        An analysis of HUASMC fibronectin receptor (integrin alpha5beta1) distribution
43 part of these effects through binding to the fibronectin receptor, integrin alpha(5)beta(1) on mesenc
44 kemia cells, a cell line expressing a single fibronectin receptor, integrin alpha5beta1, which was un
45 In this study we show that expression of the fibronectin receptor, integrin alpha8beta1 is decreased
46 , presumptive proprioceptive neurons express fibronectin receptors, integrin alpha3beta1, alpha4beta1
47                       To prevent fibronectin-fibronectin receptor interaction 100 microM RGDS peptide
48 gulated complex with alpha5beta1 integrin, a fibronectin receptor involved in cell adhesion, motility
49                         Alpha5beta1, a major fibronectin receptor, is a widely distributed integrin t
50 e show here that the alpha5beta1 integrin, a fibronectin receptor, is an efficient binder of Abeta, a
51 to known mRNAs such as those of fibronectin, fibronectin receptor, laminin receptor homolog, beta-tub
52 se include complement receptor type 3 (CR3), fibronectin receptor, mannose receptor, and transferrin
53                 The interaction of gp63 with fibronectin receptors may also play an important role in
54 CCs accumulated internalized laminin but not fibronectin receptors over 20 min, whereas on fibronecti
55 nd alpha5beta1, known as the vitronectin and fibronectin receptors, respectively.
56  endocytosis is induced by engagement of the fibronectin receptor syndecan-4.
57             The integrin alpha v beta 6 is a fibronectin receptor that is undetectable on normal kera
58 regulated levels of cell surface alpha5beta1 fibronectin receptors that resulted in increased matrix
59  it uses for binding to dendritic cells (the fibronectin receptor); the fungus experiences different
60 ression resulted in increased recruitment of fibronectin receptors to the plasma membrane.
61 hages, human DC recognized Hc yeasts via the fibronectin receptor, very late Ag-5, and not via CD18 r
62 munoreactivity for the alpha5 subunit of the fibronectin receptor was evaluated in adult rat brain wi
63                The integrin alphavbeta6 is a fibronectin receptor whose expression is not detectable