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1  PC12 cells to peptide III-7 was mediated by integrin alpha1beta1.
2 ) truncated protomer) that selectively binds integrin alpha1beta1.
3 duced pCav-1 levels only in cells expressing integrin alpha1beta1.
4 pe IV collagen, by promoting the function of integrin alpha1beta1.
5  pCav-1 is a new substrate of TCPTP and that integrin alpha1beta1 acts as a negative regulator of Cav
6 g growth factor (TGF)-beta1 and the other by integrin alpha1beta1, affect Alport glomerular pathogene
7                               How modulating integrin alpha1beta1 affinity alters collagen homeostasi
8 ibodies, we determined that adhesion through integrins alpha1beta1, alpha2beta1, alphavbeta3, and alp
9 nteractions mediated by the collagen-binding integrins, alpha1beta1, alpha2beta1, alpha10beta1 and al
10 r processes through its interaction with the integrins, alpha1beta1, alpha2beta1, alpha10beta1, and a
11 on the back skin of control and mice lacking integrin alpha1beta1 and alpha2beta1.
12 , these findings uncover a crosstalk between integrin alpha1beta1 and TbetaRII that is essential for
13                      These data suggest that integrin alpha1beta1 and TGF-beta1 may provide useful ta
14                                      If both integrin alpha1beta1 and TGF-beta1 pathways are function
15                       We now report that the integrins alpha1beta1 and alpha2beta1 are receptors for
16                         The collagen-binding integrins alpha1beta1 and alpha2beta1 have been shown to
17                   In conclusion, the loss of integrins alpha1beta1 and alpha2beta1 in mice results in
18        Mesangial cells and podocytes express integrins alpha1beta1 and alpha2beta1, which are the two
19 alpha1 and alpha2, which resulted in loss of integrins alpha1beta1 and alpha2beta1.
20                          Instead, inhibiting integrins alpha1beta1 and alpha5beta1 curtails both gale
21 IV)NC1 domain of type-IV collagen could bind integrins alpha1beta1 and alphavbeta3 expressed on melan
22 asts lack receptors and distal cells express integrins alpha1beta1 and alphaVbeta3, enabling virion a
23 r results indicate that the collagen-binding integrins, alpha1beta1 and alpha2beta1 play a central ro
24 gated the role of the major collagen-binding integrins, alpha1beta1 and alpha2beta1, in several in vi
25 te (int)) DCs expresses the collagen-binding integrin, alpha1beta1, and the E-cadherin-binding integr
26                     Thus, we have identified integrin alpha1beta1 as a modulator of glomerulosclerosi
27 ion is significantly higher in cells lacking integrin alpha1beta1 at base line and following oxidativ
28                                              Integrin alpha1beta1 binding to collagen IV, which is me
29          Cav-1 interacts with integrins, and integrin alpha1beta1 binds/activates T cell protein-tyro
30 ncogenic Kras, suggesting that both Kras and integrin alpha1beta1 cooperate to drive the growth of no
31 PARgamma axis plays a key role in regulating integrin alpha1beta1-dependent Cav-1 expression and cons
32                                              Integrin alpha1beta1-dependent endothelial cell prolifer
33 for biomechanical insult in the induction of integrin alpha1beta1-dependent Rac1-mediated mesangial c
34            Thus, our study demonstrates that integrin alpha1beta1-EGFR cross talk is a key step in ne
35 is report demonstrates a direct link between integrin alpha1beta1 function in retinal pigment epithel
36             The collagen IV binding receptor integrin alpha1beta1 has been shown to regulate lung can
37 his could explain the protective function of integrin alpha1beta1 in oxidative stress-mediated damage
38                                              Integrin alpha1beta1 is a collagen receptor abundantly e
39                                              Integrin alpha1beta1 is a collagen receptor that down-re
40                                              Integrin alpha1beta1 is a collagen-binding receptor expr
41 pand the CPP-I receptor family, showing that integrin alpha1beta1 is also a receptor for CPP-I.
42 av-1 (pCav-1) is a substrate of TCPTP and if integrin alpha1beta1 is essential for promoting TCPTP-me
43                                      Because integrin alpha1beta1 is expressed in many cell types thi
44                                              Integrin alpha1beta1 (Itgalpha1beta1) prevents kidney fi
45                                              Integrin alpha1beta1 localizes to the basal aspect of re
46 h factor receptor signaling, participates in integrin alpha1beta1-mediated EGFR activation.
47 In addition, we showed a novel pathway where integrin alpha1beta1 modulates ROS production, which in
48                                        Thus, integrin alpha1beta1 negatively regulates EGFR activatio
49                                              Integrin alpha1beta1 negatively regulates the generation
50 ression is dependent on the collagen-binding integrin alpha1beta1 on VSMCs.
51 highly increased by the addition of purified integrin alpha1beta1 or an integrin alpha1 cytoplasmic p
52                                              Integrin alpha1beta1 protects from glomerular injury by
53                                              Integrin alpha1beta1, the major collagen type IV recepto
54 how that adhesion by the collagen IV-binding integrin alpha1beta1 unexpectedly inhibited macrophage e
55                                          The integrin alpha1beta1 (very late antigen-1; CD49a/CD29) i
56                The collagen-binding receptor integrin alpha1beta1 was required for recruitment of TCP
57 rtex from Alport mice are immunopositive for integrin alpha1beta1, while only a small fraction of cir