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1 alpha2 integrin or a non-signaling chimeric alpha2 integrin.
2 omolecules, cell adhesion, and expression of alpha2 integrin.
3 e myoblast cells stably expressing the human alpha2 integrin.
4 type I collagen and this was mediated by the alpha2 integrin.
5 compared to the slow turnover of unclustered alpha2 integrin.
6 tion-blocking antibodies against alpha1- and alpha2-integrins.
7 h constitutive and TPA-induced expression of alpha2 integrin, a late megakaryocytic marker, are inhib
8 sement membrane formation instead of laminin alpha2; integrin alpha7, GalNac transferase, and ADAM12
12 stablish a direct interaction between TRPV4, alpha2 integrin, and the Src tyrosine kinase Lyn in sens
14 tion were suppressed by anti-alpha1 and anti-alpha2 integrin blocking antibodies, and systemic blocka
16 at decreased expression of the gene encoding alpha2 integrin, but not genes encoding alpha1, alpha3,
17 together, these studies demonstrate that an alpha2-integrin-collagen interaction is required for act
19 ss-of-function mutation, alpha2E336A, in the alpha2-integrin did not prevent the activation of FAK, n
21 in, either alone or with variable numbers of alpha2 integrin EF hand metal binding sites, bound colla
26 lpha7 nAChR to simultaneous up-regulation of alpha2-integrin expression and activation of Rho kinase.
27 ion kinase and paxillin with displacement of alpha2 integrin from the focal adhesion protein complex.
28 characterized the 5' flanking region of the alpha2 integrin gene and identified three distinct regul
31 We now focus on the core promoter of the alpha2 integrin gene located between bp -30 and -92 that
32 229-bp region of the distal 5' flank of the alpha2 integrin gene required for high-level enhancer ac
33 c differentiation in which expression of the alpha2 integrin gene requires signaling via the MAP kina
35 alpha7 nAChRs, we quantitated expression of alpha2-integrin gene at the mRNA and protein levels and
36 Erb-B2, which lead to downregulation of the alpha2-integrin gene expression, may proceed through the
38 cells expressing the non-signaling chimeric alpha2 integrin had negligible ability for either endocr
39 purified recombinant proteins containing the alpha2 integrin I domain, either alone or with variable
44 expression of activated, but not wild-type, alpha2 integrins in hematopoietic cells in vivo results
45 tely 40% in both cases: Cross-linking of the alpha2 integrin increased [Ca2+]i in these cells exclusi
47 ies, and systemic blockade of the alpha1 and alpha2 integrins inhibited VEGF-A-driven lymphangiogenes
48 ents mapped binding sites of the recombinant alpha2-integrin-inserted domain to the GLPGER motif of t
50 over, the recombinant inserted domain of the alpha2 integrin interacts with p176 with a relatively hi
51 eptide HEP-III is a major, specific site for alpha2 integrin-mediated binding of mesangial cells to C
54 nt cells expressing high levels of wild-type alpha2 integrin or a non-signaling chimeric alpha2 integ
55 grin promoter plays an essential role in the alpha2-integrin promoter activity and its downregulation
57 , we have used deletion mutations within the alpha2-integrin promoter inserted 5' of the chlorampheni
58 he core region (positions --64 to +1) of the alpha2-integrin promoter plays an essential role in the
59 v-ras on the transcriptional activity of the alpha2-integrin promoter were observed in nontumorigenic
60 of Erb-B2 on transcriptional activity of the alpha2-integrin promoter were observed in transient-cotr
61 face levels of activated, but not wild-type, alpha2 integrin receptors are rapidly down-regulated dur
62 We show here that the internalized clustered alpha2 integrin remains in alpha2-MVBs and is not recycl
64 ved in transient-cotransfection assays using alpha2-integrin reporter plasmids and plasmids expressin
65 Blocking monoclonal antibodies against the alpha2 integrin resulted in 70% inhibition of adhesion t
67 ypic changes elicited by reexpression of the alpha2 integrin subunit and modulates the function of ot
68 llagen was blocked by antibodies against the alpha2 integrin subunit but not by antibodies against th
69 PK kinase 1, prevented the expression of the alpha2 integrin subunit in cells induced to become megak
70 heroids up-regulate expression of CD49b, the alpha2 integrin subunit, and suppress the expression of
73 ed by pre-treatment of HEp-2 cells with anti-alpha2 integrin-subunit antibody and type I collagen, (i
75 hat addition of core3 O-glycans to beta1 and alpha2 integrin subunits in prostate cancer cells suppre
76 binding of isolated, recombinant I domain of alpha2 integrin to collagen in an ELISA assay, but not t
77 n echovirus 1 (EV1) causes redistribution of alpha2 integrin to perinuclear multivesicular bodies, al
78 sion of collagen, fibronectin, tenascin, and alpha2 integrin was detected in the TGF-beta1-expressing
79 The Raf/MEK1/ERK1/2 cascade up-regulating alpha2-integrin was activated due to both Ca2+-dependent
80 tions with blocking antibodies to alpha1 and alpha2 integrins were sufficient to inhibit both haptota
81 VEGF-A induced expression of the alpha1 and alpha2 integrins, which promoted their in vitro tube for
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