ライフサイエンスコーパス: alpha6beta1 integrin

1 n module of thrombospondin-1 is a ligand for alpha6beta1 integrin.

2 nd its receptor as well as for laminin 1 and alpha6beta1 integrin.

3 is mediated in part by activation of surface alpha6beta1 integrin.

4 ng that the peptides interact primarily with alpha6beta1 integrin.

5 were confirmed by antibody clustering of the alpha6beta1 integrins.

6 ed that microglia constitutively express the alpha6beta1 integrin, a well characterized laminin recep

7 motes fetal type II cell differentiation via alpha6beta1 integrin-ADAM17/TACE signaling pathway.

8 rin or the laminin-1/E8 domain recognized by alpha6beta1 integrin, all of which were detected and loc

9 cal adhesion kinase (FAK) has been linked to alpha6beta1 integrin and ErbB receptor signaling, and we

10 cell line that expresses alpha6beta4 but no alpha6beta1 integrin and exhibits dynamic adhesion and m

11 illin; an analogous cotransport was seen for alpha6beta1-integrin and alpha-actinin in U2OS.

12 prising the B-class scavenger receptor CD36, alpha6beta1 integrin, and CD47 (integrin-associated prot

13 of cord-like structures, inhibitable by anti-alpha6beta1 integrin antibodies.

14 ns the distinct functions of alpha4beta1 and alpha6beta1 integrins as thrombospondin receptors in mic

15 Our findings demonstrate that the alpha6beta1 integrin can activate MAP kinase, that this

16 In conclusion, the CD151-alpha6beta1 integrin complex acts as a functional unit t

17 aising cAMP levels in these neurons promotes alpha6beta1 integrin-dependent neurite outgrowth.

18 d alpha6B cytoplasmic domain variants of the alpha6beta1 integrin differentially activate p42 and p44

19 lationally regulates the amount of receptor (alpha6beta1, integrin) expressed on the surface of senso

20 Finally, netrin-4 and alpha6beta1 integrin expression colocalize in mouse embr

21 The alpha6beta1 integrin has been implicated in breast carci

22 fragment E8, i.e., the fragment to which the alpha6beta1 integrin heterodimer binds.

23 The alpha6beta1 integrin heterodimer has been implicated in

24 Staining for the alpha6beta1 integrin heterodimer increases in blood vess

25 The absence of either alpha7beta1 or alpha6beta1 integrin impairs the ability of Schwann cell

26 The ligation of available alpha6beta1 integrin in adherent LOX melanoma cells by l

27 Selective activation of alpha6beta1 integrin in microvascular endothelial cells

28 s raise the possibility that alpha1beta1 and alpha6beta1 integrins in blood vessels might be targeted

29 godendrocyte differentiation and myelination alpha6beta1-integrin interacts with hnRNP-K, an mRNA-bin

30 The alpha6beta1 integrin is a netrin-4 receptor in lymphatic

31 The alpha6beta1 integrin is also expressed by motor neurons

32 The alpha6beta1 integrin is expressed by endothelial cells,

33 Based on these results, we conclude that the alpha6beta1 integrin is not essential for sperm-egg fusi

34 ve suggested that the functional activity of alpha6beta1 integrin is regulated by protein kinase C (P

35 lays a key role in selectively strengthening alpha6beta1 integrin-mediated adhesion to laminin-1.

36 nin gamma1 subunit that in turn activates an alpha6beta1 integrin-mediated signaling pathway in NSCs.

37 alpha6beta1 integrin mediates adhesion of human microvas

38 alpha6 integrin mAb (GoH3), suggest that the alpha6beta1 integrin on mouse eggs functions as the rece

39 The expression of PECAM-1-sensitive alpha6beta1 integrins on the surface of transmigrated ne

40 studies in vivo and in vitro elucidated that alpha6beta1 integrins orchestrated extravascular directi

41 We have reported that alpha6beta1 integrin regulates the directed migration of

42 e suggest that laminin G peptides act on the alpha6beta1 integrin signaling of invasion by stimulatin

43 We suggest that activation of the alpha6beta1 integrin signaling regulates the tyrosine ph

44 d by a significant reduction at 7 days, when alpha6beta1 integrin staining is most prominent around t

45 esion to laminin is mediated entirely by the alpha6beta1 integrin, strongly suggesting that the cytok

46 Functional blocking of alpha3beta1 and alpha6beta1 integrins suppressed adhesion of LEPC to LN-

47 eceptors, with NSCs expressing low levels of alpha6beta1 integrin, syndecan-1, and lutheran, and in v

48 in determining the "outside-in" functions of alpha6beta1-integrin that follow ligand engagement.

49 its associated alpha3beta1, alpha5beta1, and alpha6beta1 integrins undergo endocytosis and accumulate

50 We found that the laminin receptor alpha6beta1 integrin, which is expressed on oligodendroc