ライフサイエンスコーパス: alpha integrin

1 ene transfer-mediated expression of a single alpha-integrin.

2 ions when compared with the VWA domains from alpha-integrins.

3 The locus encodes two isoforms of a new alpha-integrin, a molecule that dynamically mediates cel

4 nt for multiple edematous wings and inflated alpha-integrins, also show the tendrils phenotype, and l

5 erm memory in Drosophila, Volado, encodes an alpha integrin and is preferentially expressed in the mu

6 We found three alpha integrin aONs that blocked attachment to fibronect

7 ntegrin beta1 (ITGB1) pairing with different alpha-integrins as the key player mediating nHEV cell en

8 This study shows that mutations in ina-1 (alpha-integrin), as well as vab-1 (Eph receptor), and va

9 ) T cells as well as their expression of the alpha-integrin, CD103.

10 We identified the alpha integrin cDNA from Lytechinus variegatus by RT-PCR

11 majority of these migratory DCs express the alpha integrin chain CD103, and in this study we demonst

12 Endothelial cells also expressed a number of alpha-integrin chains, including alpha 4, but not alpha

13 lular binding partner of a platelet-specific alpha-integrin cytoplasmic tail.

14 pecificity, alphaSU2 was transfected into an alpha-integrin-deficient CHO cell line.

15 cription factor vab-3/Pax6 in regulating the alpha integrin genes, ina-1 and pat-2.

16 rECM culture conditions were used to compare alpha-integrin heterodimer expression in malignant and n

17 t to the distinct in vivo roles of alpha and alpha integrins in erythroid stress, suggesting that the

18 n signaling pathway and the up-regulation of alpha-integrin (ITGA2, ITGA3) were associated with the b

19 to a beta-propeller structure resembling the alpha-integrin ligand-binding domain.

20 DPW3 encodes a novel membrane-associated alpha integrin-like protein conserved in land plants.

21 findings revealed a novel and vital role of alpha integrin-like proteins in plant male reproduction.

22 , IL-1beta, tumor necrosis factor alpha (TNF-alpha)], integrin-mediated interactions [integrin subuni

23 Our analysis of C. elegans ina-1 alpha integrin mutants provides the first genetic eviden

24 thesis that two major families of vertebrate alpha integrins originated prior to the divergence of de

25 ibody directed against beta1-integrin or its alpha integrin partners reduced PA/integrin endocytosis

26 ing the transcript levels encoding the CD11b alpha integrin protein.

27 Finally, we show that the C. elegans INA-1 alpha integrin subunit associates with the PAT-3beta sub

28 Surprisingly, no associating alpha integrin subunit could be identified suggesting th

29 Recent structural and functional analyses of alpha integrin subunit I domains implicate a region in c

30 We have identified a novel alpha integrin subunit in Drosophila, that associates wi

31 sed to characterize extracellular matrix and alpha-integrin subunit expression during development.

32 Many alpha integrin subunits are cleaved during their process

33 While uncleaved alpha integrin subunits can form functional receptors th

34 examined the ability of aONs against various alpha integrin subunits to perturb cranial neural crest

35 This study examined the expression of alpha-integrin subunits and extracellular matrix ligands

36 The effect of mAbs to CD49 (alpha integrin) subunits of CD29 was also examined.

37 etic analysis of vertebrate and invertebrate alpha integrins supported the hypothesis that two major

38 eport of a naturally occurring variant of an alpha integrin that lacks the transmembrane and cytoplas

39 for radial sorting; however, which of the 11 alpha integrins that can pair with beta1 forms the funct

40 alpha-Integrin transcription is regulated by ecdysone in

41 monophyletic group of immune cell-expressed alpha integrins, which share a number of common function