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1 ene transfer-mediated expression of a single alpha-integrin.
2 ions when compared with the VWA domains from alpha-integrins.
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
7 This study shows that mutations in ina-1 (alpha-integrin), as well as vab-1 (Eph receptor), and va
9 majority of these migratory DCs express the alpha integrin chain CD103, and in this study we demonst
10 Endothelial cells also expressed a number of alpha-integrin chains, including alpha 4, but not alpha
14 rECM culture conditions were used to compare alpha-integrin heterodimer expression in malignant and n
15 t to the distinct in vivo roles of alpha and alpha integrins in erythroid stress, suggesting that the
18 thesis that two major families of vertebrate alpha integrins originated prior to the divergence of de
19 ibody directed against beta1-integrin or its alpha integrin partners reduced PA/integrin endocytosis
21 Finally, we show that the C. elegans INA-1 alpha integrin subunit associates with the PAT-3beta sub
23 Recent structural and functional analyses of alpha integrin subunit I domains implicate a region in c
25 sed to characterize extracellular matrix and alpha-integrin subunit expression during development.
28 examined the ability of aONs against various alpha integrin subunits to perturb cranial neural crest
31 etic analysis of vertebrate and invertebrate alpha integrins supported the hypothesis that two major
32 eport of a naturally occurring variant of an alpha integrin that lacks the transmembrane and cytoplas
33 for radial sorting; however, which of the 11 alpha integrins that can pair with beta1 forms the funct
35 monophyletic group of immune cell-expressed alpha integrins, which share a number of common function
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