戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  (ECs) and preventing platelet adherence and leukocyte chemotaxis.
2 L-1beta, GM-CSF, IL-6 and IL-8 and inhibited leukocyte chemotaxis.
3 ant peptides, serves as a model receptor for leukocyte chemotaxis.
4 g is important for chemoattractant-dependent leukocyte chemotaxis.
5 , Slit2 repels developing axons and inhibits leukocyte chemotaxis.
6 X3CR1 interaction and RSV G protein-mediated leukocyte chemotaxis.
7 ulate axon guidance, neuronal migration, and leukocyte chemotaxis.
8 CX3C chemokine fractalkine--and induction of leukocyte chemotaxis.
9 r phosphorylation in FPR internalization and leukocyte chemotaxis.
10 ine receptor CCR5 plays an important role in leukocyte chemotaxis and activation, and also acts as a
11 d CCR5 and their respective ligands regulate leukocyte chemotaxis and activation.
12 tional screen of Rho-GEFs for their roles in leukocyte chemotaxis and identified Arhgef5 as an import
13 s of tissue damage in periodontal disease by leukocyte chemotaxis and osteoclastic activation.
14 ics of the actin cytoskeleton, necessary for leukocyte chemotaxis and phagocytosis of microorganisms.
15 II interferon signaling, cell-cell adhesion, leukocyte chemotaxis, and angiogenesis.
16  addition, we have uncovered an inhibitor of leukocyte chemotaxis, and propose a new therapeutic appr
17  response not only through direct effects on leukocyte chemotaxis, but also through effects on the ty
18 ls with anti-N antibodies (Abs) and inhibits leukocyte chemotaxis by binding chemokines (CHKs).
19 ells and suggest that PI3Kgamma may regulate leukocyte chemotaxis by controlling the expression of ch
20 ma isoform of PI3Kinase (PI3Kgamma) controls leukocyte chemotaxis by participating in GPCR signaling,
21 n is clinically important, and yet, to date, leukocyte chemotaxis has largely been studied in vitro.
22                      Cyclophilins can induce leukocyte chemotaxis in vitro and have been detected at
23 ance, was found to inhibit chemokine-induced leukocyte chemotaxis in vitro.
24 mulation was required for platelet-dependent leukocyte chemotaxis in vitro.
25 yses, we demonstrate a two-stage process for leukocyte chemotaxis in vivo: first a "search" phase, wi
26 nce and neuronal migration, can also inhibit leukocyte chemotaxis induced by chemotactic factors.
27  reduced expression of genes associated with leukocyte chemotaxis, migration, and extravasation; >90%
28 ta(2)-integrin involved in cell adhesion and leukocyte chemotaxis, on the surface of neutrophils in a
29 te the cytoskeletal actin polymerization and leukocyte chemotaxis required for the immune function of
30 hat IDH1 mutations caused down-regulation of leukocyte chemotaxis, resulting in repression of the tum
31 mber of the CX(3)C chemokine family, induces leukocyte chemotaxis through activation of its high affi
32 Monocyte chemoattracant-1 (MCP-1) stimulates leukocyte chemotaxis to inflammatory sites, such as rheu
33 the production of inflammatory mediators and leukocyte chemotaxis to the skin.
34 R1 expression and impaired polymorphonuclear leukocyte chemotaxis toward bacterial formylpeptides are
35                                By regulating leukocyte chemotaxis via chemoattractants, miR-223 is cr
36 regulate many leukocyte functions, including leukocyte chemotaxis, via the Rho family of small GTPase
37 atinocyte-derived cytokine, no difference in leukocyte chemotaxis was observed between WT and Fer(DR/