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1  but under inflammatory conditions acts as a leukocyte adhesion molecule.
2 thelial cells to express at least one of the leukocyte adhesion molecules.
3         After X-irradiation, the endothelial leukocyte adhesion molecule 1 (ELAM-1; E-selectin) was p
4 (TNF) activates transcription of endothelial leukocyte adhesion molecule-1 (CD62E) in endothelial cel
5 ll adhesion molecule-1 (VCAM-1), endothelial-leukocyte adhesion molecule-1 (E-selectin), and intercel
6 dy 7A9 binds specifically to the endothelial leukocyte adhesion molecule-1 (E-selectin), inhibiting t
7 on of adhesion molecules such as endothelial-leukocyte adhesion molecule-1 (E-selectin), intercellula
8                    We found that endothelial leukocyte adhesion molecule-1 (ELAM-1), the earliest mar
9 hesion molecule (ICAM)-1 but not endothelial leukocyte adhesion molecule-1 expression on hepatic endo
10 higher doses required to inhibit endothelial-leukocyte adhesion molecule-1 expression.
11 ar cell adhesion molecule-1, and endothelial leukocyte adhesion molecule-1 in a time- and dose-depend
12 ar cell adhesion molecule-1, and endothelial leukocyte adhesion molecule-1 mRNA were detected by reve
13 appaB and an element, NF-ELAM-1 (endothelial leukocyte adhesion molecule-1), constitutively occupied
14  observed elevated expression of endothelial leukocyte adhesion molecule-1, a human glaucoma marker,
15 alpha (TNFalpha), tissue factor, endothelial leukocyte adhesion molecule-1, and vascular cell adhesio
16                This induction of endothelial-leukocyte adhesion molecule-1, vascular cell adhesion mo
17 sitive than changes in VCAM-1 or endothelial leukocyte adhesion molecule-1.
18 dose of natalizumab, an antibody against the leukocyte adhesion molecule alpha4 integrin, in patients
19      These alterations include expression of leukocyte adhesion molecules and decreased bioavailabili
20 xpression of chemokines, complement factors, leukocyte adhesion molecules and MHC class II, thus high
21  tumor necrosis factor-induced expression of leukocyte adhesion molecules and procoagulant tissue fac
22                 Therefore, the expression of leukocyte adhesion molecules and secretion of proinflamm
23                      The characterization of leukocyte adhesion molecules and their control by proinf
24 elial cells, their expression of ligands for leukocyte adhesion molecules, and vaso-occlusion.
25                                              Leukocyte adhesion molecules are critically involved at
26  proinflammatory cytokines and expression of leukocyte adhesion molecules by endothelial cells in res
27 ) and increased expression of membrane-bound leukocyte adhesion molecule CD11b, leading to enhanced i
28 lated the normal change in expression of the leukocyte adhesion molecules CD11b and CD62L.
29 aB-dependent reporter construct, endothelial leukocyte adhesion molecule CD25 (the 3E10 clone), were
30 mediated rolling of hard spheres coated with leukocyte adhesion molecules (cell-free system).
31                        beta(2)-Integrins are leukocyte adhesion molecules composed of alpha (CD11a, -
32                Many mutant mice deficient in leukocyte adhesion molecules display altered hematopoies
33  this report, we have determined that the EC-leukocyte adhesion molecule E-selectin is a key target f
34 may "superinduce" expression of an important leukocyte adhesion molecule, E-selectin (ELAM-1, CD62E).
35 nucleotide (ASO) targeting human endothelial leukocyte adhesion molecule, E-selectin.
36 ulatory role in cytokine induction of the EC-leukocyte adhesion molecules (ELAM) E-selectin and vascu
37                                  Endothelial leukocyte-adhesion molecule (ELAM)-1 was not detected in
38  integrin alphaMbeta2 (Mac-1, CD11bCD18) are leukocyte adhesion molecules essential for innate immuni
39                                E-selectin, a leukocyte adhesion molecule expressed on endothelium, is
40 eta2 integrins (CD11/CD18) are heterodimeric leukocyte adhesion molecules expressed on hematopoietic
41 irectly suppressed endothelial activation of leukocyte adhesion molecule expression and inflammation.
42         Preclinical investigations examining leukocyte adhesion molecules in I/R provided overwhelmin
43 anges with local expression of cytokines and leukocyte adhesion molecules in mice with disseminated c
44 othelial cell expression of cytokine-induced leukocyte adhesion molecules in vitro.
45 roke, and to study the potential role of the leukocyte adhesion molecule intercellular adhesion molec
46 ere to investigate the immunostaining of the leukocyte adhesion molecules intercellular adhesion mole
47 s that inhibit the expression of endothelial-leukocyte adhesion molecules intercellular adhesion mole
48                                              Leukocyte adhesion molecules involved in this process ha
49                A recent study shows that the leukocyte adhesion molecules known as selectins form 'ca
50                                          The leukocyte adhesion molecule L-selectin mediates lymphocy
51 orate in the biosynthesis of ligands for the leukocyte adhesion molecule L-selectin.
52 ry modification that promotes binding of the leukocyte adhesion molecule L-selectin.
53 thelium in a process mediated in part by the leukocyte adhesion molecule L-selectin.
54                                          The leukocyte adhesion molecule, L-selectin, mediates the re
55 al vascular endothelial cell ligands for the leukocyte adhesion molecule, L-selectin.
56 udy, we found that TXA(2) mimetics stimulate leukocyte adhesion molecule (LAM) expression on endothel
57 ncreased endothelial cell (EC) expression of leukocyte adhesion molecules (LAMs), which mediate monoc
58 or the synthesis of functional selectin-type leukocyte adhesion molecule ligands.
59       Reduced expression of MHC antigens and leukocyte adhesion molecules may contribute to the lack
60     E-selectin, an endothelial-cell-specific leukocyte adhesion molecule, may also function in angiog
61  whether the CD18 family (beta2-integrin) of leukocyte adhesion molecules mediates initial passage of
62 ulation of the endothelial cell cytokine and leukocyte adhesion molecule mRNAs in response to C. albi
63 ate the expression of any of the cytokine or leukocyte adhesion molecule mRNAs.
64                            TNF-alpha induces leukocyte adhesion molecules on endothelial cells (ECs),
65                            The expression of leukocyte adhesion molecules on endothelial cells is ind
66 t, Rho GTPases affect the expression of some leukocyte adhesion molecules on endothelial cells, such
67 ir ability to regulate the expression of key leukocyte adhesion molecules, on both leukocytes and end
68 ample, sulfation of tyrosine residues in the leukocyte adhesion molecule P-selectin glycoprotein liga
69 ical surface, where JAM-A played a role as a leukocyte adhesion molecule participating in transendoth
70 h AMD, there is increased immunostaining for leukocyte adhesion molecules, particularly in the periph
71                               The L-selectin leukocyte adhesion molecule plays an important role in c
72                                    All three leukocyte adhesion molecule proteins were expressed on t
73                   In contrast, the genes for leukocyte adhesion molecules showed a significant upregu
74                     E-selectin, an inducible leukocyte adhesion molecule specifically expressed by en
75 capillaries enlarged into venules expressing leukocyte adhesion molecules, sprouting angiogenesis and
76 esion, and extravasation by up-regulation of leukocyte adhesion molecules such as E-selectin and P-se
77 n and extravasation through the induction of leukocyte adhesion molecules such as ICAM-1.
78 ription or surface expression of endothelial leukocyte adhesion molecules that are readily induced by
79 e-inducible, NF-kappaB-dependent endothelial-leukocyte adhesion molecules that participate in the leu
80 x transporters, and restricted expression of leukocyte adhesion molecules, the BBB is often able to l
81 tigated the role of p75 in TNF-alpha-induced leukocyte adhesion molecules using cultured ECs derived
82                                    Increased leukocyte adhesion molecule VCAM-1 expression and leukoc
83 on of NF-kappaB and subsequent expression of leukocyte adhesion molecules (VCAM1 and ICAM1), coagulat
84 that the phenolic content of RW may modulate leukocyte adhesion molecules, whereas both ethanol and p
85 tress induces expression of endothelial cell leukocyte adhesion molecules, which are centrally import
86  T cells (Tn) are expanded in mice that lack leukocyte adhesion molecules, which have neutrophilia an
87 st and pericyte expression of chemokines and leukocyte adhesion molecules, which is linked to plaque
88  associated with endothelial upregulation of leukocyte adhesion molecules, which persist even after i
89 lming evidence that blocking the function of leukocyte adhesion molecules would be highly effective i