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1 /or top surfaces of BTN3A1 interact with its counterreceptor.
2 in, Mac-1, and a heretofore unknown platelet counterreceptor.
3 for functional pairing of human lectins with counterreceptors.
4 fy host receptors and complementing parasite counterreceptors.
5 , we identified alpha(V) integrins as ICAM-4 counterreceptors.
6 to increase its affinity for its endothelial counterreceptors.
7 ype O-glycans as found in natural L-selectin counterreceptors.
8 reted to bind to cell surface glycoconjugate counterreceptors.
9                       E-, P-, and L-selectin counterreceptor activities, leukocyte trafficking, and l
10 ns which recognize their respective cellular counterreceptors and thus are likely to be viral SLAMF d
11 ude receptors for cytokines, growth factors, counterreceptors, and extracellular matrix molecules.
12 e recently identified ICOS/B7h costimulatory counterreceptors are critical regulators of CD4(+) T cel
13 blood-borne leukocytes and their endothelial counterreceptors are frequently concentrated on the micr
14 f E-cadherin, the only known alpha(E)beta(7) counterreceptor as assessed by functional studies, flow
15               Here, we identify the platelet counterreceptor as glycoprotein (GP) Ibalpha, a componen
16 tering or retention of specific glycoprotein counterreceptors bearing these specific ligands.
17  upon the state of glycosylation of a 72-kDa counterreceptor by sialic acid residues.
18 ymphoid tissue chemokine (SLC; CCL21) to its counterreceptor, CCR7.
19 HC-class I antigen and bound to up-regulated counterreceptors CD28 and CTLA-4 on the autoinvasive CD8
20 B-1, B7-1 (CD80), and B7-2 (CD86), and their counterreceptors, CD28 or CTLA-4 (CD152), in the muscle
21 of the 6-sulfo sialyl Lewis(x) on L-selectin counterreceptors CD34, GlyCAM-1, and MAdCAM-1.
22 stribution of lipid rafts and the E-selectin counterreceptor CD44 on the monocyte surface.
23 e binding of CD2, present on T cells, to its counterreceptor CD48 facilitates adhesion, signaling, al
24 t mice to show that engagement of 2B4 by its counterreceptor, CD48, expressed on target cells leads t
25              Interaction between CD2 and its counterreceptor, CD58 (LFA-3), on opposing cells optimiz
26 ude that CD83 is an adhesion receptor with a counterreceptor expressed on monocytes and a subset of a
27 dothelium is mediated by selectins and their counterreceptors, followed by rolling of neutrophils alo
28 ecently identified CD48 as the high affinity counterreceptor for 2B4 in both mice and humans.
29 phil P-selectin ligand but is not a required counterreceptor for E-selectin under in vivo physiologic
30                                    The major counterreceptor for gal-3 on DLBCL cells was identified
31                        Mice deficient in the counterreceptor for intercellular adhesion molecule-1, t
32           However, a physiological ligand or counterreceptor for murine Thy-1 in the lymphoid compart
33 protein ligand-1 (PSGL-1) is a high-affinity counterreceptor for P-selectin on myeloid cells and acti
34 fied platelet glycoprotein (GP) Ibalpha as a counterreceptor for P-selectin.
35  Mac-1 (alphaMbeta2, CD11b/CD18) on DCs as a counterreceptor for platelet glycoprotein (GP) Ibalpha.
36 cently become apparent that CTLA-4, a second counterreceptor for the B7 family of costimulatory molec
37 ) is a member of the Ig superfamily and is a counterreceptor for the beta 2 integrins: lymphocyte fun
38                        ICAM-3 is a preferred counterreceptor for the leukocyte alpha(L)beta2 integrin
39 accharides represent components of leukocyte counterreceptors for E- and P-selectins and of L-selecti
40  during erythroid development and the likely counterreceptors for these molecules are discussed in th
41 t contribute to sulfation of such L-selectin counterreceptors has been uncertain.
42 ant for nervous system repair, this parasite counterreceptor immunoprecipitation (PcIP) assay identif
43                                   L-selectin counterreceptors in HEVs are recognized by mAb MECA-79,
44 can be readily adapted to identify receptors/counterreceptors in other T. cruzi invasion sites and in
45  with high-affinity to specific glycoprotein counterreceptors, including PSGL-1.
46 te that manipulation of lymphocyte accessory counterreceptor interactions may affect the course of Th
47 lymorphonuclear leukocytes (PMNs) with their counterreceptor, intercellular adhesion molecule-1, on t
48 s, and that interaction between CD83 and its counterreceptor is dependent upon the state of glycosyla
49  Galectin binding to a specific glycoprotein counterreceptor is regulated in part by the repertoire o
50        The identification of all CD28/CTLA-4 counterreceptors is critical to our understanding of thi
51 specific pairs of cell surface receptors and counterreceptors (ligands) including integrins, the immu
52         These results indicate that ICOS/B7h counterreceptors likely function in vivo to enhance seco
53 e data thus suggest that alpha4beta7 and its counterreceptor MAdCAM-1 represent a novel adhesion path
54 reover, HSV-1 failed to elute the biological counterreceptor MUC16 from galectin-3 affinity columns,
55 o either E- or P-selectin and is not a major counterreceptor of endothelial selectins.
56 roach, we identified galectin-3 as the major counterreceptor of GPVI on tumor cells.
57 idated CD9 and integrin beta 1 as functional counterreceptors of galectin-3 and showed that CD9 is gl
58 es Mac-1 (CD11b/CD18) on neutrophils and its counterreceptor on endothelial cells and hepatocytes, in
59 eptors for extracellular matrix proteins and counterreceptors on adjacent cells, are implicated in sy
60 diated by integrins expressed on B cells and counterreceptors on stromal cells.
61 rent to surfaces coated with either cellular counterreceptors or extracellular matrix proteins.
62 lin (Ig) after cross-linking of OX40L by its counterreceptor OX40, which is expressed on activated T
63                            Possible T. cruzi counterreceptors pulled down by the receptor-Fc bait wer
64 y decreased 6-sulfo sLe(x) on HEV L-selectin counterreceptors, relative to LSST- or Core2GlcNAcT-sing
65 n CD11b/CD18, yet the identity of epithelial counterreceptors remain elusive.
66 n host cell receptor recognition by T. cruzi counterreceptors remain largely unknown.
67 d integrin-associated protein (CD47) and its counterreceptor signal regulatory protein (SIRPalpha) on
68        Thus, cooperation of these 2 receptor/counterreceptor systems regulates the prothrombotic prop
69 n ligand 1 (PSGL-1) is a mucin-like selectin counterreceptor that binds to P-selectin, E-selectin, an
70 ha5beta1 is the first high-affinity cellular counterreceptor that has been identified for a member wi
71 nt: CG (chicken galectin)-1A, CG-8 and their counterreceptors that determine the formation, size, num
72  lymph node high endothelial venules and its counterreceptor, the Peyer's patch homing receptor, inte
73 a/CD18 (lymphocyte function antigen [LFA]-1) counterreceptors to ICAM-5, we investigated whether modu
74  can interact with cell surface glycoprotein counterreceptors to regulate placental function.
75  ANX1 competed with the endothelial integrin counterreceptor, VCAM-1, for binding to alpha 4 integrin
76                             Induction of the counterreceptor was IL-4 dependent and occurred early du
77 ipt expression of the B7 molecules and their counterreceptors was defined using reverse transcriptase
78 idity, and more uniform distribution of CD44 counterreceptor, which resulted in smooth motion of the