ライフサイエンスコーパス: counterreceptor

1 in, Mac-1, and a heretofore unknown platelet counterreceptor.

2 /or top surfaces of BTN3A1 interact with its 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 reted to bind to cell surface glycoconjugate counterreceptors.

8 ype O-glycans as found in natural L-selectin 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 cently become apparent that CTLA-4, a second counterreceptor for the B7 family of costimulatory molec

36 ) is a member of the Ig superfamily and is a counterreceptor for the beta 2 integrins: lymphocyte fun

37 ICAM-3 is a preferred counterreceptor for the leukocyte alpha(L)beta2 integrin

38 accharides represent components of leukocyte counterreceptors for E- and P-selectins and of L-selecti

39 during erythroid development and the likely counterreceptors for these molecules are discussed in th

40 t contribute to sulfation of such L-selectin counterreceptors has been uncertain.

41 ant for nervous system repair, this parasite counterreceptor immunoprecipitation (PcIP) assay identif

42 L-selectin counterreceptors in HEVs are recognized by mAb MECA-79,

43 can be readily adapted to identify receptors/counterreceptors in other T. cruzi invasion sites and in

44 with high-affinity to specific glycoprotein counterreceptors, including PSGL-1.

45 te that manipulation of lymphocyte accessory counterreceptor interactions may affect the course of Th

46 lymorphonuclear leukocytes (PMNs) with their counterreceptor, intercellular adhesion molecule-1, on t

47 s, and that interaction between CD83 and its counterreceptor is dependent upon the state of glycosyla

48 Galectin binding to a specific glycoprotein counterreceptor is regulated in part by the repertoire o

49 The identification of all CD28/CTLA-4 counterreceptors is critical to our understanding of thi

50 specific pairs of cell surface receptors and counterreceptors (ligands) including integrins, the immu

51 These results indicate that ICOS/B7h counterreceptors likely function in vivo to enhance seco

52 e data thus suggest that alpha4beta7 and its counterreceptor MAdCAM-1 represent a novel adhesion path

53 reover, HSV-1 failed to elute the biological counterreceptor MUC16 from galectin-3 affinity columns,

54 o either E- or P-selectin and is not a major counterreceptor of endothelial selectins.

55 es Mac-1 (CD11b/CD18) on neutrophils and its counterreceptor on endothelial cells and hepatocytes, in

56 eptors for extracellular matrix proteins and counterreceptors on adjacent cells, are implicated in sy

57 diated by integrins expressed on B cells and counterreceptors on stromal cells.

58 rent to surfaces coated with either cellular counterreceptors or extracellular matrix proteins.

59 lin (Ig) after cross-linking of OX40L by its counterreceptor OX40, which is expressed on activated T

60 Possible T. cruzi counterreceptors pulled down by the receptor-Fc bait wer

61 y decreased 6-sulfo sLe(x) on HEV L-selectin counterreceptors, relative to LSST- or Core2GlcNAcT-sing

62 n CD11b/CD18, yet the identity of epithelial counterreceptors remain elusive.

63 n host cell receptor recognition by T. cruzi counterreceptors remain largely unknown.

64 d integrin-associated protein (CD47) and its counterreceptor signal regulatory protein (SIRPalpha) on

65 Thus, cooperation of these 2 receptor/counterreceptor systems regulates the prothrombotic prop

66 n ligand 1 (PSGL-1) is a mucin-like selectin counterreceptor that binds to P-selectin, E-selectin, an

67 ha5beta1 is the first high-affinity cellular counterreceptor that has been identified for a member wi

68 nt: CG (chicken galectin)-1A, CG-8 and their counterreceptors that determine the formation, size, num

69 lymph node high endothelial venules and its counterreceptor, the Peyer's patch homing receptor, inte

70 a/CD18 (lymphocyte function antigen [LFA]-1) counterreceptors to ICAM-5, we investigated whether modu

71 ANX1 competed with the endothelial integrin counterreceptor, VCAM-1, for binding to alpha 4 integrin

72 Induction of the counterreceptor was IL-4 dependent and occurred early du

73 ipt expression of the B7 molecules and their counterreceptors was defined using reverse transcriptase

74 idity, and more uniform distribution of CD44 counterreceptor, which resulted in smooth motion of the