ライフサイエンスコーパス: basophilic leukemia

1 e phosphatase-inactive forms of SHP-1 in rat basophilic leukemia 2H3 (RBL-2H3) mast cell line.

2 Overexpression of Gab2 in rat basophilic leukemia 2H3 cell line cells inhibited the Fc

3 investigated the role of Gab2 using the rat basophilic leukemia 2H3 cell line mast cells.

4 The receptors were stably expressed in rat basophilic leukemia 2H3 cells and characterized for rece

5 lize the level of LAT phosphorylation in rat basophilic leukemia 2H3 cells show that Erk2 phosphoryla

6 duces an increase in 5-HT uptake Vmax in rat basophilic leukemia 2H3 cells that is enhanced by pretre

7 ing events that lead to degranulation in rat basophilic leukemia 2H3 cells.

8 A were then cotransfected with CD94 into rat basophilic leukemia 2H3 cells.

9 ctions enriched in plasma membranes from rat basophilic leukemia 2H3 mast cells.

10 n a Syk-negative variant of the RBL-2H3 (rat basophilic leukemia 2H3) mast cell line.

11 retion from transiently transfected RBL (rat basophilic leukemia)-2H3 mast cells (a tumor analog of m

12 IgE-dependent stimulation of either rat basophilic leukemia-2H3 cells (RBL-2H3 cells) or mouse b

13 In rat basophilic leukemia-2H3 cells expressing formyl peptide

14 In rat basophilic leukemia-2H3 cells expressing transfected mou

15 In rat basophilic leukemia-2H3 cells, Lyn thus plays a dual rol

16 ransfected the unique domain of Lyn into rat basophilic leukemia-2H3 mast cells and examined the cons

17 E-loaded receptors (IgE-FcepsilonRI) on rat basophilic leukemia-2H3 mast cells in contact with fluid

18 rgent sensitivity of this association on rat basophilic leukemia-2H3 mast cells, and we compare the c

19 or genetically encoded Ca(2+) sensors in rat basophilic leukemia and bone marrow-derived rat mast cel

20 release-activated Ca2+ (CRAC) channel in rat basophilic leukemia and other hematopoietic cells to rel

21 Significantly, the most prominent rat basophilic leukemia cell integrin (alpha5) avoids the pa

22 Rat basophilic leukemia cell line (RBL-2H3) stably expressin

23 In mast cells of the rat basophilic leukemia cell line (RBL-2H3), cholera toxin (

24 in a similar manner, we studied a stable rat basophilic leukemia cell line (RBL-CR1) transfected with

25 ere therefore examined using transfected rat basophilic leukemia cell lines (RBL-2H3) that expressed

26 blasts (as a model of adherent cell) and rat basophilic leukemia cells (as a model of nonadherent cel

27 In fact, CaG chemoattracts rat basophilic leukemia cells (RBL cells) expressing the hig

28 ctive channels in the plasma membrane of rat basophilic leukemia cells (RBL-2H3 m1), an immortalized

29 donoyl ethanolamide (anandamide, AEA) in rat basophilic leukemia cells (RBL-2H3) has been proposed to

30 investigated the regulation of CXCR4 in rat basophilic leukemia cells (RBL-2H3) stably transfected w

31 alcium mobilization and degranulation in rat basophilic leukemia cells and cytokine production (IL-6

32 gated through patch-clamp experiments on rat basophilic leukemia cells and fluorometric imaging plate

33 , 5-LO is localized to the cytoplasm; in rat basophilic leukemia cells and human alveolar macrophages

34 o image Annexin 2-GFP in live, secreting rat basophilic leukemia cells and in cells performing pinocy

35 s across intact cell-attached patches in rat basophilic leukemia cells and rat megakaryocytes reveale

36 on-dependently inhibited CRAC current in rat basophilic leukemia cells and thapsigargin-induced Ca(2+

37 cts more effectively with FcepsilonRI(+)-rat basophilic leukemia cells at 37 degrees C compared with

38 Examination of rat basophilic leukemia cells by both immunocytochemistry an

39 that the mitotic clock of unsynchronized rat basophilic leukemia cells has a marked precision with 80

40 inity receptor for IgE (Fc epsilonRI) on rat basophilic leukemia cells is regulated by its initiating

41 sured the extent and rate of adhesion of rat basophilic leukemia cells preincubated with anti-dinitro

42 Recent studies in Jurkat T cells and in rat basophilic leukemia cells revealed an Mg(2+)-inhibited c

43 ster ovary cells and alpha4 integrins on rat basophilic leukemia cells showed little or no associatio

44 iating Ca(2+) waves are observed in most rat basophilic leukemia cells stimulated with soluble Ag and

45 Using rat basophilic leukemia cells transfected with the human hig

46 gh affinity receptors (Fc epsilon RI) on rat basophilic leukemia cells using both single particle tra

47 we describe a study in which we incubate rat basophilic leukemia cells with a fluorescently labeled c

48 cepsilonRI-mediated calcium signaling in rat basophilic leukemia cells, a property dependent on the S

49 rent (I(crac)) in lacrimal acinar cells, rat basophilic leukemia cells, and DT40 B-lymphocytes.

50 In rat basophilic leukemia cells, emptying of the stores activa

51 ar characteristics to that recorded from rat basophilic leukemia cells, namely a similar time course

52 Here we show, in intact rat basophilic leukemia cells, that calcium responses induce

53 degranulation assay in C3aR-transfected rat basophilic leukemia cells, two were prominent agonists (

54 Using mFPR-transfected rat basophilic leukemia cells, we found that a recently iden

55 om HeLa cells expressing SERT and intact rat basophilic leukemia cells, we show that agents such as N

56 ays and degranulation tests of humanized rat basophilic leukemia cells.

57 roliferation in human Jurkat T-cells and rat basophilic leukemia cells.

58 sequent release of chemical mediators on rat basophilic leukemia cells.

59 I(CRAC) to a size comparable to that in rat basophilic leukemia cells.

60 se-activated Ca(2+) current (I(CRAC)) in rat basophilic leukemia cells.

61 a large gain in CRAC channel function in rat basophilic leukemia cells.

62 lently cross-linked IgE dimers stimulate rat basophilic leukemia cells.

63 activation of whole-cell CRAC current in rat basophilic leukemia cells.

64 usly measured in thousands of individual rat basophilic leukemia cells.

65 itutions on FPR functions in transfected rat basophilic leukemia cells.

66 um compounds in Jurkat T lymphocytes and rat basophilic leukemia cells.

67 e-labeled anti-DNP IgE on the surface of rat basophilic leukemia cells.

68 ase-activated calcium current (Icrac) in rat basophilic leukemia cells.

69 een identified in T-lymphocytes and RBL (rat basophilic leukemia) cells and named MagNuM (for Mg(2+)-

70 ibitor of mast cell degranulation in the rat basophilic leukemia mast cell model, in the passive cuta

71 ng enlargement of these vesicles in both rat basophilic leukemia mast cells and Jurkat T leukemia cel

72 find that SNAP-23 is phosphorylated when rat basophilic leukemia mast cells are triggered to degranul

73 Rat basophilic leukemia mast cells primed with fluorescent a

74 lation mutants inhibited exocytosis from rat basophilic leukemia mast cells, demonstrating that phosp

75 ) responses to antigen in IgE-sensitized rat basophilic leukemia mast cells.

76 STZ mitigated degranulation of RBL-2H3 (rat basophilic leukemia) mast cells induced by compound 48/8

77 C3a stimulated degranulation in a basophilic leukemia RBL-2H3 cell expressing wild-type C3

78 Using a basophilic leukemia RBL-2H3 cell line expressing wild-ty

79 These mutants expressed in rat basophilic leukemia RBL-2H3 cells bound LTB4 with simila

80 ion of the IgE high affinity receptor on rat basophilic leukemia RBL-2H3 cells results in activation

81 a monoclonal antibody raised against the rat basophilic leukemia RBL-2H3 cells, we identified that pl

82 man chemoattractant receptor regulation, rat basophilic leukemia RBL-2H3 cells, which are thrombin-re

83 gE receptor (FcepsilonRI) aggregation in rat basophilic leukemia RBL-2H3 cells.

84 d phospholipase C-gamma1 from lysates of rat basophilic leukemia RBL-2H3 cells.

85 (CD31), after FcepsilonRI stimulation in rat basophilic leukemia RBL-2H3 cells.

86 Coimmunoprecipitation experiments in rat basophilic leukemia (RBL 2H3) cells show that SHIP-2 int

87 pressed CD94/NKG2A-EGFP receptors in the rat basophilic leukemia (RBL) cell line.

88 In studies using transfected rat basophilic leukemia (RBL) cell lines expressing either f

89 itro with human and mouse mast cells and rat basophilic leukemia (RBL) cells and in vivo in mice.

90 ocessed appropriately, and functional in rat basophilic leukemia (RBL) cells following retroviral tra

91 Cross-linking of FcepsilonRI on rat basophilic leukemia (RBL) cells initiates a signaling ca

92 parallel studies of FcepsilonRI-bearing rat basophilic leukemia (RBL) cells transfected with constru

93 ion channel, in human and rat platelets, rat basophilic leukemia (RBL) cells, and phorbol myristate a

94 and capacitative Ca(2+) influx, we used rat basophilic leukemia (RBL) cells, vascular smooth muscle

95 gE-Fc epsilonRI) and the cytoskeleton in rat basophilic leukemia (RBL) mast cells.

96 ysteinyl leukotriene type I receptors in rat basophilic leukemia (RBL)-1 cells, large amplitude Ca(2+

97 to analyze published experiments on the rat basophilic leukemia (RBL)-2H3 cell line that seem to con

98 d, disassembled, and soluble vimentin in rat basophilic leukemia (RBL)-2H3 cells expressing human CCR

99 ist of (125)I-C3a radioligand binding to rat basophilic leukemia (RBL)-2H3 cells expressing the human

100 Surprisingly, overexpression of SphK1 in rat basophilic leukemia (RBL)-2H3 mast cells impaired degran

101 Here we show that stimulation of rat basophilic leukemia (RBL)-2H3 mast-like cells with the A

102 Rat basophilic leukemia (RBL)-SX38 cells that express human

103 and intracellular Ca2+ concentrations in rat basophilic leukemia (RBL-2H3 m1) cells.

104 lation of the CCR1 chemokine receptor, a rat basophilic leukemia (RBL-2H3) cell line was modified to

105 n-8 (CXCR1) were stably coexpressed in a rat basophilic leukemia (RBL-2H3) cell line.

106 IV-1 infection, monocytes and MAGIC5 and rat basophilic leukemia (RBL-2H3) cell lines co-expressing t

107 Rat basophilic leukemia (RBL-2H3) cells predominantly expres

108 hannels and store-operated Ca2+ entry in rat basophilic leukemia (RBL-2H3) cells.

109 of 60 phosphate units was identified in rat basophilic leukemia (RBL-2H3) mast cells using specific

110 are expressed either in the cytoplasm of rat basophilic leukemia (RBL-2H3) mucosal mast cells or anch

111 d receptor, Mas-related gene X2 (MrgX2), rat basophilic leukemia, RBL-2H3 cells, and murine BMMCs do