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1 downregulated the growth of the HMC1.2 human mast cell line.
2  reduced the viability of a canine malignant mast cell line.
3 glandin D2 production by LAD2 cells, a human mast cell line.
4 culating progenitors or with the HMC-1 human mast cell line.
5 r in neuronal exocytosis, was expressed in a mast cell line.
6 lated via Kit in a mouse bone marrow-derived mast cell line.
7 no-terminus were expressed in a Syk-negative mast cell line.
8 on in permeabilized RBL-2H3 cells, a mucosal mast cell line.
9 P-1 in rat basophilic leukemia 2H3 (RBL-2H3) mast cell line.
10 s factor alpha (TNF-alpha) by the mouse MC/9 mast cell line.
11 of the RBL-2H3 (rat basophilic leukemia 2H3) mast cell line.
12 urrent (Icrac) was investigated in the RBL-1 mast cell line.
13 FAK cDNA into a variant (3B6) of the RBL-2H3 mast cell line.
14 C, or Syp), are expressed in the RBL-2H3 rat mast cell line.
15 A2 activity, and cytokine production in this mast cell line.
16 sone on these events in a cultured (RBL-2H3) mast cell line.
17 onor progenitor cells, or using immortalized mast cell lines.
18 n and histamine synthesis in mouse and human mast cell lines.
19 m human tissues, and there are several human mast cell lines.
20 macologic inhibition of KIT in KIT-dependent mast cell lines.
21 se independent apoptosis in human and murine mast cell lines.
22 ly enhance production of cytokines in murine mast cell lines.
23       17-AAG promotes cell death of both HMC mast cell lines.
24 ent on cell activation signals in both T and mast cell lines.
25 bitor EXEL-0862 against 2 subclones of human mast cell line-1 (HMC-1)-HMC-1.1, harboring the juxtamem
26  sites across 121 proteins in the MCP5 mouse mast cell line and 179 modification sites on 117 protein
27 effect of artesunate was examined in RBL-2H3 mast cell line and in mature human cultured mast cells.
28 ll lines and have been identified in a human mast cell line and in situ in human gastrointestinal str
29    shRNA-mediated knockdown of MrgX2 in LAD2 mast cell line and primary CD34(+) cell-derived mast cel
30 on kinase family, was present in the RBL-2H3 mast cell line and was rapidly tyrosine-phosphorylated a
31 d dose-dependent proapoptotic effect in both mast cell lines and caused a significant reduction in ma
32 on of Siglec-9 and Siglec-9 ligands on human mast cell lines and human primary mast cells by real-tim
33 ntly induced degranulation of the human LAD2 mast-cell line and cord blood-derived human mast cells (
34                  We found that LAD2, a human mast cell line, and CD34(+) cell-derived primary mast ce
35 IL-10 and vIL-10 were compared in B cell and mast cell lines, and demonstrated that the inability of
36 ytometry using peripheral blood eosinophils, mast cell lines, and Siglec-8-transduced cells in the pr
37             We have isolated a unique murine mast cell line, B6M, that is phenotypically similar to i
38 r survival and growth of the IC2-mKit(D814Y) mast cell line both in vitro and in vivo.
39 C) and peritoneal mast cells, as well as two mast cell lines (C57 and MCP-5), constitutively expresse
40 of intact and permeabilized RBL-2H3 (mucosal mast cell line) cells.
41                   p161 was purified from the mast cell line CFTL-12 by affinity chromatography and su
42        The cloned growth, factor-independent mast cell line Cl.MC/C57.1 was also studied.
43 , we have isolated and characterized primary mast cell lines derived from the upper airways of normal
44  addition, two mutations were found in three mast cell lines derived from two additional dogs.
45                                              Mast cell lines expressing either wild-type (WT) Kit, a
46                   Mouse and canine malignant mast cell lines expressing various Kit mutations, normal
47         Transient transfections of the human mast cell line HMC-1 and the T cell line Jurkat with rep
48 ional MrgX1 and MrgX2 but the immature human mast cell line HMC-1 does not.
49          We previously showed that the human mast cell line HMC-1 expresses A2A and A2B receptors, an
50      Extending this observation to the human mast cell line HMC-1, we show that these mast cells also
51 human basophil cell line KU812 and the human mast cell line HMC-1.
52 h mesenteric windows (ex vivo) and the human mast cell line HMC-1.
53 d in the SCF receptor gain-of-function human mast cell line HMC-1.
54                 Treatment with 17-AAG of the mast cell line HMC-1.2, harboring the Asp816Val and Val5
55           PAI-1 was secreted by both a human mast cell line (HMC)-1 and primary cultured human mast c
56 stine, and in several other tissues and in a mast cell line (HMC-1) that also expresses gamma-tryptas
57             To test this hypothesis, a human mast cell line (HMC-1) that normally expresses receptors
58  levels of IL-6 secreted from human leukemic mast cell line (HMC-1).
59 tions of human mast cells, we analyzed human mast cell lines (HMC-1 and LAD2) depleted of RGS13 by sp
60 marrow-cultured human mast cells and a human mast cell line, HMC-1, as demonstrated by intracytoplasm
61                   However, an immature human mast cell line, HMC-1, that lacks functional MrgX2 did n
62                              We used a human mast cell line, HMC-1, to determine if mast cells can in
63 ng and biological responses, we used a human mast cell-line, HMC-1, that natively expresses both rece
64 esent in eosinophils, basophils, and a human mast cell line (HMC1), whereas MBP2 is only detected in
65 d signaling pathways activated in the murine mast cell line IC2 infected with either wild-type (IC2-m
66 ation of both airway and bone marrow derived mast cell lines in response to inflammatory and hematopo
67                                        Tumor mast cell lines, in contrast, expressed persistently hig
68  surface receptors on MMC-34 cells, a murine mast cell line, induces the synthesis and secretion of p
69               We demonstrated that the human mast cell line Laboratory of Allergic Diseases 2 (LAD2)
70                    Whole-blood basophils and mast cell line Laboratory of Allergic Diseases 2 sensiti
71      Cord blood-derived mast cells and human mast cell line LAD-2 challenged by SUCNR1 ligands were a
72 MRGPRX2-dependent degranulation of the human mast cell line LAD2 (Laboratory of Allergic Diseases-2).
73                        We found that a human mast cell line LAD2 and CD34(+) cell-derived primary mas
74 c IgG and tested its activation of the human mast cell line LAD2.
75 re, HDPs stimulated degranulation in a human mast cell line (LAD2) and in RBL-2H3 cells stably expres
76        To identify such a receptor two human mast cell lines, LAD2 and LUVA, were selected that diffe
77 tudied for their ability to activate a human mast cell line (LUVA) as determined by cysteinyl leukotr
78                                    The human mast cell line (LUVA) was used to model MC(TC)s or MC(T)
79 ession of kinase-inactive MKK7 in the murine mast cell line MC/9 inhibits c-Jun NH(2)-terminal kinase
80                                   The murine mast cell line, MC/9, synthesizes and secretes TNF-alpha
81 tured murine mast cells (BMCMC) and a murine mast cell line (MCP-5) employing flow cytometry and thro
82 one marrow-derived cultured mast cells and a mast cell line, MCP-5.
83 se phosphatase genes was screened in a mouse mast cell line, MMC-1.
84 n microvascular endothelial cell line, human mast cell line, mouse cardiac Sca1-positive stromal cell
85 recognizes c-kit endogenously expressed by a mast cell line or hematopoietic progenitor cells, and sp
86 ctivated by antigen cross-linking in a mouse mast cell line passively sensitized with ovalbumin-speci
87                                      The rat mast cell line RBL-2H3 contains both phospholipase D (PL
88         The secretion process of the mucosal mast cell line RBL-2H3 was imaged using infrared three p
89  the function of InsP4 in Ca2+ influx in the mast cell line RBL-2H3, and we show that InsP4 inhibits
90 lpha subunit was overexpressed in a cultured mast cell line (RBL-2H3) known to contain G alpha z.
91 tigen clustering of Fc epsilon RI on the rat mast-cell line (RBL-2H3) activates a sphingosine kinase
92                         Cells of the mucosal mast cell line, RBL-2H3, are normally stimulated to degr
93 eceptor for IgE (FcepsilonRI) on the mucosal mast cell line, RBL-2H3, results in the rapid and persis
94 y receptors for IgE, Fc epsilon RI, on a rat mast cell line, RBL-2H3, stimulated transcription of the
95  receptors on the widely studied rat mucosal mast cell line, RBL-2H3.
96 uman mast cells as well as the rat and human mast cell lines, RBL-2H3 and HMC-1, produce the heparan
97 n that occur after cannabinoid exposure in a mast cell line, RBL2H3.
98 igh affinity IgE receptor (FcepsilonRI) in a mast cell line resulted in activation of the p42 and the
99         Overexpression of Vav in the RBL-2H3 mast cell line resulted in the constitutive tyrosine pho
100         Expression of human SNAP-23 in a rat mast cell line significantly enhanced exocytosis, and th
101                                 Furthermore, mast cell lines stably expressing MrgX2 responded to LL-
102                                      A mouse mast cell line that endogenously expresses mouse mast ce
103         Studies were conducted in two rodent mast cell lines that were stimulated with Ag via Fcepsil
104                                      Mucosal mast cells lining the stomach and small intestine rapidl
105                               In the RBL-2H3 mast cell line, the interaction of PKC-delta with Lyn re
106 nd jejunum of the BALB/c mouse, the V3 mouse mast cell line was used to investigate the developmental
107 hereas maintenance of high activity in tumor mast cell lines was not dependent on intracellular signa
108  cells (RBL-2H3 m1), an immortalized mucosal mast cell line, was studied at the single-channel level
109                                       In two mast cell lines, we observed mRNA and protein expression
110  cord blood-derived mast cells and the HMC-1 mast cell line were exposed to RSV or UV-inactivated RSV
111                  IgE-stripped basophils or a mast cell line were used in passive sensitization activa
112                                    Pulmonary mast cell lines were capable of proliferating in respons
113               The results from the pulmonary mast cell lines were compared with those from bone marro
114                                  The primary mast cell lines were grown and maintained by incubation
115   Finally, IL-3-independent mastocytomas and mast cell lines were resistant to apoptosis induced by I
116                Using 2 subclones of the HMC1 mast cell line, which both express KIT with an identical
117 ner and decreased cell proliferation in both mast cell lines with higher activity against HMC-1.2 cel

 
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