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1  the adjunct solitary from the term solitary mastocytoma.
2 ammary adenocarcinoma, glioma, leukemia, and mastocytoma.
3 ntaneous transformation ex vivo; and P815, a mastocytoma.
4 n a malignant fashion, unlike human solitary mastocytomas.
5 y (n = 20), autoimmune (n = 36) and lymphoma/mastocytoma/adenocarcinoma (n = 12).
6 s in both primary mast cells and transformed mastocytomas, although with a smaller IC(50) value in th
7  interfere with the GVT effect, because P815 mastocytoma and most importantly primary Bcr-Abl-transfo
8 ate chymase and tryptase mRNA levels between mastocytoma and non-mast cells.
9  mice transplanted with the immunogenic P815 mastocytoma and showed that it significantly enhanced th
10 ponse against two B7- tumors, the mouse P815 mastocytoma and the E7C3 melanoma, requires host-derived
11                    Finally, IL-3-independent mastocytomas and mast cell lines were resistant to apopt
12  analyses of non-T cells, including B cells, mastocytoma, and fibroblasts, by Northern blot analysis
13 cyte cell lines, including T and B lymphoma, mastocytoma, and macrophage lines.
14 dicted from a cDNA clone we sequenced from a mastocytoma cDNA library.
15                        NECA increases canine mastocytoma cell cAMP, Ca2+, and inositol trisphosphate
16 r experiments using highly purified enzymes, mastocytoma cell chymase activated 92-kD progelatinase i
17 gical inhibition of CD39 in a cultured human mastocytoma cell line (HMC-1) and murine bone marrow-der
18                           Compared to the C2 mastocytoma cell line harboring a Kit exon 11 mutation,
19 F) was expressed on the surface of the mouse mastocytoma cell line P815 to target tumor cell-associat
20                          We found the dog C2 mastocytoma cell line to be the richest source yet descr
21                We established a novel canine mastocytoma cell line, NI-1, from a patient suffering fr
22 ty, we immunized PLRP2-deficient mice with a mastocytoma cell line, P815, and determined the ability
23 d to clone the full-length cDNA from a mouse mastocytoma cell line.
24 d from fibrosarcoma, lymphoma, melanoma, and mastocytoma cell lines.
25 hat a metallogelatinase is secreted from dog mastocytoma cells and directly activated by exocytosed m
26 iments, animals also received host-type P815 mastocytoma cells at the time of BMT.
27         Animals also received host-type P815 mastocytoma cells at the time of BMT.
28            Like BR cells, the C2 line of dog mastocytoma cells constitutively secrete progelatinase B
29                           Although canine BR mastocytoma cells contain A1AR, A2BAR, and A3AR, degranu
30  with different cell types, including murine mastocytoma cells in suspension culture, adherent NIH 3T
31                                          Dog mastocytoma cells incubated with 12-O-tetradecanoylphorb
32                                    In dog BR mastocytoma cells incubated with phorbol ester, high ste
33 nase activity secreted by the BR line of dog mastocytoma cells reveals a phorbol-inducible, approxima
34              These data demonstrate that dog mastocytoma cells secrete a metalloproteinase related to
35                                    Thus, dog mastocytoma cells secrete DPPI that is active at the pH
36 e presence of B7/BBl-transfected P815 murine mastocytoma cells underscoring an SLE-associated defect
37                             Degranulation of mastocytoma cells using ionophore A23187 greatly acceler
38                                         P815 mastocytoma cells were used as cell-associated antigens
39 t form expressed in pineal gland and in P815 mastocytoma cells with a molecular weight of 51 kDa.
40              Coincubation of chymase-rich BR mastocytoma cells with Ala-Ala-Pro-Phe-chloromethylketon
41 coded by an abundant 4.6-kilobase mRNA, like mastocytoma cells, has 70% amino acid sequence identity
42    The current work demonstrates that dog BR mastocytoma cells, HMC-1 cells, and murine bone marrow-d
43 xtracellular roles, we purified MC-DPPI from mastocytoma cells.
44 duced degranulation of the BR line of canine mastocytoma cells.
45 o, but it has no such effect on lymphoma and mastocytoma cells.
46 privileged central nervous system using P511 mastocytoma cells.
47 s the regulation of gelatinase expression in mastocytoma cells.
48  not detectable in nonresponder lymphoma and mastocytoma cells.
49 denosine-mediated degranulation of canine BR mastocytoma cells; and (iii) the BR cell A2BAR couples t
50 ain a cDNA encoding the complete sequence of mastocytoma gelatinase B, a 2.3-kilobase clone encoding
51 o- and carboxyl-terminal halves of the above mastocytoma holoenzyme.
52 ned posttransplant relapse of the DBA/2 P815 mastocytoma in a murine model of MHC-matched, minor hist
53 tumor-specific CTL response against the P815 mastocytoma in the peritoneal cavity of preimmunized mic
54                NI-1 cells were found to form mastocytoma lesions in NOD/SCID IL-2Rgamma(null) mice an
55 ncoding progelatinase was isolated from a BR mastocytoma library.
56 strongly suggest that the above enzymes from mastocytoma, liver, and trachea, per se, are not solely
57 rowth in mice in a highly tumorigenic murine mastocytoma model.
58 DTRs autoimmune (n = 18) and NDSTRs lymphoma/mastocytoma (n = 12) and 68 dogs for IL-2; healthy (n =
59 om rat liver (NDST1) and another from murine mastocytoma (NDST2).
60  CM, and 10 patients presented with solitary mastocytoma of the skin.
61                              In transplanted mastocytoma- or melanoma-bearing hosts, STAT5CA greatly
62        Cellular accumulation was enhanced in mastocytomas over primary mast cells, suggesting a mecha
63 + B lymphoblastoid cell lines and the murine mastocytoma p815 transfected with CD80 or CD86.
64 phoma (A20) cells, but not class II(-) mouse mastocytoma (P815) cells, supported IL-2 secretion of hy
65 15 minutes, in DBA/2 mice bearing either the mastocytoma, P815, which expresses the naturally occurri
66  NH2-terminal 13 amino acids of the purified mastocytoma progelatinase are 50-67% identical to those
67 liver NDANST that are conserved in the mouse mastocytoma protein produced three important findings re
68 d NIH 3T3 and some murine cancer cells (e.g. mastocytoma, sarcoma, and lymphoma), while lacking on ot
69 hows that cultured BR cells derived from dog mastocytomas secrete the 92-kDa proenzyme form of gelati
70 also following in vitro exposure of the P815 mastocytoma (that is negative for both B7-1 and B7-2 sur
71 timal primary tumor-specific CTL to the P815 mastocytoma, the EL4 thymoma, and the Lewis lung carcino
72                                           In mastocytomas, this pathway may facilitate tumor invasion
73 hibitor, dasatinib, on the c-KIT mutant P815 mastocytoma tumor were substantially dependent on T cell
74 y isolated from cells of a heparin-producing mastocytoma tumor.
75 t of mast cell neoplasms, we examined canine mastocytomas, which are among the most common tumors of