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1 ase (PAcP) is a prostate epithelium-specific differentiation antigen.
2 nduced expression of GpIIb, a megakaryocytic differentiation antigen.
3 cell resistance in part owing to the loss of differentiation antigens.
4  TSC1 or TSC2 gene function express melanoma differentiation antigens.
5 endocrine status, hypoxia, and oncofetal and differentiation antigens.
6 otic expression plasmids encoding melanocyte differentiation antigens.
7 lass I-restricted epitopes of two melanocyte differentiation antigens.
8 CD8+ T cell precursors specific for melanoma differentiation antigens.
9 s, albeit with a loss of tolerance to normal differentiation antigens.
10 tumor antigens are normal, nonmutated tissue differentiation antigens.
11 ns are nonmutated, poorly immunogenic tissue differentiation antigens.
12 and as a ligand for the CD21 and CD11b/CD11c differentiation antigens.
13  and gp75, are well-characterized melanocyte differentiation antigens.
14 clonal antibodies directed against leukocyte differentiation antigens.
15                                    Thymocyte differentiation antigen 1 (Thy1) was identified as a spe
16 , CD45, Lys76, Ly(-6c) and Ly(6c), thymocyte differentiation antigen 1, and discoidin domain receptor
17 ed to expand the marrow immature granulocyte differentiation antigen-1 cell pool and demonstrated few
18 y, recovery of the marrow mature granulocyte differentiation antigen-1 cell population after E. coli
19 n, and expansion the of immature granulocyte differentiation antigen-1 precursor cell population.
20  antigen-1 was induced in sorted granulocyte differentiation antigen-1, stem cell antigen-1' cells by
21  inhibited by an antibody against cluster of differentiation antigen 14 (CD14), an adhesion molecule
22 sulting in the down-regulation of cluster of differentiation antigen 4 (CD4) and major histocompatibi
23 ic acid-inducible gene-I (RIG-I) or melanoma differentiation antigen 5 and suppressed the downstream
24 n the intracellular adapter molecule myeloid differentiation antigen 88 (MyD88), which is required fo
25 ce deficient in the adaptor molecule myeloid differentiation antigen 88 (MyD88), which is required no
26  immunization of mice against the melanocyte differentiation antigen, a tyrosinase-related protein (T
27  directed against overexpressed self-derived differentiation antigens after a nonmyeloablative condit
28 ese antigens are mainly melanoma/ melanocyte differentiation antigens, although mutated intracellular
29          The role of CD4 on immature MK as a differentiation antigen and/or receptor for the human im
30       Many of these antigens are non-mutated differentiation antigens and are expressed by virtually
31  other fusion oncoproteins, myeloid-specific differentiation antigens and minor histocompatibility an
32                                              Differentiation antigens are prototypes of these self an
33                Self-antigens, in the form of differentiation antigens, are commonly recognized by the
34 roach was demonstrated using viral and self-(differentiation) antigens as models.
35 e refractory also to T cells recognizing non-differentiation antigens, as well as to BRAF + MEK inhib
36  responses, depending on the stage of B cell differentiation, antigen binding affinity, and duration
37                      The murine B-lymphocyte differentiation antigen BP-1/6C3 has been identified as
38 ids encoding xenogeneic orthologues of tumor differentiation antigens can break immune ignorance and
39 inations against cancer have mainly targeted differentiation antigens, cancer-testis antigens, and ov
40 al-derived factor (PEDF), and serum monocyte differentiation antigen (CD-14) to predict whether a giv
41 er biomarker panel, including serum monocyte differentiation antigen (CD-14), ETS-related gene protei
42 single cells expressing the mature leukocyte differentiation antigen CD11b can also incorporate the t
43 or for IgG (Fc gamma RI/CD64) and the B-cell differentiation antigens CD19 and CD37.
44 -bound peptides from two leukemia-associated differentiation antigens; CD20 and the previously undesc
45 4.14.5; DPP IV), also known as the leukocyte differentiation antigen CD26 when found as an extracellu
46 cted against the cell surface myelomonocytic differentiation antigen CD33.
47 aries similar to those observed in the human differentiation antigen CD69.
48 immunoblastic lymphomas, with loss of B-cell differentiation antigens, clonal immunoglobulin heavy ch
49                           CD14 is a monocyte differentiation antigen expressed by myeloid-derived cel
50  antigen receptor (CAR) specific for CD19, a differentiation antigen expressed in B cells and B linea
51                            Nonmutated tissue differentiation antigens expressed by tumors are attract
52 er recombinant DNA vaccines targeting tissue differentiation antigens expressed by tumors.
53 nt and synthetic vaccines that target tissue differentiation antigens expressed by tumors.
54                     Analysis of cytokine and differentiation antigen expression in human natural kill
55 CD8(+) T-cell responses against the melanoma differentiation antigens gp100 and tyrosinase-related pr
56 ce immune responses to five mouse melanocyte differentiation antigens, gp100, MART-1, tyrosinase, and
57 vity is essential for recruitment of myeloid differentiation antigen (Gr-1)-positive BMDCs, whereas V
58 oclonal antibodies that target hematopoietic differentiation antigens have been developed to treat he
59  in the expression of the cortical thymocyte differentiation antigen HTA 1 were derived from the T-ce
60 0% stained positively for the ED2 macrophage differentiation antigen, identifying them as perivascula
61 m untreated patients and increases monocytic differentiation antigens in some.
62              NI-1 cells expressed several MC differentiation antigens, including tryptase, Kit, and a
63 Immunohistochemical expression of melanocyte differentiation antigens, including tyrosinase-related-p
64     CD73, originally defined as a lymphocyte differentiation antigen, is thought to function as a cos
65 gnated Mndal (for MNDA-like, myeloid nuclear differentiation antigen-like), was absent in the suscept
66          Vaccine strategies targeting tissue differentiation antigens may be valuable in cancers aris
67  leads to increased expression of melanocyte differentiation antigens (MDA).
68 r/testis antigen, NY-ESO-1, and the melanoma differentiation antigen, Melan-A by human DC subsets.
69 s led to the recognition of a new melanocyte differentiation antigen, Melan-A(MART-1).
70 rent solid tumors known to express the tumor-differentiation antigen mesothelin.
71 e CCS/MSP included those encoding melanocyte differentiation antigens, MITF, SOX10, ERBB3, and FGFR1.
72      Reduced levels of human myeloid nuclear differentiation antigen (MNDA) gene transcripts have bee
73  that the PYHIN protein myeloid cell nuclear differentiation antigen (MNDA) is required for IFNalpha
74 s, including gp100 and TRP1 (melanoma tissue differentiation antigens), NY-ESO-1 (cancer/testis antig
75           A recently described breast tissue differentiation antigen, NY-BR-1, is expressed in >80% b
76                             Cells expressing differentiation antigens of mature NK cells (CD56, CD16,
77 w melanoma-associated antigens that is not a differentiation antigen or a mutated protein.
78 and stromal cells and, subsequently, myeloid differentiation antigen-positive (Gr-1(+)) myeloid cell
79 oid dendritic cells and myeloid cell nuclear differentiation antigen-positive neutrophil precursors.
80  additional presence of myeloid cell nuclear differentiation antigen-positive precursor neutrophils.
81 TCR, CD3, and CD4, but little or no Thy-1, a differentiation antigen present on the great majority of
82                              Mesothelin is a differentiation antigen present on the surface of ovaria
83 erse processes including cell-cycle control, differentiation, antigen presentation, and the stress re
84 le tumor types-transcriptional regulation of differentiation, antigen receptor signaling, tyrosine ki
85 inase family proteins are well characterized differentiation antigens recognized by antibodies and T
86 ogically normal intestine but also expressed differentiation antigens required for normal lymphoid ho
87 based vaccine vector expressing a melanocyte differentiation antigen resulted in T cell-dependent lon
88  only to one other known protein, the T cell differentiation antigen Rt6.
89 n this study, we expressed an anti-thymocyte differentiation antigen-scFv (Thy1-scFv) as a fusion pro
90 mmunotherapy to break tolerance against self-differentiation antigens shared by tumors.
91 ose (patient-derived) melanoma cell lines to differentiation antigen-specific cytotoxic T cells and o
92                        Mesothelin is a tumor differentiation antigen that is highly expressed in many
93 trategy to search the dbEST database to find differentiation antigens that are expressed by cancers a
94                          Examination of cell differentiation antigens that are up-regulated in FR(+)
95 active immunization against a relevant tumor differentiation antigen, the brown locus protein gp75.
96 , in variable proportions, all other NK cell differentiation antigens; the second subset expressed on
97 -primed memory T cells recognized melanocyte differentiation antigens TRP-2/DCT and gp100 and persist
98                          Like other melamona differentiation antigens, TRP-2 was only expressed in me
99 isting of residues 180-188 of the melanocyte differentiation antigen tyrosinase-related protein (TRP)
100 tricted CD4+ TCR specific for the melanocyte differentiation antigen tyrosinase-related protein 1 (Ty
101  monoclonal antibody TA99 targeting melanoma differentiation antigen tyrosinase-related protein-1 (Ty
102 investigate immune responses to a melanocyte differentiation antigen, tyrosinase-related protein 1 (o
103 class II-restricted processing of melanocyte differentiation antigen, tyrosinase-related protein 1 (T
104    In this paper we identify a normal tissue differentiation antigen, tyrosinase-related protein 2 (T
105  Two proteins (caldesmon and myeloid nuclear differentiation antigen) were only weakly expressed in l
106 odel of tolerance maintained to a melanocyte differentiation antigen where tolerance can be broken by
107              Increased expression of PSMA, a differentiation antigen with folate hydrolase activity,
108                           Targeting the CD33 differentiation antigen with gemtuzumab ozogamicin was t

 
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