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1 d in various human tumors, defining SSX as a cancer/testis antigen.
2 TRAG-3 has been reported to be a cancer/testis antigen.
3 demethylation of endogenous retroviruses and cancer testis antigens.
4 topes predominantly from differentiation and cancer-testis antigens.
5 mmon regulatory mechanisms for this group of cancer-testis antigens.
6 and in some cases shared differentiation or cancer-testis antigens.
7 t SPAN-Xb is a novel member of the family of cancer/testis antigens aberrantly expressed by, and capa
8 er 1, is characterized by high expression of cancer testis antigen and proliferation-associated genes
9 ssed in the medulloblastoma include PRAME, a cancer-testis antigen and potential targets for immunoth
10 action between melanoma antigen-11 (MAGE-11) cancer-testis antigen and the major HIF-alpha hydroxylat
11 -PCR analysis demonstrates that SPAN-Xb is a cancer/testis antigen and shows a restricted normal tiss
12 ecific traits included expression of several cancer/testis antigens and the c-kit proto-oncogene thro
13 tissue differentiation antigens), NY-ESO-1 (cancer/testis antigen) and survivin (inhibitor of apopto
16 sine residue at position 124 of the NY-ESO-1 cancer/testis antigen as the acceptor site for the forma
23 Here, we describe the de novo induction of a cancer/testis antigen (CTA) for immunotherapy of tumors
25 es in the tumor lines, 6 were members of the cancer/testis antigen (CTAG) gene group including 5 MAGE
32 -expressed in soma-derived human cancers as "cancer/testis antigens" (CTAs), and piRNA (PIWI-interact
33 al transition; (c) coordinated activation of cancer/testis antigens; (d) coordinated down-regulation
38 ssion of MAGEA2, and related members of this cancer-testis antigen family, is upregulated in tamoxife
42 AG-1, TAG-2a, TAG-2b, and TAG-2c) of a novel cancer/testis antigen gene have been identified and are
43 rough this analysis, we show that a class of cancer testis antigen genes undergoes CpG island hypomet
44 ubtypes and two of the AD subtypes expressed cancer testis antigen genes, whereas three AD subtypes e
46 nduce helper T cells against melanocytic and cancer-testis antigens, has been shown to induce specifi
47 ed immunohistochemical analysis for TILs and cancer testis antigens in 117 cases of epithelial ovaria
48 ntigen-specific T-cell responses against six cancer-testis antigens in peripheral blood lymphocytes f
52 state-associated gene 4 (PAGE4), an X-linked cancer/testis antigen, is highly up-regulated in the epi
53 suggested by identifying reactivation of the cancer-testis antigens MAGE and RAGE in ACHN cells after
57 mor shrinkage with antibody responses to the cancer-testis antigen NY-ESO-1, changes in peripheral-bl
59 Salmonella typhimurium engineered to deliver cancer/testis antigen NY-ESO-1 through type III secretio
61 815, which expresses the naturally occurring cancer/testis antigen P1A, or the corresponding tumor P1
63 y expressed antigen in melanoma (PRAME) is a cancer-testis antigen that is expressed in many cancers
64 sts of more than 60 genes, many of which are cancer-testis antigens that are highly expressed in canc
65 breakpoint (SSX) proteins comprise a set of cancer-testis antigens that are upregulated in MHC class
66 ESO-1 thus represents the first example of a cancer/testis antigen that is a also damage-associated m
67 ene 4 (PAGE4) is an intrinsically disordered cancer/testis antigen that is up-regulated in the fetal
68 een subpopulations of TILs and expression of cancer testis antigens was investigated, as well as betw
69 ively strong immunogenicity of a non-mutated cancer/testis antigen, we found that NY-ESO-1 forms poly
71 l 94 amino acids of L552S are identical to a cancer testis antigen, XAGE-1, found in Ewing's sarcoma.
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