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1 of the melanocyte, possibly tyrosinase or a tyrosinase-related protein.
2 ified, forming a family of proteins known as tyrosinase related proteins.
3 ified, forming a family of proteins known as tyrosinase-related proteins.
4 been conserved in vertebrate tyrosinases and tyrosinase-related proteins.
5 ther lentivector delivering a self/tumor Ag, tyrosinase related protein 1 (TRP1), could stimulate eff
6 % of vesicles demonstrated colocalization of tyrosinase related protein 1 and 3-(2, 4-dinitroanilino)
7 (pJ/pJ and pcp/p6H) showed colocalization of tyrosinase related protein 1 and 3-(2,4-dinitroanilino)-
9 ses to a melanocyte differentiation antigen, tyrosinase-related protein 1 (or gp75), which is the pro
10 to controlling tyrosinase (albino locus) and tyrosinase-related protein 1 (TR-P1/gp75/brown locus), b
11 ch CD4+ T cells recognize a novel epitope in tyrosinase-related protein 1 (TRP-1), an antigen express
14 eine change at a highly conserved residue in tyrosinase-related protein 1 (TYRP1) as a major determin
15 erved in the number of NC-Ms [melanin(+) and tyrosinase-related protein 1 (TYRP1)(+) cells], the diff
16 fficking of a known AP-3 cargo, CD63, and of tyrosinase-related protein 1 (Tyrp1), a melanosomal memb
17 similar in color to mice with a mutation in tyrosinase-related protein 1 (Tyrp1), a mouse model for
18 chromosome 2 where a strong candidate gene, tyrosinase-related protein 1 (TYRP1), has also been mapp
19 c for the melanocyte differentiation antigen tyrosinase-related protein 1 (Tyrp1), then constructed b
20 uestions, a mutated self-antigen, designated tyrosinase-related protein 1 (Tyrp1)-WM, derived from Ty
22 dendritic morphology and down-regulation of tyrosinase-related protein 1 (TYRP1/gp75), a melanocyte
24 Both BRG1 and Mitf could be localized to the tyrosinase-related protein 1 and tyrosinase promoters by
25 recognized an epitope expressed in both the tyrosinase-related protein 1 and tyrosinase-related prot
26 ab27b colocalizes with the melanosome marker tyrosinase-related protein 1 and with myosin Va at the c
27 on in A-188 cells caused both tyrosinase and tyrosinase-related protein 1 to be localized to large gr
28 esults in mistranslocation of tyrosinase and tyrosinase-related protein 1 to large granular complexes
29 proteins (including TYR (tyrosinase), TYRP1 (tyrosinase-related protein 1), DCT (tyrosinase-related p
32 perinuclear vesicles carrying tyrosinase and tyrosinase-related protein 1, consistent with a role in
33 was 100% penetrance in the progeny from the tyrosinase-related protein 1-mGluR5 lines generated from
38 I-IV melanoma were assessed for tyrosinase, tyrosinase-related proteins 1 and 2, Pmel 17, and MART-1
42 epitope (ISPNSVFSQWRVVCDSLEDYD) derived from tyrosinase-related protein-1 (TRP-1) using a predictive
43 iated antigens, glycoprotein 100 (gp100) and tyrosinase-related protein-1 (TRP-1), respectively, into
45 st the melanosome membrane glycoprotein gp75/tyrosinase-related protein-1 (TYRP-1) of melanocytes lea
47 ressing Cre-recombinase under control of the tyrosinase-related protein-1 (Tyrp1) promoter, which is
48 lanocytes accumulate the melanosomal protein tyrosinase-related protein-1 (Tyrp1), but not other mela
53 9 targeting melanoma differentiation antigen tyrosinase-related protein-1 (Tyrp1; gp75) and active im
54 The MAAs studied included tyrosinase (Tyr), tyrosinase-related protein-1 and -2 (TRP-1 and TRP-2), g
56 o the M-box promoter elements of tyrosinase, tyrosinase-related protein-1 and dopachrome tautomerase/
57 MTS from the mouse brown locus product gp75/tyrosinase-related protein-1 and full-length OVA as a re
60 the skin of transgenic mice using either the Tyrosinase-Related Protein-1 or the keratin-14 (K14) pro
62 e, melanoma antigen recognized by T cells-1, tyrosinase-related protein-1, and tyrosinase-related pro
63 dautochrome tautomerase, pMel 17/Silver and tyrosinase-related protein-1, but lack expression of the
64 er melanosomal proteins, such as tyrosinase, tyrosinase-related protein-1, dopachrome tautomerase, an
65 Immunity to the brown locus protein, gp75/ tyrosinase-related protein-1, was investigated in a syng
68 lanocyte differentiation antigens, including tyrosinase-related-protein-1 and gp100/pmel17, was marke
71 nses against the murine B16 melanoma using a tyrosinase-related protein 2 (TRP-2) peptide as a model
72 ify a normal tissue differentiation antigen, tyrosinase-related protein 2 (TRP-2), expressed by the m
75 CD8+ T cells specific for the self/tumor Ag tyrosinase-related protein 2 (TRP2) are readily detected
79 in both the tyrosinase-related protein 1 and tyrosinase-related protein 2 Ags in the context of the H
80 melanoma Ags MART-1, gp100, tyrosinase, and tyrosinase-related protein 2 as evaluated by specific cy
82 , TYRP1 (tyrosinase-related protein 1), DCT (tyrosinase-related protein 2), MART1 (melanoma antigens
83 ombined with a tumor-associated peptide from tyrosinase-related protein 2, our combined adjuvant appr
84 -boost vaccination with the melanoma antigen tyrosinase-related protein 2, which also showed a signif
85 toward targets loaded with a K(b)-restricted tyrosinase-related protein 2-derived peptide correlated
87 melanoma differentiation antigens gp100 and tyrosinase-related protein 2/dopachrome tautomerase and
88 ctors encoding the endogenous tumor Ags (TA) tyrosinase-related protein-2 (TRP-2) and glycoprotein 10
89 -associated Ags for the B16 murine melanoma: tyrosinase-related protein-2 (TRP-2) and the endogenous
90 ibody responses to a melanocyte autoantigen, tyrosinase-related protein-2 (TRP-2), as it is highly ex
91 -Dopachrome tautomerase (l-DCT), also called tyrosinase-related protein-2 (TRP-2), is a melanoma anti
92 transgene specific for the melanoma antigen tyrosinase-related protein-2 (TRP-2, Dct) harbor T cells
93 o an immunodominant CTL epitope derived from tyrosinase-related protein-2 administered with CpG-ODN a
95 related protein-1 and dopachrome tautomerase/tyrosinase-related protein-2 and transactivate these gen
97 ients (29%) expressed IgG antibody titers to tyrosinase-related protein-2 compared to four of 28 non-
98 SOX10 acts as a critical transactivator of tyrosinase-related protein-2 during melanoblast developm
100 combined with melanocyte differentiation Ag tyrosinase-related protein-2 peptide-based vaccination,
101 effect is most pronounced in a setting where tyrosinase-related protein-2 peptide-pulsed DCs alone ar
103 enes vaccine expressing the melanoma antigen tyrosinase-related protein-2 to protect mice against int
107 immunity against a murine melanoma self Ag, tyrosinase-related protein-2, using DCs transduced with
108 tomerase gene (Dct) and its protein product, tyrosinase-related protein-2, was studied in the culture
109 disrupting the intracellular trafficking of tyrosinase-related proteins and lysosome-associated memb
110 numbers of random mutations in two syngeneic tyrosinase-related proteins are used to immunize black m
111 oplasmic sequence, which is conserved in the tyrosinase related protein family and through vertebrate
112 tional levels that induces production of the tyrosinase-related proteins that have a significant role
113 Melanocyte differentiation Ags, including tyrosinase-related protein (TRP) 1, are relevant to both
114 st the melanocyte differentiation antigen, a tyrosinase-related protein (TRP) gp75(TRP-1) (the brown
115 Two T cell epitopes derived from tumor Ags, tyrosinase-related protein (TRP)-1 and TRP-2, were shown
116 me tautomerase, that the melanogenic protein tyrosinase-related protein (TRP)-1 can oxidize (HO)2IndC
117 we combined peptide vaccines with mAb to the tyrosinase-related protein (TRP)-1 surface Ag for the tr
118 open-reading frame sequences of tyrosinase, tyrosinase-related protein (TRP)-1, TRP-2, and melanoma-
119 recognize HLA-A2-restricted CTL epitopes in tyrosinase-related protein (TRP)-2 (clone MR7) and NY-ES
121 isoaspartic acid within the melanoma antigen tyrosinase-related protein (TRP)-2 peptide-(181-188) mak
122 ining the MHC class I-presented self-peptide tyrosinase-related protein (TRP)-2(180-188) and CpG-cont
124 ion antigens, gp100, MART-1, tyrosinase, and tyrosinase-related proteins (TRP) 1 and TRP-2, we observ
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