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1 BSAP (Pax5) is an essential transcription factor for ear
2 BSAP activated the promoter in transfected cells, and th
3 BSAP failed to trans-activate CD19 promoter constructs i
4 BSAP has been shown previously to be important for B cel
5 BSAP knockdown led to an increase in the expression of m
6 BSAP may play an additional role later in development, s
7 BSAP regulates transcription of several genes expressed
8 As a paradigm for these interactions, Pax-5 (BSAP) assembles ternary complexes with Ets proteins on t
9 observed for the transcription factors Pax-5/BSAP, Bob-1, and Ikaros, but this was not a general prop
11 ivator protein (BSAP) site, the low affinity BSAP site, a SP1/Egr-1 site termed the CD19 GC box, and
15 gulate 3'alpha E(hs1,2), including Oct-1 and BSAP, were identified, and their contribution to 3'alpha
17 and functional interactions between AML1 and BSAP and suggest that AML1 is an important factor for re
18 ivity in transfection studies where AML1 and BSAP synergistically activate blk promoter transcription
19 ranscription factor gene PAX5 (also known as BSAP) are a hallmark of B cell precursor acute lymphobla
21 ts indicates that sequences flanking a and b BSAP-binding sites are essential for appropriate regulat
22 We demonstrate a direct connection between BSAP and B-lymphocyte-induced maturation protein 1 (Blim
24 d repression, a physical interaction between BSAP and octamer-binding proteins was demonstrated using
26 t CD72 promoter activity was up-regulated by BSAP in plasmacytoma cells and T cells in a dose-depende
27 present in J chain-expressing plasma cells, BSAP repression could be overridden by positive-acting f
28 ied in both pro- and pre-B cells, while CRE, BSAP, and PU.1/pip sites within the 3'kappa enhancer und
31 ors necessary for B lineage differentiation (BSAP, E12, E47, and Id) provide further support for desi
35 ed with retrovirus constitutively expressing BSAP/Pax5A began myeloid cell differentiation, but like
37 and have shown that the transcription factor BSAP (B-cell-specific activator protein) directly intera
38 gene PAX-5 encodes the transcription factor BSAP (B-cell-specific activator protein), which plays a
39 hat the B-cell-specific transcription factor BSAP (Pax-5) could bind to a conserved sequence critical
40 y, we reported that the transcription factor BSAP (PAX-5) regulates the murine RAG-2 promoter in B-ce
41 ll immune response, the transcription factor BSAP maintains its activator functions but is relieved o
42 hat the B cell-specific transcription factor BSAP/Pax5 binds to a second site, CBF2, in the E2RE.
43 of the B-cell-specific transcription factor BSAP/Pax5A in regulating B-lymphoid-restricted gene expr
44 identified as the Pax5 transcription factor, BSAP, which recognizes a negative regulatory motif in th
45 ndent mechanism whereby activator motifs for BSAP had a 20-fold higher binding affinity than represso
46 different amounts of expression plasmids for BSAP showed that CD72 promoter activity was up-regulated
47 Previous studies have suggested a role for BSAP-interacting proteins in the regulation of the funct
51 ific transcription factors including Ikaros, BSAP, PU.1, and octamer binding proteins, as well as DNA
56 l zone lymphoma cases showed negative or low BSAP levels, and 17 of 24 (71%) large B-cell lymphomas d
57 ormal lymphoid tissues showed strong nuclear BSAP expression in mantle zone B cells, less intense rea
59 of B, T, and myeloid cells, while absence of BSAP results in an early block in B-cell differentiation
63 lly, we provide evidence that the binding of BSAP prevents USF and B-MEF2 from interacting with the J
65 he N-terminal paired (DNA-binding) domain of BSAP also conferred nuclear localization when coupled to
66 The NLS sequence in the central domain of BSAP binds to the C-terminal 98-amino acid fragment of i
70 's lymphoma (NHL), a detailed examination of BSAP expression in NHL has not been previously reported.
75 ering RNA-mediated repression, the levels of BSAP were decreased in vitro in the NZB-derived malignan
79 its effects on switching, overexpression of BSAP inhibits germline alpha RNA expression and the tran
89 e-regulated expression system to overexpress BSAP in the surface IgM+ I.29 mu B cell line, a mouse ce
93 n (NTx), bone-specific alkaline phosphatase (BSAP), and phylloquinone concentrations were measured at
95 5/B cell lineage specific activator protein (BSAP) is a B lineage-specific regulator that controls th
96 y B cell lineage-specific activator protein (BSAP) site, the low affinity BSAP site, a SP1/Egr-1 site
98 t B-cell lineage specific activator protein (BSAP), also known as paired box 5 (PAX5), controls MCOLN
99 B cell lineage-specific activator protein (BSAP), encoded by the Pax 5 gene, is a critical modulato
100 B-cell lineage-specific activator protein (BSAP), encoded by the Pax-5 gene, is critical for B-cell
101 n factor, B-cell-specific activator protein (BSAP), represses the murine immunoglobulin heavy-chain 3
104 soform of B cell-specific activator protein (BSAP, or Pax5) in MM cells while performing differential
106 3' enhancer and associated binding proteins, BSAP represses PU.1 function by a distinct mechanism.
107 epression of Pax-5 is sufficient to regulate BSAP targets CD19 and J chain and is necessary but not s
108 e transcription of the germline epsilon RNA, BSAP has been hypothesized to be involved in regulation
109 olation on a multimerized PU.1 binding site, BSAP targets a portion of the PU.1 transactivation domai
111 cted to lymphomas of B-cell lineage and that BSAP expression varies in B-cell subsets and subtypes of
119 d the promoter in transfected cells, and the BSAP site was occupied in a tissue-specific manner in vi
124 T- and null-cell lymphomas reacted with the BSAP antisera, whereas in Hodgkin's disease, 2 of 4 (50%
129 ighest levels of hXBP-1 mRNA were found when BSAP was not expressed, in pre-Pro-B cells and in plasma
131 tes the enhancer in pre-B and B cells, while BSAP is a repressor in pre-B cells and an activator at t
133 ition of histone deacetylation combined with BSAP knockdown increased miR-15a/16-1 expression, and al
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