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1  functionally and directly interact with the TATA box binding protein.
2 tion, and exhibited a down-regulation of the TATA box binding protein.
3 g on the bent DNA environment induced by the TATA box-binding protein.
4 at encodes an ATP-dependent inhibitor of the TATA box-binding protein.
5 iation directed by YY1 in the absence of the TATA box-binding protein.
6 ed by a polyglutamine tract expansion in the TATA box-binding protein.
7 ific interaction of double-stranded DNA with TATA box-binding protein.
8 s-1, lymphoid-enhancer binding factor 1, and TATA-box binding protein.
9  genes are the most prominent targets of the TATA-box binding protein.
10 t with) binding of the constitutively active TATA box-binding proteins.
11 into the co-evolution hypothesis of MBF1 and TATA-box-binding proteins.
12      The tethering domain interacts with the TATA box binding protein and directs the repressor compl
13  is a multiprotein complex consisting of the TATA box binding protein and multiple tightly associated
14                          TFIID comprises the TATA box-binding protein and a set of highly conserved a
15  is a multiprotein complex consisting of the TATA box-binding protein and multiple TATA box-binding p
16 DNA through interactions with promoter-bound TATA box-binding protein and transcription factor IIB.
17 r TFIID is a multisubunit complex comprising TATA-box binding protein and associated factors (TAFIIs)
18         This "mini-TFIIA" interacts with the TATA-box binding protein and can overcome repression of
19                     TFIIA interacts with the TATA-box binding protein and can overcome repression of
20 to provide key insights in two examples: the TATA-box binding protein and glutamate dehydrogenase fam
21 archaeal general transcription factors, TBP (TATA-box binding protein) and TFB (archaeal homologue of
22 y with the general transcription factor TBP (TATA-box binding protein), and these two factors bind co
23          Yeast TFIID is composed of TBP, the TATA box binding protein, and 14 distinct TBP-associated
24    Specifically the altered specificity TBP (TATA box binding protein) assay has been used to analyze
25                                    In yeast, TATA box binding protein associated factors (TAF(II)s) a
26                                Serial first [TATA box binding protein-associated factor (TBP)] and th
27 ractors identified the PHD finger of TAF3, a TATA box binding protein-associated factor with importan
28 actor kinase that is most closely related to TATA box binding protein-associated factor, 250 kDa (TAF
29 her protein complexes, including a subset of TATA box binding protein-associated factors (TAFIIs) and
30 HD finger (BRPF) family member BRPF2 and the TATA box binding protein-associated factors TAF1 and TAF
31 ion of TFIID in a simple system, we depleted TATA box-binding protein-associated factor (TAF)1 from D
32 nsus recognition element for the human TFIID TATA box-binding protein-associated factor TAFII31 and c
33 ne of its targets, hTAF(II)31 (a human TFIID TATA box-binding protein-associated factor).
34  its target protein, hTAFII31 (a human TFIID TATA box-binding protein-associated factor).
35                       A complex of two TFIID TATA box-binding protein-associated factors (TA FIIs) is
36 of the TATA box-binding protein and multiple TATA box-binding protein-associated factors (TAF(II)s).
37                                          The TATA box-binding protein-associated factors (TAFs) are t
38 tial functional redundancy between TRAPs and TATA box-binding protein-associated factors in TFIID.
39 ent of activation by TR does not require the TATA box-binding protein-associated factors of TFIID.
40 are either independent or dependent on TAFs (TATA-box Binding Protein-Associated Factors).
41        These findings demonstrate how mutant TATA box-binding protein at the endogenous level affects
42 be overcome by cooperative interactions with TATA-box-binding protein at a U6 promoter but not at a U
43                                       Mutant TATA box-binding protein binds more tightly to the trans
44 hat are physically and genetically linked to TATA box-binding protein can provide an explanation for
45                Neuronal expression of mutant TATA box-binding protein causes age-dependent neurologic
46  complex intermediate consisting of TBP, the TATA box-binding protein component of TFIID and TFIID, v
47    However, UBF recruits the pol I-specific, TATA box-binding protein containing complex SL1 and pol
48 e proximal sequence element, which binds the TATA box-binding protein-containing complex SNAPc.
49                             In solution, the TATA box binding protein from S. cerevisiae (yTBP) is on
50                       The interaction of the TATA-box binding protein from the thermophilic and halop
51  model that expresses one copy of the mutant TATA box-binding protein gene, which encodes a 105-gluta
52 nalysis of the heat-shock gene hsp82 and the TATA-box-binding protein gene tbp in multiple bdelloid s
53 nscription presumably by preventing archaeal TATA-box binding protein, general transcription factor T
54                            Surfaces of human TATA box-binding protein (hsTBP) required for activated
55 ption when working alone (i.e., that bearing TATA box-binding protein) is strongly influenced by prom
56                                         TBP (TATA-box binding protein) is a central transcription fac
57                               Interestingly, TATA box-binding protein occupancy was greater at Pol II
58 f protein-protein interactions with TBP, the TATA box-binding protein of TFIID, and TEF-1, an enhance
59  in Acanthamoeba castellanii is regulated by TATA box binding protein promoter binding factor (TPBF),
60                  The transcription activator TATA box-binding protein promoter-binding factor (TPBF)
61                       Here we show that TBP (TATA box-binding protein)-related factor TRF2, but not T
62  approach and identified the Drosophila TBP (TATA-box-binding protein)-related factor 2 (TRF2) as an
63 biochemistry, and genetics to show that TBP (TATA-box-binding protein)-related factor 2 (TRF2) select
64 t of proteins (e.g alpha-synuclein, insulin, TATA-box binding protein, Sup35, p53), independent of th
65                                          The TATA box binding protein TBP is highly conserved and the
66                                          The TATA box binding protein TBP plays a universally importa
67                      Interaction between the TATA box-binding protein TBP and TFIIB is critical for t
68 homologs for two of the TFIIIB subunits, the TATA box-binding protein TBP and the TFIIB-related facto
69 ranscription factor TFIID is composed of the TATA box binding protein (TBP) and a set of conserved TB
70 s is TFIID, a 700-kD complex composed of the TATA box binding protein (TBP) and a set of phylogenetic
71 lyamides inhibit the DNA binding activity of TATA box binding protein (TBP) and basal transcription b
72 III (Pol III) transcription factor (TFIIIB); TATA box binding protein (TBP) and Brf1 are the other su
73 tion factor IIIB (TFIIIB) is composed of the TATA box binding protein (TBP) and class III gene-specif
74  The transcription factor TFIID contains the TATA box binding protein (TBP) and multiple TBP-associat
75 ranscription factor TFIID is composed of the TATA box binding protein (TBP) and multiple TBP-associat
76 n of histone H3 at Lys-4, and recruitment of TATA box binding protein (TBP) and RNA polymerase II, bu
77 arge multiprotein complex is composed of the TATA box binding protein (TBP) and several TBP-associate
78 ce that inducibly express one copy of mutant TATA box binding protein (TBP) at different ages by tamo
79 esses trpEGCFBAD transcription by preventing TATA box binding protein (TBP) binding to the TATA box s
80 form of DNA observed in the complex with the TATA box binding protein (TBP) could be completed by mod
81 activating protein complex (SNAP(c)) and the TATA box binding protein (TBP) for basal transcription,
82 rity of primary and secondary structure, the TATA box binding protein (TBP) from Pw binds thermodynam
83 the thermodynamics of the interaction of the TATA box binding protein (TBP) from Pyrococcus woesei (P
84                         Transcription of the TATA box binding protein (TBP) gene in Acanthamoeba cast
85 agments ( approximately 160 bp) bound by the TATA box binding protein (TBP) have demonstrated the for
86                                          The TATA box binding protein (TBP) is a central component of
87                                          The TATA box binding protein (TBP) is the platform for assem
88  Previous work has shown that binding of the TATA box binding protein (TBP) to the TATA box is a rate
89 lex (PIC) primarily through contact with the TATA box binding protein (TBP), an interaction mediated
90 ry complex of Negative Cofactor 2 (NC2), the TATA box binding protein (TBP), and DNA has been determi
91 ive target, the general transcription factor TATA box binding protein (TBP), and the biological relev
92             Rb binds and represses Brf-1 and TATA box binding protein (TBP), subunits of RNA pol III-
93 study, 14-3-3 proteins are shown to bind the TATA box binding protein (TBP), transcription factor IIB
94 etail the interactions of initiation factors TATA box binding protein (TBP), transcription factor IIB
95          Here we report the cloning of human TATA box binding protein (TBP)-associated factor 20 (TAF
96                      We demonstrate that the TATA box binding protein (TBP)-containing component of X
97 RT), and binding domains for USF, TFIIB, and TATA box binding protein (TBP).
98 eral negative regulators which interact with TATA box binding protein (TBP).
99 rs, both through direct interaction with the TATA box binding protein (TBP).
100 rations of SNAPc contain variable amounts of TATA box binding protein (TBP).
101 iated via an interaction between p53 and the TATA box binding protein (TBP).
102 eneral transcription machinery proteins, the TATA box binding protein (TBP).
103                The TATA box is recognized by TATA box binding protein (TBP).
104 tion factor D (TFIID) complex is composed of TATA box-binding protein (TBP) and 13 TBP-associated fac
105 oter depends on a TATA box that recruits the TATA box-binding protein (TBP) and a proximal sequence e
106 r TFIID is a multisubunit complex comprising TATA box-binding protein (TBP) and associated factors (T
107 n initiation factor TFIID, consisting of the TATA box-binding protein (TBP) and many TBP-associated f
108  is a multimeric protein complex composed of TATA box-binding protein (TBP) and many TBP-associated f
109 ID is a multiprotein complex composed of the TATA box-binding protein (TBP) and multiple TBP-associat
110 se I, and chemical cross-linking assays with TATA box-binding protein (TBP) and Rep68 indicate that b
111                                          The TATA box-binding protein (TBP) and TBP-associated factor
112 which are bound by the transcription factors TATA box-binding protein (TBP) and TFB.
113                                          How TATA box-binding protein (TBP) and the TBP-associated fa
114           Taken together with its binding to TATA box-binding protein (TBP) and transcription factor
115 pha DNA-binding domain binds directly to the TATA box-binding protein (TBP) and, through this interac
116                       In addition, c-Rel and TATA box-binding protein (TBP) appeared to occupy the pr
117 found to be dependent not upon the canonical TATA box-binding protein (TBP) but instead upon the TBP-
118 nt regulator of basal transcription, removes TATA box-binding protein (TBP) from TATA sites in vitro.
119 box significantly reduced the recruitment of TATA box-binding protein (TBP) in the adult cells, but n
120 vating function in vivo and interaction with TATA box-binding protein (TBP) in vitro.
121                       Here, we show that the TATA box-binding protein (TBP) interacts with the Cnd2 k
122                                          The TATA box-binding protein (TBP) is an essential component
123                                          The TATA box-binding protein (TBP) is required by all three
124                                          The TATA box-binding protein (TBP) plays an essential role i
125            Cocrystal structures of wild-type TATA box-binding protein (TBP) recognizing 10 naturally
126 e components of selective recognition of the TATA box-binding protein (TBP) to a TATA box sequence th
127                                   Fusing the TATA box-binding protein (TBP) to other DNA-binding doma
128                       The recruitment of the TATA box-binding protein (TBP) to promoters in vivo is o
129                           The recruitment of TATA box-binding protein (TBP) to promoters is one of th
130                                              TATA box-binding protein (TBP) was not detectable in the
131 ssays that binding interactions of the human TATA box-binding protein (TBP) were disrupted on 2-chlor
132 or early growth response factor-1 (EGR1) and TATA box-binding protein (TBP) were identified on the he
133 30) interacts with the DNA binding domain of TATA box-binding protein (TBP) which exists in the same
134                           Interaction of the TATA box-binding protein (TBP) with promoters of RNA pol
135           It consists of three subunits: the TATA box-binding protein (TBP), a TFIIB-related factor,
136 s of the RNA polymerase (I, II, or III), the TATA box-binding protein (TBP), and transcription factor
137  and PACAP reduce the phosphorylation of the TATA box-binding protein (TBP), resulting in a reduction
138 en shown previously that ICP4 interacts with TATA box-binding protein (TBP), TFIIB, and the TBP-assoc
139 n complex (OC) composed of the promoter DNA, TATA box-binding protein (TBP), transcription factor B (
140 -initiation complex containing promoter DNA, TATA box-binding protein (TBP), transcription factor TFI
141 nd IIA (TFIIA) to promoter DNA and induces a TATA box-binding protein (TBP)-associated factor-depende
142                                              TATA box-binding protein (TBP)-associated factors (TAFs)
143 endent transcription in vivo and dissociates TATA box-binding protein (TBP)-DNA complexes in vitro.
144 eraction with both the polymerase and with a TATA box-binding protein (TBP)-promoter DNA complex orie
145 iption factor IID components hTAF(II)130 and TATA box-binding protein (TBP).
146 ied to TATA box DNA and its complex with the TATA box-binding protein (TBP).
147 ular cofactors, including p300, pRb, and the TATA box-binding protein (TBP).
148 moter, a process which is independent of the TATA box-binding protein (TBP).
149 rotein and mRNA of TFIIIB subunits, Brf1 and TATA box-binding protein (TBP).
150 assays revealed that the IR2P interacts with TATA box-binding protein (TBP).
151  upon the TATA box DNA binding properties of TATA box-binding protein (TBP).
152 for a requirement for cognate binding of the TATA box-binding protein (TBP).
153 nits contribute to overall functions of this TATA box-binding protein (TBP)/TBP-associated factor (TA
154 t1 (modifier of transcription 1) dissociates TATA box-binding protein (TBP):DNA complexes, offering a
155 ly of a preinitiation complex containing the TATA- box binding protein (TBP), transcription factor B
156                                              TATA-box binding protein (TBP) (but not transcription fa
157 der these experimental conditions identified TATA-Box Binding Protein (TBP) and Importin 8 (IPO8) to
158             Repressors compete with archaeal TATA-box binding protein (TBP) and TFB for the TATA-box
159  to correlate with IEP86 binding to both the TATA-box binding protein (TBP) and the transcription fac
160  of the polyglutamine (polyQ) tract in human TATA-box binding protein (TBP) causes the neurodegenerat
161 lyzes the three-dimensional structure of the TATA-box binding protein (TBP) from the hyperthermophili
162                                              TATA-box binding protein (TBP) is an essential factor th
163                                          The TATA-box binding protein (TBP) is required by eukaryotic
164 pression of the general transcription factor TATA-box binding protein (TBP) leads to increased RNA sy
165              Regions on the surface of human TATA-box binding protein (TBP) required for activated tr
166 ole of SAGA components in the recruitment of TATA-box binding protein (TBP) to SAGA-dependent promote
167 ), which is nucleated through binding of the TATA-box binding protein (TBP) to the promoter.
168 d steps in crystal complexes of DNA with the TATA-box binding protein (TBP).
169 activating protein complex (SNAP(c)) and the TATA-box binding protein (TBP).
170 TA element transcriptional regulator and the TATA-box binding protein (TBP).
171 ranscription factor TFIID is composed of the TATA-box-binding protein (TBP) and a set of TBP-associat
172 ral transcription factor TFIID comprises the TATA-box-binding protein (TBP) and approximately 14 TBP-
173 0 (Rplp0), non-POU domain containing (Nono), TATA-box-binding protein (Tbp) and eukaryotic translatio
174 tiation complex, the interaction between the TATA-box-binding protein (TBP) and its binding site, the
175 iption initiation factor TFIIIB contains the TATA-box-binding protein (TBP) and polymerase III-specif
176 or 1, a multisubunit complex composed of the TATA-box-binding protein (TBP) and three TBP-associated
177              Here we consider the concept of TATA-box-binding protein (TBP) family proteins as "syste
178                                              TATA-box-binding protein (TBP) is a highly conserved RNA
179 hin SPT3, a protein which interacts with the TATA-box-binding protein (TBP), suggesting that RSP5 and
180 l transcription factor complex formed by the TATA-box-binding protein (TBP), the transcription factor
181                                   Drosophila TATA-box-binding protein (TBP)-related factor 2 (TRF2) i
182                                              TATA-box-binding protein (TBP)-related factor 3, TRF3 (a
183 romoters by mimicking and replacing cellular TATA-box-binding protein (TBP).
184 he basal transcription factors TFIIF and the TATA-box-binding protein (TBP).
185 expanded polyglutamine (polyQ) repeat in the TATA-box-binding protein (TBP).
186                              Here we analyse TATA-box-binding-protein (TBP) occupancy of 30 yeast pro
187  190 kDa, as well as variable amounts of the TATA box binding protein, TBP.
188  SNAP(c), and a TATA box, which recruits the TATA box-binding protein, TBP.
189  both the ubiquitous coactivator CBP and the TATA box-binding protein, TBP.
190 sal transcription factor TFIID comprises the TATA-box-binding protein, TBP, and associated factors, t
191 omoters, is made up of three components: the TATA box-binding protein, the TFIIB-related Brf, and the
192  polymerase II (RNAPII), enhanced binding of TATA box-binding protein to RNAPII and selectively promo
193 rotein-protein interactions involving Pax-6, TATA-box-binding protein (TPB), and retinoblastoma prote
194 -initiation complex by M. thermautotrophicus TATA-box-binding protein, transcription factor B, and RN
195          The 27-kDa subunit of TFIIIB or the TATA box binding protein was photoaffinity labeled at bp
196 vage agent to specific residues in the yeast TATA box binding protein (yTBP), we demonstrate that, in

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