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1  RNA aptamers that bind to the yeast general transcription factor TFIIB.
2 e resistant to DNase and exclude the general transcription factor TFIIB.
3 rotein physically interacts with the general transcription factor TFIIB.
4 own function that interacts with the general transcription factor TFIIB.
5 that involves its interaction with the basal transcription factor TFIIB.
6 s of the corepressor complex and the general transcription factor TFIIB.
7 in disassembly is the release of the general transcription factor TFIIB, although the mechanism of re
8 metazoans carries a structural homology with transcription factor TFIIB and can bind DNA on its own.
9 s well as reduced recruitment of the general transcription factor TFIIB and increased overall histone
10 abnormal interaction of TBP with the general transcription factor TFIIB and induces neurodegeneration
11 ion element (BRE), so named because eukaryal transcription factor TFIIB and its archaeal orthologue T
12 activation domain interacts with the general transcription factor TFIIB and that this interaction is
13 romoter DNA, TATA box-binding protein (TBP), transcription factor TFIIB and the polymerase.
14 0 protein interacted directly with the basal transcription factors TFIIB and TBP and that the EICP0 p
15 l specificity, reminiscent of the effects of transcription factors TFIIB and TFIIA reported previousl
16  complexes containing the additional general transcription factors TFIIB and TFIIA.
17                                              Transcription factors TFIIB and TFIIF are both required
18                                          The transcription factors TFIIB, Brf1, and Brf2 share relate
19 al Pol requires structurally related general transcription factors TFIIB, Brf1, and TFB, respectively
20 ce similarity with the polymerase II general transcription factor TFIIB, but it is the carboxy-termin
21  A structure of an RNA polymerase II-general transcription factor TFIIB complex at 4.5 angstrom resol
22 n the presence of an antibody to the general transcription factor TFIIB, indicating the transcription
23                                  The general transcription factor TFIIB is a highly conserved and ess
24                                  The general transcription factor TFIIB is a key component in the euk
25                         However, the general transcription factor TFIIB is presumed to be universally
26                                  The general transcription factor TFIIB is required for accurate init
27                                          The transcription factor TFIIB plays a central role in prein
28                                  The general transcription factor TFIIB plays a central role in prein
29                                  The general transcription factor TFIIB plays a crucial role in the a
30 HP1alpha droplets, but molecules such as the transcription factor TFIIB show no preference.
31              Notably, a missense mutation in transcription factor TFIIB suppresses gene looping, yet
32 ystem reconstituted with recombinant general transcription factors (TFIIB, TBP, TFIIE, TFIIF), a reco
33 II), the TATA box-binding protein (TBP), and transcription factors TFIIB, TFIIE, and TFIIF (for Pol I
34 , ICP4 was unable to interact with the basal transcription factors, TFIIB, TFIIE, TFIIF, and TFIIH an
35 bstitution [serine-53 --> proline (S53P)] in transcription factor TFIIB that impairs activation of th
36 3 to 249 directly interacts with the general transcription factor TFIIB, the activator protein Sp1, a
37 eover, looping is dependent upon the general transcription factor TFIIB: the E62K (glutamic acid 62 -
38 archaeal homologue of the eukaryotic general transcription factor TFIIB) to initiate basal transcript
39 bes positioned on the surface of the general transcription factor TFIIB were used to probe the archit
40 ators physically interacted with the general transcription factor TFIIB when the genes were activated
41                Here we show that the general transcription factor TFIIB, which is required for the in