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1 ith RBP-JK, which then recruits EBNA2 to the transcription initiation complex.
2 component of the RNA polymerase II (RNAP II) transcription initiation complex.
3  a model of the RbpA-SID in the context of a transcription initiation complex.
4 of the transcription bubble to stabilize the transcription initiation complex.
5 ncover the organization of the Spx-activated transcription initiation complex.
6 rotein-protein interactions in assembly of a transcription initiation complex.
7 RNA pol II) C-terminal domain (CTD) within a transcription initiation complex.
8 D played an important role in assembling the transcription initiation complex.
9  the RNA polymerase surface in this archaeal transcription initiation complex.
10 ts a model for the organization of a minimal transcription initiation complex.
11 t mechanisms to stably recruit TBP to the U6 transcription initiation complex.
12 s depending on the accurate formation of the transcription initiation complex.
13 II) carboxy-terminal domain (CTD) within the transcription initiation complex.
14 ss to RNA polymerase II and its accompanying transcription initiation complex.
15  an inseparable cassette for assembly of the transcription initiation complex.
16 er in nonglial cells by interaction with the transcription initiation complex.
17 s with other viral components of the reverse transcription initiation complex.
18 CTD that is stimulated by the formation of a transcription initiation complex.
19 ns subsequent to the formation of a specific transcription initiation complex.
20 f the 5S RNA gene and supports assembly of a transcription initiation complex.
21 he RNA polymerase active site to destabilize transcription initiation complexes.
22 matin-bound E2F may be a signpost for active transcription initiation complexes.
23 described models of eukaryotic and bacterial transcription initiation complexes.
24 e key factors for the assembly of eukaryotic transcription initiation complexes.
25 hich lacks an intrinsic ability to form open transcription initiation complexes.
26 te to its ability to promote the assembly of transcription initiation complexes.
27 entially required to enhance the assembly of transcription initiation complexes.
28 ied in yeast and mammalian RNA polymerase II transcription initiation complexes.
29 quencing), we identify approximately 160,000 transcription initiation complexes across the human K562
30 ore recognition element (CRE) that stabilize transcription initiation complexes also occur in transcr
31 ed binds to and inhibits the function of the transcription initiation complex and also recruits prote
32 f proteins required for the formation of the transcription initiation complex and chromatin remodelin
33 capable of efficiently assembling the pol II transcription initiation complex and directly participat
34 his association occurs in the context of the transcription initiation complex and is blocked by the C
35 stitute a minimal set for the formation of a transcription initiation complex and may represent the p
36  upon formation of a catalytically competent transcription initiation complex and remains closed duri
37         These data indicate that the reverse transcription initiation complex and RNA packaging appar
38   Mutant tRNA genes defective in assembly of transcription initiation complexes and a temperature-sen
39 nct core promoter domains, nucleate distinct transcription initiation complexes and initiate at disti
40 he TFIIA-TBP-DNA complex and in higher order transcription-initiation complexes, and we have mapped t
41 rt crystal structures of human mitochondrial transcription initiation complexes assembled on both lig
42 on by accelerating the rate and/or extent of transcription initiation complex assembly.
43 n and is the first and rate-limiting step of transcription initiation complex assembly.
44  stable binding of various components of the transcription initiation complex at promoters.
45 lay an important role in the assembly of the transcription initiation complex at the late gene promot
46 ting transcription and efficiently stabilize transcription initiation complexes at both distal and pr
47 portant implications for the architecture of transcription initiation complexes at CRP-dependent prom
48 (TBP) and nucleate the assembly of the snRNA transcription initiation complex, but little is known ab
49 istone H3 and possibly other proteins in the transcription initiation complex by CARM1 occurs along w
50 ions in formation of catalytically competent transcription initiation complex by measuring initiation
51  arguments have allowed modeling of archaeal transcription initiation complexes by comparison with re
52  phosphorylation-independent assembly of the transcription initiation complex can occur at elevated c
53 cumstances, assembly of stable ("committed") transcription initiation complexes can freeze far-from-e
54 D structure of an intact activator-dependent transcription initiation complex comprising the Escheric
55 es at 2.9 and 3.0 A resolution of functional transcription initiation complexes comprising Thermus th
56 jannaschii RNAP system to probe the archaeal transcription initiation complex, consisting of promoter
57 r YY1 lie in close proximity to those of the transcription initiation complex containing TFIID, so th
58 we present the crystal structures of E. coli transcription initiation complexes containing a complete
59  we determined crystal structures of Thermus transcription initiation complexes containing CarD.
60                  RNAPII that associates with transcription initiation complexes contains an unphospho
61 ation is becoming available for fragments of transcription initiation complexes (e.g. RNAP, TBP-TFB-D
62 IF-IA at Ser-635, precluding the assembly of transcription initiation complexes for rDNA.
63   Transcription factor IID (TFIID) nucleates transcription initiation complex formation by direct cor
64 e show that a common site on TBP is used for transcription initiation complex formation by RNA polyme
65 cription factors are required for productive transcription initiation complex formation.
66  transcriptional repressive element prevents transcription initiation complex formation.
67                                              Transcription initiation complexes formed by bacterial R
68                             To address this, transcription initiation complexes have been formed with
69        Thus, yFACT functions in establishing transcription initiation complexes in addition to the pr
70 ol element to facilitate the assembly of the transcription initiation complex including SL1 and Pol I
71 ion of CDK9 at threonine 29 (T29) in the HIV transcription initiation complex, inhibiting CDK9 kinase
72 rmediates, we have found that this steadfast transcription-initiation complex inhibits replication fo
73 imiting step that controls conversion of the transcription initiation complex into a transcription el
74                                    The TFIID transcription initiation complex is composed of TBP and
75 ee of taxon specificity, suggesting that the transcription initiation complex is highly conserved.
76      These data suggest that the assembly of transcription initiation complexes is dynamic and can be
77        The formation of a minimal functional transcription initiation complex on a TATA-box-containin
78  the organization of the human mitochondrial transcription initiation complex on the light-strand pro
79 ct AR or p160 coactivator recruitment to the transcription initiation complex on the prostate-specifi
80  transcription by inhibiting assembly of the transcription initiation complex on the US3 promoter.
81   The molecular architecture of RNAP II-like transcription initiation complexes remains opaque due to
82 tes that the two factors can act on the same transcription initiation complex simultaneously.
83 rase (RNAP) secondary channel, modifying the transcription initiation complex so that promoters with
84 -E2 binds specifically to a component of the transcription initiation complex, TATA binding protein a
85  (NER) and function in the RNA polymerase II transcription initiation complex TFIIH.
86 olution structures of components of the core transcription initiation complex that assembles at RNA p
87 gest that cyclopentenone interferes with the transcription initiation complex that assembles over the
88 est that PBP-1 and PBP-2 are components of a transcription initiation complex that assembles within t
89  gene expression involves the formation of a transcription initiation complex that includes RNA polym
90 otein (TBP) is an essential component of the transcription initiation complex that recognizes and bin
91          We present the structure of de novo transcription initiation complex that reveals unique con
92 s that target formation of the pre-catalytic transcription initiation complex-the decisive step in ge
93 he nascent transcripts are released from the transcription initiation complex, thereby reducing the l
94 olution crystal structure of a mycobacterial transcription initiation complex (TIC) with RbpA as well
95 e we report the crystal structures of E coli transcription initiation complexes (TICs) containing the
96  (NRs) and help the NRs to recruit an active transcription initiation complex to the promoters of tar
97 erates via the mutually exclusive binding of transcription initiation complexes to closely opposed fo
98 elongation complex, similar to sigma2 in the transcription initiation complex, to stabilize the junct
99                             The formation of transcription initiation complexes upon addition of dexa
100 in single molecules of abortively initiating transcription initiation complexes, we show that initial
101 ised by an activator to form an intermediate transcription initiation complex where full DNA melting
102 25D)/human nuclear vitamin D receptor (hVDR) transcription initiation complex, where the activation h
103 owing efficient incorporation of RNAPII into transcription initiation complexes, which results in inc
104 .76 A-resolution crystal structure of an Msm transcription initiation complex with a promoter DNA fra

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