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1 component of the RNA polymerase II (RNAP II) transcription initiation complex.
2 s for Rpc53's CBR in assembly of the pol III transcription initiation complex.
3 s depending on the accurate formation of the transcription initiation complex.
4 ith RBP-JK, which then recruits EBNA2 to the transcription initiation complex.
5 a model of the RbpA-SID in the context of a transcription initiation complex.
6 of the transcription bubble to stabilize the transcription initiation complex.
7 ncover the organization of the Spx-activated transcription initiation complex.
8 rotein-protein interactions in assembly of a transcription initiation complex.
9 RNA pol II) C-terminal domain (CTD) within a transcription initiation complex.
10 D played an important role in assembling the transcription initiation complex.
11 the RNA polymerase surface in this archaeal transcription initiation complex.
12 ts a model for the organization of a minimal transcription initiation complex.
13 t mechanisms to stably recruit TBP to the U6 transcription initiation complex.
14 II) carboxy-terminal domain (CTD) within the transcription initiation complex.
15 ss to RNA polymerase II and its accompanying transcription initiation complex.
16 an inseparable cassette for assembly of the transcription initiation complex.
17 er in nonglial cells by interaction with the transcription initiation complex.
18 s with other viral components of the reverse transcription initiation complex.
19 CTD that is stimulated by the formation of a transcription initiation complex.
20 ns subsequent to the formation of a specific transcription initiation complex.
21 f the 5S RNA gene and supports assembly of a transcription initiation complex.
22 information that facilitates the binding of transcription initiation complexes.
23 d the different interactions of Np(4)As with transcription initiation complexes.
24 g activities and aid in specific assembly of transcription initiation complexes.
25 he RNA polymerase active site to destabilize transcription initiation complexes.
26 matin-bound E2F may be a signpost for active transcription initiation complexes.
27 described models of eukaryotic and bacterial transcription initiation complexes.
28 e key factors for the assembly of eukaryotic transcription initiation complexes.
29 hich lacks an intrinsic ability to form open transcription initiation complexes.
30 te to its ability to promote the assembly of transcription initiation complexes.
31 entially required to enhance the assembly of transcription initiation complexes.
32 ied in yeast and mammalian RNA polymerase II transcription initiation complexes.
33 quencing), we identify approximately 160,000 transcription initiation complexes across the human K562
34 ore recognition element (CRE) that stabilize transcription initiation complexes also occur in transcr
35 ed binds to and inhibits the function of the transcription initiation complex and also recruits prote
36 f proteins required for the formation of the transcription initiation complex and chromatin remodelin
37 capable of efficiently assembling the pol II transcription initiation complex and directly participat
38 his association occurs in the context of the transcription initiation complex and is blocked by the C
39 stitute a minimal set for the formation of a transcription initiation complex and may represent the p
40 upon formation of a catalytically competent transcription initiation complex and remains closed duri
42 Mutant tRNA genes defective in assembly of transcription initiation complexes and a temperature-sen
43 nct core promoter domains, nucleate distinct transcription initiation complexes and initiate at disti
44 rase II (Pol II) involves the formation of a transcription initiation complex, and a transition to an
45 he TFIIA-TBP-DNA complex and in higher order transcription-initiation complexes, and we have mapped t
46 rt crystal structures of human mitochondrial transcription initiation complexes assembled on both lig
47 Our findings provide new insights into the transcription initiation complex assembly on the 5S rRNA
51 lay an important role in the assembly of the transcription initiation complex at the late gene promot
52 ting transcription and efficiently stabilize transcription initiation complexes at both distal and pr
53 portant implications for the architecture of transcription initiation complexes at CRP-dependent prom
54 (TBP) and nucleate the assembly of the snRNA transcription initiation complex, but little is known ab
55 istone H3 and possibly other proteins in the transcription initiation complex by CARM1 occurs along w
56 ions in formation of catalytically competent transcription initiation complex by measuring initiation
57 arguments have allowed modeling of archaeal transcription initiation complexes by comparison with re
58 phosphorylation-independent assembly of the transcription initiation complex can occur at elevated c
59 cumstances, assembly of stable ("committed") transcription initiation complexes can freeze far-from-e
60 D structure of an intact activator-dependent transcription initiation complex comprising the Escheric
61 es at 2.9 and 3.0 A resolution of functional transcription initiation complexes comprising Thermus th
62 jannaschii RNAP system to probe the archaeal transcription initiation complex, consisting of promoter
63 r YY1 lie in close proximity to those of the transcription initiation complex containing TFIID, so th
64 we present the crystal structures of E. coli transcription initiation complexes containing a complete
68 ation is becoming available for fragments of transcription initiation complexes (e.g. RNAP, TBP-TFB-D
70 Transcription factor IID (TFIID) nucleates transcription initiation complex formation by direct cor
71 e show that a common site on TBP is used for transcription initiation complex formation by RNA polyme
77 ol element to facilitate the assembly of the transcription initiation complex including SL1 and Pol I
78 ion of CDK9 at threonine 29 (T29) in the HIV transcription initiation complex, inhibiting CDK9 kinase
79 rmediates, we have found that this steadfast transcription-initiation complex inhibits replication fo
80 imiting step that controls conversion of the transcription initiation complex into a transcription el
82 ee of taxon specificity, suggesting that the transcription initiation complex is highly conserved.
87 the organization of the human mitochondrial transcription initiation complex on the light-strand pro
88 ct AR or p160 coactivator recruitment to the transcription initiation complex on the prostate-specifi
89 transcription by inhibiting assembly of the transcription initiation complex on the US3 promoter.
90 The molecular architecture of RNAP II-like transcription initiation complexes remains opaque due to
93 rase (RNAP) secondary channel, modifying the transcription initiation complex so that promoters with
94 -E2 binds specifically to a component of the transcription initiation complex, TATA binding protein a
96 olution structures of components of the core transcription initiation complex that assembles at RNA p
97 gest that cyclopentenone interferes with the transcription initiation complex that assembles over the
98 est that PBP-1 and PBP-2 are components of a transcription initiation complex that assembles within t
99 gene expression involves the formation of a transcription initiation complex that includes RNA polym
100 otein (TBP) is an essential component of the transcription initiation complex that recognizes and bin
102 ained cryo-electron microscopy structures of transcription initiation complexes that reveal a previou
103 s that target formation of the pre-catalytic transcription initiation complex-the decisive step in ge
104 he nascent transcripts are released from the transcription initiation complex, thereby reducing the l
105 s required for assembly of the TFIID general transcription initiation complex, thereby regulating glo
106 olution crystal structure of a mycobacterial transcription initiation complex (TIC) with RbpA as well
107 e we report the crystal structures of E coli transcription initiation complexes (TICs) containing the
108 terative initiation, which may stabilize the transcription initiation complex to stimulate gene trans
109 (NRs) and help the NRs to recruit an active transcription initiation complex to the promoters of tar
110 erates via the mutually exclusive binding of transcription initiation complexes to closely opposed fo
111 elongation complex, similar to sigma2 in the transcription initiation complex, to stabilize the junct
113 eraction within the human mitochondrial core transcription initiation complex, was 74% lower in septi
114 in single molecules of abortively initiating transcription initiation complexes, we show that initial
115 ised by an activator to form an intermediate transcription initiation complex where full DNA melting
116 25D)/human nuclear vitamin D receptor (hVDR) transcription initiation complex, where the activation h
117 owing efficient incorporation of RNAPII into transcription initiation complexes, which results in inc
118 .76 A-resolution crystal structure of an Msm transcription initiation complex with a promoter DNA fra