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1 cts as a positive regulator for YAP-mediated transcriptional machinery.
2 c protein function communicates with nuclear transcriptional machinery.
3 a complex array of repressive and activating transcriptional machinery.
4 accessibility of underlying DNA sequences to transcriptional machinery.
5 ions between transcription factors and basal transcriptional machinery.
6 f the start site could influence activity of transcriptional machinery.
7 s of gonad-selective components of the basal transcriptional machinery.
8 tokine genes that allow accessibility to the transcriptional machinery.
9 n these pathways as the conduit to the basic transcriptional machinery.
10 essibility and leads to recruitment of basal transcriptional machinery.
11 nt that relays neural activity to the muscle transcriptional machinery.
12 g upstream signaling pathways with the basal transcriptional machinery.
13 bility to recruit specific components of the transcriptional machinery.
14 mass complexes associated with viral reverse transcriptional machinery.
15 n is still able to bind to its target in the transcriptional machinery.
16 3 and ERalpha binding and recruitment of the transcriptional machinery.
17 tween the yeast nuclear pore complex and the transcriptional machinery.
18 regions to transcription factors and to the transcriptional machinery.
19 ds to enhancement of elongation by the basal transcriptional machinery.
20 gene and seems to act as a regulator of the transcriptional machinery.
21 6 activation domain to the RNA polymerase II transcriptional machinery.
22 st that AID is recruited to S regions by the transcriptional machinery.
23 ncer-bound factors (activators) and the core transcriptional machinery.
24 the recruitment of coactivators or the basal transcriptional machinery.
25 ppropriate response to the RNA polymerase II transcriptional machinery.
26 ing interactions between Sp1 and the general transcriptional machinery.
27 tive signal that is transmitted to the basal transcriptional machinery.
28 ripts, perhaps through interactions with the transcriptional machinery.
29 w transmission of the hormonal signal to the transcriptional machinery.
30 es to the nucleus to initiate the downstream transcriptional machinery.
31 hat Groucho may also interact with the basal transcriptional machinery.
32 possibly through specific recruitment of the transcriptional machinery.
33 tors, which keep the locus accessible to the transcriptional machinery.
34 nifying effects of activators on the general transcriptional machinery.
35 n strains bearing three modifications of the transcriptional machinery.
36 requirements for different components of the transcriptional machinery.
37 e activity directly to the RNA polymerase II transcriptional machinery.
38 subcomplex of the RNA polymerase II (PolII) transcriptional machinery.
39 cyclin-dependent kinase associated with the transcriptional machinery.
40 eir dependence on specific components of the transcriptional machinery.
41 ivates a previously unobserved target in the transcriptional machinery.
42 ell type-specific component of the mammalian transcriptional machinery.
43 omplex of Smad4 with components of the basic transcriptional machinery.
44 more than one mechanism of interaction with transcriptional machinery.
45 the interaction of these receptors with the transcriptional machinery.
46 iated coactivators and the RNA polymerase II transcriptional machinery.
47 al degeneracy in the highly complex metazoan transcriptional machinery.
48 interacting with coactivators and the basal transcriptional machinery.
49 t constantly required to give signals to the transcriptional machinery.
50 repression even in the presence of exogenous transcriptional machinery.
51 romatin modification and disabling the basal transcriptional machinery.
52 y of repair enzymes, and the fidelity of the transcriptional machinery.
53 g specific protein-protein contacts with the transcriptional machinery.
54 ning and a direct interaction with the basal transcriptional machinery.
55 ment of coactivators that interface with the transcriptional machinery.
56 essential for connecting STAT5 to the basal transcriptional machinery.
57 s an adapter between EBNA-2 and the cellular transcriptional machinery.
58 in the eukaryotic RNA polymerase II (RNAPII) transcriptional machinery.
59 accessibility of the nucleosomal DNA to the transcriptional machinery.
60 volved in interactions with other members of transcriptional machinery.
61 cription factors and components of the basal transcriptional machinery.
62 ific glucagon gene expression with the basal transcriptional machinery.
63 A-binding domain fused to a component of the transcriptional machinery.
64 tial component of the RNA polymerase II core transcriptional machinery.
65 perhaps rendering it less accessible to the transcriptional machinery.
66 ple the Snf1 kinase signaling pathway to the transcriptional machinery.
67 odifications, disrupting the assembly of the transcriptional machinery.
68 domain and several components of the general transcriptional machinery.
69 ced in the direction of transcription by the transcriptional machinery.
70 nes, acting broadly by removing stops on the transcriptional machinery.
71 ogeny in the absence of functional bacterial transcriptional machinery.
72 matin structure and to prevent access to the transcriptional machinery.
73 atalysing modifications of translational and transcriptional machinery.
74 roteins and defines DNA accessibility to the transcriptional machinery.
75 sponses via interactions with the endogenous transcriptional machinery.
76 romoter, where it perhaps interacts with the transcriptional machinery.
77 eactive oxygen species perturb the beta-cell transcriptional machinery.
78 not due to the simple steric blockage of the transcriptional machinery.
79 chromatin to make the promoter accessible to transcriptional machinery.
80 etic changes that facilitate assembly of the transcriptional machinery.
81 lates transcription through interaction with transcriptional machinery.
82 plex, and TAF1, an element of the core TFIID transcriptional machinery.
83 ed chromatin regions prevent the activity of transcriptional machinery.
84 e between upstream regulators and the Pol II transcriptional machinery.
85 stone acetyltransferase p300, and downstream transcriptional machinery.
86 rans-acting factors, chromatin, and the core transcriptional machinery.
87 ting that their interactions are mediated by transcriptional machinery.
88 litating assembly of other components of the transcriptional machinery.
89 , without affecting the recruitment of basal transcriptional machinery.
90 hich directly impacts the recruitment of the transcriptional machinery.
91 ts role as linker coactivator of Sp1 and the transcriptional machinery.
92 ls from transcription factors to the general transcriptional machinery.
93 ng and activating distinct components of the transcriptional machinery.
94 A through interaction with components of the transcriptional machinery.
95 pecies are synthesized by different cellular transcriptional machineries.
96 igenetic modifications, which influences the transcriptional machinery aberrant in many human disease
97 ch is demonstrated to be sufficient to allow transcriptional machinery access to the HO promoter (in
98 e findings identify a surprising link in the transcriptional machinery across a large evolutionary di
99 er, IVMA provided a better definition of the transcriptional machinery activated during chronic and r
100 However, it now appears that the "basal" transcriptional machinery also contributes to specificit
101 s and underscore the conserved nature of the transcriptional machinery among eukaryotic organisms.
102 volved in mRNA processing associate with the transcriptional machinery and are in proximity to DNA.
103 recruiting other required components of the transcriptional machinery and as a histone acetyltransfe
104 ription factors with components of the basal transcriptional machinery and by augmenting the access o
105 a functional link between recruitment of the transcriptional machinery and changes in large-scale chr
106 a detailed analysis of the interplay between transcriptional machinery and chromatin on the RANTES pr
107 show that the human basal RNA polymerase II transcriptional machinery and core promoter are inherent
108 findings support a relationship between the transcriptional machinery and establishment of the repli
109 epigenetic modifications that influences the transcriptional machinery and is aberrant in many human
110 BP) is a central component of the eukaryotic transcriptional machinery and is the target of positive
112 This renders the gene inaccessible to the transcriptional machinery and prevents induction of the
113 ives us insight into the interaction between transcriptional machinery and promoter elements, and may
114 t the promoter that contain both the general transcriptional machinery and promoter-specific factors.
115 AhR TAD makes multiple interactions with the transcriptional machinery and protein conformation plays
116 bunit composition of a core component of the transcriptional machinery and provide a paradigm for how
117 RG1 with Tax additionally recruits the basal transcriptional machinery and removes some of the core h
118 refore, it might fail to stabilize the basal transcriptional machinery and repress transactivation.
119 en increasingly implicated in control of the transcriptional machinery and serves as an intracellular
120 ting as bridging molecules between the basal transcriptional machinery and specific DNA-binding trans
121 esulting in recruitment of components of the transcriptional machinery and subsequent gene transcript
122 nactivates Rob by blocking its access to the transcriptional machinery and that inducers activate Rob
124 the ADs of p53, which binds both the general transcriptional machinery and the repressor protein MDM2
125 usly required for recruitment of the general transcriptional machinery and transcription for at least
126 comprised of RNA Polymerase II (RNA Pol II) transcriptional machinery and we demonstrate Psi is a po
127 etail of how FOXP3 itself interacts with the transcriptional machinery and which components of the FO
128 concert, or perhaps in competition, with the transcriptional machinery and with chromatin modifiers t
129 ancer-bound transcription factors, the basal transcriptional machinery, and a chromosomally integrate
130 gene promoter, affects the assembly of basal transcriptional machinery, and increases the recruitment
131 provides a link between beta-catenin and the transcriptional machinery, and possibly mediates the onc
132 the three-dimensional chromatin space, same transcriptional machinery, and similar Histone3 methylat
133 ctivator binds cooperatively to DNA with the transcriptional machinery, and the constitutively active
134 tructure that influence its accessibility by transcriptional machinery, and we are continuing to deve
135 t the former can touch multiple sites on the transcriptional machinery, and we propose that that diff
138 ion initiation conformational changes in the transcriptional machinery are required to accommodate th
141 Results suggest that proteins of the plastid transcriptional machinery are specifically protected fro
142 potential to interact with the host DNA and transcriptional machinery as part of their mode of actio
144 ce suggest that it sees targets in the yeast transcriptional machinery at least partially distinct fr
145 to target genes and links CLOCK-BMAL1 to the transcriptional machinery at target-gene promoters.
147 on, providing blueprints for the assembly of transcriptional machinery at transcription start sites (
149 es by interacting with some component of the transcriptional machinery binding to the promoter, an in
152 SWI/SNF is necessary for recruitment of RNA transcriptional machinery, but not for binding of transc
153 molecules such as Ca2+, H2O2, and SA affect transcriptional machinery by altering the expression and
154 during nutrient starvation directly targets transcriptional machinery by binding to the principal si
155 een DNA-bound proteins and components of the transcriptional machinery can activate transcription.
157 g to the promoter so that recruitment of the transcriptional machinery can be effected "at a distance
158 polymerases themselves and highlighting how transcriptional machinery can vary across bacterial gene
159 l view of the functional relationships among transcriptional machinery, chromatin structure and gene
160 These changes in gene expression, related to transcriptional machinery, chromatin structure, and the
162 ecific transcription factors and the general transcriptional machinery contribute to the selectivity
163 thalamus, TTF1 remains active as part of the transcriptional machinery controlling female sexual deve
164 that degradation of the most active cellular transcriptional machinery couples cellular growth and pr
165 etal lung mesenchyme by interfering with the transcriptional machinery critical for lung morphogenesi
168 uggests the similarity between mycobacterial transcriptional machinery during growth in SCID and in b
169 n of plastid genes and genes for the plastid transcriptional machinery during leaf senescence Loss-of
171 ons, fewer promoters compete for the limited transcriptional machinery, effectively increasing the co
172 epts, including a recent approach for global transcriptional machinery engineering (gTME), which has
173 e, we demonstrate the combined use of global transcriptional machinery engineering and a high-through
175 se indicated that the subversion of the cell transcriptional machinery for the purpose of HIV-1 repli
176 sh that CK2 acts as a switch, converting the transcriptional machinery from functioning on one type o
177 tion mechanism of the HS2 enhancer-assembled transcriptional machinery from the enhancer through the
179 on activators (comprising a component of the transcriptional machinery fused to a DNA binding domain)
180 a fusion protein bearing a component of the transcriptional machinery fused to a DNA-binding domain,
181 coded as methylated CpG dinucleotides to the transcriptional machinery, give rise to the debilitating
184 ing strains, but global engineering of their transcriptional machinery has produced better outcomes.
186 ween transcriptional repressors and the core transcriptional machinery in bacteria and archaea are su
187 tial link between small RNA pathways and the transcriptional machinery in Caenorhabditis elegans.
188 Our results identify a role for essential transcriptional machinery in driving tumorigenesis and d
190 of the E2E promoter by the RNA polymerase II transcriptional machinery in infected cells limits trans
192 h coactivators and components of the general transcriptional machinery in order to regulate target ge
194 es a protein, pX, which abducts the cellular transcriptional machinery in several ways including dire
197 econdary structure, or interactions with the transcriptional machinery in vivo, which are not impaire
198 nal activators work by recruiting to DNA the transcriptional machinery, including protein complexes r
199 human BRCA1 tumor suppressor interacts with transcriptional machinery, including RNA polymerase II (
200 sii may interact with and activate host cell transcriptional machinery independently of the involveme
201 f such an experiment, the ordinary activator-transcriptional machinery interaction is replaced by a h
203 oming increasingly clear that the eukaryotic transcriptional machinery is adapted to exploit the pres
205 genes responsible for cell specification to transcriptional machinery is dependent on chromatin remo
206 in which the recruitment and assembly of the transcriptional machinery is directed by gene- and cell-
207 A-bound activators and the RNA polymerase II transcriptional machinery is inhibited by the adenovirus
208 C or colder, at which temperature mammalian transcriptional machinery is largely inactive, thereby e
209 ng of the three factors is abrogated and the transcriptional machinery is no longer efficiently recru
211 a critical component of the TGFbeta-induced transcriptional machinery, is shown here to be essential
212 ot only does TAZ couple phospho-Smads to the transcriptional machinery, it is also essential for thei
213 egment into the nuclear matrix and away from transcriptional machinery, leading to repression of basa
214 and Period2 (Per2) genes, components of the transcriptional machinery maintaining a clock rhythm.
215 hromatin modification and recruitment of the transcriptional machinery, many questions remain unanswe
216 ssociated protein, RbpA, suggesting that the transcriptional machinery may also be modified in respon
217 various components of the replicational and transcriptional machinery may be interfered with due to
218 findings suggest that mutations in the core transcriptional machinery may facilitate the evolution o
219 g RNA structure and recruitment of competing transcriptional machinery, may affect gene expression fr
220 horylation and ubiquitination enzymes, basal transcriptional machinery members, and RNA processing fa
222 oded (NEP and PEP) components of the plastid transcriptional machinery, mRNA and protein levels of so
223 nucleosomes; however, regulatory factors and transcriptional machinery must gain access to chromatin
224 signals and coordinate the activation of the transcriptional machinery necessary for differentiation
225 n among components of both chromatin and the transcriptional machinery, nucleosome depletion at promo
226 t apoptotic cells target the proinflammatory transcriptional machinery of macrophages with which they
231 by changes in the recruitment of the general transcriptional machinery or by post-POLR2A recruitment
232 ng to promoter elements and activating basal transcriptional machinery) or an indirect mechanism (via
233 ecific DNA binding activators to the general transcriptional machinery, or that help activators and t
234 nts, can be independently interpreted by the transcriptional machinery, possibly through successive e
235 cate that T(reg) cells use components of the transcriptional machinery, promoting a particular type o
236 interaction between splicing factors and the transcriptional machinery provides an intriguing link be
237 ayed by musicians (transcription factors and transcriptional machinery) reading the score encoded in
238 complexity and functional diversification of transcriptional machineries recognizing distal enhancers
239 ichia coli, bacteriophage T4 usurps the host transcriptional machinery, redirecting it to the express
241 n activator) gene; and reprogramming of host transcriptional machinery regulating a variety of cellul
242 during infection, HHV-8 reprograms the host transcriptional machinery regulating a variety of cellul
243 nk between FGF signaling and crystallin gene transcriptional machinery remains to be established.
244 on factor IIH (TFIIH) is part of the general transcriptional machinery required by RNA polymerase II
245 ilitate the subsequent access of the general transcriptional machinery required for transcriptional i
246 fic genes through interaction with NRSF/REST transcriptional machinery, resulting in the transition f
247 cribe the interaction of BRCA1 with the core transcriptional machinery (RNA polII); (iii) describe ho
248 inks sister chromatids but also inhibits the transcriptional machinery's interaction with and movemen
250 their interaction with key components of the transcriptional machinery, such as CREB-binding protein,
251 While additional components of the RNAPII transcriptional machinery, such as TFIIB and CDK7, are r
253 e are few examples of core components of the transcriptional machinery that are directly controlled b
255 FOXO1 as the molecular node of an intricate transcriptional machinery that confers the signal of duo
256 e expression, is a critical component in the transcriptional machinery that controls sensory neuron s
257 describe a simple modification of the yeast transcriptional machinery that extends the success of si
258 a direct link between ERK signaling and the transcriptional machinery that governs pluripotency.
259 sponse to corticosterone by impacting on the transcriptional machinery that is regulated by classical
260 t NO, directly or indirectly, may modify the transcriptional machinery that is responsible for the in
261 of how miR-155 causes disruption of the BCL6 transcriptional machinery that leads to up-regulation of
262 ur work sheds light on new components of the transcriptional machinery that maintain steady-state lev
263 differentiation of Th2 cells, as part of the transcriptional machinery that regulates IL-4 production
264 ations, or by directly manipulating the host transcriptional machinery that regulates the induction o
266 ovide a foundation for identification of the transcriptional machinery that specifies neurotrophin re
267 ng activity of Taf1, a component of the core transcriptional machinery that was recently reported to
268 or advances in characterizing the eukaryotic transcriptional machinery, the function of promoter-spec
269 the accessibility of promoter regions to the transcriptional machinery, the kinetics of assembly of t
270 ranscription factors interact with the basal transcriptional machinery through the transcriptional co
271 cetyltransferase is a component of the viral transcriptional machinery throughout the replicative cyc
277 omes away from p63 binding sites and recruit transcriptional machinery to control tissue differentiat
278 ng factor that enhances accessibility of the transcriptional machinery to DNA within a repressive chr
280 es a platform of interactions with the basal transcriptional machinery to facilitate transcription in
281 own to regulate gene expression by assisting transcriptional machinery to gain access to their sites
282 ral oncoprotein Tax, which utilizes cellular transcriptional machinery to perform this function.
283 ranscription factors that co-opt the general transcriptional machinery to sustain the oncogenic state
285 tivators) recruiting components of the basal transcriptional machinery to the DNA, eventually leading
286 molecule capable of recruiting the necessary transcriptional machinery to the HBV nucleocapsid promot
287 ory factor-3, CREB binding protein/p300, and transcriptional machinery to the murine ifnb1 promoter d
289 iator elements, which attract and direct the transcriptional machinery to the transcription start sit
291 300, which regulates NF-kappaB and the basal transcriptional machinery, to increase HIV gene expressi
292 atellite cell metabolism with changes in the transcriptional machinery toward myogenic commitment.
296 gnal relay from PRR complexes to the nuclear transcriptional machinery via intracellular kinase casca
297 ss signaling and that Armadillo recruits the transcriptional machinery via multiple contact sites, wh
298 il recently, it was thought that the general transcriptional machinery was largely invariant and reli
299 ils of how influenza viruses hijack the host transcriptional machinery, we aim to uncover novel targe
300 st that L1s have evolved to present the host transcriptional machinery with a minimally disruptive pr
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