コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 A1 represses DNMT3a expression via HDAC1/YY1 transcription factor complex.
2 he subcellular localization of the Rtg1/Rtg3 transcription factor complex.
3 tinct biological activities of the NF-kappaB transcription factor complex.
4 locator (ARNT/HIF-1beta) to form an AhR/ARNT transcription factor complex.
5 ity by inducing a unique conformation in the transcription factor complex.
6 hway signaling which converges upon the AP-1 transcription factor complex.
7 that were reconstituted by rapamycin into a transcription factor complex.
8 able to independently bind its corresponding transcription factor complex.
9 meric, basic helix-loop-helix/leucine zipper transcription factor complex.
10 , in assembly of a myeloid-restricted, basal transcription factor complex.
11 p65 (RelA) forms the prototypical NF-kappaB transcription factor complex.
12 ceptor (AhR)/AhR nuclear translocator (ARNT) transcription factor complex.
13 strongly inhibited binding of the respective transcription factor complex.
14 its stabilization and the formation of HIF-1 transcription factor complex.
15 lipogenic genes through the Mondo/ChREBP-Mlx transcription factor complex.
16 NFATc2 is critical for assembly of this transcription factor complex.
17 erning is dependent on the WER-GL3/EGL3-TTG1 transcription factor complex.
18 forms part of the activator protein 1 (AP-1) transcription factor complex.
19 through activation of the beta-catenin/TCF4 transcription factor complex.
20 ression of HIF1 (hypoxia-inducible factor 1) transcription factor complex.
21 (PRC1), binds directly to the Runx1/CBFbeta transcription factor complex.
22 ative affinities to any DNA sequence for any transcription factor complex.
23 being directly responsive to a core Pol III transcription factor complex.
24 d Rbpj, no neural targets are known for this transcription factor complex.
25 (TCF)-lymphoid enhancer factor (LEF) family transcription factor complex.
26 dependent activation of the GABP(alpha/beta) transcription factor complex.
27 re also recruited, possibly as components of transcription factor complexes.
28 embers of the Jun family to form active AP-1 transcription factor complexes.
29 xpression also alters the composition of E2F transcription factor complexes.
30 dinated assembly and disassembly of distinct transcription factor complexes.
31 toplasmic inhibitor of select NF-kappa B/Rel transcription factor complexes.
32 lterations in the expression of E2F and AP-1 transcription factor complexes.
33 rk of genes under the direct control of SOC1 transcription factor complexes.
34 art by the coordinated action of a series of transcription factor complexes.
35 d, and Hth binding sites mediate cooperative transcription factor complexes.
36 ignal transduction machinery, ribosomes, and transcription factor complexes.
37 ted assembly of Smad-containing multiprotein transcription factor complexes.
38 ter activity and altered binding of specific transcription factor complexes.
39 1 association with c-Jun, a component of the transcription factor complex, activator protein 1 (AP-1)
40 nctions through a stable AML1-ETO-containing transcription factor complex (AETFC) that contains sever
41 BTF122 is a subunit of the Xenopus CCAAT box transcription factor complex and a member of a family of
42 with inhibition of the canonical NF-kappaB1 transcription factor complex and activation of the alter
43 form part of the activating protein-1 (AP-1) transcription factor complex and are implicated in regul
44 cell fates are determined by a MYB-bHLH-WD40 transcription factor complex and are regulated by many i
45 Fos, a key component of the ubiquitous AP-1 transcription factor complex and as such could influence
46 al component of the activator protein (AP)-1 transcription factor complex and can promote contact-ind
47 e due to decreased activation of the E2F1/Dp transcription factor complex and delayed progression thr
48 member of the multimeric activator protein 1 transcription factor complex and plays an important role
49 l cycle progression, including the E2F-1/DP1 transcription factor complex and the retinoblastoma tumo
52 e the DNA binding subunits of MBF cell-cycle transcription factor complexes and contain an N terminal
53 )17 responses through the activation of AP-1 transcription factor complexes and the histone deacetyla
54 ells in culture, to dissociate the p130-E2F4 transcription factor complex, and to stimulate ATP hydro
58 ological action of the eukaryotic NF-kappa B transcription factor complex are tightly regulated throu
59 tions suggests that NLI-dependent LIM domain transcription factor complexes are involved in communica
60 protein, and the heterodimeric RUNX1/CBFbeta transcription factor complex, are critical for definitiv
62 egulation involving chromatin accessibility, transcription factor complex assembly, and protein phosp
64 cells to enhancer occupancy by the BATF-IRF4 transcription factor complex at varying strengths of TCR
65 e demonstrate that this protein is part of a transcription factor complex binding to extended sequenc
70 same signal transduction components (R-Smad transcription factor complexes), but whether and how the
71 n is therefore accompanied by replacement of transcription factor complexes by a repressive chromatin
72 ets of Cln3/CDK, we analyzed the SBF and MBF transcription factor complexes by multidimensional prote
73 physically interacted with Aiolos to form a transcription factor complex capable of inducing the exp
74 athways (the Rb-like protein RBF and the E2F transcription factor complex components dE2F and dDP) co
75 ulated by a conserved anthocyanin-regulating transcription factor complex consisting of a MYB, a bHLH
78 This is the first example of a eukaryotic transcription factor complex containing both a MADS-box
79 nism whereby mutations in BRCA1, via a novel transcription factor complex containing BRCA1, c-Myc, an
80 st that Hmo1 is required for the assembly of transcription factor complexes containing Fhl1 and Ifh1
82 -like antigen 1 (FOSL1), a component of AP-1 transcription factor complexes, contributes to the regul
83 acute leukemia that affect the AML-1/CBFbeta transcription factor complex create dominant inhibitory
87 Area III contains a binding site for PTF1, a transcription factor complex essential for pancreas deve
89 d extends the argument that CO utilizes NF-Y transcription factor complexes for the activation of FLO
90 d intrinsic signals to control heterodimeric transcription factor complex formation provides a robust
91 the 2.1-A crystal structure of the archaeal transcription factor complex formed by the TATA-box-bind
92 appaB elements that are activated by a novel transcription factor complex formed when U-STAT3 binds t
93 ted Gabpa, the DNA-binding component of this transcription factor complex, from mouse embryonic fibro
99 T cells and implicates the integrity of this transcription factor complex in developmental events ess
101 amined the expression of members of the AP-1 transcription factor complex in response to stimulation
103 The Core Binding Factor is a heterodimeric transcription factor complex in vertebrates that is comp
104 r the nucleus and combine with TCF to form a transcription factor complex in which TCF binds DNA and
106 nce for the functional role of highly mobile transcription factor complexes in transcription regulati
107 otein complexes, in particular chromatin and transcription factor complexes, in a rapid and robust ma
108 ) is a prerequisite for the formation of the transcription factor complex interferon-stimulated gene
116 tion factor c-Jun, which is part of the AP-1 transcription factor complex, is also important for mono
118 which led to activation of a heterotrimeric transcription factor complex known as IFN-stimulated gen
120 ic helix-loop-helix-leucine zipper (bHLHZip) transcription factor complex MondoA-Mlx plays a central
121 tains an inverted CCAAT box motif, binds the transcription factor complex NF-Y (also referred to as C
122 of these cytokines is often regulated by the transcription factor complex, nuclear factor-kappa B (NF
123 PTF1 is an atypical basic helix-loop-helix transcription factor complex of pancreatic acinar cells
126 characterize the DNA binding activity of Hox transcription factor complexes on eight experimentally v
127 this stage of myelopoiesis, the formation of transcription factor complexes on the promoter was compl
128 s that CIITA is required for the assembly of transcription factor complexes on the promoters of this
129 TA1 indicating the recruitment of CTCF/GATA1 transcription factor complex onto the HPIP promoter.
130 otein c-Jun, a major constituent of the AP-1 transcription factor complex, or expression of a c-Jun-s
131 These data provide evidence that Fos/Jun transcription factor complexes play a role in modulating
132 cts genetically with: (1) genes for multiple transcription factor complexes predominantly involving M
133 udy of the structural details of an archaeal transcription factor complex presents the opportunity to
134 along with an E protein and Rbpj, forms the transcription factor complex PTF1-J that is essential fo
136 onse gene c-fos, these pathways activate the transcription factor complex serum response factor (SRF)
137 hrough the hypoxia-inducible factor (HIF), a transcription factor complex stabilized under low oxygen
138 oid receptor (GR) can tether to inflammatory transcription factor complexes, such as NFkappaB and AP-
139 ltorphin also increased accumulation of AP-1 transcription factor complexes, suggesting that DOR1 aug
140 compared with other Stat protein-containing transcription factor complexes suggests distinct roles f
141 eractions between proteins that comprise the transcription factor complex TFIIH raises the possibilit
143 heterodimerize, thereby generating an active transcription factor complex that commits mated cells to
145 or GA binding protein (GABP) is a tetrameric transcription factor complex that contains GABPalpha and
146 anding of the complexity and dynamics of the transcription factor complex that forms at the MT-I prom
147 the primary blue-light photoreceptor and the transcription factor complex that initiates light-regula
148 ore binding factor [CBF]) is a heterodimeric transcription factor complex that is frequently involved
149 appaB corresponds to an inducible eukaryotic transcription factor complex that is negatively regulate
150 embly and activation of the RUNX2-TAZ master transcription factor complex that is required for osteob
151 rticipate as components of a multi-component transcription factor complex that is required for regula
152 hese results suggest the presence of a novel transcription factor complex that mediates the glucose-r
153 are targets of the DREAM complex, which is a transcription factor complex that regulates expression o
154 ucleoprotein complex configuration, and that transcription factor complexes that bind the same enhanc
155 ed a series of multisubunit, tissue-general, transcription factor complexes that bound to the GHF3 ac
156 sult of decreased expression of unidentified transcription factor complexes that interact with PRE1 a
157 itions with overexpressed E2F and Cabut, two transcription factor complexes that promote ectopic cell
158 2 is a component of multisubunit DNA-binding transcription factor complexes that regulate gene expres
159 is a component of activator protein-1 (AP-1) transcription factor complexes that regulates processes
160 nserved chromatin-remodeling and homeodomain transcription factor complexes that work with somi-1 to
161 ster, where it targets the Mcm1p-Fkh2p-Ndd1p transcription factor complex, through direct phosphoryla
162 d with MAPK signaling through the c-Jun/AP-1 transcription factor complex to activate CD73 transcript
163 lated the binding of the activator protein-1 transcription factor complex to the cyclic AMP response
164 evealed the binding of such a p204-pRb-Cbfa1 transcription factor complex to the promoter of the oste
166 al systems to be mediated through binding of transcription factor complexes to TRE and EpRE elements.
167 ATA binding protein (TBP) interacts with two transcription factor complexes, upstream activating fact
169 and the transcriptional activity of the AP-1 transcription factor complex were markedly reduced in th
171 binds a multi-protein hematopoietic-specific transcription factor complex which includes GATA-1, SCL/
172 ding factor alpha subunit of a heterodimeric transcription factor complex which plays critical roles
173 before forming the heterodimeric NFATc3-FosB transcription factor complex, which bound the proximal A
174 un is a component of the activator protein-1 transcription factor complex, which is involved in cellu
175 n and interaction with the TEA domain (TEAD) transcription factor complex, which led to upregulated e
176 forms part of the activator protein 1 (AP-1) transcription factor complex, which plays a pivotal role
177 th Jun family proteins to create active AP-1 transcription-factor complexes, which bind to DNA specif
178 in is a target gene of beta-catenin-Tcf, the transcription factor complex whose activity is thought t
179 he nucleus where it functions in a bipartite transcription factor complex, whose targets include inva
180 nd adaptation to iron starvation by the same transcription factor complex with activating and repress
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。