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1  rapid receptor-to-nucleus communication and transcription control.
2 hly dynamic chromatin interactions linked to transcription control.
3  that OriP enhancer shares aspects of HSV IE transcription control.
4 tion and DOT1L-mediated H3K79 methylation in transcription control.
5 djacent to a CpG-islands implicated in TERRA transcription control.
6 ing, a recently recognized important step of transcription control.
7 s, including Gli2 and Gli3, that function in transcription control.
8 ication of ligand binding is central to LacI transcription control.
9 l integration at the level of cis-regulatory transcription control.
10 nd AT8 within proximity is important for the transcription control.
11 t is most likely, however, to be involved in transcription control.
12 exes, thereby regulating their activities in transcription control.
13 s MLL fusion partners belies a dependency on transcription control.
14 of various domains of the leader RNA in this transcription control.
15 phase-separation model has been proposed for transcription control.
16  regulatory processes in the cell, including transcription control.
17          Mediator is a universal adaptor for transcription control.
18 y molecule by uridylation-induced, antisense transcription-controlled 3'-5' exonucleolytic degradatio
19                          sigma(54)-dependent transcription controls a wide range of stress-related ge
20 RB) is a critical regulator of E2F-dependent transcription, controlling a multitude of protumorigenic
21 of ENL in leukaemia pathogenesis and dynamic transcription control, a chemical genetic strategy was d
22  a richly detailed tapestry of signaling and transcription, controlling an important T cell developme
23  chromatin remodeling is a necessary step in transcription control and its memory, genome integrity,
24                                              Transcription control and RNA binding are the primary fu
25 regulatory modules as units of developmental transcription control, and also of evolution, in the ass
26 chinery governing cell cycle progression and transcription control are often homologous in yeast and
27 ecades has revealed the key pillars of HIV-1 transcription control at the initiation and elongation s
28                                              Transcription control at the melting step is not yet und
29 accessibility model is that cis-elements and transcription control binding of the recombination-activ
30 7 which was an indirect effect of c-myc gene transcription control by Ada3.
31 NA strand might be an essential component of transcription control by ppGpp.
32 nor did Stat1 and c-Jun cooperate in driving transcription controlled by the alpha(2)-macroglobulin e
33 c/Rho signalling pathways that regulate gene transcription controlled by the c-fos promoter, the c-fo
34 ated, which led to the dysregulation of gene transcription controlled by these pathways.
35 on is tuned by the frequency and the rate of transcription, controlled by the RNA polymerase and NTP
36 ral proteins involved in translation, global transcription control, cell-cycle control, stress respon
37 ation of RNA polymerase II (RNAPII)-mediated transcription controls cellular phenotypes such as cance
38    Dopamine receptor genes are under complex transcription control, determining their unique regional
39      However, the key domains by which CASZ1 transcription controls developmental processes and neuro
40 hich are helicases, perform diverse roles in transcription control, DNA repair, and chromosome segreg
41                                     Positive transcription control elements associated with two DNase
42 n close proximity to consensus sequences for transcription control elements within the thrombomodulin
43      Our analysis suggests that many complex transcription-control functions of the type encountered
44 ch strongly resembles the kor (kil override) transcription control genes identified previously on Str
45      Although critical roles of eRNA in gene transcription control have been increasingly realized, t
46 a telomeric reporter gene, a rare example of transcription control in an organism with widespread and
47 limiting the genome-wide adoption of complex transcription control in bacteria.
48  potential synthetic aneuploidy mechanism of transcription control in cancer.
49 plications of our findings for combinatorial transcription control in eukaryotes are discussed.
50 s on the transcript and the implications for transcription control in other regulatory systems are di
51 ly the consequence of E2F-dependent negative transcription control in quiescent cells.
52 racts with the Pax6 gene in Rb cells through transcription control in the 5'-flanking region upstream
53 teins provide a basis for the specificity of transcription control in the Rb/E2F pathway.
54 nce-dependent behavioral plasticity and gene transcription control in vivo.
55                   These results suggest that transcription control is relatively inexact but that the
56 signaling and a potent modulator of hormonal transcription control, is one candidate for regulating t
57 though multiple RBPs have been implicated in transcription control, it has remained unclear how exten
58                           In most organisms, transcription control makes a major contribution to diff
59 nal conservation of a DPE-dependent, general transcription control mechanism between Drosophila and h
60 ated gene network might result from a non-AR transcription control mechanism common to these genes.
61 , it was found that transcriptional and post-transcription control mechanisms determine potencies and
62  regulation involves many different types of transcription control mechanisms, including mechanisms b
63 15 genes have complex genomic structures and transcription control mechanisms.
64 with PDZ-binding motif (TAZ), as the central transcription control module of the Hippo pathway, have
65 ct to mutation constrain the organization of transcription control networks?
66 work has provided evidence for E2F-dependent transcription control of both G1/S- and G2/M-regulated g
67 g protein Hfq has a central role in the post-transcription control of gene expression in many bacteri
68           However, little is known about the transcription control of the human SNCA gene in the brai
69 holipid synthesis regulation by zinc and the transcription control of the PIS1 gene.
70 to uncover evidence for much higher upstream transcription control of transcription factors themselve
71 uire specific cellular functions such as RNA transcription control or even become part of protein cod
72 ions and how they are shaping the eukaryotic transcription control paradigm into one of promiscuous s
73  bioinformatic strategy was used to quantify transcription control pathway activity based on the rela
74 regulation of the pro-inflammatory NF-kappaB transcription control pathway and downregulation of the
75 d activity of the pro-inflammatory NF-kappaB transcription control pathway compared to the active con
76 ith increased activation of pro-inflammatory transcription control pathways (i.e., activator protein-
77  implicate sympathetic nervous system-linked transcription control pathways as candidate mediators of
78  controls) showed: (i) decreased activity of transcription control pathways involved in adrenergic an
79 it is often of interest to identify upstream transcription control pathways mediating observed change
80 le, rapid and sensitive tool for identifying transcription control pathways mediating observed gene e
81                                      Several transcription control pathways were significantly upregu
82 s study shows how the activity of an ancient transcription controlling phosphoswitch became dependent
83                       Rate-limiting steps of transcription control Pol II recruitment, site and degre
84 is the interaction site for many enzymes and transcription control proteins and as a result, developm
85 CTC-binding factor was enriched at the EBNA2 transcription control region in type I but not type III
86  first exon of E1a and a deletion within the transcription control region of E1b.
87                                          The transcription control region of the archetype strain of
88 shed through binding of the repressor to the transcription control region of the biotin biosynthetic
89 was performed using specific primers for the transcription control regions of BKV, JCV, and SV40, res
90 e novel repressor sites is highly present in transcription control regions of FeS genes.
91  potential binding sites are identified from transcription control regions of genes of interest.
92 scribed to identify regulatory motifs in the transcription control regions of genes that exhibit simi
93 ed that identify sequence motifs enriched in transcription control regions of genes that share simila
94 ence features (words) present in presumptive transcription control regions.
95 of all genes that contain the motif in their transcription control regions.
96               Indirect readout mechanisms of transcription control rely on the recognition of DNA sha
97            Also, unique sequences, including transcription control sequences, are often subject to ca
98 lex region that spans a variety of potential transcription control signals.
99 arcinogenic mechanisms such as altering gene transcription, controlling stem cell differentiation to
100 e decompaction and then compaction represses transcription, controls stochastic fate specification.
101 ve been well characterized, other aspects of transcription control, such as pausing/elongation, are p
102 eport here a robust, tunable, and reversible transcription control system for endogenous genes.
103 al benefits and mechanistic differences this transcription control system offers.
104 l, and also of evolution, in the assembly of transcription control systems.
105 n3 and Swi4 levels mediated by ECB-dependent transcription controls the timing of the G(1)-to-S phase
106 .2 and to find chromatin landmarks there for transcription control, unannotated genes and chromatin s
107 nsights into the mechanisms of SRF-dependent transcription control via chaperone-like activity.
108          Included are only examples in which transcription control was modified by the insert.
109 ing, small molecule sensing, and integrative transcription control were amplified selectively.
110 is addressed, the full impact of research on transcription control will be realized throughout the fi

 
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