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1 y effectors) through alteration of the local nucleosomal structure.
2 stones but does not form a regular repeating nucleosomal structure.
3 e endotoxin response through modification of nucleosomal structure.
4 a more extensive disruption of the canonical nucleosomal structure.
5 in the same number of nucleosomes as well as nucleosomal structure.
6 in by initiating the destabilization of core nucleosomal structure.
7 NF-E2 site was associated with disruption of nucleosomal structure.
8 xt but do not reflect changes in first order nucleosomal structure.
9 on and transcription, and repair or regulate nucleosomal structure.
10  UV radiation are thought to destabilize the nucleosomal structure.
11 iptional regulation have been shown to alter nucleosomal structure.
12 ependent upon the maintenance of appropriate nucleosomal structure.
13 one chaperone that destabilizes and restores nucleosomal structure.
14  1, and UHRF1, but it does require an intact nucleosomal structure.
15 e in solution and when they are wrapped into nucleosomal structures.
16 ons are incorporated into nuclease-resistant nucleosomal structures.
17 type topo IIalpha promoter but disrupted the nucleosomal structure about as much as did the binding o
18 e gene; identify discrete, sequence-specific nucleosomal structures above the level of the canonical
19                         Intricate control of nucleosomal structure and assembly governs access of RNA
20 e regulation of chromatin dynamics, altering nucleosomal structure and DNA accessibility.
21 NF-E2 is critical both for alteration of the nucleosomal structure and for activation of the TXAS pro
22  genes with GC-rich promoters, a more labile nucleosomal structure and roles in chromatin regulation,
23 s located, is associated with alterations of nucleosomal structure at the regions of promoter and rep
24 get coactivators and corepressors and affect nucleosomal structure by inducing histone modifications.
25                          Their assembly into nucleosomal structures confers specialized functions to
26 nd H4 indicates that DNA is constrained into nucleosomal structures containing either mutant or wild-
27                            The compaction of nucleosomal structures creates a barrier for DNA-binding
28 nuclei and macronuclei contain H3 in typical nucleosomal structures, defects in nuclear divisions wer
29 that the HSV-1 genome is found in an ordered nucleosomal structure during latent infection.
30 ive system that has not evolved to deal with nucleosomal structures: Escherichia coli.
31 hese data propose a role for modification of nucleosomal structure in inflammatory cytokine gene tran
32                               Maintenance of nucleosomal structure in the cell nuclei is essential fo
33 hesize that binding of CBF that disrupts the nucleosomal structure in the topo II alpha promoter is a
34 of the structural constraints imposed by the nucleosomal structure, integrase gains access to the sci
35                    The packaging of DNA into nucleosomal structures limits access for templated proce
36 four CBF-binding sites disrupted the regular nucleosomal structure not only in the promoter region co
37 ndent chromatin remodeler that maintains the nucleosomal structure of chromatin, but the determinants
38 cture, and therefore, we have delineated the nucleosomal structure of RNR3 in the repressed and derep
39 a chromatin-mediated process specific to the nucleosomal structure of the integrated constructs.
40  protein binding in native chromatin and the nucleosomal structure of the PBRU and proximal promoter
41                            Surprisingly, the nucleosomal structure of the T7-transcribed hsp82 gene r
42                  Nevertheless, an underlying nucleosomal structure of the Tec elements can be demonst
43 dy asks whether RA induces alteration in the nucleosomal structure of this gene promoter that has no
44                  The assembly of specialized nucleosomal structures on methylated DNA helps to explai
45 a partial unfolding or other perturbation of nucleosomal structure, rather than the loss of nucleosom
46              The analysis of polyamide-bound nucleosomal structures reveals other discrepancies in th
47  containing four binding sites disrupted the nucleosomal structure, similarly as observed in the topo
48 Pol II-driven transcription by destabilizing nucleosomal structure so that one histone H2A-H2B dimer
49 ow that hSWI/SNF and ATP generate an altered nucleosomal structure that is stable in the absence of S
50 oter represents a novel class of specialized nucleosomal structures that links rapid transcriptional
51 y transfected promoter that has a disordered nucleosomal structure, though significantly less well th
52 that contributes to IKKalpha modification of nucleosomal structure through phosphorylation of histone
53    DNA is arranged and indexed through these nucleosomal structures to adjust local chromatin compact
54 rus (MMTV) promoter, which adopts an ordered nucleosomal structure, to investigate the impact of a sp
55 ars to be packaged into a nuclease-resistant nucleosomal structure, whereas the R, U5, and gag leader