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1 g a specifically localized altered or normal dinucleosome.
2 leosomal histone-DNA interactions within the dinucleosome.
3 2 molecule bridging two nucleosomes within a dinucleosome.
4 nd spacing activities of ISW1a when bound to dinucleosomes.
5 36 on histone 3 (H3K36me), and Rpd3S prefers dinucleosomes.
6 pacing and a propensity to form close-packed dinucleosomes.
7 owing for the assembly of mononucleosomes or dinucleosomes.
8 ucleosomes favor the formation of long-lived dinucleosomes 4-fold as much as the acetylated ones.
9  interactions of the tail domains in a model dinucleosome and determine the propensity of each of the
10  atomistic molecular dynamics simulations of dinucleosomes and histone tails in explicit solvent and
11   Here, we show that the binding of Rpd3S to dinucleosomes and its catalytic activity are sensitive t
12 omes, and in some conditions ordered stacked dinucleosomes and mononucleosomes with a disordered gyre
13 es in association of these proteins with the dinucleosome are reflected in the efficiency with which
14                           Here, we show that dinucleosomes are the preferred ZMET2 substrate, with DN
15 l chromatin fragment (purified reconstituted dinucleosome) as a substrate to analyze cohesin interact
16 able of forming dinucleosomes, revealed that dinucleosomes assembled on hybrid sequences show a prefe
17 nucleosomes assembled on supercoiled DNA and dinucleosomes assembled on linear DNA, but Zta-stimulate
18 also generates abundant structurally altered dinucleosomes, called altosomes, on polynucleosomal temp
19 es a structural mechanism for formation of a dinucleosome complex specific to the linker histone H5,
20   We find that the Bdf1/SWR1 complex forms a dinucleosome complex that is selective for the +1 and +2
21 tone H1, histone B4 or HMG1 into a synthetic dinucleosome containing two 5S rRNA genes.
22  array length shows that systems as short as dinucleosomes demonstrate significant self-association,
23 ein gel electrophoresis shows that telomeric dinucleosomes from soluble chromatin contain H1.
24 as the highest-affinity interaction with the dinucleosome; histone B4 and HMG1 associate with signifi
25 sion of T(3) induced strong positioning of a dinucleosome in the TSH alpha proximal promoter that was
26 when they were reconstituted into monomer or dinucleosomes in vitro.
27 find that binding of a linker histone to the dinucleosome increased the association of the H3 and H4
28 hromatin, with high levels of closely packed dinucleosomes involving the second (+2) nucleosome.
29                             The formation of dinucleosomes is strongly Mg(2+)-dependent, and unacetyl
30 ocopies loss of Ioc4, resulting in increased dinucleosome levels with only a weak effect on nucleosom
31 n the chicken ovalbumin gene sequence with a dinucleosome-like period facilitates nucleosome array fo
32 t neither enzyme is capable of resolving all dinucleosomes on its own.
33 lecular "gaps" and generating closely spaced dinucleosomes on replicated DNA.
34 stimulation of H3 methylation by H1 requires dinucleosomes or oligonucleosome substrates.
35  a nucleosome repeat that is one-half of the dinucleosome oscillation period value, as computed by Fo
36 region of DNA possessing a strong, in-phase, dinucleosome period oscillation in the motif period-10 n
37  oscillations in period-10 VWG counts with a dinucleosome period were found in vertebrate DNA regions
38                  Employing a model system of dinucleosomes rather than mononucleosomes, we demonstrat
39 W1a's dinucleosome specificity, we find that dinucleosome recognition is required by ISW1a for proper
40 2,000 nuclear proteins with over 80 modified dinucleosomes representing promoter, enhancer and hetero
41 SW1b and Chd1 make additive contributions to dinucleosome resolution, such that neither enzyme is cap
42 ed for normal nucleosome spacing but not for dinucleosome resolution.
43  We conclude that the nucleosome spacing and dinucleosome resolving activities of ISW1b and Chd1 are
44 ong with nonspecific DNA, capable of forming dinucleosomes, revealed that dinucleosomes assembled on
45       Here, the cryo-EM structure of PRC2 on dinucleosomes reveals how binding of its catalytic subun
46 trimethylation contributes to ISW1b-mediated dinucleosome separation.
47 rmore, asymmetric incorporation of uH2B into dinucleosomes showed that the enhancement of methylation
48                                 Hence, a VWG dinucleosome signal is plausible.
49 utational analysis and uncoupling of ISW1a's dinucleosome specificity, we find that dinucleosome reco
50 than from the destabilization of a compacted dinucleosome state.
51                                              Dinucleosome studies resulted in the discovery of two ef
52 A sensitive assay for competitive binding of dinucleosome substrates revealed that SWR1 preferentiall
53 pulations and asymmetrically ADP-ribosylated dinucleosome substrates, and that nucleosome serine ADPr
54 than two stacked nucleosomes or side-by-side dinucleosomes, suggesting that groups of more than two n
55                       We demonstrate using a dinucleosome template that acetylation of the core histo
56        We found that histone H1 binds to the dinucleosome template with a dissociation constant (KD)
57                                  Remarkably, dinucleosome templates support transcription when H3K4me
58                                   We created dinucleosome templates using the albumin enhancer sequen
59  condensed telomeric tetranucleosome and its dinucleosome unit.
60 2 complex exhibits a dramatic preference for dinucleosomes when compared with mononucleosomes and tha
61 ucleosome spacing and resolving close-packed dinucleosomes, whereas ISW1a plays only a minor role.