ライフサイエンスコーパス: dinucleosome

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1 g a specifically localized altered or normal dinucleosome.

2 leosomal histone-DNA interactions within the dinucleosome.

3 36 on histone 3 (H3K36me), and Rpd3S prefers dinucleosomes.

4 ucleosomes favor the formation of long-lived dinucleosomes 4-fold as much as the acetylated ones.

5 interactions of the tail domains in a model dinucleosome and determine the propensity of each of the

6 atomistic molecular dynamics simulations of dinucleosomes and histone tails in explicit solvent and

7 Here, we show that the binding of Rpd3S to dinucleosomes and its catalytic activity are sensitive t

8 es in association of these proteins with the dinucleosome are reflected in the efficiency with which

9 l chromatin fragment (purified reconstituted dinucleosome) as a substrate to analyze cohesin interact

10 nucleosomes assembled on supercoiled DNA and dinucleosomes assembled on linear DNA, but Zta-stimulate

11 also generates abundant structurally altered dinucleosomes, called altosomes, on polynucleosomal temp

12 es a structural mechanism for formation of a dinucleosome complex specific to the linker histone H5,

13 We find that the Bdf1/SWR1 complex forms a dinucleosome complex that is selective for the +1 and +2

14 tone H1, histone B4 or HMG1 into a synthetic dinucleosome containing two 5S rRNA genes.

15 array length shows that systems as short as dinucleosomes demonstrate significant self-association,

16 ein gel electrophoresis shows that telomeric dinucleosomes from soluble chromatin contain H1.

17 as the highest-affinity interaction with the dinucleosome; histone B4 and HMG1 associate with signifi

18 sion of T(3) induced strong positioning of a dinucleosome in the TSH alpha proximal promoter that was

19 when they were reconstituted into monomer or dinucleosomes in vitro.

20 find that binding of a linker histone to the dinucleosome increased the association of the H3 and H4

21 The formation of dinucleosomes is strongly Mg(2+)-dependent, and unacetyl

22 n the chicken ovalbumin gene sequence with a dinucleosome-like period facilitates nucleosome array fo

23 stimulation of H3 methylation by H1 requires dinucleosomes or oligonucleosome substrates.

24 a nucleosome repeat that is one-half of the dinucleosome oscillation period value, as computed by Fo

25 region of DNA possessing a strong, in-phase, dinucleosome period oscillation in the motif period-10 n

26 oscillations in period-10 VWG counts with a dinucleosome period were found in vertebrate DNA regions

27 Employing a model system of dinucleosomes rather than mononucleosomes, we demonstrat

28 rmore, asymmetric incorporation of uH2B into dinucleosomes showed that the enhancement of methylation

29 Hence, a VWG dinucleosome signal is plausible.

30 than from the destabilization of a compacted dinucleosome state.

31 A sensitive assay for competitive binding of dinucleosome substrates revealed that SWR1 preferentiall

32 We demonstrate using a dinucleosome template that acetylation of the core histo

33 We found that histone H1 binds to the dinucleosome template with a dissociation constant (KD)

34 We created dinucleosome templates using the albumin enhancer sequen

35 2 complex exhibits a dramatic preference for dinucleosomes when compared with mononucleosomes and tha

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