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1 ughout the nucleus but was excluded from the chromocenter.
2 tuin 1 (Sirt1) protein from contact with the chromocenter.
3 ns of all polytene chromosomes into a single chromocenter.
4 r ectopic binding to autosomal sites and the chromocenter.
5 ids and Brdt and Sirt1 overlapped around the chromocenters.
6 centromeric heterochromatin) into peripheral chromocenters.
7 teracting domain [CRID]) to redirect LANA to chromocenters.
8 ated genomic loci in vivo and is enriched in chromocenters.
9 binds heterochromatic satellite repeats and chromocenters.
10 eterochromatin compaction within conspicuous chromocenters.
11 he aberrant spermatid nuclei is a fragmented chromocenter, a structure comprised of peri-centromeric
12 within G1-phase nuclei, we demonstrate that chromocenters acquire the property of late replication c
13 he formation and/or maintenance of an intact chromocenter and implicate this structure in proper remo
14 ene chromosomes revealed localization at the chromocenter and to the 49 CD region on the right arm of
15 s of POU5F1 (also known as OCT4) protein and chromocenters, and the conversion of the chromatin lands
17 orescence microscopy revealed densely packed chromocenters associated with H3K9me3-a conserved marker
18 t of late replication, and removing HP1 from chromocenters by competition with Me3K9H3 peptides did n
20 D2 inhibits heterochromatin association into chromocenters, coincident with losses in cytosine methyl
21 Furthermore, KRP5 overexpression increases chromocenter decondensation and endoreduplication in the
22 HP1 binding at chromocenters, replication of chromocenter DNA was advanced by 10-15% of the length of
27 ication, HP1 binding, and aggregation at the chromocenter, in successive steps coordinated with devel
28 or locus of lambda 20p1.4 hybridization, the chromocenter, is found juxtaposed to the nuclear envelop
29 acultatively condenses in cycling cells into chromocenters negative both for histone H3 dimethylated
30 e and morphology but a synergistic effect on chromocenter number (reduction) and whole-plant morpholo
31 s also displace HP1 from the heterochromatic chromocenter of polytene chromosomes in larval salivary
32 of euchromatic bands and the heterochromatic chromocenter of polytene chromosomes, and the H2Av antib
33 During spermiogenesis, SUMO-1 localized in chromocenters of certain round spermatids and perinuclea
34 ssion and reduced amount of cenH3 protein at chromocenters of meristematic nuclei, anaphase bridges d
35 like and/or dMBD-likeDelta is present at the chromocenter on larval polytene chromosomes as well as a
36 equired for LANA to colocalize with MeCP2 at chromocenters, regions of extensive pericentric heteroch
37 lication results in DNA damage and extensive chromocenter remodeling into unique structures we have n
38 t to, or "paints," major satellite blocks as chromocenters replicate, where topoisomerase is also enr
39 e for K9H3 trimethylation and HP1 binding at chromocenters, replication of chromocenter DNA was advan
40 e chromosomes, HP2 and HP1 colocalize at the chromocenter, telomeres, and the small fourth chromosome
41 a), suggesting that the presence of multiple chromocenters was correlated with a spread of heterochro
42 s studies in genetic models where fragmented chromocenters were observed in spermatids, the Brdt(BD1/
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