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1 e histone modification that is a hallmark of facultative heterochromatin.
2 me3) to assemble transcriptionally repressed facultative heterochromatin.
3 sal of this process results in reassembly of facultative heterochromatin.
4  HP1 is important for normal localization of facultative heterochromatin.
5 ociated with silenced developmental genes at facultative heterochromatin.
6 ethyltransferase complexes to form localized facultative heterochromatin.
7 r in mediating a switch from constitutive to facultative heterochromatin.
8 iptional repression through the spreading of facultative heterochromatin.
9  X chromosomes packaged into euchromatin and facultative heterochromatin.
10 ellular differentiation and the formation of facultative heterochromatin.
11 nt functions in maintaining the stability of facultative heterochromatin.
12 rate histone H2A variant that is enriched on facultative heterochromatin.
13 ve X chromosome (Xi) to mediate formation of facultative heterochromatin.
14 ructures, in the regulation and formation of facultative heterochromatin.
15 modifications that have been associated with facultative heterochromatin.
16 s 20 methylation, a mark of constitutive and facultative heterochromatin.
17 ted at Lys9 is also a distinguishing mark of facultative heterochromatin.
18 de' involved in establishing and maintaining facultative heterochromatin.
19 PcG-targeted gene silencing via formation of facultative heterochromatin.
20 on acts as an additional layer of control in facultative heterochromatin.
21 me positioning is critical for repression of facultative heterochromatin.
22 n linked to the formation and maintenance of facultative heterochromatin, although the underlying mec
23 ding complexes that mediate the formation of facultative heterochromatin and are required for silenci
24 he hornwort transposons were associated with facultative heterochromatin and euchromatin and formed t
25 c shells of pericentromeric heterochromatin, facultative heterochromatin and euchromatin in the inver
26 ntral to the formation of H3K27me3-decorated facultative heterochromatin and gene silencing.
27 erall highly paired and are characterized by facultative heterochromatin and insulated topological do
28 plex 2 (PRC2), deposits the H3K27me3 mark of facultative heterochromatin and is required for stem cel
29            We explore the connection between facultative heterochromatin and replication control and
30                         Cbx7 associates with facultative heterochromatin and, more specifically, is e
31 d X chromosome inactivation in female cells (facultative heterochromatin), and the stable shutdown of
32 obility, redistributes both constitutive and facultative heterochromatin, and induces differential ge
33 with both H3K27me3, an integral component of facultative heterochromatin, and MCM2, an integral compo
34 e underlying the resolution and formation of facultative heterochromatin, and they demonstrate that B
35         Cellular long, noncoding RNAs induce facultative heterochromatin, and this study shows that t
36 proteins, but the chromatin modifications of facultative heterochromatin are less clear.
37                        Stem cells have lower facultative heterochromatin as defined by trimethylation
38 required for Erh1 binding, causes defects in facultative heterochromatin assembly and gene silencing
39 ltransferase G9a directly interact to induce facultative heterochromatin assembly and regulate epigen
40 on (H3K9me2), a modification associated with facultative heterochromatin assembly and the resulting t
41 ese analyses reveal the role of Shelterin in facultative heterochromatin assembly at late origins, wh
42 ontrol gene expression through RNA decay and facultative heterochromatin assembly.
43 lex (EMC), to promote meiotic mRNA decay and facultative heterochromatin assembly.
44 l1-Red1 core and the exosome are involved in facultative heterochromatin assembly; however, the exact
45                                 Formation of facultative heterochromatin at specific genomic loci is
46 matin modification associated with repressed facultative heterochromatin, but the mechanism of this r
47 ing the appearance of specialized domains of facultative heterochromatin called senescence-associated
48 escence is often characterized by domains of facultative heterochromatin, called senescence-associate
49 cent cells accumulate specialized domains of facultative heterochromatin, called Senescence-Associate
50                       Specialized domains of facultative heterochromatin, called senescence-associate
51                    This indicates a role for facultative heterochromatin, coincident with high DMC1 a
52 self-aggregated and cocompartmentalized with facultative heterochromatin, contrasting with their sepa
53  Current models indicate circadian-regulated facultative heterochromatin (CRFH) is a conserved mechan
54 3 lysine 9 trimethylation (H3K9Me3), whereas facultative heterochromatin displays DNA hypomethylation
55                          Reversibly silenced facultative heterochromatin domains are often enriched f
56 matin block and by the presence of prominent facultative heterochromatin domains that are localized a
57 t of typical histone methylation patterns in facultative heterochromatin domains.
58  by preventing transcriptional activation of facultative heterochromatin during differentiation.
59 tions, with H3K27me3, which is indicative of facultative heterochromatin, exhibiting the highest enri
60                                              Facultative heterochromatin (fHC) concerns the developme
61 rd "facultas" literally means "opportunity." Facultative heterochromatin (fHC) then designates genomi
62 ovo cytosine methylation events required for facultative heterochromatin formation and higher-order h
63 nation, to promote premature termination and facultative heterochromatin formation at meiotic genes.
64  gene expression and found that RelB induces facultative heterochromatin formation by directly intera
65 lexe-1 plays a key role in the initiation of facultative heterochromatin formation in somatic cells.
66 ss of chromatin accessibility, suggestive of facultative heterochromatin formation.
67 ers, that serve to demarcate the boundary of facultative heterochromatin formation.
68 le for chromatin modulations associated with facultative heterochromatin formation.
69 stemic inflammatory (SSI), the generation of facultative heterochromatin from euchromatin reversibly
70          Hence, CTCF is required to insulate facultative heterochromatin from impinging euchromatin t
71 tify genes required to maintain silencing at facultative heterochromatin genes in Neurospora crassa a
72 erochromatin and stably active, euchromatin, facultative heterochromatin has the capacity to alternat
73 omise the integrity of both constitutive and facultative heterochromatin in an age-dependent manner b
74 pressive complex 2 is a prominent feature of facultative heterochromatin in both fungi and higher euk
75 egrate single DSB systems in euchromatin and facultative heterochromatin in Drosophila melanogaster a
76 ntified multiple loci which act similarly to facultative heterochromatin in eukaryotes, normally sile
77 n, with a primary role in RNA degradation at facultative heterochromatin in human cells.
78 omosome (Xi), the most extensive instance of facultative heterochromatin in mammals, replicates later
79 n is developmentally up-regulated to promote facultative heterochromatin in mature rod photoreceptors
80 lation is a factor required for silencing of facultative heterochromatin in N. crassa, and perhaps in
81  3, modifications that are characteristic of facultative heterochromatin in plants, increase at FLC c
82 barley whereby intergenic H3K27me3 specifies facultative heterochromatin in the telomere-proximal reg
83 e there are different mechanisms for forming facultative heterochromatin in vertebrates.
84  27 on histone H3 (H3K27me) marks repressed "facultative heterochromatin," including developmentally
85                           The arrangement of facultative heterochromatin into spatially and temporall
86                                              Facultative heterochromatin is a cytological manifestati
87                  Therefore, the formation of facultative heterochromatin is dependent on factors that
88                                Repression of facultative heterochromatin is essential for development
89 ucture and is associated with transcription, facultative heterochromatin is essential to silence deve
90 ression via dicer-independent siRNA-mediated facultative heterochromatin is largely independent of, a
91                 In Neurospora, the rhythm in facultative heterochromatin is mediated by the frequency
92                                              Facultative heterochromatin is of particular interest, b
93  throughout the genome, yet association with facultative heterochromatin is specifically promoted by
94                The most extensive example of facultative heterochromatin is the mammalian inactive X
95 thylated on lysine 27 (H3K27me3), a mark for facultative heterochromatin, is lost on the inactive X c
96                            Here, we describe facultative heterochromatin islands in fission yeast and
97                    Previously, we identified facultative heterochromatin islands in the fission yeast
98 s in the distribution of H3K27me; regions of facultative heterochromatin lost H3K27me3, while regions
99  and a site associated with the formation of facultative heterochromatin, lysine 27 (H3K27).
100  H3K4me2 also partially colocalizes with the facultative heterochromatin mark H3K27me3, and loss of H
101 n the B compartment near the nuclear lamina, facultative heterochromatin marked by H3K27me3 spans bot
102  clusters in F. fujikuroi are located within facultative heterochromatin marked by trimethylated lysi
103  the LAT region showed reduced levels of the facultative heterochromatin marker (H3K27me3) along with
104 es, we demonstrated that a redistribution of facultative heterochromatin marks in regions usually occ
105 tutive heterochromatin, but association with facultative heterochromatin mediated by Polycomb-group (
106 xamined histone modifications and HP1 in the facultative heterochromatin of nucleated erythrocytes an
107      Here we report that, as observed in the facultative heterochromatin of the inactive X chromosome
108 modifications that normally characterize the facultative heterochromatin of the inactive X-chromosome
109  the other one localized to the more plastic facultative heterochromatin, or next to it.
110 data show that ISW is a key component of the facultative heterochromatin pathway in Neurospora, and t
111                To identify components of the facultative heterochromatin pathway, we performed a targ
112  often near centromeres and telomeres, where facultative heterochromatin plays a role in transcriptio
113 scriptional interference and the blocking of facultative heterochromatin propagation by transcription
114        Additionally, self-attraction between facultative heterochromatin regions facilitates the form
115                                              Facultative heterochromatin regulates gene expression, b
116 Whether the specific chromatin properties of facultative heterochromatin require distinct DSB repair
117                     We conclude that DSBs in facultative heterochromatin require dUtx-mediated loss o
118 utive heterochromatin segment and a 16.17-kb facultative heterochromatin segment that form part of th
119 We reported that gene-selective formation of facultative heterochromatin silences transcription of ac
120                                              Facultative heterochromatin silencing at frq functions i
121                                              Facultative heterochromatin tends to switch from the rep
122 ker histone plays a role in establishing the facultative heterochromatin territory and architecture i
123                                              Facultative heterochromatin that changes during cellular
124 g in the formation of extraordinarily stable facultative heterochromatin that is faithfully propagate
125 ex 1 (PRC1) is instrumental for establishing facultative heterochromatin that is repressive to transc
126 ion of a viral noncoding RNA can also induce facultative heterochromatin to promote lytic gene silenc
127 3K27 tri-methylation (H3K27me3) are marks of facultative heterochromatin which maintains transcriptio
128 n genome safeguarded by conserved domains of facultative heterochromatin, which we term regions under
129 small (~10 kb) sub-domain of hypoacetylated, facultative heterochromatin within the acetylated sub-TA

 
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