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1 ccompanying paper that mes-6 encodes another Polycomb group protein.
2                        mes-2 encodes another Polycomb group protein.
3 also involved in epigenetic silencing by the Polycomb group proteins.
4 rs and epigenetic gene silencing mediated by Polycomb group proteins.
5 even in the presence of normal levels of all Polycomb group proteins.
6 al repressors: the gap gene products and the Polycomb group proteins.
7  silencing is mediated, at least in part, by Polycomb Group proteins.
8        Both silencing activities depend upon Polycomb Group proteins.
9  genes previously epigenetically silenced by Polycomb group proteins.
10 of chromatin-remodeling complexes, including Polycomb group proteins.
11 glycosylases and repressive targeting by the Polycomb group proteins.
12 lation of histone H3 on lysine 27 (H3K27) by Polycomb group proteins.
13  paternal and maternal genomes as well as by Polycomb group proteins.
14 keletal or chromatin tethers as well as with polycomb group proteins.
15 H3 at lysine 27 (H3K27me) as directed by the Polycomb group proteins.
16 core ES transcriptional circuitry, including Polycomb group proteins.
17 tions, expanding the regulatory diversity of polycomb group proteins.
18 ber of transcriptional repressors, including Polycomb-group proteins.
19 homologs of the Drosophila chromatin-binding Polycomb-group proteins.
20  basis of epigenetic maintenance mediated by Polycomb-group proteins.
21 e been identified that mediate the action of Polycomb-group proteins.
22 complex 1 (PRC1) comprise a core assembly of Polycomb group proteins and additional factors that incl
23                                              Polycomb group proteins and associated histone marks are
24  chromatin states mediated by the Drosophila Polycomb group proteins and is physically associated wit
25 t that, contrary to the prevailing view, the Polycomb group proteins and methyltransferase complexes
26 se genes are subjected to repression by both Polycomb group proteins and SetDB1, and loss of either r
27                                          The Polycomb group proteins and the associated H3K27me3 hist
28  generation of ChIP-seq data for SWI/SNF and Polycomb group proteins and the transcriptional represso
29                                    CBX7 is a polycomb group protein, and despite being implicated in
30 ypermethylation, recruitment, and binding of polycomb-group proteins, and histone heterochromatin mod
31                                              Polycomb group proteins are critical to maintaining gene
32                                              Polycomb group proteins are essential for early developm
33                                              Polycomb group proteins are essential regulators of deve
34                                Trithorax and polycomb group proteins are generally thought to antagon
35                                              Polycomb group proteins are important for maintaining ge
36                                          The Polycomb group proteins are involved in maintenance of t
37                                              Polycomb group proteins are required for long-term repre
38                                          The polycomb group proteins are required for the stable main
39                                          The Polycomb group proteins are responsible for long-term re
40 of the SC gene corona and depletion of other Polycomb group proteins are similarly associated with po
41                                              Polycomb group proteins are transcriptional repressors r
42                                              Polycomb group proteins are transcriptional repressors t
43                                          The Polycomb group proteins are transcriptional repressors t
44 acetylglucosamine transferase (OGT), and the polycomb group proteins ASXL1 and ASXL2 in vivo.
45 a link between an Abd-type Hox protein and a Polycomb group protein at the level of direct protein-pr
46 ver faster at sites for trithorax-group than polycomb-group protein binding, suggesting that nucleoso
47                                          The Polycomb group protein Bmi-1 is an essential regulator o
48                                              Polycomb group proteins Bmi-1 and Ring1B are core subuni
49                                          The polycomb group protein BMI1 has been shown to support no
50                                          The polycomb group protein BMI1 is an important regulator of
51                   Herein, we report that the Polycomb group protein BMI1 is enriched at heterochromat
52                                              Polycomb group protein BMI1 plays an important role in c
53 ruiting not only MLL complexes, but also the polycomb group protein Bmi1.
54 MUC1-C regulated nuclear localization of the polycomb group proteins BMI1 and EZH2, which formed comp
55  suggest, more generally, that Trithorax and Polycomb group proteins can cooperate with one another t
56                                          The polycomb group protein CBX2 is an important epigenetic r
57           Our data suggest a novel role of a polycomb group protein Cbx4 controlling CTL differentiat
58 in turn is required for the stability of the Polycomb group protein complex.
59                                   PRC1-class Polycomb group protein complexes are essential for devel
60                                              Polycomb group proteins comprise a family of evolutionar
61                                              Polycomb group proteins control a hierarchy of gene expr
62                                              Polycomb-group proteins control many fundamental biologi
63                        Here we show that the polycomb group protein EED, a core component of PRC2, ph
64 sferase EHMT2 (also known as G9A) or for the Polycomb group protein EED, involved in repressive H3K9m
65                  These findings suggest that Polycomb group proteins Eed and Ezh2 functionally intera
66 -3, WDR5, L2DTL (also known as CDT2) and the Polycomb-group protein EED (also known as ESC).
67             Despite evidence implicating the Polycomb group protein, Eed (embryonic ectoderm developm
68 al germ cells (PGCs), (iii) highly express a polycomb group protein enhancer of zeste drosophila homo
69                                          The Polycomb group protein Enhancer of Zeste has been shown
70  through gene expression profiling, that the polycomb group protein enhancer of zeste homolog 2 (EZH2
71 ast cancer with heightened expression of the Polycomb group protein Enhancer of Zeste Homolog 2 (EZH2
72                                 Although the polycomb group protein Enhancer of Zeste Homolog 2 (EZH2
73                                          The Polycomb group protein enhancer of zeste homolog 2 (EZH2
74                             Among these, the polycomb group protein enhancer of Zeste homologue 2 (EZ
75  encodes a protein similar to the Drosophila Polycomb group protein, Enhancer of zeste, and in the ac
76                                  In animals, Polycomb group proteins ensure the stable inheritance of
77 otein, a mammalian homolog of the Drosophila Polycomb group protein Esc, as a bait in the yeast two-h
78        Molecular analyses establish that the polycomb group protein EZH2 (enhancer of zeste homolog 2
79      Recent work suggests a link between the polycomb group protein EZH2 and mediation of gene silenc
80 en-responsive elements (ARE) and dictated by Polycomb group protein EZH2 and repressive chromatin rem
81 ever, constitutive repression of CCN3 by the Polycomb group protein EZH2 disrupted this negative feed
82 4) in Genes & Development of the role of the polycomb group protein Ezh2 in muscle stem cells, and di
83         We report that the expression of the Polycomb group protein EZH2 increases in histologically
84                                              Polycomb group protein Ezh2 is a histone H3 Lys-27 histo
85                                          The polycomb group protein Ezh2 is a histone methyltransfera
86                                          The Polycomb Group Protein EZH2 is a transcriptional repress
87                                              Polycomb group protein Ezh2 is an essential epigenetic r
88                                              Polycomb group protein Ezh2, one of the key regulators o
89 inase in FLB1 and a differentially localized Polycomb group protein Ezh2, which is mostly nuclear in
90                   AR activation recruits the polycomb group protein EZH2, which subsequently catalyze
91 ogenesis is to suppress transcription of the Polycomb group protein, EZH2, thereby de-repressing gene
92  DNA methyltransferase MET1, and/or the core Polycomb group protein FIE.
93                           It is thought that Polycomb group proteins form heteromeric complexes and c
94                                          The Polycomb group proteins foster gene repression profiles
95 uces dorsal mesoderm by releasing repressive polycomb group proteins from chromatin, bound to the Sta
96                        Recently, the role of Polycomb group proteins has been studied in the specific
97                                              Polycomb group proteins have a critical role in silencin
98                                              Polycomb group proteins have an essential role in the ep
99                               Many mammalian Polycomb-group proteins have also been identified and sh
100 ng of DAB2IP is a key mechanism by which the polycomb-group protein histone-lysine N-methyltransferas
101 ranscriptional regulator, and EMF2 encodes a Polycomb group protein homolog.
102                                              Polycomb group proteins HPC2 and BMI-1 and the corepress
103 ur results suggest a role of Sfmbt and other Polycomb group proteins in downregulating the expression
104  results predict that the MES proteins, like Polycomb group proteins in Drosophila, function as a com
105  silent set of miRNA genes is co-occupied by Polycomb group proteins in ES cells and shows tissue-spe
106            Consistent with the known role of Polycomb group proteins in regulating gene expression, M
107 the importance of histone methylation by the polycomb group proteins in the mouse circadian clock mec
108          To begin to analyze the function of Polycomb-group proteins in Xenopus development, we have
109 sive complex 1-like), is composed of several Polycomb-group proteins including Ring1, Ring2, Bmi1 and
110 ver, we demonstrate that endogenous E2F6 and polycomb group proteins, including RYBP, Ring1, MEL-18,
111          HSI2 and HSL1 recruit components of polycomb-group proteins, including CURLY LEAF (CLF) and
112 ng protein homologous to Drosophila SFMBT, a Polycomb group protein involved in epigenetic regulation
113 ion of transcriptional silencing mediated by Polycomb group proteins is sufficient to induce an irrev
114 t the H2A-K119 ubiquitin E3 ligase Ring1b, a Polycomb group protein, is enriched on Xi in female trop
115  third thoracic segments, which requires the Polycomb group proteins, is disrupted by most chromosoma
116  miR-16 levels down-regulated BMI1 and other polycomb group proteins like RING1A, RING1B, EZH2 and al
117 ession of three other structurally unrelated Polycomb-group proteins: M33, XBmi-1, and mPh2.
118 by histone deacetylases and that mediated by polycomb group proteins may act either independently or
119                                              Polycomb group proteins mediate heritable transcriptiona
120 s provide a framework for an RNAi-dependent, Polycomb group protein-mediated heterochromatin formatio
121 trimethylation (H3K27me3) has been linked to polycomb-group-protein-mediated suppression of Hox genes
122        As predicted from its similarity to a Polycomb group protein, MES-2 localizes to nuclei.
123 is study investigates the effect of Bmi-1, a polycomb group protein, on radiation-induced senescence
124 racterisation indicates that MEDEA encodes a Polycomb-group protein, particularly intriguing as MEDEA
125                            Here, we analyzed Polycomb group protein (PcG) complex integrity in respon
126 ction of methylation-prone genes compared to Polycomb group protein (PcG) marking in embryonic stem c
127 biquitous transcription factor and mammalian Polycomb Group protein (PcG) with important functions fo
128 m chromatin and found candidates that impact polycomb group protein (PcG)-regulated gene expression i
129 ue of Molecular Cell) have demonstrated that Polycomb group proteins (PcG) and the Kcnq1ot1 regulator
130                                              Polycomb group proteins (PcG) are required for proper de
131                                              Polycomb group proteins (PcG) are transcriptional repres
132                                              Polycomb group proteins (PcG) function as transcriptiona
133                                              Polycomb group proteins (PcG) repress homeotic genes in
134                                              Polycomb group proteins (PcG), polycomb repressive compl
135              Hox genes are also repressed by polycomb group proteins (PcG), though how these proteins
136                              We identify the polycomb group protein Pcgf1 as an epigenetic regulator
137                                              Polycomb group proteins (PCGs) are involved in repressio
138                                          The Polycomb group proteins (PcGs) play a vital role through
139 strate that p53 influences expression of the Polycomb-group protein PHC1, which functions as a transc
140                           Here, we show that polycomb group proteins play a central role in repressin
141 eversible chromatin interactions mediated by Polycomb-group proteins play an important role in these
142                                              Polycomb-group proteins play critical roles in gene sile
143 ncer contains multiple binding sites for the Polycomb group protein Pleiohomeotic (PHO).
144         One of the required sites is for the Polycomb group protein Pleiohomeotic and another is GAGA
145 n of alternative fate genes by retaining the Polycomb Group protein Pleiohomeotic at Ubx targeted gen
146 g activity depends on a binding site for the Polycomb-group protein Pleiohomeotic (Pho) and on pho ge
147 e interaction between the SAM domains of the polycomb group proteins polyhomeotic (Ph) and Sex-comb-o
148                                              Polycomb group proteins preserve body patterning through
149                                              Polycomb group proteins represent a conserved family of
150                                          How polycomb group proteins repress gene expression in vivo
151 tioning in Arabidopsis thaliana We show that Polycomb-group proteins repress nucellus degeneration be
152 rotein interacts directly with E(Z), another Polycomb Group protein required for silencing of the hom
153 me3 modifications catalyzed by Trithorax and Polycomb group proteins, respectively.
154 ingle-cell genome-wide interaction data on a polycomb-group protein, RING1B, and the associated trans
155 3 and is essential for proper recruitment of Polycomb group protein Rnf2.
156         In this manuscript, we show that the Polycomb group protein Sfmbt, the Drosophila ortholog of
157                                              Polycomb-group proteins silence gene expression through
158         However, Enhancer of Zeste and other Polycomb group proteins stay primarily localized at thei
159 results indicate that combined modulation of polycomb group proteins, such as EZH2, along with TrxG p
160   The products of these genes are similar to Polycomb group proteins, suggesting possible mechanisms
161 es are a subset of those described for other Polycomb-group proteins, suggesting that E(Z) may also p
162 epress reporter gene expression and bind the Polycomb group protein SUZ12 and the DNA methyltransfera
163 strated that RA-mediated displacement of the polycomb group protein SUZ12 from a RARE was inhibited i
164 s including age-specific hypermethylation in polycomb group protein target genes and the upregulation
165                           The specificity of polycomb group protein targeting is incompletely underst
166                 First, we show that SCML2, a Polycomb group protein that associates with PRC1.2 (cont
167                                Psc encodes a Polycomb group protein that functions as a central compo
168                      The CBX7 gene encodes a polycomb group protein that is known to be downregulated
169 was correlated with higher levels of Bmi1, a polycomb group protein that is known to regulate the Ink
170                                   EZH 2 is a polycomb group protein that mediates repression of gene
171 ransferase, Ezh2 (enhancer of zeste 2), is a Polycomb group protein that plays important roles in man
172                                      Rather, Polycomb group proteins that are expressed from the mate
173 ubtypes and multiple myeloma, linked several polycomb group proteins that could be targeted by small
174 of bmi-1 is homologous to certain Drosophila Polycomb group proteins that regulate homeotic gene expr
175  is a mammalian homolog of Drosophila SCM, a Polycomb-group protein that associates with PRC1.
176 lated by trans-acting factors related to the Polycomb-group proteins that have long been known as reg
177 e range of action of repressors, such as the Polycomb group proteins, throughout the euchromatic regi
178  Since E(Z) is required for binding of other Polycomb Group proteins to chromosomes, these results su
179                 Embryonic stem cells rely on Polycomb group proteins to reversibly repress genes requ
180 adian rhythms and extend the activity of the polycomb group proteins to the core clockwork mechanism
181 ransferases and repressing proteins, such as Polycomb group proteins; upon differentiation, DNMT acti
182 ensitive silencing are related properties of Polycomb-group proteins, whereas their activities are ge
183 on the mechanism of histone modification via Polycomb Group Proteins, which evolved in tandem with th
184 ereas VRN2 encodes a homologue of one of the Polycomb group proteins, which maintain the silencing of
185 he mark trimethyl H3K27, we examined whether Polycomb group proteins, which methylate H3K27, were pre
186 ppression as an alternative to regulation by Polycomb-group proteins, which coordinate embryonic germ
187 g how these configurations are stabilized by Polycomb group proteins will advance our understanding o

 
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