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Mouse polycomb proteins bind differentially to methylated histone H3 and RNA and are enriched in facultative heterochromatin
scientific journal article
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scholarly article
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stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
title
Mouse polycomb proteins bind differentially to methylated histone H3 and RNA and are enriched in facultative heterochromatin
(English)
1 reference
stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
main subject
Chromobox 6
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GOA release 2020-03-11
Chromobox 7
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GOA release 2020-03-11
Chromobox 4
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GOA release 2020-03-11
Chromobox 8
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GOA release 2020-03-11
Chromobox 2
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GOA release 2020-03-11
author
Charles David Allis
series ordinal
6
object named as
C. David Allis
1 reference
stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
Jesus Gil
object named as
Jesus Gil
series ordinal
4
0 references
Edith Heard
series ordinal
5
object named as
Edith Heard
1 reference
stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
author name string
Emily Bernstein
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
Elizabeth M. Duncan
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
Osamu Masui
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3
1 reference
stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
language of work or name
English
0 references
publication date
1 April 2006
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PubMed
PubMed ID
16537902
retrieved
31 January 2017
published in
Molecular and Cellular Biology
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stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
volume
26
1 reference
stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
page(s)
2560–2569
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stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
issue
7
1 reference
stated in
PubMed
PubMed ID
16537902
retrieved
31 January 2017
cites work
Stable X chromosome inactivation involves the PRC1 Polycomb complex and requires histone MACROH2A1 and the CULLIN3/SPOP ubiquitin E3 ligase
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PubMed Central
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Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation
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Molecular basis for the discrimination of repressive methyl-lysine marks in histone H3 by Polycomb and HP1 chromodomains
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Structural basis for specific binding of Polycomb chromodomain to histone H3 methylated at Lys 27
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Structure of HP1 chromodomain bound to a lysine 9-methylated histone H3 tail
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Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain
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PubMed Central
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Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins
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PubMed Central
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Chromatin association of human origin recognition complex, cdc6, and minichromosome maintenance proteins during the cell cycle: assembly of prereplication complexes in late mitosis
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Regulation of HP1-chromatin binding by histone H3 methylation and phosphorylation
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WDR5 associates with histone H3 methylated at K4 and is essential for H3 K4 methylation and vertebrate development
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Epigenetic regulation of cellular memory by the Polycomb and Trithorax group proteins
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RNA meets chromatin
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Developmentally regulated alterations in Polycomb repressive complex 1 proteins on the inactive X chromosome
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Differential histone H3 Lys-9 and Lys-27 methylation profiles on the X chromosome
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PubMed Central
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29 September 2017
Recent advances in X-chromosome inactivation
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PubMed Central
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29 September 2017
HP1 and the dynamics of heterochromatin maintenance
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PubMed Central
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29 September 2017
Coordinated methyl and RNA binding is required for heterochromatin localization of mammalian HP1alpha
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PubMed Central
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29 September 2017
The dMi-2 chromodomains are DNA binding modules important for ATP-dependent nucleosome mobilization
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29 September 2017
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29 September 2017
Dynamic relocalization of histone MacroH2A1 from centrosomes to inactive X chromosomes during X inactivation
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29 September 2017
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PubMed Central
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29 September 2017
Distinct contributions of histone H3 lysine 9 and 27 methylation to locus-specific stability of polycomb complexes
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PubMed Central
reference URL
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PubMed Central
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27 November 2018
Establishment of histone h3 methylation on the inactive X chromosome requires transient recruitment of Eed-Enx1 polycomb group complexes
1 reference
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PubMed Central
reference URL
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27 November 2018
Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA component
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27 November 2018
Methylation of histone H3 at Lys-9 is an early mark on the X chromosome during X inactivation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430336
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27 November 2018
Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430336
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27 November 2018
Activation of transcription through histone H4 acetylation by MOF, an acetyltransferase essential for dosage compensation in Drosophila.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1430336
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27 November 2018
Ring1b-mediated H2A ubiquitination associates with inactive X chromosomes and is involved in initiation of X inactivation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/16537902
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1128/MCB.26.7.2560-2569.2006
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3069040
OpenCitations bibliographic resource ID
3069040
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3069040
PMCID
1430336
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3069040
PubMed ID
16537902
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3069040
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