about
Transcriptional regulation by the repressor of estrogen receptor activity via recruitment of histone deacetylasesComposition and histone substrates of polycomb repressive group complexes change during cellular differentiationTransdifferentiation. Sequential histone-modifying activities determine the robustness of transdifferentiationRegulation of transcription through acetylation of H3K122 on the lateral surface of the histone octamerThe Polycomb complex PRC2 and its mark in lifePRC2 is dispensable for HOTAIR-mediated transcriptional repressionSilencing of human polycomb target genes is associated with methylation of histone H3 Lys 27.Jarid2 Methylation via the PRC2 Complex Regulates H3K27me3 Deposition during Cell Differentiation.Suz12 binds to silenced regions of the genome in a cell-type-specific mannerChromatin regulated interchange between polycomb repressive complex 2 (PRC2)-Ezh2 and PRC2-Ezh1 complexes controls myogenin activation in skeletal muscle cells.Histone deacetylase inhibition and estrogen signalling in human breast cancer cells.ERalpha and ERbeta expression and transcriptional activity are differentially regulated by HDAC inhibitors.Steps toward understanding the inheritance of repressive methyl-lysine marks in histones.Impaired PRC2 activity promotes transcriptional instability and favors breast tumorigenesisImprinting control regions (ICRs) are marked by mono-allelic bivalent chromatin when transcriptionally inactive.Cdyl, a new partner of the inactive X chromosome and potential reader of H3K27me3 and H3K9me2.Chromatin in the nuclear landscape.Association between EZH2 expression, silencing of tumor suppressors and disease outcome in solid tumors.The Multiple Facets of PRC2 Alterations in Cancers.Legionella pneumophila effector RomA uniquely modifies host chromatin to repress gene expression and promote intracellular bacterial replication.Mechanisms Regulating PRC2 Recruitment and Enzymatic Activity.Versatile and precise gene-targeting strategies for functional studies in mammalian cell lines.Ezh2 requires PHF1 to efficiently catalyze H3 lysine 27 trimethylation in vivo.Modulating BAP1 expression affects ROS homeostasis, cell motility and mitochondrial function.Histone propionylation is a mark of active chromatin.Histone deacetylase inhibition and estrogen receptor alpha levels modulate the transcriptional activity of partial antiestrogens.Prdm3 and Prdm16 are H3K9me1 methyltransferases required for mammalian heterochromatin integrity.A meiotic XPF-ERCC1-like complex recognizes joint molecule recombination intermediates to promote crossover formation.Chromatin biology: Breaking into the PRC2 cage.Uveal melanoma cells are resistant to EZH2 inhibition regardless of BAP1 status.A Family of Vertebrate-Specific Polycombs Encoded by the LCOR/LCORL Genes Balance PRC2 Subtype Activities.Reprogrammation épigénétique des cellules hôtes parLegionella pneumophilaHistone variants H2A.Z and H3.3 coordinately regulate PRC2-dependent H3K27me3 deposition and gene expression regulation in mES cellsJarid2 Is Implicated in the Initial Xist-Induced Targeting of PRC2 to the Inactive X ChromosomeBAP1 complex promotes transcription by opposing PRC1-mediated H2A ubiquitylation
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Q24292875-FC8B1DC3-72D9-4794-8EF4-669C7485B7DBQ24293278-1BB19701-1568-46FD-9038-C796317FF9B2Q24302015-36EDC110-4579-4963-B7A3-EB7541F904CDQ24317494-CB1203B6-7B40-4318-AA46-1C593CE9AF18Q29547358-A8D589F3-635A-4B60-99AF-952F1EAEBC24Q33563215-4C9CCA41-BC28-4B0F-AE5E-C555D0185C9FQ33979536-87C1F5F5-E944-4A02-A7CC-188DC809D50CQ34043035-EE4DF0D6-2626-470F-9D55-FB57A32D799BQ34703113-AECA6F3A-F657-4395-8167-D1CFE3D0CE82Q35232680-02D894C2-9A65-4FF8-A0BF-EB43FA3F0734Q35864090-551D696D-2980-4786-9D19-5EAC759E0C7FQ36083466-52EE3EB6-16C0-467B-807C-552C5D45E575Q36238555-278C419C-4E0B-4A50-A371-B57EE096236BQ36424889-A580C01F-2A8B-482C-8047-7090739CABA7Q36532744-30093AA0-45CA-4672-879C-86208919C9C1Q37469472-B223FC40-F7EB-4564-9E38-02450A01E4F7Q37866556-BAC97B26-A858-4121-BD52-08B484D404C0Q38758038-27BAAF3A-4F04-4388-93D4-7880CE525DAEQ38981219-F8A8035E-D6A4-4358-B19B-9B5E9B3F1733Q39163703-15870E1E-32EE-4459-BB08-66F04DE328BDQ39291860-EF77C88E-B943-4E51-83FF-0E12D3CF45D1Q39303208-6719A3DA-3177-46C5-AA8A-8DAD0E007EF9Q40011376-A527784B-E1EB-4023-9DA0-A40022419AB5Q42700777-F0CC3C6E-F941-4755-9E74-918BCFC7CA92Q43065475-D7C3534F-00FA-4132-8DC4-C3DA853FBF0DQ44836071-C9F1CAD4-B7DF-4DEF-AD9A-4DFEE61DEB3CQ45262911-767D05D7-4E50-4F50-ABF0-664AFCE01DF7Q50027177-42D6EA2B-EC21-4EA1-BAA7-2AFDAF908F09Q50458426-09D2CAB5-0863-4BE6-B770-9C689BDFB83BQ51716300-498E8786-CD65-43E5-96FA-F37A74D76F88Q52328745-01ACDB62-9D14-4C66-889F-A675DBF4E3A4Q57954103-69C2ED36-C4F3-48A8-B44C-55086F4D590BQ58701573-03CEA93C-1D63-4414-9DD2-592A98D1FB8FQ60483619-3D1EB1FD-44E9-4CDF-A1A5-373522C8F95CQ61124903-03242645-D46B-4008-A1FE-3588800D5085
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description
chercheur français
@fr
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Raphael Margueron
@ast
Raphael Margueron
@en
Raphael Margueron
@es
Raphael Margueron
@fr
Raphael Margueron
@nl
type
label
Raphael Margueron
@ast
Raphael Margueron
@en
Raphael Margueron
@es
Raphael Margueron
@fr
Raphael Margueron
@nl
prefLabel
Raphael Margueron
@ast
Raphael Margueron
@en
Raphael Margueron
@es
Raphael Margueron
@fr
Raphael Margueron
@nl
P106
P21
P31
P496
0000-0002-9093-7977