Strategy for "detoxification" of a cancer-derived histone mutant based on mapping its interaction with the methyltransferase PRC2
about
Histone H3 mutations--a special role for H3.3 in tumorigenesis?A histone H3K9M mutation traps histone methyltransferase Clr4 to prevent heterochromatin spreadingFunctionally defined therapeutic targets in diffuse intrinsic pontine gliomaHistones: at the crossroads of peptide and protein chemistry.Catalytically Important Residues of E6AP Ubiquitin Ligase Identified Using Acid-Cleavable Photo-Cross-LinkersTargeted Histone Peptides: Insights into the Spatial Regulation of the Methyltransferase PRC2 by using a Surrogate of Heterotypic Chromatin.Mutations in chromatin machinery and pediatric high-grade gliomaStructural basis of oncogenic histone H3K27M inhibition of human polycomb repressive complex 2.S-adenosyl methionine is necessary for inhibition of the methyltransferase G9a by the lysine 9 to methionine mutation on histone H3.Histone Lysine-to-Methionine Mutations Reduce Histone Methylation and Cause Developmental Pleiotropy.Oncogenic Mechanisms of Histone H3 Mutations.Comment on "Structural basis of histone H3K27 trimethylation by an active polycomb repressive complex 2".The role of histone modifications and telomere alterations in the pathogenesis of diffuse gliomas in adults and children.Potential New Therapies for Pediatric Diffuse Intrinsic Pontine Glioma.Characterization of H3.3K36M as a tool to study H3K36 methylation in cancer cells.Transcriptional Dependencies in Diffuse Intrinsic Pontine Glioma.Histone lysine methyltransferase structure activity relationships that allow for segregation of G9a inhibition and anti-Plasmodium activity† †The authors declare no competing interests. ‡ ‡Electronic supplementary information (ESI) available: SuppleHistone lysine methyltransferase structure activity relationships that allow for segregation of G9a inhibition and anti-Plasmodium activity.Structure, mechanism, and regulation of polycomb repressive complex 2.ISWI chromatin remodellers sense nucleosome modifications to determine substrate preference.Oncohistones: drivers of pediatric cancers.Live-cell single-molecule dynamics of PcG proteins imposed by the DIPG H3.3K27M mutation.Multiple modes of PRC2 inhibition elicit global chromatin alterations in H3K27M pediatric glioma
P2860
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P2860
Strategy for "detoxification" of a cancer-derived histone mutant based on mapping its interaction with the methyltransferase PRC2
description
2014 nî lūn-bûn
@nan
2014 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Strategy for "detoxification" ...... ith the methyltransferase PRC2
@ast
Strategy for "detoxification" ...... ith the methyltransferase PRC2
@en
Strategy for "detoxification" ...... ith the methyltransferase PRC2
@nl
type
label
Strategy for "detoxification" ...... ith the methyltransferase PRC2
@ast
Strategy for "detoxification" ...... ith the methyltransferase PRC2
@en
Strategy for "detoxification" ...... ith the methyltransferase PRC2
@nl
prefLabel
Strategy for "detoxification" ...... ith the methyltransferase PRC2
@ast
Strategy for "detoxification" ...... ith the methyltransferase PRC2
@en
Strategy for "detoxification" ...... ith the methyltransferase PRC2
@nl
P2093
P2860
P356
P1476
Strategy for "detoxification" ...... ith the methyltransferase PRC2
@en
P2093
C David Allis
Manuel M Müller
Tom W Muir
Zachary Z Brown
P2860
P304
13498-13501
P356
10.1021/JA5060934
P407
P577
2014-09-19T00:00:00Z