about
Ribosomal Antibiotics: Contemporary ChallengesInduced-fit tightens pleuromutilins binding to ribosomes and remote interactions enable their selectivityThe structure of ribosome-lankacidin complex reveals ribosomal sites for synergistic antibioticsPromiscuous RNA binding by Polycomb repressive complex 2.A dimeric state for PRC2Toward a consensus on the binding specificity and promiscuity of PRC2 for RNA.The recruitment of chromatin modifiers by long noncoding RNAs: lessons from PRC2.RNA Duplex Map in Living Cells Reveals Higher-Order Transcriptome StructureTargeting of Polycomb Repressive Complex 2 to RNA by Short Repeats of Consecutive Guanines.The evolving ribosome: from non-coded peptide bond formation to sophisticated translation machinery.The Proto-Ribosome: an ancient nano-machine for peptide bond formationStructural basis for cross-resistance to ribosomal PTC antibiotics.Ribosome's mode of function: myths, facts and recent results.Ancient machinery embedded in the contemporary ribosome.The heat shock protein YbeY is required for optimal activity of the 30S ribosomal subunit.Targeting PRC2: RNA offers new opportunities.The Ribosomal Protein uL22 Modulates the Shape of the Protein Exit Tunnel.Structural basis of specific H2A K13/K15 ubiquitination by RNF168RNA exploits an exposed regulatory site to inhibit the enzymatic activity of PRC2
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P50
description
researcher ORCID ID = 0000-0002-1085-6094
@en
name
Chen Davidovich
@ast
Chen Davidovich
@en
Chen Davidovich
@es
Chen Davidovich
@nl
type
label
Chen Davidovich
@ast
Chen Davidovich
@en
Chen Davidovich
@es
Chen Davidovich
@nl
prefLabel
Chen Davidovich
@ast
Chen Davidovich
@en
Chen Davidovich
@es
Chen Davidovich
@nl
P31
P496
0000-0002-1085-6094