VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q83379226 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000059.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q83379226‏
024 ‎‡a 0000-0003-0985-6617‏ ‎‡2 orcid‏
035 ‎‡a (OCoLC)Q83379226‏
100 0 ‎‡a Emmanuel Smith‏ ‎‡c researcher‏ ‎‡9 en‏
400 0 ‎‡a Emmanuel Smith‏ ‎‡c wetenschapper‏ ‎‡9 nl‏
670 ‎‡a Author's Coregulator control of androgen receptor action by a novel nuclear receptor-binding motif‏
670 ‎‡a Author's Crystallographic Structure of Truncated CCL21 and the Putative Sulfotyrosine-Binding Site‏
670 ‎‡a Author's Fragment-based optimization of small molecule CXCL12 inhibitors for antagonizing the CXCL12/CXCR4 interaction.‏
670 ‎‡a Author's Hematein, a casein kinase II inhibitor, inhibits lung cancer tumor growth in a murine xenograft model‏
670 ‎‡a Author's Insights into POT1 structural dynamics revealed by cryo-EM‏
670 ‎‡a Author's Ligand-Induced Proton Transfer and Low-Barrier Hydrogen Bond Revealed by X-ray Crystallography‏
670 ‎‡a Author's Structural analysis of a novel small molecule ligand bound to the CXCL12 chemokine‏
670 ‎‡a Author's Structure-based design of potent and ligand-efficient inhibitors of CTX-M class A β-lactamase‏
670 ‎‡a Author's Structure-Based Identification of Novel Ligands Targeting Multiple Sites within a Chemokine-G-Protein-Coupled-Receptor Interface‏
670 ‎‡a Author's Structures of Pseudomonas aeruginosa LpxA Reveal the Basis for Its Substrate Selectivity‏
909 ‎‡a (orcid) 0000000309856617‏ ‎‡9 1‏
919 ‎‡a structuresofpseudomonasaeruginosalpxarevealthebasisforitssubstrateselectivity‏ ‎‡A Structures of Pseudomonas aeruginosa LpxA Reveal the Basis for Its Substrate Selectivity‏ ‎‡9 1‏
919 ‎‡a structurebasedidentificationofnovelligandstargetingmultiplesiteswithinachemokinegproteincoupledreceptorinterface‏ ‎‡A Structure-Based Identification of Novel Ligands Targeting Multiple Sites within a Chemokine-G-Protein-Coupled-Receptor Interface‏ ‎‡9 1‏
919 ‎‡a structurebaseddesignofpotentandligandefficientinhibitorsofctx1000classaβlactamase‏ ‎‡A Structure-based design of potent and ligand-efficient inhibitors of CTX-M class A β-lactamase‏ ‎‡9 1‏
919 ‎‡a structuralanalysisofanovelsmallmoleculeligandboundtothecxcl12chemokine‏ ‎‡A Structural analysis of a novel small molecule ligand bound to the CXCL12 chemokine‏ ‎‡9 1‏
919 ‎‡a ligandinducedprotontransferandlowbarrierhydrogenbondrevealedby10raycrystallography‏ ‎‡A Ligand-Induced Proton Transfer and Low-Barrier Hydrogen Bond Revealed by X-ray Crystallography‏ ‎‡9 1‏
919 ‎‡a insightsintopot1structuraldynamicsrevealedbycryoem‏ ‎‡A Insights into POT1 structural dynamics revealed by cryo-EM‏ ‎‡9 1‏
919 ‎‡a hemateinacaseinkinase2inhibitorinhibitslungcancertumorgrowthinamurinexenograftmodel‏ ‎‡A Hematein, a casein kinase II inhibitor, inhibits lung cancer tumor growth in a murine xenograft model‏ ‎‡9 1‏
919 ‎‡a fragmentbasedoptimizationofsmallmoleculecxcl12inhibitorsforantagonizingthecxcl12cxcr4interaction‏ ‎‡A Fragment-based optimization of small molecule CXCL12 inhibitors for antagonizing the CXCL12/CXCR4 interaction.‏ ‎‡9 1‏
919 ‎‡a crystallographicstructureoftruncatedccl21andtheputativesulfotyrosinebindingsite‏ ‎‡A Crystallographic Structure of Truncated CCL21 and the Putative Sulfotyrosine-Binding Site‏ ‎‡9 1‏
919 ‎‡a coregulatorcontrolofandrogenreceptoractionbyanovelnuclearreceptorbindingmotif‏ ‎‡A Coregulator control of androgen receptor action by a novel nuclear receptor-binding motif‏ ‎‡9 1‏
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏