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