11 articles for MJ Scanlon
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Ligand-induced conformational change of Plasmodium falciparum AMA1 detected using 19F NMR.

La Trobe University
Characterization of the drug binding specificity of rat liver fatty acid binding protein.

Monash University (Parkville Campus)
Conformational selection of inhibitors and substrates by proteolytic enzymes: implications for drug design and polypeptide processing.

University of Queensland
Probing the fibrate binding specificity of rat liver fatty acid binding protein.

Monash University
Rapid Elaboration of Fragments into Leads Applied to Bromodomain-3 Extra-Terminal Domain.

Monash University (Parkville Campus)
Elaboration of a benzofuran scaffold and evaluation of binding affinity and inhibition of Escherichia coli DsbA: A fragment-based drug design approach to novel antivirulence compounds.

La Trobe University
Substituted 1-methyl-4-phenylpyrrolidin-2-ones - Fragment-based design of N-methylpyrrolidone-derived bromodomain inhibitors.

Monash University (Parkville Campus)
Rapid Elaboration of Fragments into Leads by X-ray Crystallographic Screening of Parallel Chemical Libraries (REFiL

Monash University (Parkville Campus)
Design, Synthesis, and Characterization of Cyclic Peptidomimetics of the Inducible Nitric Oxide Synthase Binding Epitope That Disrupt the Protein-Protein Interaction Involving SPRY Domain-Containing Suppressor of Cytokine Signaling Box Protein (SPSB) 2 and Inducible Nitric Oxide Synthase.

Monash University
Synthesis and elaboration of N-methylpyrrolidone as an acetamide fragment substitute in bromodomain inhibition.

Monash University (Parkville Campus)
Synthesis and biological evaluation of novel EG5 inhibitors.

University of Leipzig