A. Lawson

Molecular Biology · 2012–2014

A researcher in the Science corpus: 2 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

Whom A. Lawson trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

  1. J. Wells
  2. Arthur Christopoulos

Who trusts A. Lawson overall

  1. Zhuoran Qiao
  2. Gideon Lapidoth

Papers from A. Lawson's perspective

Ordered by how strongly the researchers A. Lawson trusts endorse each paper. Same corpus, a different order for every researcher.

  1. Implications of protein flexibility for drug discovery
  2. A common mechanism underlying promiscuous inhibitors from virtual and high-throughput screening. (Journal of Medicinal Chemistry)
  3. Drug-like properties and the causes of poor solubility and poor permeability. (Journal of pharmacological and toxicological methods)
  4. Virtual exploration of the small-molecule chemical universe below 160 Daltons.
  5. Allosteric binding sites on cell-surface receptors: novel targets for drug discovery (Nature reviews. Drug discovery)
  6. The druggable genome (Nature reviews. Drug discovery)
  7. Is There a Difference between Leads and Drugs? A Historical Perspective (Journal of chemical information and computer sciences)
  8. An inhibitor of Bcl-2 family proteins induces regression of solid tumours (Nature)
  9. Predicting druggable binding sites at the protein-protein interface.
  10. Protein–protein docking benchmark version 4.0 (Proteins: Structure, Function, and Bioinformatics)

Their papers