W. Jahnke
Nature reviews. Drug discovery · 2016
A researcher in the Science corpus: 1 paper; trusts 0 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Papers from W. Jahnke's perspective
Ordered by how strongly the researchers W. Jahnke trusts endorse each paper. Same corpus, a different order for every researcher.
- Ligand efficiency: a useful metric for lead selection. (Drug Discovery Today)
- A 'rule of three' for fragment-based lead discovery?
- Selective Inhibition of Oncogenic KRAS Output with Small Molecules Targeting the Inactive State. (Cancer Discovery)
- An inhibitor of Bcl-2 family proteins induces regression of solid tumours (Nature)
- Crystal structure of the human β2 adrenergic G-protein-coupled receptor
- The role of ligand efficiency metrics in drug discovery
- ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets (Nature Medicine)
- Molecular Interaction Studies Using Microscale Thermophoresis (Assay and drug development technologies)
- Vemurafenib: the first drug approved for BRAF-mutant cancer (Nature reviews. Drug discovery)
- Structure of a β1-adrenergic G protein-coupled receptor (Nature)
Their papers
- Twenty years on: the impact of fragments on drug discovery (2016) — 798 citations