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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Robert Powers

Department of Chemistry

University of Nebraska-Lincoln

Lincoln

NE 68588-0304 USA

USA

[email]@unl.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Chemistry, University of Nebraska-Lincoln, Lincoln, NE 68588-0304 USA, USA. 2005 - 2011

References

  1. Searching the protein structure database for ligand-binding site similarities using CPASS v.2. Powers, R., Copeland, J.C., Stark, J.L., Caprez, A., Guru, A., Swanson, D. BMC. Res. Notes (2011) [Pubmed]
  2. NMR metabolomics and drug discovery. Powers, R. Magn. Reson. Chem (2009) [Pubmed]
  3. The application of FAST-NMR for the identification of novel drug discovery targets. Powers, R., Mercier, K.A., Copeland, J.C. Drug Discov. Today (2008) [Pubmed]
  4. Functional genomics and NMR spectroscopy. Powers, R. Comb. Chem. High Throughput Screen. (2007) [Pubmed]
  5. Design and characterization of a functional library for NMR screening against novel protein targets. Mercier, K.A., Germer, K., Powers, R. Comb. Chem. High Throughput Screen. (2006) [Pubmed]
  6. Comparison of protein active site structures for functional annotation of proteins and drug design. Powers, R., Copeland, J.C., Germer, K., Mercier, K.A., Ramanathan, V., Revesz, P. Proteins (2006) [Pubmed]
  7. Solution structure of Archaeglobus fulgidis peptidyl-tRNA hydrolase (Pth2) provides evidence for an extensive conserved family of Pth2 enzymes in archea, bacteria, and eukaryotes. Powers, R., Mirkovic, N., Goldsmith-Fischman, S., Acton, T.B., Chiang, Y., Huang, Y.J., Ma, L., Rajan, P.K., Cort, J.R., Kennedy, M.A., Liu, J., Rost, B., Honig, B., Murray, D., Montelione, G.T. Protein Sci. (2005) [Pubmed]
 
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