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Michael P. Johnson

Neuroscience Department

Lilly Research Laboratories

Lilly Corporate Center

Indianapolis

USA

[email]@lilly.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Neuroscience Department, Lilly Research Laboratories, Lilly Corporate Center, Indianapolis, USA. 1999 - 2005
  • Neuroscience Department, Eli Lilly and Company, Indianapolis, IN 46285, USA. 2002
  • Hoechst Marion Roussel, CNS Research, Cincinnati, OH 45215, USA. 1998

References

  1. Metabotropic glutamate 2 receptor potentiators: receptor modulation, frequency-dependent synaptic activity, and efficacy in preclinical anxiety and psychosis model(s). Johnson, M.P., Barda, D., Britton, T.C., Emkey, R., Hornback, W.J., Jagdmann, G.E., McKinzie, D.L., Nisenbaum, E.S., Tizzano, J.P., Schoepp, D.D. Psychopharmacology (Berl.) (2005) [Pubmed]
  2. Allosteric modulators of metabotropic glutamate receptors: lessons learnt from mGlu1, mGlu2 and mGlu5 potentiators and antagonists. Johnson, M.P., Nisenbaum, E.S., Large, T.H., Emkey, R., Baez, M., Kingston, A.E. Biochem. Soc. Trans. (2004) [Pubmed]
  3. Discovery of allosteric potentiators for the metabotropic glutamate 2 receptor: synthesis and subtype selectivity of N-(4-(2-methoxyphenoxy)phenyl)-N-(2,2,2- trifluoroethylsulfonyl)pyrid-3-ylmethylamine. Johnson, M.P., Baez, M., Jagdmann, G.E., Britton, T.C., Large, T.H., Callagaro, D.O., Tizzano, J.P., Monn, J.A., Schoepp, D.D. J. Med. Chem. (2003) [Pubmed]
  4. Modulation of stress-induced and stimulated hyperprolactinemia with the group II metabotropic glutamate receptor selective agonist, LY379268. Johnson, M.P., Chamberlain, M. Neuropharmacology (2002) [Pubmed]
  5. Changes in rat serum corticosterone after treatment with metabotropic glutamate receptor agonists or antagonists. Johnson, M.P., Kelly, G., Chamberlain, M. J. Neuroendocrinol. (2001) [Pubmed]
  6. Blockade of pilocarpine-induced cerebellar phosphoinositide hydrolysis with metabotropic glutamate antagonists: evidence for an indirect control of granule cell glutamate release by muscarinic agonists. Johnson, M.P., Kelly, G.M., Chamberlain, M. Neurosci. Lett. (2000) [Pubmed]
  7. Phosphoinositide hydrolysis in vivo with group I metabotropic glutamate receptor agonists. Johnson, M.P., Chamberlain, M., Kelly, G.M. Brain Res. (1999) [Pubmed]
  8. Temporal dependent neuroprotection with propentofylline (HWA 285) in a temporary focal ischemia model. Johnson, M.P., McCarty, D.R., Chmielewski, P.A. Eur. J. Pharmacol. (1998) [Pubmed]
  9. MDL 101,002, a free radical spin trap, is efficacious in permanent and transient focal ischemia models. Johnson, M.P., McCarty, D.R., Velayo, N.L., Markgraf, C.G., Chmielewski, P.A., Ficorilli, J.V., Cheng, H.C., Thomas, C.E. Life Sci. (1998) [Pubmed]
 
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