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

Laurence J. Egan

Division of Gastroenterology and Hepatology

Mayo Clinic

Rochester

Minnesota 55905

USA

[email]@mayo.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, USA. 1999 - 2004
  • Clinical Pharmacology Unit, Division of Gastroenterology and Hepatology and Division of Biostatistics, Mayo Clinic, Rochester, USA. 2003

References

  1. Advances in the treatment of Crohn's disease. Egan, L.J., Sandborn, W.J. Gastroenterology (2004) [Pubmed]
  2. Drug interactions in gastroenterology: mechanisms, consequences, and how to avoid. Egan, L.J. Clin. Gastroenterol. Hepatol. (2004) [Pubmed]
  3. CYP2C19 pharmacogenetics in the clinical use of proton-pump inhibitors for gastro-oesophageal reflux disease: variant alleles predict gastric acid suppression, but not oesophageal acid exposure or reflux symptoms. Egan, L.J., Myhre, G.M., Mays, D.C., Dierkhising, R.A., Kammer, P.P., Murray, J.A. Aliment. Pharmacol. Ther. (2003) [Pubmed]
  4. Inhibition of interleukin-1-stimulated NF-kappaB RelA/p65 phosphorylation by mesalamine is accompanied by decreased transcriptional activity. Egan, L.J., Mays, D.C., Huntoon, C.J., Bell, M.P., Pike, M.G., Sandborn, W.J., Lipsky, J.J., McKean, D.J. J. Biol. Chem. (1999) [Pubmed]
 
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