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Joel P. Berger

Department of Molecular Endocrinology

Merck Research Laboratories

Rahway

New Jersey 07065

USA

[email]@merck.com

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Molecular Endocrinology, Merck Research Laboratories, Rahway, New Jersey 07065, USA. 1996 - 2005
  • RY80N-C31, Merck Research Laboratories, 126 East Lincoln Avenue, Rahway, USA. 2003

References

  1. PPARs: therapeutic targets for metabolic disease. Berger, J.P., Akiyama, T.E., Meinke, P.T. Trends Pharmacol. Sci. (2005) [Pubmed]
  2. Distinct properties and advantages of a novel peroxisome proliferator-activated protein [gamma] selective modulator. Berger, J.P., Petro, A.E., Macnaul, K.L., Kelly, L.J., Zhang, B.B., Richards, K., Elbrecht, A., Johnson, B.A., Zhou, G., Doebber, T.W., Biswas, C., Parikh, M., Sharma, N., Tanen, M.R., Thompson, G.M., Ventre, J., Adams, A.D., Mosley, R., Surwit, R.S., Moller, D.E. Mol. Endocrinol. (2003) [Pubmed]
  3. The mechanisms of action of PPARs. Berger, J., Moller, D.E. Annu. Rev. Med. (2002) [Pubmed]
  4. Physiological and therapeutic roles of peroxisome proliferator-activated receptors. Berger, J., Wagner, J.A. Diabetes Technol. Ther. (2002) [Pubmed]
  5. Peroxisome proliferator-activated receptor-gamma ligands inhibit adipocyte 11beta -hydroxysteroid dehydrogenase type 1 expression and activity. Berger, J., Tanen, M., Elbrecht, A., Hermanowski-Vosatka, A., Moller, D.E., Wright, S.D., Thieringer, R. J. Biol. Chem. (2001) [Pubmed]
  6. A PPARgamma mutant serves as a dominant negative inhibitor of PPAR signaling and is localized in the nucleus. Berger, J., Patel, H.V., Woods, J., Hayes, N.S., Parent, S.A., Clemas, J., Leibowitz, M.D., Elbrecht, A., Rachubinski, R.A., Capone, J.P., Moller, D.E. Mol. Cell. Endocrinol. (2000) [Pubmed]
  7. Novel peroxisome proliferator-activated receptor (PPAR) gamma and PPARdelta ligands produce distinct biological effects. Berger, J., Leibowitz, M.D., Doebber, T.W., Elbrecht, A., Zhang, B., Zhou, G., Biswas, C., Cullinan, C.A., Hayes, N.S., Li, Y., Tanen, M., Ventre, J., Wu, M.S., Berger, G.D., Mosley, R., Marquis, R., Santini, C., Sahoo, S.P., Tolman, R.L., Smith, R.G., Moller, D.E. J. Biol. Chem. (1999) [Pubmed]
  8. A high-capacity assay for activators of glucose incorporation into glycogen in L6 muscle cells. Berger, J., Hayes, N.S. Anal. Biochem. (1998) [Pubmed]
  9. Thiazolidinediones produce a conformational change in peroxisomal proliferator-activated receptor-gamma: binding and activation correlate with antidiabetic actions in db/db mice. Berger, J., Bailey, P., Biswas, C., Cullinan, C.A., Doebber, T.W., Hayes, N.S., Saperstein, R., Smith, R.G., Leibowitz, M.D. Endocrinology (1996) [Pubmed]
 
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