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Citation: Je. Rivier et al., Design of potent dicyclic (4-10/5-8) gonadotropin releasing hormone (GnRH)antagonists, J MED CHEM, 43(5), 2000, pp. 784-796

Authors: Rivier, JE Porter, J Cervini, LA Lahrichi, SL Kirby, DA Struthers, RS Koerber, SC Rivier, CL

Citation: Je. Rivier et al., Design of monocyclic (1-3) and dicyclic (1-3/4-10) gonadotropin releasing hormone (GnRH) antagonists, J MED CHEM, 43(5), 2000, pp. 797-806

Authors: Rivier, JE Jiang, GC Struthers, RS Koerber, SC Porter, J Cervini, LA Kirby, DA Craig, AG Rivier, CL

Citation: Je. Rivier et al., Design of potent dicyclic (1-5/4-10) gonadotropin releasing hormone (GnRH)antagonists, J MED CHEM, 43(5), 2000, pp. 807-818

Authors: Koerber, SC Rizo, J Struthers, RS Rivier, JE

Citation: Sc. Koerber et al., Consensus bioactive conformation of cyclic GnRH antagonists defined by NMRand molecular modeling, J MED CHEM, 43(5), 2000, pp. 819-828

Authors: Millar, RP Zhu, YF Chen, C Struthers, RS

Citation: Rp. Millar et al., Progress towards the development of nonpeptide orally-active gonadotropin-releasing hormone (GnRH) antagonists: therapeutic implications, BR MED B, 56(3), 2000, pp. 761-772