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Journal of Medicinal Chemistry|April 16, 2008
Ring size of somatostatin analogues (ODT-8) modulates receptor selectivity and binding affinityJudit Erchegyi, Christy Rani R Grace, Manoj Samant, et al.
Journal of Medicinal Chemistry|April 16, 2008
Ring size in octreotide amide modulates differently agonist versus antagonist binding affinity and selectivityChristy Rani R Grace, Judit Erchegyi, Manoj Samant, et al.
Journal of Medicinal Chemistry|December 12, 2003
Novel sst(4)-selective somatostatin (SRIF) agonists. 1. Lead identification using a betide scanJean Rivier, Judit Erchegyi, Carl Hoeger, et al.
Journal of Peptide Science : an Official Publication of the European Peptide Society|December 21, 2005
Conformational analysis of a potent SSTR3-selective somatostatin analogue by NMR in water solutionMargarida Gairí, Pilar Saiz, Sergio Madurga, et al.
Journal of Medicinal Chemistry|April 9, 2009
Novel, potent, and radio-iodinatable somatostatin receptor 1 (sst1) selective analoguesJudit Erchegyi, Renzo Cescato, Christy Rani R Grace, et al.
Journal of Medicinal Chemistry|December 12, 2003
Novel sst(4)-selective somatostatin (SRIF) agonists. 2. Analogues with beta-methyl-3-(2-naphthyl)alanine substitutions at position 8Judit Erchegyi, Botond Penke, Lajos Simon, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 24, 2006
Radiolabeled somatostatin receptor antagonists are preferable to agonists for in vivo peptide receptor targeting of tumorsMihaela Ginj, Hanwen Zhang, Beatrice Waser, et al.
Journal of Medicinal Chemistry|January 22, 2005
Somatostatin receptor 1 selective analogues: 2. N(alpha)-Methylated scanJudit Erchegyi, Carl A Hoeger, William Low, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|August 2, 2012
Unexpected sensitivity of sst2 antagonists to N-terminal radiometal modificationsMelpomeni Fani, Friederike Braun, Beatrice Waser, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 5, 2015
Characterization of a Pachymedusa dacnicolor-Sauvagine analog as a new high-affinity radioligand for corticotropin-releasing factor receptor studiesMarilyn H Perrin, Laura A Tan, Joan M Vaughan, et al.
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