U. G. Sahm

Synthesis of 153N-6 analogues and structure-function analysis at murine melanocortin-1 (MC1) receptors

C. Pouton, U. G. Sahm, G. W. Olivier, 1999, Peptides.

Synthesis and biological evaluation of alpha-MSH analogues substituted with alanine.

C. Pouton, S. H. Moss, U. G. Sahm, 1994, Peptides.

Synthesis and biological evaluation of α-MSH analogues substituted with alanine

C. Pouton, S. H. Moss, U. G. Sahm, 1994, Peptides.

The melanocortin (MC3) receptor from rat hypothalamus: Photoaffinity labelling and binding of alanine‐substituted α‐MSH analogues

S. H. Moss, C. W. Pouton, U. G. Sahm, 1994, FEBS letters.

Binding and Biological Activity of C-Terminally Modified Melanocortin Peptides: A Comparison Between Their Actions at Rodent MC1 and MC3 Receptors

C. Pouton, R. G. Kinsman, U. G. Sahm, 1997, Peptides.

Influence of α-MSH terminal amino acids on binding affinity and biological activity in melanoma cells

C. Pouton, U. G. Sahm, S. Branch, 1994, Peptides.

Identification of a melanocortin receptor expressed by murine brain microvascular endothelial cells in culture.

C. Pouton, U. G. Sahm, S. Branch, 1995, Microvascular research.

Development of an Oral Formulation for Oestrone 3-O-Sulphamate, a Potent Sulphatase Inhibitor

B. Potter, A. Purohit, M. Reed, 1996 .

Pharmacokinetics of oestrone-3-O-sulphamate

B. Potter, A. Purohit, M. Reed, 1996, The Journal of Steroid Biochemistry and Molecular Biology.