Authors:
Polevaya, L
Mavromoustakos, T
Zoumboulakis, P
Grdadolnik, SG
Roumelioti, P
Giatas, N
Mutule, I
Keivish, T
Vlahakos, DV
Iliodromitis, EK
Kremastinos, DT
Matsoukas, J
Citation: L. Polevaya et al., Synthesis and study of a cyclic angiotensin II antagonist analogue revealsthe role of pi-pi* interactions in the C-terminal aromatic residue for agonist activity and its structure resemblance with AT(1) non-peptide antagonists, BIO MED CH, 9(6), 2001, pp. 1639-1647
Authors:
Lindblom, J
Opmane, B
Mutulis, F
Mutule, I
Petrovska, R
Klusa, V
Bergstrom, L
Wikberg, JES
Citation: J. Lindblom et al., The MC4 receptor mediates alpha-MSH induced release of nucleus accumbens dopamine, NEUROREPORT, 12(10), 2001, pp. 2155-2158
Authors:
Prusis, P
Muceniece, R
Mutule, I
Mutulis, F
Wikberg, JES
Citation: P. Prusis et al., Design of new small, cyclic melanocortin receptor-binding peptides using molecular modelling: Role of the His residue in the melanocortin peptide core, EUR J MED C, 36(2), 2001, pp. 137-146
Authors:
Muceniece, R
Mutule, I
Mutulis, F
Prusis, P
Szardenings, M
Wikberg, JES
Citation: R. Muceniece et al., Detection of regions in the MC1 receptor of importance for the selectivityof the MC1 receptor super-selective MS04/MS05 peptides, BBA-PROT ST, 1544(1-2), 2001, pp. 278-282
Authors:
Schioth, HB
Muceniece, R
Mutulis, F
Bouifrouri, AA
Mutule, I
Wikberg, JES
Citation: Hb. Schioth et al., Further pharmacological characterization of the selective melanocortin 4 receptor antagonist HS014: comparison with SHU9119, NEUROPEPTID, 33(3), 1999, pp. 191-196
Authors:
Skuladottir, GV
Jonsson, L
Skarphedinsson, JO
Mutulis, F
Muceniece, R
Raine, A
Mutule, I
Helgason, J
Prusis, P
Wikberg, JES
Schioth, HB
Citation: Gv. Skuladottir et al., Long term orexigenic effect of a novel melanocortin 4 receptor selective antagonist, BR J PHARM, 126(1), 1999, pp. 27-34