Smart Grid Standardisation: Contributions and Opportunities of EU Horizon 2020 Projects von Mutule, Antoskova, I., Carroll, P., Papadimitriou, C., Morch, A., Efthymiou, V.

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Microwave-promoted automated synthesis of a coumarin library von Katkevičs, M., Kontijevskis, A., Mutule, I., Sūna, E.

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Melanocortin Receptors: Ligands and Proteochemometrics Modeling von WIKBERG, J. E.S., MUTULIS, F., MUTULE, I., VEIKSINA, S., LAPINSH, M., PETROVSKA, R., PRUSIS, P.

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The novel adrenergic agonist ATR-127 targets skeletal muscle and brown adipose tissue to tackle diabesity and steatohepatitis von Talamonti, Emanuela, Davegardh, Jelena, Kalinovich, Anastasia, van Beek, Sten M.M., Dehvari, Nodi, Halleskog, Carina, Bokhari, Hamza M., Hutchinson, Dana S., Ham, Seungmin, Humphrys, Laura J., Dijon, Nicola C., Motso, Aikaterini, Sandstrom, Anna, Zacharewicz, Evelyn, Mutule, Ilga, Suna, Edgars, Spura, Jana, Ditrychova, Karolina, Stoddart, Leigh A., Holliday, Nicholas D., Wright, Shane C., Lauschke, Volker M., Nielsen, Soren, Scheele, Camilla, Cheesman, Elizabeth, Hoeks, Joris, Molenaar, Peter, Summers, Roger J., Pelcman, Benjamin, Yakala, Gopala K., Bengtsson, Tore

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The novel adrenoceptor agonist ATR-127 targets skeletal muscle and brown adipose tissue to counter diabesity and hepatic steatosis von Yakala, GK, Talamonti, E, Kalinovich, A, van Beek, SMM, Holliday, ND, Suna, E, Mutule, I, Wright, SC, Lauschke, VM, Nielsen, S, Scheele, C, Summers, RJ, Hoeks, J, Pelcman, B, Bengtsson, T

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Further pharmacological characterization of the selective melanocortin 4 receptor antagonist HS014: comparison with SHU9119 von Schiöth, H.B., Muceniece, R., Mutulis, F., Bouifrouri, A.A., Mutule, I., Wikberg, J.E.S.

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The MC4 receptor mediates α-MSH induced release of nucleus accumbens dopamine von Lindblom, Jonas, Opmane, Baiba, Mutulis, Felikss, Mutule, Ilze, Petrovska, Ramona, Klusa, Vija, Bergström, Lena, Wikberg, Jarl E. S

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Discovery of a novel superpotent and selective melanocortin-4 receptor antagonist (HS024): evaluation in vitro and in vivo von Kask, A, Mutulis, F, Muceniece, R, Pähkla, R, Mutule, I, Wikberg, J E, Rägo, L, Schiöth, H B

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Co-operative regulation of ligand binding to melanocortin receptor subtypes: Evidence for interacting binding sites von Kopanchuk, Sergei, Veiksina, Santa, Petrovska, Ramona, Mutule, Ilze, Szardenings, Michael, Rinken, Ago, Wikberg, Jarl E.S.

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New Substituted Piperazines as Ligands for Melanocortin Receptors. Correlation to the X-ray Structure of “THIQ” von Mutulis, Felikss, Yahorava, Sviatlana, Mutule, Ilze, Yahorau, Aleh, Liepinsh, Edvards, Kopantshuk, Sergei, Veiksina, Santa, Tars, Kaspars, Belyakov, Sergey, Mishnev, Anatoly, Rinken, Ago, Wikberg, Jarl E. S

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Long term orexigenic effect of a novel melanocortin 4 receptor selective antagonist von Skuladottir, Gudrun V, Jonsson, Logi, Skarphedinsson, Jon O, Mutulis, Felikss, Muceniece, Ruta, Raine, Amanda, Mutule, Ilze, Helgason, Johannes, Prusis, Peteris, Wikberg, Jarl E S, Schiöth, Helgi B

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Novel selective melanocortin 4 receptor antagonist induces food intake after peripheral administration von Schiöth, Helgi B., Kask, Ants, Mutulis, Felikss, Muceniece, Ruta, Mutule, Ilga, Mutule, Ilze, Mandrika, Ilona, Wikberg, Jarl E.S.

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N-alkylated dipeptide amides and related structures as imitations of the melanocortins’ active core von Mutulis, Felikss, Mutule, Ilze, Liepinsh, Edvards, Yahorau, Aleh, Lapinsh, Maris, Kopantshuk, Sergei, Veiksina, Santa, Rinken, Ago, Wikberg, Jarl E.S.

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Synthesis and study of a cyclic angiotensin II antagonist analogue reveals the role of pi--pi interactions in the C-terminal aromatic residue for agonist activity and its structure... von Polevaya, L, Mavromoustakos, T, Zoumboulakis, P, Golic Grdadolnik, S, Roumelioti, P, Giatas, N, Mutule, I, Keivish, T, Vlahakos, D V, Iliodromitis, E K, Kremastinos, D T, Matsoukas, J

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Design of new small cyclic melanocortin receptor-binding peptides using molecular modelling: Role of the His residue in the melanocortin peptide core von Prusis, Peteris, Muceniece, Ruta, Mutule, Ilze, Mutulis, Felikss, Wikberg, Jarl E.S.

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New C-protective group for peptide synthesis. Application of 2-(1-adamantyl)-propanol-2 esters von Mutulis, F, Mutule, I, Balodis, J, Sekacis, I, Brivkalne, L, Cipens, G

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Subtype selective binding properties of substituted linear melanocyte stimulating hormone analogues von Schiöth, Helgi B, Tesfaye, Aster, Mutulis, Felikss, Rudzish, Richard, Mutule, Ilze, Muceniece, Ruta, Watanobe, Hajime, Wikberg, Jarl E.S

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The MC sub(4) receptor mediates alpha -MSH induced release of nucleus accumbens dopamine von Lindblom, J, Opmane, B, Mutulis, F, Mutule, I, Petrovska, R, Klusa, V, Bergstroem, L, Wikberg, JES

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Thyrotropin releasing hormone (TRH) selectively binds and activates the melanocortin 1 receptor von Schiöth, Helgi B, Prusis, Peteris, Muceniece, Ruta, Mutulis, Felikss, Mutule, Ilze, Wikberg, Jarl E.S

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Cyclic analogues of bradykinin. II: Synthesis of cyclic derivatives of kallidin von MUTULIS, F. K, CHIPENS, G. I, LANDO, O. E, MUTULE, I. E

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