Antinociceptive effects of two deltorphins analogs in the tail-immersion test in rats von Kotlinska, J.H., Gibula-Bruzda, E., Witkowska, E., Chung, N.N., Schiller, P.W., Izdebski, J.

Volltext

Mechanisms Implicated in the Reduced Fat Mass and Improved Glucose Homeostasis Observed in Obese Mice Treated with a Prorenin/Renin Receptor Blocker von Tan, P, Blais, C, Michel, C, Kajla, S, Nguyen, T.M.D, Schiller, P.W, Gutkowska, J, Lavoie, J.L

Volltext

Characterization of specific receptors for atrial natriuretic factor in bovine adrenal zona glomerulosa von De Léan, A., Gutkowska, J., McNicoll, N., Schiller, P.W., Cantin, M., Genest, J.

Volltext

Novel highly potent mu-opioid receptor antagonist based on endomorphin-2 structure von Fichna, J, do-Rego, J.C, Janecki, T, Staniszewska, R, Poels, Jeroen, Vanden Broeck, Jozef, Costentin, J, Schiller, P.W, Janecka, A

Volltext

An All D-Amino Acid Opioid Peptide with Central Analgesic Activity from a Combinatorial Library von Dooley, C. T., Chung, N. N., Wilkes, B. C., Schiller, P. W., Bidlack, J. M., Pasternak, G. W., Houghten, R. A.

Volltext

Receptor binding, biological, and immunological properties of chemically deglycosylated pituitary lutropin von Sairam, M.R., Schiller, P.W.

Volltext

Deltorphin analogs restricted via a urea bridge: structure and opioid activity von Ciarkowski, J., Zieleniak, A., Rodziewicz-Motowidło, S., Rusak, Ł., Chung, N.N., Czaplewski, C., Witkowska, E., Schiller, P.W., Izdebski, J.

Volltext

Synthesis and biological evaluation of constrained analogues of the opioid peptide H-Tyr-d-Ala-Phe-Gly-NH2 using the 4-amino-2-benzazepin-3-one scaffold von Ballet, S., Frycia, A., Piron, J., Chung, N.N., Schiller, P.W., Kosson, P., Lipkowski, A.W., Tourwé, D.

Volltext

A chimeric opioid peptide with mixed μ agonist/δ antagonist properties von Weltrowska, G., Lemieux, C., Chung, N.N., Schiller, P.W.

Volltext

Cyclic enkephalin analogs containing various para ‐substituted phenylalanine derivatives in place of Tyr 1 are potent opioid agonists von Weltrowska, G., Lemieux, C., Chung, N.N., Schiller, P.W.

Volltext

Type and location of fluorescent probes incorporated into the potent μ-opioid peptide [Dmt1]DALDA affect potency, receptor selectivity and intrinsic efficacy von Schiller, P.W., Berezowska, I., Weltrowska, G., Chen, H., Lemieux, C., Chung, N.N.

Volltext

Radiosynthesis and in vivo evaluation of the pseudopeptide δ-opioid antagonist [ 125I]-ITIPP(ψ) von Collier, T.L, Schiller, P.W, Waterhouse, R.N

Volltext

Novel endomorphin-2 analogs with μ-opioid receptor antagonist activity von Kruszynski, R., Fichna, J., Do-Rego, J.-C., Chung, N.N., Schiller, P.W., Kosson, P., Costentin, J., Janecka, A.

Volltext

Synthesis and biological evaluation of constrained analogues of the opioid peptide H‐Tyr‐ d ‐Ala‐Phe‐Gly‐NH 2 using the 4‐amino‐2‐benzazepin‐3‐one scaffold von Ballet, S., Frycia, A., Piron, J., Chung, N.N., Schiller, P.W., Kosson, P., Lipkowski, A.W., Tourwé, D.

Volltext

Cyclic enkephalin analogs containing various para-substituted phenylalanine derivatives in place of Tyr1 are potent opioid agonists von Weltrowska, G., Lemieux, C., Chung, N.N., Schiller, P.W.

Volltext

TIPP[ψ], a highly selective δ ligand von Visconti, L.M., Standifer, K.M., Schiller, P.W., Pasternak, G.W.

Volltext

Synthesis and characterization of ruthenium complexes containing tridentate P[sub 3]O[sub 9][sup 3[minus]], Nb[sub 2]W[sub 4]O[sub 19][sup 4[minus]], and CpTiW[sub 5]O[sub 18][sup... von Day, V.W., Eberspacher, T.A., Klemperer, W.G., Ygasaki, A., Zhong, B., Planalp, R.P., Schiller, P.W.

Volltext

Effects of morphine, H‐Tyr‐ d ‐Arg‐Phe‐Lys‐NH 2 (DALDA) and B‐HT920 on non‐cholinergic nerve‐mediated bronchoconstriction in pithed guinea‐pigs von Rechtman, M.P., Boura, A.L.A., King, R.G., Olley, J.E., Schiller, P.W.

Volltext

Isolation, Structure, and Synthesis of a Human Seminal Plasma Peptide with Inhibin-Like Activity von Ramasharma, K., Sairam, M. R., Seidah, N. G., Chrétien, M., Manjunath, P., Schiller, P. W., Yamashiro, D., Li, Choh Hao

Volltext

TIPP analogs: Highly selective δ opioid antagonists with subnanomolar potency and first known compounds with mixed μ agonist/δ antagonist properties von Schiller, P.W., Weltrowska, G., Nguyen, TM-D, Chung, N, Lemieux, C., Wilkes, B.C.

Volltext