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Authors:
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Mouillac, B
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Citation: E. Carnazzi et al., Design, synthesis and pharmacological characterization of a potent radioiodinated and photoactivatable peptidic oxytocin antagonist, J MED CHEM, 44(18), 2001, pp. 3022-3030
Authors:
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Paquet, JL
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Citation: P. Bedos et al., A rational approach to the design and synthesis of a new bradykinin B-1 receptor antagonist, J MED CHEM, 43(12), 2000, pp. 2387-2394
Authors:
Cotte, N
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Citation: N. Cotte et al., Conserved aromatic residues in the transmembrane region VI of the V-1a vasopressin receptor differentiate agonist vs. antagonist ligand binding, EUR J BIOCH, 267(13), 2000, pp. 4253-4263
Authors:
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Citation: M. Jimenez-estrada et al., Two novel Diels-Alder adducts from Hippocratea celastroides roots and their insecticidal activity, CAN J CHEM, 78(2), 2000, pp. 248-254
Authors:
Yang, YS
Mitta, G
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Citation: Ys. Yang et al., Solution structure and activity of the synthetic four-disulfide bond Mediterranean mussel defensin (MGD-1), BIOCHEM, 39(47), 2000, pp. 14436-14447
Authors:
Malliavin, TE
Desvaux, H
Aumelas, A
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Delsuc, MA
Citation: Te. Malliavin et al., Quantitative measurement of longitudinal and transverse cross-relaxation rates: An application to the analysis of the internal dynamics of ranalexin in water and trifluoroethanol, J MAGN RES, 140(1), 1999, pp. 189-199
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Aumelas, A
Chiche, L
Kubo, S
Chino, N
Watanabe, TX
Kobayashi, Y
Citation: A. Aumelas et al., The chimeric peptide [Lys(-2)-Arg(-1)]-sarafotoxin-S6b, composed of the endothelin pro-sequence and sarafotoxin, retains the salt-bridge staple between Arg(-1) and Asp8 previously observed in [Lys(-2)-Arg(-1)]-endothelin - Implications of this salt-bridge in the contractile activity and the oxidative folding reaction, EUR J BIOCH, 266(3), 1999, pp. 977-985