Balestre MN - Search Results

1

The D136A mutation of the V2 vasopressin receptor induces a constitutive activity which permits discrimination between antagonists with partial agonist and inverse agonist activities.

Morin D, Cotte N, Balestre MN, Mouillac B, Manning M, Breton C, Barberis C. Morin D, et al. Among authors: balestre mn. FEBS Lett. 1998 Dec 28;441(3):470-5. doi: 10.1016/s0014-5793(98)01585-3. FEBS Lett. 1998. PMID: 9891993 Free article.

2

Tyr115 is the key residue for determining agonist selectivity in the V1a vasopressin receptor.

Chini B, Mouillac B, Ala Y, Balestre MN, Trumpp-Kallmeyer S, Hoflack J, Elands J, Hibert M, Manning M, Jard S, et al. Chini B, et al. Among authors: balestre mn. EMBO J. 1995 May 15;14(10):2176-82. doi: 10.1002/j.1460-2075.1995.tb07211.x. EMBO J. 1995. PMID: 7774575 Free PMC article.

3

Identification of agonist binding sites of vasopressin and oxytocin receptors.

Mouillac B, Chini B, Balestre MN, Jard S, Barberis C, Manning M, Tribollet E, Trumpp-Kallmeyer S, Hoflack J, Elands J, et al. Mouillac B, et al. Among authors: balestre mn. Adv Exp Med Biol. 1995;395:301-10. Adv Exp Med Biol. 1995. PMID: 8713980

4

Molecular basis for agonist selectivity in the vasopressin/oxytocin receptor family.

Chini B, Mouillac B, Ala Y, Balestre MN, Cotte N, Trumpp-Kallmeyer S, Hoflack J, Elands J, Hibert M, Manning M, et al. Chini B, et al. Among authors: balestre mn. Adv Exp Med Biol. 1995;395:321-8. Adv Exp Med Biol. 1995. PMID: 8713982

5

Two aromatic residues regulate the response of the human oxytocin receptor to the partial agonist arginine vasopressin.

Chini B, Mouillac B, Balestre MN, Trumpp-Kallmeyer S, Hoflack J, Hibert M, Andriolo M, Pupier S, Jard S, Barberis C. Chini B, et al. Among authors: balestre mn. FEBS Lett. 1996 Nov 18;397(2-3):201-6. doi: 10.1016/s0014-5793(96)01135-0. FEBS Lett. 1996. PMID: 8955347 Free article.

6

Identification of residues responsible for the selective binding of peptide antagonists and agonists in the V2 vasopressin receptor.

Cotte N, Balestre MN, Phalipou S, Hibert M, Manning M, Barberis C, Mouillac B. Cotte N, et al. Among authors: balestre mn. J Biol Chem. 1998 Nov 6;273(45):29462-8. doi: 10.1074/jbc.273.45.29462. J Biol Chem. 1998. PMID: 9792651 Free article.

7

Mapping peptide antagonist binding sites of the human V1a and V2 vasopressin receptors.

Mouillac B, Phalipou S, Cotte N, Balestre MN, Hibert M, Manning M, Barberis C. Mouillac B, et al. Among authors: balestre mn. Adv Exp Med Biol. 1998;449:359-61. doi: 10.1007/978-1-4615-4871-3_45. Adv Exp Med Biol. 1998. PMID: 10026825 No abstract available.

8

Conserved aromatic residues in the transmembrane region VI of the V1a vasopressin receptor differentiate agonist vs. antagonist ligand binding.

Cotte N, Balestre MN, Aumelas A, Mahé E, Phalipou S, Morin D, Hibert M, Manning M, Durroux T, Barberis C, Mouillac B. Cotte N, et al. Among authors: balestre mn. Eur J Biochem. 2000 Jul;267(13):4253-63. doi: 10.1046/j.1432-1033.2000.01472.x. Eur J Biochem. 2000. PMID: 10866830 Free article.

9

The binding site of neuropeptide vasopressin V1a receptor. Evidence for a major localization within transmembrane regions.

Mouillac B, Chini B, Balestre MN, Elands J, Trumpp-Kallmeyer S, Hoflack J, Hibert M, Jard S, Barberis C. Mouillac B, et al. Among authors: balestre mn. J Biol Chem. 1995 Oct 27;270(43):25771-7. doi: 10.1074/jbc.270.43.25771. J Biol Chem. 1995. PMID: 7592759 Free article.

10

Characterization of a novel, linear radioiodinated vasopressin antagonist: an excellent radioligand for vasopressin V1a receptors.

Barbeis C, Balestre MN, Jard S, Tribollet E, Arsenijevic Y, Dreifuss JJ, Bankowski K, Manning M, Chan WY, Schlosser SS, et al. Barbeis C, et al. Among authors: balestre mn. Neuroendocrinology. 1995 Aug;62(2):135-46. doi: 10.1159/000126998. Neuroendocrinology. 1995. PMID: 8584113

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