J. Maffrand

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Effects of divalent cations and of a calcimimetic on adrenocorticotropic hormone release in pituitary tumor cells.

D. Gully, J. Maffrand, C. Lair, 1997, Biochemical and biophysical research communications.

Binding of [3H] SR 49059, a potent nonpeptide vasopressin V1a antagonist, to rat and human liver membranes.

G. Le Fur, C. Serradeil-Le Gal, J. Maffrand, 1994, Biochemical and biophysical research communications.

Biochemical and Pharmacological Properties of SR 49059 , a New , Potent , Nonpeptide Antagonist of Rat and Human Vasopressin Via Receptors

Ala, C. S. Gal, S., 2022 .

Binding properties of a selective tritiated vasopressin V2 receptor antagonist, [H]-SR 121463.

G. Guillon, C. Serradeil-Le Gal, M. Pascal, 2000, Kidney international.

Characterization and localization of leptin receptors in the rat kidney

J. Maffrand, G. Le Fur, C. Serradeil-Le Gal, 1997, FEBS letters.

Endothelin action in rat liver. Receptors, free Ca2+ oscillations, and activation of glycogenolysis.

P. Cobbold, J. Hanoune, S. Lotersztajn, 1991, The Journal of clinical investigation.

Purification and Characterization of the Human SR 31747A-binding Protein

S. Galiègue, P. Casellas, P. Ferrara, 1997, The Journal of Biological Chemistry.

Autoradiographic localization of vasopressin V1a receptors in the rat kidney using [3H]-SR 49059.

G. Le Fur, C. Serradeil-Le Gal, J. Maffrand, 1996, Kidney international.

Effects of SR 49059, a non‐peptide antagonist of vasopressin V1a receptors, on vasopressin‐induced coronary vasoconstriction in conscious rabbits

C. S. Gal, G. Fur, J. Maffrand, 1995, Fundamental & clinical pharmacology.

Effect of a new, potent, non-peptide V1a vasopressin antagonist, SR 49059, on the binding and the mitogenic activity of vasopressin on Swiss 3T3 cells.

P. Casellas, G. Le Fur, C. Serradeil-Le Gal, 1994, Biochemical pharmacology.

Protective effects of SR 57746A in central and peripheral models of neurodegenerative disorders in rodents and primates

P. Soubrié, R. Steinberg, G. Fur, 1993, Neuroscience.

[3H]SR 48692, the first nonpeptide neurotensin antagonist radioligand: characterization of binding properties and evidence for distinct agonist and antagonist binding domains on the rat neurotensin receptor.

M. Mas, D. Gully, P. Kitabgi, 1995, Molecular pharmacology.

A nonpeptide vasopressin V1a receptor antagonist, SR 49059, does not prevent cisplatin‐induced emesis in piglets

L. Grélot, J. Maffrand, C. Serradeil-Le Gal, 2001, Fundamental & clinical pharmacology.

Effect of SR121463, a selective non-peptide vasopressin V2 receptor antagonist, in a rabbit model of ocular hypertension.

G. Le Fur, C. Serradeil-Le Gal, A. Barbier, 2000, Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics.

Biochemical and pharmacological activities of SR 144190, a new potent non-peptide tachykinin NK2 receptor antagonist

P. Soubrié, E. Naline, G. Néliat, 1997, Neuropeptides.

Involvement of protein kinase C in the mitogenic and chemotaxis effects of basic fibroblast growth factor on bovine cerebral cortex capillary endothelial cells

J. Herbert, J. Maffrand, I. Daviet, 1990, FEBS letters.

[3H]-SR 27897B: a selective probe for autoradiographic labelling of CCK-A receptors in the brain.

D. Gully, J. Maffrand, J. Zajac, 1996, Journal of receptor and signal transduction research.

Peripheral biological activity of SR 27897: a new potent non-peptide antagonist of CCKA receptors.

D. Gully, G. Néliat, G. Le Fur, 1993, European journal of pharmacology.

Activation of mitogen-activated protein kinase couples neurotensin receptor stimulation to induction of the primary response gene Krox-24.

P. Casellas, D. Gully, J. Monroe, 1996, The Biochemical journal.

Neurotensin is an antagonist of the human neurotensin NT2 receptor expressed in Chinese hamster ovary cells.

P Ferrara, P. Soubrié, P. Casellas, 1998, European journal of pharmacology.

Glycosaminoglycans enhance megakaryocytopoiesis by modifying the activities of hematopoietic growth regulators

J. Maffrand, M. Pascal, M. Petitou, 1996, Journal of cellular physiology.

SR 25989 inhibits healing of a mechanical wound of confluent human saphenous vein endothelial cells which is modulated by standard heparin and growth factors

J. Herbert, J. Maffrand, J. Cazenave, 1994, Journal of cellular physiology.

Neuropharmacological profile of non‐peptide neurotensin antagonists

P. Soubrié, D. Gully, F. Jeanjean, 1995, Fundamental & clinical pharmacology.

The cannabinoid CB1 receptor antagonist SR141716 increases Acrp30 mRNA expression in adipose tissue of obese fa/fa rats and in cultured adipocyte cells.

P. Soubrié, F. Oury-Donat, J. Maffrand, 2003, Molecular pharmacology.

The arterial wall: a new pharmacological and therapeutic target *

J. Elghozi, B. Dupuis, J. Elghozi, 1995, Fundamental & clinical pharmacology.

ADP Receptor Induced Activation of Guanine Nucleotide Binding Proteins in Rat Platelet Membranes– An Effect Selectively Blocked by the Thienopyridine Clopidogrel

K. Jakobs, J. Maffrand, P. Ohlmann, 1992, Thrombosis and Haemostasis.

Effect of the neurotensin receptor antagonist SR48692 on rat blood pressure modulation by neurotensin.

D. Gully, M. Canton, W. Rostène, 1996, Life sciences.

Effect of SR-49059, a vasopressin V1a antagonist, on human vascular smooth muscle cells.

J. Herbert, G. Le Fur, P. Schaeffer, 1995, The American journal of physiology.

NEW POTENT AND SELECTIVE NON-PEPTIDE ANTAGONISTS OF NEUROTENSIN RECEPTORS

D. Gully, F. Jeanjean, J. Maffrand, 1995, European Journal of Medicinal Chemistry.

Neurotensin receptor interaction with dopaminergic systems in the guinea-pig brain shown by neurotensin receptor antagonists.

D. Gully, R. Boigegrain, M. Héaulme, 1994, European journal of pharmacology.

Selective blockade of vasopressin V2 receptors reveals significant V2-mediated water reabsorption in Brattleboro rats with diabetes insipidus.

L. Bankir, G. Le Fur, N. Bouby, 2001, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.