检索结果 - Claude Barberis

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  1. 1
    Pharmacological characterization of two specific binding sites for neurohypophyseal hormones in hippocampal synaptic plasma membranes of the rat.

    Pharmacological characterization of two specific binding sites for neurohypophyseal hormones in hippocampal synaptic plasma membranes of the rat. 由 S. Audigier, Claude Barberis

    出版 1985
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  2. 2
    Structural bases of vasopressin/oxytocin receptor function

    Structural bases of vasopressin/oxytocin receptor function 由 Claude Barberis, Bernard Mouillac, Thierry Durroux

    出版 1998
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    Revisão
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  3. 3
    Heterodimerization of V1a and V2 vasopressin receptors determines the interaction with β-arrestin and their trafficking patterns

    Heterodimerization of V1a and V2 vasopressin receptors determines the interaction with β-arrestin and their trafficking patterns 由 Sonia Terrillon, Claude Barberis, Michel Bouvier

    出版 2004
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  4. 4
    A radioiodinated linear vasopressin antagonist: A ligand with high affinity and specificity for V<sub>1a</sub> receptors

    A radioiodinated linear vasopressin antagonist: A ligand with high affinity and specificity for V<sub>1a</sub> receptors 由 Anne Schmidt, S. Audigier, Claude Barberis, Serge Jard, M. Manning, Aleksandra S. Kołodziejczyk, W. H. Sawyer

    出版 1991
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  5. 5
    Molecular cloning and expression of a fifth muscarinic acetylcholine receptor

    Molecular cloning and expression of a fifth muscarinic acetylcholine receptor 由 C F Liao, Axel P. N. Themmen, Rolf H. Joho, Claude Barberis, M Birnbaumer, Lutz Birnbaumer

    出版 1989
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  6. 6
    The D136A mutation of the V<sub>2</sub>vasopressin receptor induces a constitutive activity which permits discrimination between antagonists with partial agonist and inverse agonist activities

    The D136A mutation of the V<sub>2</sub>vasopressin receptor induces a constitutive activity which permits discrimination between antagonists with partial agonist and inverse agonis... 由 Denis Morin, Nathalie de la Cotte, Marie‐Noëlle Balestre, Bernard Mouillac, Maurice Manning, Christophe Breton, Claude Barberis

    出版 1998
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  7. 7
    The Binding Site of Neuropeptide Vasopressin V1a Receptor

    The Binding Site of Neuropeptide Vasopressin V1a Receptor 由 Bernard Mouillac, Bice Chini, Marie‐Noëlle Balestre, Jack Elands, Susanne Trumpp-Kallmeyer, Jan Hoflack, Marcel Hibert, Serge Jard, Claude Barberis

    出版 1995
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  8. 8
    Two aromatic residues regulate the response of the human oxytocin receptor to the partial agonist arginine vasopressin

    Two aromatic residues regulate the response of the human oxytocin receptor to the partial agonist arginine vasopressin 由 Bice Chini, Bernard Mouillac, Marie‐Noëlle Balestre, Susanne Trumpp-Kallmeyer, Jan Hoflack, Marcel Hibert, Maria Andriolo, Sandrine Pupier, Serge Jard, Claude Barberis

    出版 1996
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  9. 9
    Glutaminase is essential for the growth of triple-negative breast cancer cells with a deregulated glutamine metabolism pathway and its suppression synergizes with mTOR inhibition

    Glutaminase is essential for the growth of triple-negative breast cancer cells with a deregulated glutamine metabolism pathway and its suppression synergizes with mTOR inhibition 由 Michael Lampa, Heike Arlt, Timothy He, Beatriz Muñoz, Jason Reeves, Bailin Zhang, Joshua Murtie, Gejing Deng, Claude Barberis, Dietmar Hoffmann, Hong Cheng, Jack Pollard, Christopher Winter, Victoria M. Richon, Carlos Garcia-Escheverria, Francisco Adrián, Dmitri Wiederschain, Lakshmi Srinivasan

    出版 2017
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  10. 10
    Functional studies of twelve mutant V2 vasopressin receptors related to nephrogenic diabetes insipidus

    Functional studies of twelve mutant V2 vasopressin receptors related to nephrogenic diabetes insipidus 由 Yahya S. Al‐Awthan, Didier Morin, Bernard Mouillac, Nancy Sabatier, R. Vargas, Nathalie de la Cotte, M Déchaux, Corinne Antignac, Marie‐Françoise Arthus, Michèle Lonergan, Michelle Turner, M N Balestre, G. Alonso, Marcel Hibert, Claude Barberis, Geoffrey N. Hendy, Daniel G. Bichet, Serge Jard

    出版 1998
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  11. 11
    Characterization of SR 121463A, a highly potent and selective, orally active vasopressin V2 receptor antagonist.

    Characterization of SR 121463A, a highly potent and selective, orally active vasopressin V2 receptor antagonist. 由 C. Serradeil‐Le Gal, C Lacour, G Valette, Georges Garcia, Loïc Foulon, G Galindo, Lise Bankir, Brigitte Pouzet, Gilles Guillon, Claude Barberis, D Chicot, Serge Jard, P. Vilain, Corinne Garcia, E. Marty, Danielle Raufaste, Gabrielle Brossard, Dino Nisato, Jean‐Pierre Maffrand, G. Le Fur

    出版 1996
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