Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Hélène Orcel"'
Autor:
Julie Sauvant, Jean-Christophe Delpech, Karine Palin, Nadia De Mota, Jennifer Dudit, Agnès Aubert, Hélène Orcel, Pascale Roux, Sophie Layé, Françoise Moos, Catherine Llorens-Cortes, Agnès Nadjar
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e87421 (2014)
Normal aging is associated with vasopressin neuron adaptation, but little is known about its effects on the release of apelin, an aquaretic peptide colocalized with vasopressin. We found that plasma vasopressin concentrations were higher and plasma a
Externí odkaz:
https://doaj.org/article/9d061029a0304ac48f86863adfd67f4b
Autor:
Henri J. Vial, Marie L. Ancelin, Noureddine Elabbadi, Hélène Orcel, Hye-Jeong Yeo, Catherine Gumila
Publikováno v:
Memorias do Instituto Oswaldo Cruz, Vol 89, Pp 91-97 (1994)
We have developed a model for designing antimalarial drugs based on interference with an essential metabolism developed by Plasmodium during its intraerythrocytic cycle, phospholipid (PL) metabolism. The most promising drug interference is choline tr
Externí odkaz:
https://doaj.org/article/d7cbf43d6db5431d99deafac5809094b
Autor:
Julien Bous, Aurélien Fouillen, Hélène Orcel, Stefano Trapani, Xiaojing Cong, Simon Fontanel, Julie Saint-Paul, Joséphine Lai-Kee-Him, Serge Urbach, Nathalie Sibille, Rémy Sounier, Sébastien Granier, Bernard Mouillac, Patrick Bron
Publikováno v:
Science Advances
Science Advances, 2022, 8 (35), pp.eabo7761. ⟨10.1126/sciadv.abo7761⟩
Science Advances, 2022, 8 (35), pp.eabo7761. ⟨10.1126/sciadv.abo7761⟩
Arrestins interact with G protein-coupled receptors (GPCRs) to stop G protein activation and to initiate key signaling pathways. Recent structural studies shed light on the molecular mechanisms involved in GPCR-arrestin coupling, but whether this pro
Autor:
Patrick Bron, Stefano Trapani, Hélène Orcel, Julien Bous, Nicolas Floquet, Remy Sounier, Cedric Leyrat, Aurelie Ancelin, Julie Saint-Paul, Sébastien Granier, Gérald Gaibelet, Joséphine Lai-Kee-Him, Hélène Déméné, Bernard Mouillac, Maxime Louet
Publikováno v:
Science Advances
Science Advances, American Association for the Advancement of Science (AAAS), 2021, 7 (21), pp.eabg5628. ⟨10.1126/sciadv.abg5628⟩
Science Advances, 2021, 7 (21), pp.eabg5628. ⟨10.1126/sciadv.abg5628⟩
Science Advances, American Association for the Advancement of Science (AAAS), 2021, 7 (21), pp.eabg5628. ⟨10.1126/sciadv.abg5628⟩
Science Advances, 2021, 7 (21), pp.eabg5628. ⟨10.1126/sciadv.abg5628⟩
Structures of the AVP-V2R-Gs protein complex provide molecular insights into the function of this clinically relevant target.
The antidiuretic hormone arginine-vasopressin (AVP) forms a signaling complex with the V2 receptor (V2R) and the Gs pro
The antidiuretic hormone arginine-vasopressin (AVP) forms a signaling complex with the V2 receptor (V2R) and the Gs pro
Autor:
Julien Bous, Aurelie Ancelin, Nicolas Floquet, Hélène Orcel, Joséphine Lai-Kee-Him, Stefano Trapani, Julie Saint-Paul, Hélène Déméné, Sébastien Granier, Patrick Bron, Maxime Louet, Remy Sounier, Gérald Gaibelet, Bernard Mouillac, Cedric Leyrat
Arginine-vasopressin (AVP) is a neurohypophysial peptide known as the antidiuretic hormone. It forms an active signalling complex with the V2 receptor (V2R) and the Gs protein, promoting a cAMP/PKA-dependent aquaporin insertion in apical membranes of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14a5993c6f47ec20e9d586f9877003a8
https://doi.org/10.1101/2020.12.22.424028
https://doi.org/10.1101/2020.12.22.424028
Autor:
Empar Vengut-Climent, Eleuterio Álvarez, Rocío Recio, Noureddine Khiar, Miguel López-Lázaro, José Manuel Calderón-Montaño, Hélène Orcel, Bernard Mouillac, Inmaculada Fernández
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2017, 138, pp.644-660. ⟨10.1016/j.ejmech.2017.06.056⟩
instname
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2017, 138, pp.644-660. ⟨10.1016/j.ejmech.2017.06.056⟩
A library of 5-arylthiosubstituted 2-amino-4,6-diaryl-3-cyano-4H-pyrans has been synthesized as a new family of non-peptide NK1 receptor ligands by a one-pot cascade process. Their biological effects via interaction with the NK1 receptor were experim
Autor:
Sanja Perkovska, Hélène Orcel, Bernard Mouillac, Thierry Durroux, Maria-Angeles Ventura, Floriane Hemery, Nadine Laguette, Christiane Mendre, C Méjean, Juan Li, Mohammed Akli Ayoub, Maithé Corbani
Publikováno v:
Traffic
Traffic, Wiley, 2018, 19 (1), pp.58-82. ⟨10.1111/tra.12535⟩
Traffic, Wiley, 2018, 19 (1), pp.58-82. ⟨10.1111/tra.12535⟩
International audience; The signaling pathway of G protein-coupled receptors is strongly linked to their trafficking profile. Little is known about the molecular mechanisms involved in the vasopressin receptor V1b subtype (V1b R) trafficking and its
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5abf872dbdcff73ec30e505464ac27e3
https://hal.archives-ouvertes.fr/hal-02391128
https://hal.archives-ouvertes.fr/hal-02391128
Autor:
Sabrina Sigismeau, Loïc Quinton, Hélène Orcel, Jérôme Nevoux, Nicolas Gilles, Steve Peigneur, Ralph Witzgall, Justyna Ciolek, Laura Droctové, Enrico A. Stura, Gilles Mourier, Fabrice Beau, Edwin De Pauw, Marc Lombès, Laura Vera, Denis Servent, Helen Reinfrank, Jan Tytgat, Bernard Mouillac, Christiane Mendre, Say Viengchareun
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2017, 114 (27), pp.7154-7159. ⟨10.1073/pnas.1620454114⟩
Proceedings of the National Academy of Sciences of the United States of America, 2017, 114 (27), pp.7154-7159. ⟨10.1073/pnas.1620454114⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2017, 114 (27), pp.7154-7159. ⟨10.1073/pnas.1620454114⟩
Proceedings of the National Academy of Sciences of the United States of America, 2017, 114 (27), pp.7154-7159. ⟨10.1073/pnas.1620454114⟩
International audience; Polycystic kidney diseases (PKDs) are genetic disorders that can cause renal failure and death in children and adults. Lowering cAMP in cystic tissues through the inhibition of the type-2 vasopressin receptor (V2R) constitutes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96c2bc7082628374c5642168569897e5
https://hal.umontpellier.fr/hal-02050051
https://hal.umontpellier.fr/hal-02050051
Autor:
Laura Albizu, Alain Rabié, Thierry Durroux, Bernard Mouillac, Christiane Mendre, Hervé Ansanay, Sanja Perkovska, Hélène Orcel
Publikováno v:
Molecular Pharmacology
Molecular Pharmacology, American Society for Pharmacology and Experimental Therapeutics, 2009, 75 (3), pp.637-47. ⟨10.1124/mol.108.049031⟩
Molecular Pharmacology, 2009, 75 (3), pp.637-47. ⟨10.1124/mol.108.049031⟩
Molecular Pharmacology, American Society for Pharmacology and Experimental Therapeutics, 2009, 75 (3), pp.637-47. ⟨10.1124/mol.108.049031⟩
Molecular Pharmacology, 2009, 75 (3), pp.637-47. ⟨10.1124/mol.108.049031⟩
International audience; We show here that the rat vasopressin V(1b) receptor simultaneously activates both the G(q/11)-inositol phosphate (IP) and G(s)-cAMP pathways when transiently expressed in Chinese hamster ovary, human embryonic kidney (HEK) 29