Zobrazeno 1 - 10
of 149
pro vyhledávání: '"Jean Claude Meunier"'
Autor:
Andreas Zimmer, Nurulain Zaveri, Yung H. Wong, Hiroshi Ueda, John R. Traynor, Lawrence Toll, Eric J. Simon, Toni S. Shippenberg, Stefan Schulz, Philip S. Portoghese, Jean-Claude Meunier, Dominique Massot, Davide Malfacini, Lee-Yuan Liu-Chen, Mary-Jeanne Kreek, Ian Kitchen, Brigitte Kieffer, Eamonn Kelly, Stephen Husbands, Graeme Henderson, Volker Höllt, Christopher Evans, Lakshmi A. Devi, Brian M. Cox, Mark Connor, Olivier Civelli, MacDonald J. Christie, Charles Chavkin, Girolamo Caló, Michael Bruchas, Anna Borsodi
Publikováno v:
IUPHAR/BPS Guide to Pharmacology CITE. 2023
Opioid and opioid-like receptors are activated by a variety of endogenous peptides including [Met]enkephalin (met), [Leu]enkephalin (leu), β-endorphin (β-end), α-neodynorphin, dynorphin A (dynA), dynorphin B (dynB), big dynorphin (Big dyn), nocice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee9382e24df4bdd47b46cff68280622f
https://doi.org/10.2218/gtopdb/f50/2023.1
https://doi.org/10.2218/gtopdb/f50/2023.1
Autor:
Eric J. Simon, Nurulain T. Zaveri, Dominique Massot, Brian M. Cox, Lawrence Toll, Lakshmi A. Devi, Toni S. Shippenberg, Eamonn Kelly, John R. Traynor, Philip S. Portoghese, Mary Jeanne Kreek, Brigitte L. Kieffer, Hiroshi Ueda, Andreas Zimmer, Volker Höllt, Graeme Henderson, Charles Chavkin, Stephen M. Husbands, MacDonald J. Christie, Michael R. Bruchas, Mark Connor, Ian Kitchen, Girolamo Calò, Anna Borsodi, Stefan Schulz, Olivier Civelli, Jean-Claude Meunier, Lee-Yuan Liu-Chen, Yung Hou Wong, Christopher J. Evans
Publikováno v:
IUPHAR/BPS Guide to Pharmacology CITE. 2021
Opioid and opioid-like receptors are activated by a variety of endogenous peptides including [Met]enkephalin (met), [Leu]enkephalin (leu), β-endorphin (β-end), α-neodynorphin, dynorphin A (dynA), dynorphin B (dynB), big dynorphin (Big dyn), nocice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ba854d07718d1e3fc306a2322a4bbca
https://doi.org/10.2218/gtopdb/f50/2021.3
https://doi.org/10.2218/gtopdb/f50/2021.3
Autor:
Brian M. Cox, Eamonn Kelly, Girolamo Calo, Stephen M. Husbands, Mark Connor, Nurulain T. Zaveri, Jean-Claude Meunier, Anna Borsodi, Lee-Yuan Liu-Chen, Volker Höllt, Graeme Henderson, Eric J. Simon, Toni S. Shippenberg, Hiroshi Ueda, Olivier Civelli, Philip S. Portoghese, Mary Jeanne Kreek, Andreas Zimmer, MacDonald J. Christie, Yung Hou Wong, John R. Traynor, Stefan Schulz, Charles Chavkin, Brigitte L. Kieffer, Michael R. Bruchas, Ian Kitchen, Christopher J. Evans, Dominique Massot, Lawrence Toll, Lakshmi A. Devi
Publikováno v:
IUPHAR/BPS Guide to Pharmacology CITE. 2019
Opioid and opioid-like receptors are activated by a variety of endogenous peptides including [Met]enkephalin (met), [Leu]enkephalin (leu), β-endorphin (β-end), α-neodynorphin, dynorphin A (dynA), dynorphin B (dynB), big dynorphin (Big dyn), nocice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fbdce74a9095db9e72a9fe6ea0cd891
https://doi.org/10.2218/gtopdb/f50/2019.4
https://doi.org/10.2218/gtopdb/f50/2019.4
Autor:
Pascal Demange, Brice Bes, Alain Milon, Lionel Moulédous, Honoré Mazarguil, Jean-Claude Meunier, Bruno Vincent
Publikováno v:
Journal of Peptide Science. 14:1183-1194
The second extracellular loop (ECL2) of the Noc receptor has been proposed to be involved in ligand binding and selectivity. The interaction of Noc with a constrained cyclic synthetic peptide, mimicking the ECL2, has been studied using fluorescence a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12d5cf2439fd0d452231672dee0bc297
https://doi.org/10.1002/psc.1057
https://doi.org/10.1002/psc.1057
Autor:
A. Puget, Honoré Mazarguil, Jocelyne Polastron, Philippe Jauzac, Mireille Mur, Jean-Claude Meunier
Publikováno v:
Journal of Neurochemistry. 62:898-906
A human neuroblastoma cell line, SK-N-BE, was shown to express a substantial amount of opioid receptors (200-300 fmol/mg of protein). A ligand binding profile of these receptors revealed that they could belong to two distinct subtypes of delta-opioid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73ffe7fdd5e6bb0c119f3cfea7826acc
https://doi.org/10.1046/j.1471-4159.1994.62030898.x
https://doi.org/10.1046/j.1471-4159.1994.62030898.x
Publikováno v:
Hepatology. 44:844-849
The effects of the addition of clonidine to diuretics on the mobilization of ascites in the short term (diuretic response and requirement of diuretics) and the long term (readmissions for tense ascites and requirement of diuretics) were examined in p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f76aa39dfc6cfc5d57f9ea4a2b7c5d2
https://doi.org/10.1002/hep.21355
https://doi.org/10.1002/hep.21355
Autor:
Anna Magyar, Özge Gündüz, Sándor Benyhe, László Kocsis, Andás Z. Rónai, Brice Bes, Anna Borsodi, Jean Claude Meunier, Erzsébet Kató, Mahmoud Al-Khrasani, Géza Tóth, György Orosz
Publikováno v:
Regulatory Peptides. 122:199-207
In search for effective antagonist structures for the nociceptin (NOP) receptor, a number of N-acylated oligopeptides, including N-acyl tetra- and pentapeptides selective for the kappa-opioid receptor, as well as N-acyl hexapeptides bearing the Ac-Ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a199711746913aa5f3df7cc0a2ed43e9
https://doi.org/10.1016/j.regpep.2004.06.019
https://doi.org/10.1016/j.regpep.2004.06.019
Publikováno v:
Endocrinology. 145:2876-2885
To better understand opioid receptor-like 1 (ORL1) internalization, we fused the C terminus of ORL1, the nociceptin (noc) receptor, to the N terminus of a green fluorescent protein and used the fusion protein to characterize receptor endocytosis in l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f840cf89370223f9452c3f08976c5e04
https://doi.org/10.1210/en.2004-0062
https://doi.org/10.1210/en.2004-0062
Autor:
Jean-Claude Meunier, Brice Bes
Publikováno v:
Biochemical and Biophysical Research Communications. 310:992-1001
The interaction of Ac-Arg-Tyr-Tyr-Arg-Trp-Arg-NH(2) (HP1), a high-affinity partial agonist of the opioid receptor like (ORL1) receptor, has been investigated using the photo-labile analogue [p-benzoyl-L-Phe (Bpa)(2)]-HP1. In recombinant CHO cells exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::157865bc033538e094823467dec6abd3
https://doi.org/10.1016/j.bbrc.2003.09.113
https://doi.org/10.1016/j.bbrc.2003.09.113
Autor:
Jean-Claude Meunier
Publikováno v:
American Journal of PharmacoGenomics. 3:117-130
Nociceptin/orphanin FQ (noc/oFQ) is the first novel bioactive substance to have been discovered by the implementation of a functional genomics/reverse pharmacology approach. The neuropeptide was indeed identified in brain extracts as the natural liga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c74672986ef7f302809dd190ddba3f8c
https://doi.org/10.2165/00129785-200303020-00005
https://doi.org/10.2165/00129785-200303020-00005