Zobrazeno 1 - 10
of 1 029
pro vyhledávání: '"Arrang, J. M."'
Autor:
Arrang, J.‐M.1 (AUTHOR), Armand, V.1 (AUTHOR) vincent.armand@parisdescartes.fr
Publikováno v:
Pharmacology Research & Perspectives. Oct2024, Vol. 12 Issue 5, p1-9. 9p.
Akademický článek
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Publikováno v:
Journal of Neurochemistry; Jan2000, Vol. 74 Issue 1, p339-346, 8p, 3 Charts, 5 Graphs
Autor:
Benoy A; Neural Circuits Laboratory, Biosciences Institute, Newcastle University, Newcastle, UK., Ramaswamy S; Neural Circuits Laboratory, Biosciences Institute, Newcastle University, Newcastle, UK.; Theoretical Sciences Visiting Program (TSVP), Okinawa Institute of Science and Technology Graduate University, Onna, Japan.
Publikováno v:
The European journal of neuroscience [Eur J Neurosci] 2024 Aug; Vol. 60 (4), pp. 4597-4623. Date of Electronic Publication: 2024 Jul 20.
Autor:
Rouleau, A, Ligneau, X, Tardivel-Lacombe, J, Morisset, S, Gbahou, F, Schwartz, J -C, Arrang, J -M
Constitutive activity of the recombinant and native rat and human H(3) receptors (H(3)Rs) was studied using H(3)R-mediated [(35)S]GTPgamma[S] binding and [(3)H]-arachidonic acid release. Ciproxifan, an inverse agonist at the rat H(3)R (rH(3)R), decre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca7fe733a374c3618cba3cdc3853b345
https://europepmc.org/articles/PMC1573152/
https://europepmc.org/articles/PMC1573152/
Akademický článek
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Autor:
Ligneau, X, Morisset, S, Tardivel-Lacombe, J, Gbahou, F, Ganellin, C R, Stark, H, Schunack, W, Schwartz, J -C, Arrang, J -M
Starting from the sequence of the human histamine H(3) receptor (hH(3)R) cDNA, we have cloned the corresponding rat cDNA. Whereas the two deduced proteins show 93.5% overall homology and differ only by five amino acid residues at the level of the tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e456bdb37a4c3412dd79d3f00978d0de
https://europepmc.org/articles/PMC1572469/
https://europepmc.org/articles/PMC1572469/
Autor:
Séverine MORISSET, Sahm, U. G., Traiffort, E., Tardivel-Lacombe, J., Arrang, J. M., Schwartz, J. C.
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics
Journal of Pharmacology and Experimental Therapeutics, American Society for Pharmacology and Experimental Therapeutics, 1999, 288 (2), pp.590-6
ResearcherID
Journal of Pharmacology and Experimental Therapeutics, American Society for Pharmacology and Experimental Therapeutics, 1999, 288 (2), pp.590-6
ResearcherID
International audience; Clozapine and olanzapine behave as weak H3-receptor antagonists in vitro with Ki values around 1 and 50 microM, respectively. Despite these modest apparent affinities, both compounds given orally to mice, nearly doubled steady
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::35d0b07e54e10f61d33990c3fb1e62a8
https://hal.archives-ouvertes.fr/hal-00347619
https://hal.archives-ouvertes.fr/hal-00347619
Autor:
Wu, Yuxin1,2 (AUTHOR), Jensen, Niels2,3 (AUTHOR), Rossner, Moritz J.2,3 (AUTHOR), Wehr, Michael C.1,2 (AUTHOR) michael.wehr@med.uni-muenchen.de
Publikováno v:
International Journal of Molecular Sciences. May2024, Vol. 25 Issue 10, p5474. 23p.