Zobrazeno 1 - 10
of 31
pro vyhledávání: '"E. Heuillet"'
Autor:
F. Petitet, M. Saffroy, E. Heuillet, Jacques Glowinski, Jean-Claude Beaujouan, Yvette Torrens
Publikováno v:
British Journal of Pharmacology. 108:793-800
1. This study was undertaken to compare the potency and selectivity of the nonpeptide (RP 67580, (+/-)-CP-96,345 and its chloro-derivative [(+/-)-cis-3-(2-chlorobenzylamino)-2-benzhydrylquinuclidine] (CP-C1)) and peptide (GR 71,251 and spantide) neur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54e345fcbb520524d1d799255d26eddc
https://doi.org/10.1111/j.1476-5381.1993.tb12880.x
https://doi.org/10.1111/j.1476-5381.1993.tb12880.x
Publikováno v:
Carcinogenesis. 11:1175-1182
The early stages of the carcinogenic process induced by aflatoxin B1 (AFB1) in rat liver during 24 weeks of feeding and the resulting tumours have been studied with respect to cytokeratin (CK) expression. A previously uncharacterized monoclonal antib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbd94e3ec7689165658c843e3e365b1e
https://doi.org/10.1093/carcin/11.7.1175
https://doi.org/10.1093/carcin/11.7.1175
Autor:
Adam Doble, Jean-Luc Malleron, Jacques Lavayre, Serge Mignani, Gervais Neliat, François Petitet, E. Heuillet, Jean-Charles Blanchard
Publikováno v:
European journal of pharmacology. 314(1-2)
The dopamine D4 receptor is a potential target for novel antipsychotic drugs. Most available compounds with affinity for the dopamine D4 receptor also bind to dopamine D2 receptors. This report describe the affinity of the 5-HT2A receptor antagonist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3380721b69fe0984ab180271b23036ff
https://pubmed.ncbi.nlm.nih.gov/8957240
https://pubmed.ncbi.nlm.nih.gov/8957240
Autor:
Brigitte Amiranoff, Hervé Dubois, Adam Doble, Zakia Bouaiche, Jean Menager, Jean-Charles Blanchard, Philippe Dugay, Noelli Munoz, Jacques Lavayre, Andre Crespo, E. Heuillet
Publikováno v:
European journal of pharmacology. 269(2)
The human galanin receptor has been characterized pharmacologically from the Bowes melanoma cell line. Using porcine [125I]galanin as the radioligand, a single population of non-interacting high-affinity binding sites (KD = 0.05 ± 0.01 nM; Bmax = 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6932f653c1137314f9e6e27e6857b301
https://pubmed.ncbi.nlm.nih.gov/7531645
https://pubmed.ncbi.nlm.nih.gov/7531645
Autor:
L, Pradier, J, Ménager, J, Le Guern, M D, Bock, E, Heuillet, V, Fardin, C, Garret, A, Doble, J F, Mayaux
Publikováno v:
Molecular pharmacology. 45(2)
The hexapeptide [pGlu6,Pro9]substance P (SP)6-11, septide, has been shown to be an agonist as potent as SP in eliciting smooth muscle contraction in several in vitro preparations, while being a poor competitor of labeled SP binding. These results, as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f50f05a170ec8a8fba9378712f49978b
https://pubmed.ncbi.nlm.nih.gov/7509440
https://pubmed.ncbi.nlm.nih.gov/7509440
Publikováno v:
Journal of neurochemistry. 61(5)
— In the human astrocytoma cell line U 373 MG, application of substance P (SP) leads to a transient increase in cytosolic calcium concentration and to a biphasic current response in voltage-clamped cells. Using these two functional assays we have c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dd432b7fca1a153b00c9de9afb94d37
https://pubmed.ncbi.nlm.nih.gov/7693869
https://pubmed.ncbi.nlm.nih.gov/7693869
Autor:
J. Ménager, E. Heuillet
Publikováno v:
Neuropeptides. 26:26-27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c037a120f2e4bc1e2a1c840d8e963024
https://doi.org/10.1016/0143-4179(94)90200-3
https://doi.org/10.1016/0143-4179(94)90200-3
Autor:
T. Rouyer, Michel Reibaud, M. Pasquet, Assunta Imperato, E. Heuillet, M.C.D. Dubroeucq, F. Perrot
Publikováno v:
European Neuropsychopharmacology. 7:S167
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d635cabac46623084a58e5e5863609b6
https://doi.org/10.1016/s0924-977x(97)88551-3
https://doi.org/10.1016/s0924-977x(97)88551-3
Autor:
V. Fardin, A. Carruette, J. Menager, M. Bock, O. Flamand, F. Foucault, E. Heuillet, S.M. Moussaoui, M. Tabart, J.F. Peyronel, C. Garret
Publikováno v:
Neuropeptides. 26:34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffab2a1cfb88956e75c20dfc23262d14
https://doi.org/10.1016/0143-4179(94)90218-6
https://doi.org/10.1016/0143-4179(94)90218-6
Autor:
A. Doble, J.-C. Blanchard, P. Dugay, E. Heuillet, B. Amiranoff, Z. Boualche, N. Munoz, I. Gravier, A. Crespo, J. Ménager, J. Lavayre, F.F. Clerc
Publikováno v:
Neuropeptides. 24:242
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3983d23c0e1215f850d2b4f38cbce163
https://doi.org/10.1016/0143-4179(93)90266-d
https://doi.org/10.1016/0143-4179(93)90266-d