Zobrazeno 1 - 4
of 4
pro vyhledávání: '"MESH: Receptors, sigma"'
Autor:
E. E. Baulieu, François P. Monnet, Marie-Pierre Morin-Surun, T. Collin, Monique Denavit-Saubié
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, 1999, 96 (14), pp.8196-9
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 1999, 96 (14), pp.8196-9
Most physiological effects of σ 1 receptor ligands are sensitive to pertussis toxin, suggesting a coupling with cell membrane-bound G proteins. However, the cloning of the σ 1 receptor has allowed the identification of an intracellular protein anch
Autor:
Vandier Christophe, Besson Pierre, Ouadid-Ahidouch Halima, Ahidouch Ahmed, Soriani Olivier, Le Guennec Jean-Yves
Publikováno v:
Recent Pat Anticancer Drug Discov
Recent Pat Anticancer Drug Discov, 2007, 2 (3), pp.189-202
Recent Patents Anticancer Drug Discov
Recent Patents Anticancer Drug Discov, 2007, 2 (3), pp.189-202
Recent Pat Anticancer Drug Discov, 2007, 2 (3), pp.189-202
Recent Patents Anticancer Drug Discov
Recent Patents Anticancer Drug Discov, 2007, 2 (3), pp.189-202
International audience; Cancer is one of the leading causes of mortality in the world. This is a complex disease involving many steps with proper signalling pathways. Early detection and treatment of cancers have increased survival and improved clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba7d47653b39b23e005cacb3a9fda74e
https://www.hal.inserm.fr/inserm-00662369
https://www.hal.inserm.fr/inserm-00662369
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics
Journal of Pharmacology and Experimental Therapeutics, American Society for Pharmacology and Experimental Therapeutics, 2003, 307 (2), pp.705-12. ⟨10.1124/jpet.103.053447⟩
Journal of Pharmacology and Experimental Therapeutics, American Society for Pharmacology and Experimental Therapeutics, 2003, 307 (2), pp.705-12. ⟨10.1124/jpet.103.053447⟩
International audience; Intracellular calcium concentration ([Ca2+]i) plays a major role in neuronal excitability, especially that triggered by the N-methyl-d-aspartate (NMDA)-sensitive glutamatergic receptor. We have previously shown that sigma1 rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f88ccb990423fc4ac4a777fb35c5fdaa
https://hal.archives-ouvertes.fr/hal-00374393
https://hal.archives-ouvertes.fr/hal-00374393
Autor:
Marc Poirot, Sylvie Daunes, Jean-Charles Faye, Wayne D. Bowen, Berthold J Vilner, Blandine Kedjouar, Alain Klaebe
Publikováno v:
Biochemical Pharmacology
Biochemical Pharmacology, 1999, 58, pp.1927-39
Biochemical Pharmacology, Elsevier, 1999, 58, pp.1927-39
Biochemical Pharmacology, 1999, 58, pp.1927-39
Biochemical Pharmacology, Elsevier, 1999, 58, pp.1927-39
1-Benzyl-4-(N-2-pyrrolidinylethoxy)benzene (PBPE) is a cytotoxic derivative of the antitumoral drug tamoxifen. PBPE binds with high-affinity and specificity to the microsomal antiestrogen-binding site (AEBS). PBPE, as well as some other high-affinity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c87edff330fa8a49b4bf7e6243c2d7a
https://www.hal.inserm.fr/inserm-00090780
https://www.hal.inserm.fr/inserm-00090780