Zobrazeno 1 - 10
of 29
pro vyhledávání: '"A. L. Jaton"'
Autor:
A. L. Jaton, P. Gull, H. O. Kalkman, D. Hoyer, C. Rüdeberg, Stephan Urwyler, A. K. Dixon, R. Markstein
Publikováno v:
Journal of Neural Transmission. 103:17-30
SDZ GLC-756, a novel octahydrobenzo[g]quinoline derivative, is equipotent in displacing [3H]SCH23390 from dopamine D1 receptors and [3H]205-501 from dopamine D2 receptor binding sites. It blocks dopamine sensitive adenylate cyclase with the same pote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::662d64fbe6528d92a2cebcd1eb4f20b2
https://doi.org/10.1007/bf01292613
https://doi.org/10.1007/bf01292613
Autor:
Van Nguyen-Tran, Sarah P. Gerber, S. Renee Commerford, Peter McNamara, Chad Schwartzkopf, Beatriz N. Dardik, Yu Alice Chen, Jesper Gromada, Frederique Chaperon, Hong Liu, Sandra Teixeira, Xiaohui He, H. Martin Seidel, Anneliese L. Jaton, Thomas Hollenbeck, Laura H. Jacobson
Publikováno v:
Naunyn-Schmiedeberg's archives of pharmacology. 384(6)
Pharmacologic antagonism of cannabinoid 1 receptors (CB1 receptors) in the central nervous system (CNS) suppresses food intake, promotes weight loss, and improves the metabolic profile. Since the CB1 receptor is expressed both in the CNS and in perip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f77bce869ee802cf335483dc176bafc2
https://pubmed.ncbi.nlm.nih.gov/21947251
https://pubmed.ncbi.nlm.nih.gov/21947251
Autor:
H. P. Weber, A. R. Dravid, J. M. Vigouret, H. O. Kalkman, A. Hofmann, A. L. Jaton, J. Nozulak, Malcolm D. Walkinshaw
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c43ee61ed74d5129a0ace578dbcc3b55
https://doi.org/10.1002/chin.199223193
https://doi.org/10.1002/chin.199223193
Autor:
Anton Neuenschwander, Stephan A. Kaeser, Tristan Bolmont, Paolo Paganetti, Jorge Ghiso, Claudia Schaefer, Dominic M. Walsh, Paul M. Mathews, Melanie Meyer-Luehmann, Jean-Marie Vigouret, Ellen Kilger, Lary C. Walker, Mathias Jucker, Dorothee Abramowski, Peter Frey, Janaky Coomaraswamy, Anneliese L. Jaton, Matthias Staufenbiel
Publikováno v:
Science (New York, N.Y.). 313(5794)
Protein aggregation is an established pathogenic mechanism in Alzheimer's disease, but little is known about the initiation of this process in vivo. Intracerebral injection of dilute, amyloid-beta (Abeta)-containing brain extracts from humans with Al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bffd1f7afc980b49144699f272abccd9
https://pubmed.ncbi.nlm.nih.gov/16990547
https://pubmed.ncbi.nlm.nih.gov/16990547
Publikováno v:
Schizophrenia Research. 60:357
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5038fc0d24b8ef60d2d5e74b5742e21
https://doi.org/10.1016/s0920-9964(03)80170-6
https://doi.org/10.1016/s0920-9964(03)80170-6
Publikováno v:
Journal of Neural Transmission. 69:179-199
CK 204-933 displaces [3H]dopamine and [3H]spiperone with high affinity from D-1 and D-2 recognition sites in membranes of calf caudate. Results from functional in vitro tests suggest that it is a partial agonist at D-1 receptors and an antagonist at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::995a873aaedbdfbb7c287ac35d1f889d
https://doi.org/10.1007/bf01244340
https://doi.org/10.1007/bf01244340
Publikováno v:
Hormone research. 9(4)
The effects of drugs which interfere with alpha-adrenergic and dopaminergic mechanisms, involved in GH and PRL secretion, have been analyzed in urethane anesthetized rats. Clonidine induced a dose-dependent release of GH (0.0032--0.1 mg/kg i.v.) as w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::859ed4732a424cb0911157b8a8ed82be
https://pubmed.ncbi.nlm.nih.gov/669571
https://pubmed.ncbi.nlm.nih.gov/669571
Autor:
A L, Jaton, J M, Vigouret
Publikováno v:
Journal de pharmacologie. 16
Rats were trained in 4 consecutive trials to obtain a liquid reward in a labyrinth system. Drugs were given s.c. 2-4 hours before each trial, and starting time (ST), running time (RT) and number of errors (NE) were recorded on the fourth trial. Hyder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2947b566a122b94cde804602b9044ec4
https://pubmed.ncbi.nlm.nih.gov/4094447
https://pubmed.ncbi.nlm.nih.gov/4094447
Publikováno v:
British journal of pharmacology. 56(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a6dea8dfe5772f8c8c9752342796d875
https://pubmed.ncbi.nlm.nih.gov/944059
https://pubmed.ncbi.nlm.nih.gov/944059