Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Yaw Senyah"'
Autor:
Yaw Senyah, Richard Bruce Lamptey
Publikováno v:
Library & Archival Security. 24:83-102
This case study aims at a critical examination of the security risks to which staff of Kwame Nkrumah University of Science and Technology (KNUST) Library are exposed and measures put in place to deal with them. It also assesses the personal safety me
Autor:
Salituro Francesco G, Vicki L. Taylor, Barry W. Siegel, Bruce M. Baron, John H. Kehne, Yaw Senyah, Harrison Boyd L, H.Steven White, Paul L.M. Van Giersbergen, Phillip L. Nyce, Christopher J. Schmidt, Michael Murawsky, Gina M. Fadayel, Timothy C. McCloskey
Publikováno v:
European Journal of Pharmacology. 323:181-192
MDL 105,519, ( E )-3-(2-phenyl-2-carboxyethenyl)-4,6-dichloro-1 H -indole-2-carboxylic acid, is a potent and selective inhibitor of [ 3 H]glycine binding to the NMDA receptor. MDL 105,519 inhibits NMDA ( N -methyl- d -aspartate)-dependent responses i
Autor:
M. A. Staeger, Yaw Senyah, Miller Francis P, Timothy C. McCloskey, Ann Marie L. Ogden, Herbert J. Ketteler, John M. Kane, John H. Kehne, Dalton Christopher R, P. A. Chmielewski, Mark W. Dudley, Jerry A. Miller
Publikováno v:
ChemInform. 25
Autor:
Michal Arad, Jeanne Stemmelin, Caroline Cohen, Yaw Senyah, Beth Borowsky, Philippe Pichat, Stevens Rachel, Amaya De Levie, Segev Barak, Odessa Giardino, Guy Griebel, Geoffrey B. Varty, Robert E. Featherstone, Ina Weiner, Mark D. Black, Nancy Rogacki
Publikováno v:
Psychopharmacology. 215(1)
The psychotomimetic effects of cannabis are believed to be mediated via cannabinoid CB1 receptors. Furthermore, studies have implicated CB1 receptors in the pathophysiology of schizophrenia.These studies investigated the effects of the CB1 receptor a
Autor:
John M. Kane, Yaw Senyah, Timothy C. McCloskey, Herbert J. Ketteler, John H. Kehne, Michael G. Palfreyman
Publikováno v:
Neuroscience letters. 147(1)
Disrupted glycinergic inhibition in the brainstem and spinal cord may contribute to some of the alterations in reflex control seen in patients with spastic disorders. MDL 27,531, which acts functionally like a glycine agonist in its capacity to selec
Autor:
Ann Marie Ogden, John H. Kehne, John M. Kane, Stephen F. Chaney, Donald L. Braun, Miller Francis P, Michael G. Palfreyman, Mark W. Dudley, Abdulmuniem Abdallah, Herbert J. Ketteler, Yaw Senyah
1. Strychnine-sensitive glycine receptors are primarily localized in the brainstem and spinal cord where they are the major mediators of postsynaptic inhibition. A compound which acts functionally like a glycine receptor agonist would be potentially
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44a2f43190754ee7179cb6781f0673df
https://europepmc.org/articles/PMC1907658/
https://europepmc.org/articles/PMC1907658/