Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Laura B. Rosen"'
Autor:
Patricio O’Donnell, Cheng Dong, Venkatesha Murthy, Mahnaz Asgharnejad, Xiaoming Du, Ann Summerfelt, Hong Lu, Lin Xu, Jens R. Wendland, Eduardo Dunayevich, Derek L. Buhl, Robert Litman, William P. Hetrick, L. Elliot Hong, Laura B. Rosen
Publikováno v:
Neuropsychopharmacology. 48:1052-1059
Several attempts have been made to enhance N-methyl-D-aspartate (NMDA) receptor function in schizophrenia, but they have yielded mixed results. Luvadaxistat, a D-amino acid oxidase (DAAO) inhibitor that increases the glutamate co-agonist D-serine lev
Autor:
Christopher Lines, M. Gail Murphy, Chantal Mahon, John J. Renger, Hong Sun, John A. Wagner, Kate Mostoller, W. Joseph Herring, Catherine MacLeod, Gary G. Kay, Lingling Han, Valerie Schulz, Junshui Ma, Kevin R. Brown, Laura B. Rosen
Publikováno v:
The Journal of Clinical Pharmacology. 53:1294-1302
Histaminergic neurons are regulators of the sleep-wake cycle. We evaluated the alerting effects of MK-7288 (10, 20 mg), a novel histamine-3 receptor inverse agonist (H3RIA), along with modafinil (200 mg), a standard treatment, in a randomized, double
Autor:
Scott A. Monk, Laura B. Rosen, Alan R. Kugler, Pankaj Daga, Jamie Mullen, Naidong Ye, David M. Bender, Margaret Minkwitz
Publikováno v:
Clinical Pharmacology in Drug Development
The relative bioavailability of lanabecestat administered as 2 tablet formulations versus an oral solution was investigated. This phase 1 single‐center, open‐label, randomized, 3‐period crossover study involved healthy male and nonfertile femal
Autor:
Samantha Budd Haeberlein, Alan R. Kugler, Tina Olsson, Robert C. Alexander, Naidong Ye, Muir Russell, Justine Maltby, Laura B. Rosen, Susanna Eketjäll, Ronald Goldwater, Gvido Cebers, Larry Ereshefsky, David Han
Publikováno v:
Journal of Alzheimer's disease : JAD. 55(3)
AZD3293 (LY3314814) is a promising new potentially disease-modifying BACE1 (β-secretase) inhibitor in Phase III clinical development for the treatment of Alzheimer's disease. Reported here are the first two Phase I studies: (1) a single ascending do
Autor:
Anthony L. Gotter, Vladimir Svetnik, Arie Struyk, Pamela L. Tannenbaum, Mark S. Forman, Nicole Calder, Susan L. Garson, John J. Renger, Christopher J. Winrow, Joanne Stevens, Anthony J. Roecker, Laura B. Rosen, W. Joseph Herring, Ka Lai Yee, Inge De Lepeleire, Xiaodong Li, Paul J. Coleman, Steven V. Fox, Charles M. Harrell
Publikováno v:
Scientific Reports
Orexin neuropeptides regulate sleep/wake through orexin receptors (OX1R, OX2R); OX2R is the predominant mediator of arousal promotion. The potential for single OX2R antagonism to effectively promote sleep has yet to be demonstrated in humans. MK-1064
Autor:
Chantal Mahon, Terence G. Hamill, K Butterfield, Guy Bormans, John A. Wagner, Michel Koole, Fang Liu, J De Hoon, Richard Hargreaves, P Zappacosta, I De Lepeleire, P. D Mozley, Ruben Declercq, W Xie, Yang Liu, Inge Derdelinckx, K. Van Laere, M. G Murphy, Laura B. Rosen, Daniel Tatosian, Craig R. Shadle, S M Sanabria Bohorquez
Publikováno v:
Clinical Pharmacology & Therapeutics. 92:243-250
The type 1 neurokinin receptor (NK1R) antagonist aprepitant and its i.v. prodrug fosaprepitant have been approved for prevention of acute and delayed nausea and vomiting associated with chemotherapy. This study evaluated the magnitude and duration of
Autor:
John J. Renger, John Palcza, Nagaaki Sato, Robert Iannone, A Buntinx, B R Bloem, R H Hargreaves, Rik C. Schoemaker, K S Koblan, Laura B. Rosen, Adam F. Cohen, J.M.A. van Gerven, Chodakewitz Jeffrey A, Keith Gottesdiener, Remco W. M. Zoethout, Sabrina Marsilio, Shigeru Tokita, Gail Murphy, K Van Dyck, E D Louis
Publikováno v:
Journal of Psychopharmacology, 26, 2, pp. 292-302
Journal of Psychopharmacology, 26(2), 292-302
Journal of Psychopharmacology, 26, 292-302
Journal of Psychopharmacology, 26(2), 292-302
Journal of Psychopharmacology, 26, 292-302
Item does not contain fulltext Essential tremor (ET) is a common movement disorder. Animal studies show that histaminergic modulation may affect the pathological processes involved in the generation of ET. Histamine-3 receptor inverse agonists (H3RIA
Autor:
Hong, Sun, Catherine, MacLeod, Kate, Mostoller, Chantal, Mahon, Lingling, Han, John J, Renger, Junshui, Ma, Kevin R, Brown, Valerie, Schulz, Gary G, Kay, W Joseph, Herring, Christopher, Lines, Laura B, Rosen, M Gail, Murphy, John A, Wagner
Publikováno v:
Journal of clinical pharmacology. 53(12)
Histaminergic neurons are regulators of the sleep-wake cycle. We evaluated the alerting effects of MK-7288 (10, 20 mg), a novel histamine-3 receptor inverse agonist (H3RIA), along with modafinil (200 mg), a standard treatment, in a randomized, double
Autor:
Eric Mangin, Hong Sun, Junshui Ma, Gail Murphy, Ka Lai Yee, Xiaodong Li, Laura B. Rosen, Darren Wilbraham, Christopher Lines, Nicole Lewis, William P. Kennedy, Chodakewitz Jeffrey A, Nicole Calder, Susan Ermlich
Publikováno v:
Sleep. 36(2)
Study objectives Suvorexant (MK-4305) is an orexin receptor antagonist being developed for the treatment of insomnia. This report describes the effects of nighttime administration of suvorexant on polysomnography (PSG) sleep parameters in healthy you
Autor:
Laura B. Rosen, Michael E. Greenberg
Publikováno v:
Proceedings of the National Academy of Sciences. 93:1113-1118
To understand the mechanisms by which electrical activity may generate long-term responses in the nervous system, we examined how activation of voltage-sensitive calcium channels (VSCCs) can stimulate the Ras/mitogen-activated protein kinase (MAPK) s