Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Thomas H. Large"'
Autor:
Una Campbell, Kerry L. Spear, Taleen Hanania, Seth C. Hopkins, Liming Shao, John Emmerson Campbell, Emer Leahy, Philip Jones, Nina Dedic, Kenneth S. Koblan, Thomas H. Large, Robert Lew
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics. 371:1-14
For the past 50 years, the clinical efficacy of antipsychotic medications has relied on blockade of dopamine D2 receptors. Drug development of non-D2 compounds, seeking to avoid the limiting side effects of dopamine receptor blockade, has failed to d
Autor:
Nina, Dedic, Philip G, Jones, Seth C, Hopkins, Robert, Lew, Liming, Shao, John E, Campbell, Kerry L, Spear, Thomas H, Large, Una C, Campbell, Taleen, Hanania, Emer, Leahy, Kenneth S, Koblan
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 371(1)
For the past 50 years, the clinical efficacy of antipsychotic medications has relied on blockade of dopamine D
Autor:
Q. Kevin Fang, John Emmerson Campbell, Una Campbell, Philip Jones, Noel Aaron Powell, Vadim Alexandrov, Emily Sabath, Liming Shao, Kerry L. Spear, Irene Morganstern, Thomas H. Large, Taleen Hanania, Hua M. Zhong
Publikováno v:
MedChemComm. 7:1093-1101
Phenotypic drug discovery (PDD) is increasingly being recognized as a viable compliment to target-based drug discovery (TDD). By measuring functional changes, typically at a systems level, PDD can facilitate the identification of compounds having a d
Publikováno v:
ASSETS
With millions of players worldwide, Minecraft has become a rich context for playing, socializing and learning for children. However, as is the case with many video games, players must rely heavily on vision to navigate and participate in the game. We
Publikováno v:
Lecture Notes in Computer Science ISBN: 9783319938455
AIED (2)
AIED (2)
In this paper, we propose that the artificial intelligence in education (AIED) community lead the charge in leveraging multimodal interfaces, in conjunction with artificial intelligence, to advance learning interfaces and experiences that are more in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::effc6ebc5281e51ff2f6278db17b1b9b
https://doi.org/10.1007/978-3-319-93846-2_73
https://doi.org/10.1007/978-3-319-93846-2_73
Autor:
Michael Klimas, David Borsook, Alexandre Coimbra, David Bleakman, Richard Hargreaves, Lino Becerra, Jaymin Upadhyay, Jeffrey L. Evelhoch, William Z. Potter, Richard Baumgartner, Smriti Iyengar, Thomas H. Large, Adam J. Schwarz, Edward George
Publikováno v:
Drug Discovery Today. 17:964-973
Substance P (SP) and neurokinin-1 receptors (NK-1R) are localized within central and peripheral sensory pain pathways. The roles of SP and NK-1R in pain processing, the anatomical distribution of NK-1R and efficacy observed in preclinical pain studie
Autor:
Julie Anderson, Richard Hargreaves, David Borsook, Jordan Lemme, David Bleakman, Jaymin Upadhyay, Lino Becerra, Jeffrey L. Evelhoch, Thomas H. Large
Publikováno v:
Journal of neuroscience methods. 253
To date, the blood oxygenated-level dependent (BOLD) functional magnetic resonance imaging (fMRI) technique has enabled an objective and deeper understanding of pain processing mechanisms embedded within the human central nervous system (CNS). In ord
Autor:
G. Erik Jagdmann, Joseph P. Tizzano, David O. Callagaro, Darryle D. Schoepp, Michael P. Johnson, Thomas H. Large, James A. Monn, Thomas C. Britton, Melvyn Baez
Publikováno v:
Journal of Medicinal Chemistry. 46:3189-3192
This report describes recently discovered novel allosteric modulators of metabotropic glutamate2 (mGlu2) receptors. These pyridylmethylsulfonamides (e.g., 3) potentiate glutamate, shifting agonist potency by 2-fold. This effect was specific for mGlu2
Autor:
Q. K. Fang, Lawrence Chun, Thomas H. Large, Loredano Pollegioni, Michelle L. R. Heffernan, Larry W. Hardy, Ryan T. Terry-Lorenzo, Scott P. Brown, M. A. Orsini, Kerry L. Spear
Publikováno v:
Bioscience Reports, Vol 34, Iss 4, p e00133 (2014)
Bioscience Reports
Bioscience Reports
The NMDAR (N-methyl-D-aspartate receptor) is a central regulator of synaptic plasticity and learning and memory. hDAAO (human D-amino acid oxidase) indirectly reduces NMDAR activity by degrading the NMDAR co-agonist D-serine. Since NMDAR hypofunction
Publikováno v:
Experimental Neurology. 148:558-567
Growth factors, including members of the neurotrophin family, are expressed by neuronal and glial elements following injury to the CNS. In order to assess the capacity for glial cells to respond to neurotrophins at sites of chronic injury, full-lengt