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Journal of Neurotrauma|May 28, 2010
Glial cell-mediated deterioration and repair of the nervous system after traumatic brain injury in a rat model as assessed by positron emission tomographyIwae Yu, Motoki Inaji, Jun Maeda, et al.
Synapse (New York, N.Y.)|June 29, 2007
Progressive changes of pre- and post-synaptic dopaminergic biomarkers in conscious MPTP-treated cynomolgus monkeys measured by positron emission tomographyYuji Nagai, Shigeru Obayashi, Kiyoshi Ando, et al.
Psychopharmacology|September 20, 2007
Neurobehavioral protection by single dose l-deprenyl against MPTP-induced parkinsonism in common marmosetsKiyoshi Ando, Jun Maeda, Motoki Inaji, et al.
Synapse (New York, N.Y.)|August 19, 2003
Effects of endogenous agonists, glycine and D-serine, on in vivo specific binding of [11C]L-703,717, a PET radioligand for the glycine-binding site of NMDA receptorsTerushi Haradahira, Takashi Okauchi, Jun Maeda, et al.
Bioorganic & Medicinal Chemistry|May 22, 2003
N-[18F]fluoroethyl-4-piperidyl acetate ([18F]FEtP4A): A PET tracer for imaging brain acetylcholinesterase in vivoMing-Rong Zhang, Kenji Furutsuka, Jun Maeda, et al.
Biochemical and Biophysical Research Communications|December 19, 2020
Alleviation of the chronic stress response attributed to the antioxidant and anti-inflammatory effects of electrolyzed hydrogen waterDi Hu, Danxi Li, Mika Shigeta, et al.
Nuclear Medicine Communications|February 22, 2005
In-vivo PET imaging of inducible D2R reporter transgene expression using [11C]FLB 457 as reporter probe in living ratsWinn Aung, Takashi Okauchi, Masaaki Sato, et al.
Biological & Pharmaceutical Bulletin|April 2, 2004
Synthesis of 11C-labelled bis(phenylalkyl)amines and their in vitro and in vivo binding properties in rodent and monkey brainsShigeki Sasaki, Fumie Kurosaki, Terushi Haradahira, et al.
Synapse (New York, N.Y.)|March 4, 2011
In vivo and in vitro imaging of I₂ imidazoline receptors in the monkey brainKazunori Kawamura, Jun Maeda, Akiko Hatori, et al.
Nuclear Medicine and Biology|February 2, 2002
Syntheses and pharmacological evaluation of two potent antagonists for dopamine D4 receptors: [11C]YM-50001 and N-[2-[4-(4-Chlorophenyl)-piperizin-1-yl]ethyl]-3-[11C]methoxybenzamideMing-Rong Zhang, Terushi Haradahira, Jun Maeda, et al.
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