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Plos One|August 6, 2011
Impaired cognitive function and altered hippocampal synapse morphology in mice lacking Lrrtm1, a gene associated with schizophreniaNoriko Takashima, Yuri S Odaka, Kazuto Sakoori, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 8, 2009
X11-like protein deficiency is associated with impaired conflict resolution in miceYoshitake Sano, Veravej G Ornthanalai, Kazuyuki Yamada, et al.
Glia|June 15, 2010
Glycosphingolipid synthesis in cerebellar Purkinje neurons: roles in myelin formation and axonal homeostasisShun Watanabe, Shogo Endo, Eriko Oshima, et al.
Neuroscience Research|March 18, 2008
Behavioral and gene expression analyses of Wfs1 knockout mice as a possible animal model of mood disorderTadafumi Kato, Mizuho Ishiwata, Kazuyuki Yamada, et al.
The EMBO Journal|November 7, 2009
Social isolation stress induces ATF-7 phosphorylation and impairs silencing of the 5-HT 5B receptor geneToshio Maekawa, Seungjoon Kim, Daisuke Nakai, et al.
Biochemical and Biophysical Research Communications|August 16, 2011
Comparative characterization of GPRC5B and GPRC5CLacZ knockin mice; behavioral abnormalities in GPRC5B-deficient miceTakamitsu Sano, Yeon-Jeong Kim, Eriko Oshima, et al.
Frontiers in Molecular Neuroscience|May 26, 2022
Leucine-Rich Repeats and Transmembrane Domain 2 Controls Protein Sorting in the Striatal Projection System and Its Deficiency Causes Disturbances in Motor Responses and Monoamine DynamicsMisato Ichise, Kazuto Sakoori, Kei-Ichi Katayama, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 19, 2011
ERK2 contributes to the control of social behaviors in miceYasushi Satoh, Shogo Endo, Takahiro Nakata, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 9, 2013
Rines E3 ubiquitin ligase regulates MAO-A levels and emotional responsesMiyuki Kabayama, Kazuto Sakoori, Kazuyuki Yamada, et al.
Annals of Clinical and Translational Neurology|December 26, 2014
Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletionsSatoshi Fuke, Mizue Kametani, Kazuyuki Yamada, et al.
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