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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 3, 2009
Mice with altered myelin proteolipid protein gene expression display cognitive deficits accompanied by abnormal neuron-glia interactions and decreased conduction velocitiesHisataka Tanaka, Jianmei Ma, Kenji F Tanaka, et al.
Plos One|March 9, 2010
Comprehensive behavioral analysis of calcium/calmodulin-dependent protein kinase IV knockout miceKeizo Takao, Koichi Tanda, Kenji Nakamura, et al.
Molecular Brain|June 5, 2014
Enhanced stability of hippocampal place representation caused by reduced magnesium block of NMDA receptors in the dentate gyrusYuichiro Hayashi, Yoko Nabeshima, Katsunori Kobayashi, et al.
Cell|July 1, 2009
Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autismJin Nakatani, Kota Tamada, Fumiyuki Hatanaka, et al.
Journal of Neurochemistry|March 2, 2022
Perturbation of monoamine metabolism and enhanced fear responses in mice defective in the regeneration of tetrahydrobiopterinKatsuya Miyajima, Yusuke Sudo, Sho Sanechika, et al.
Molecular Brain|September 23, 2008
Alpha-CaMKII deficiency causes immature dentate gyrus, a novel candidate endophenotype of psychiatric disordersNobuyuki Yamasaki, Motoko Maekawa, Katsunori Kobayashi, et al.
Brain & Development|January 13, 2021
Clinical manifestations and epilepsy treatment in Japanese patients with pathogenic CDKL5 variantsYu Kobayashi, Jun Tohyama, Yukitoshi Takahashi, et al.
Journal of Medical Genetics|March 8, 2019
Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencingKazuhiro Iwama, Takeshi Mizuguchi, Eri Takeshita, et al.
Human Mutation|November 1, 2020
Efficient detection of copy-number variations using exome data: Batch- and sex-based analysesYuri Uchiyama, Daisuke Yamaguchi, Kazuhiro Iwama, et al.
Journal of Medical Genetics|August 1, 2020
Prenatal clinical manifestations in individuals with COL4A1/2 variantsToshiyuki Itai, Satoko Miyatake, Masataka Taguri, et al.
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