Oral

[1O07m-1] Neurodevelopment Disorder

Wed. Jul 29, 2020 9:00 AM - 10:00 AM Room 7

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[1O07m-1-01] Genetic dissection identifies Necdin as a driver gene in 15q11-q13 duplication syndrome

*KOTA TAMADA^1,2, Keita Fukumoto^1,2, Tsuyoshi Toya^1,3, Nobuhiro Nakai¹, Janak Awasthi^1,4, Shinji Tanaka⁵, Shigeo Okabe⁵, Spitz Francois⁶, Toru Takumi^1,2,4,7 (1. Lab. for Mental Biology, RIKEN CBS, 2. Grad Sch Biomed Sci, Hiroshima Univ, 3. Grad Sch Pharm, Keio Univ, 4. Grad Sch Sci and Engineering, Saitama Univ, 5. Dept Cell Neurobiol, Grad Sch Med, Univ of Tokyo, Tokyo, Japan, 6. Institut Pasteur, Paris, France, 7. Grad Sch Med, Kobe Univ)

[1O07m-1-02] A viral based treatment of synaptic and behavioral deficits of the mouse with an autism associated mutation of neuroligin3

*TAKUMA MORI¹, Xueshan Cao², Taiga Kurihara², Emi Suzuki², Guo Qi², Katsuhiko Tabuchi^1,2 (1. Inst. Biomedical Sciences, Shinshu Unviersity, 2. Dept. Mol. Cell. Physiol., Shinshu University, Nagano, Japan)

[1O07m-1-03] A deficiency of CAPS2 in mice causes a deficit in release of social neuropeptide oxytocin, resulting in impaired social behavior

Awardees for Travel Award

*Shuhei Fujima¹, Ryosuke Yamaga¹, Haruka Minami¹, Rina Maniwa¹, Yo Shinoda², Manabu Abe³, Kenji Sakimura³, Yoshitake Sano¹, Teiichi Furuichi¹ (1. Dept. of Appl. Biol. Sci., Fac. Of Sci. and Technol., Tokyo Univ. of Sci., Chiba, Japan, 2. Dept. of Env. Health, Sch. Of Pharm., Tokyo Univ. of Pharm. And Life Sci., Hachioji, Japan, 3. Dept. of Cellular Neurobiology. BRI, Niigata Univ., Niigata, Japan)

[1O07m-1-04] The whole exon sequence trio analyses of Preserved speech variant of Rett syndrome patient.

*Kenji Orimoto¹, Toyojiro Matsuishi², Kotaro Yuge³, Shin-ichi Horike⁴, Makiko Meguro⁴ (1. Dept Gen Med, Fureai Higashi-totsuka Hospital, Kangawa, Japan, 2. Cogn Mol Res Inst of Brain Dis, Univ of Kurume University , 3. Dept Pediatr, Sch of Med, Univ of Kurume, 4. Div of Func Genomics, Adv Sci Res Ctr, Univ Of Kanazawa)

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