セッション詳細
[2S06a]Connecting dots of CNV-linked structural and functional phenotypes from humans to mice
2025年7月25日(金) 14:10 〜 16:10
第6会場（301A）
オーガナイザー：Noboru Hiroi（Department of Pharmacology, UT Health San Antonio）、Carrie E Bearden（Department of Psychiatry and Behavioral Sciences, UCLA）
[2S06a-1]The development of children at high neuropsychiatric genomic risk: clinical outcomes and behavioural dimensions
*Samuel John Rupert Allen Chawner1 (1. Cardiff University)
[2S06a-2]Developmental dysconnectivity in a genetic risk model for schizophrenia
*Carrie E Bearden1, Filomena G Alvino2, Silvia Gini2, Marco Pagani2,5, David Sastre-Yugue2,6, Noemi Barsotti7, E De Guzman2, Charles Schleifer1, Alexia Stuefer2,6, Leila Kushan1, Caterina Montani2, Alberto Galbusera2, Francisco Papaleo8,3, Michael V Lombardo8, Massimo Pasqualetti2,7, Alessandro Gozzi , A Minetti4, Alessandro Gozzi2 (1. Departments of Psychiatry and Biobehavioral Sciences and Psychology, Semel Institute for Neuroscience and Human Behavior, University of California at Los Angeles, Los Angeles, 2. Functional Neuroimaging Laboratory, Istituto Italiano di Tecnologia, Center for Neuroscience and Cognitive Systems, University of Trento, Rovereto, Italy, 3. Genetics of Cognition Laboratory, Neuroscience area, Istituto Italiano di Tecnologia, Genova, Italy, 4. Department of Biology, Unit of Cell and Developmental Biology, University of Pisa, Pisa, Italy, 5. IMT School for Advanced Studies, Lucca, Italy, 6. Center for Mind and Brain Sciences, University of Trento, Rovereto, Italy, 7. Centro per l’Integrazione della Strumentazione Scientifica dell’Università di Pisa (CISUP), Pisa, Italy, 8. Laboratory for Autism and Neurodevelopmental Disorders, Center for Neuroscience and Cognitive Systems, Istituto Italiano di Tecnologia, Rovereto, Italy)
[2S06a-3]Cytoarchitectural alterations in a mouse model of the 22q11.2 microdeletion syndrome
*田畑 秀典1、森 大輔2,5、松木 亨3、吉崎 嘉一4、浅井 真人4、中山 敦雄3、尾崎 紀夫5,6、永田 浩一1 (1. 愛知県医療療育総合センター、発達障害研究所、分子病態研究部、2. 名古屋大学、脳とこころの研究センター、3. 愛知県医療療育総合センター、発達障害研究所、細胞病態研究部、4. 愛知県医療療育総合センター、発達障害研究所、障害モデル研究部、5. 名古屋大学大学院医学系研究科、精神疾患病態解明学、6. 東海国立大学機構、糖鎖生命コア研究所)
[2S06a-4]Investigating abnormalities in top-down cortical processing and behavior in a model of the 22q11.2 deletion
*Renata Batista-Brito1 (1. Albert Einstein College of Medicine)
[2S06a-5]TBX1, a gene encoded in 22q11.2 copy number variation, contributes to structural, cellular, and behavioral deficits via neonatal and embryonic neurogenesis
*Noboru Hiroi1, Takeshi Hiramoto1, Shuken Boku2, Akira Sumiyoshi4,3, Risa Kato5, Takahira Yamauchi1, Takeshi Takano1, Emily T. Averyt1, Takaki Tanifuji1, Gina Kang1, Marisa Esparza1, Yukiko J Hiroi1, Rie Ryoke3, Hiroi Nonaka3, Akihiro Machida5, Kensaku Nomoto5, Kazutaka Mogi5, Takefumi Kikusui5, Ryuta Kawashima3, Jason Pugh1 (1. UT Health San Antonio, San Antonio, USA, 2. Kumamoto University, Kumamoto, Japan, 3. Tohoku University, Miyagi, Japan, 4. NIRS-QST, Chiba, Japan, 5. Azabu University, Kanagawa, Japan)