Art

J-GLOBAL ID：201902223476597474   Reference number：19A1343443

Further evidence of a causal association between AGO1, a critical regulator of microRNA formation, and intellectual disability/autism spectrum disorder

マイクロRNA形成の重要な調節因子AGO1と知的障害/自閉症スペクトラム障害との因果関係の更なる証拠【JST・京大機械翻訳】

Author (8)： Sakaguchi Asami (Department of Pediatrics, Yokohama Municipal Citizen’s Hospital, Kanagawa, Japan) ,  Sakaguchi Asami (Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan) ,  Yamashita Yukio (Department of Pediatrics, Yokohama Municipal Citizen’s Hospital, Kanagawa, Japan) ,  Ishii Tomohiro (Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan) ,  Uehara Tomoko (Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan) ,  Kosaki Kenjiro (Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan) ,  Takahashi Takao (Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan) ,  Takenouchi Toshiki (Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan)
Material： European Journal of Medical Genetics  (Eur J Med Genet)
Volume： 62  Issue： 6  Page： Null  Publication year： 2019 
JST Material Number： A1224A  ISSN： 1769-7212  Document type： Article
Article type： 原著論文  Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)

Abstract/Point： Among the many regulators of m...

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Thesaurus term： chromosome ,  computed tomography ,  *intelligence disorder ,  phenotype ,  calcification ,  seizure(disease) ,  variation(biology) ,  *causality ,  *autism ,  mutation ,  scanning ,  globus pallidus
Semi thesaurus term： 小児期 ,  *自閉症スペクトラム障害 ,  *マイクロRNA , 【Automatic Indexing@JST】

Author keywords (5)： AGO1 ,  microRNAs ,  Intellectual disability ,  Autism ,  Calcification

JST classification (2)： Genetic variation  (EC01030Y) ,  Congenital diseases,deformities in general.  (GD03010V)

Terms in the title (6)： マイクロRNA ,  調節因子 ,  知的障害 ,  自閉症スペクトラム障害 ,  因果関係 ,  証拠