Juntendo University · Graduate School of Medicine / Faculty of Medicine

Research keywords一卵性双生児疾患不一致例・GRP94・双極性障害・合理的配慮・統合失調症・リチウム・リンパ芽球・バルプロ酸・XBP1・WFS1

This is a public-data preview. Personalized fit, contact angles, and saved workflows require sign-in.

• Expression of mitochondrial complex I subunit gene NDUFV2 in the lymphoblastoid cells derived from patients with bipolar disorder and schizophrenia.
• Identification and functional characterization of the extremely long allele of the serotonin transporter-linked polymorphic region.
• Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder in Japanese and the National Institute of Mental Health pedigrees.
• Identification of candidate genes involved in the etiology of sporadic Tourette syndrome by exome sequencing.

• 一卵性双生児統合失調症不一致例及び健常一致例の遺伝子発現解析
• 双生児法を用いた統合失調症脳病態に対する遺伝・環境要因の解明
• 統合失調症脳における微小循環・慢性炎症関連分子のジェネティックニューロパソロジー
• 多発家系・一卵性双生児不一致例の解析による精神疾患・発達障害の新規候補遺伝子同定

• Official profile