✦ LIBER ✦

An association of the polymorphic repeat of tetranucleotide (TCAT) in the first intron of the human tyrosine hydroxylase gene with schizophrenia in a Japanese sample

✍ Scribed by A. Kurumaji; T. Kuroda; K. Yamada; T. Yoshikawa; M. Toru

Publisher: Springer
Year: 2001
Tongue: English
Weight: 67 KB
Volume: 108
Category: Article
ISSN: 1435-1463
DOI: 10.1007/s007020170069

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Lack of association of the (AAAT)6 allel

Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism

✍ Plank, Sara M. ;Copeland-Yates, Susan A. ;Sossey-Alaoui, Khalid ;Bell, Jennifer 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 68 KB

Association studies of the CT repeat pol

Association studies of the CT repeat polymorphism in the 5? upstream region of the cholecystokinin B receptor gene with panic disorder and schizophrenia in Japanese subjects

✍ Hattori, Eiji ;Yamada, Kazuo ;Toyota, Tomoko ;Yoshitsugu, Kiyoshi ;Toru, Michio 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 83 KB 👁 3 views

## Abstract The tetrapeptide of cholecystokinin (CCK), CCK‐4, is known to induce panic attacks in human subjects, while CCK‐8 is reported to have a therapeutic effect on schizophrenia symptoms. Recently, we have identified a novel microsatellite polymorphism in the 5′ upstream region of the CCK gen

An association study between two missens

An association study between two missense variations of the benzodiazepine receptor (peripheral) gene and schizophrenia in a Japanese sample

✍ A. Kurumaji; H. Nomoto; T. Yoshikawa; Y. Okubo; M. Toru 📂 Article 📅 2000 🏛 Springer 🌐 English ⚖ 389 KB

Novel polymorphism in the promoter and c

Novel polymorphism in the promoter and coding regions of the human cholecystokinin B receptor gene: An association analysis with schizophrenia

✍ Tachikawa, Hirokazu; Harada, Shoji; Kawanishi, Yoichi; Okubo, Takehito; Shiraish 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 38 KB 👁 3 views

Genetic variations in the 5-untranslated region and the coding region of the CCK-B receptor (CCK-BR) gene were investigated in healthy controls. Novel variants (-215 C→A, Leu37Phe, Arg319Glu) were found in addition to the mutations (Val125Iso, His207His, Arg215His, 2491 C→A) reported previously. In

A deletion polymorphism due to alu-alu r

A deletion polymorphism due to alu-alu recombination in intron 2 of the retinoblastoma gene: Association with human gliomas

✍ Paul G. Rothberg; Satish Ponnuru; Darren Baker; John F. Bradley; Arnold I. Freem 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 91 KB 👁 2 views

The retinoblastoma gene (RB) encodes a tumor suppressor that is inactivated in a number of different types of cancer. We searched for gross alterations of this gene in tumors of the central nervous system by using Southern blot hybridization. A common alteration was found in several tumors and was m

A novel association of a polymorphism in

A novel association of a polymorphism in the first intron of adiponectin gene with type 2 diabetes, obesity and hypoadiponectinemia in Asian Indians

✍ Karani S. Vimaleswaran; Venkatesan Radha; Kandaswamy Ramya; Hunsur Narayan Sathi 📂 Article 📅 2008 🏛 Springer 🌐 English ⚖ 324 KB