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J-GLOBAL ID：200902274768598791   Reference number：09A0712795

Isolation of ON Bipolar Cell Genes via hrGFP-coupled Cell Enrichment Using the mGluR6 Promoter

hrGFP結合細胞増殖を介したON双極細胞遺伝子のmGluR6プロモーターを用いた単離

Author (7)： NAKAJIMA Yoshiaki (Kyoto Univ., Kyoto) ,  MORIYAMA Masaki (Kyoto Univ., Kyoto) ,  HATTORI Masakazu (Kyoto Univ., Kyoto) ,  HATTORI Masakazu (Kitasato Univ., Kanagawa) ,  MINATO Nagahiro (Kyoto Univ., Kyoto) ,  NAKANISHI Shigetada (Kyoto Univ., Kyoto) ,  NAKANISHI Shigetada (Osaka Bioscience Inst., Osaka, JPN)
Material： Journal of Biochemistry  (JB)
Volume： 145  Issue： 6  Page： 811-818  Publication year： Jun. 01, 2009 
JST Material Number： W1920A  ISSN： 0021-924X  CODEN： JOBIAO  Document type： Article
Article type： 原著論文  Country of issue： United Kingdom (GBR)  Language： ENGLISH (EN)

Thesaurus term： *retina ,...
Semi thesaurus term： Cacna2d3 ,...

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JST classification (3)： Basic ophthalmology  (GP01020C) ,  Structure and chemistry of genes  (EC02020U) ,  Congenital diseases,deformities in general.  (GD03010V)

Reference (55)：

• KOLB, H. The architecture of functional neural circuits in the vertebrate retina. The Proctor Lecture. Invest. Ophthalmol. Vis. Sci. 1994, 35, 2385-2404
• MASLAND, R. H. The fundamental plan of the retina. Nat. Neurosci. 2001, 4, 877-886
• NAKAJIMA, Y. Molecular characterization of a novel retinal metabotropic glutamate receptor mGluR6 with a high agonist selectivity for L-2-amino-4-phosphonobutyrate. J. Biol. Chem. 1993, 268, 11868-11873
• DRYJA, T. P. Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6. Proc. Natl Acad. Sci. USA. 2005, 102, 4884-4889
• ZEITZ, C. Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram. Invest. Ophthalmol. Vis. Sci. 2005, 46, 4328-4335

Terms in the title (5)： 細胞増殖 ,  双極細胞 ,  遺伝子 ,  プロモーター ,  単離