15 results for author:"Kou I." in Literature citations
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| SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern Chinese. Fan Y.H., Song Y.Q., Chan D., Takahashi Y., Ikegawa S., Matsumoto M., Kou I., Cheah K.S., Sham P., Cheung K.M. et al. J. Hum. Genet. 57:244-246(2012) · Mapped (3) |
| A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis. Takahashi Y., Kou I., Takahashi A., Johnson T.A., Kono K., Kawakami N., Uno K., Ito M., Minami S., Yanagida H. et al. Nat. Genet. 43:1237-1240(2011) · Mapped (3) |
| Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese. Kou I., Takahashi A., Urano T., Fukui N., Ito H., Ozaki K., Tanaka T., Hosoi T., Shiraki M., Inoue S. et al. PLoS ONE 6:E19641-E19641(2011) · UniProtKB (1) |
| Asporin expression is highly regulated in human chondrocytes. Duval E., Bigot N., Hervieu M., Kou I., Leclercq S., Galera P., Boumediene K., Bauge C. Mol. Med. 17:816-823(2011) · Mapped (12) |
| New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study. Nakajima M., Takahashi A., Kou I., Rodriguez-Fontenla C., Gomez-Reino J.J., Furuichi T., Dai J., Sudo A., Uchida A., Fukui N. et al. PLoS ONE 5:e9723-e9723(2010) · Mapped (179) |
| Binding characteristics of the osteoarthritis-associated protein asporin. Kou I., Nakajima M., Ikegawa S. J. Bone Miner. Metab. 28:395-402(2010) · UniProtKB (1) · Mapped (2) |
| Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation. Murakami T., Saito A., Hino S., Kondo S., Kanemoto S., Chihara K., Sekiya H., Tsumagari K., Ochiai K., Yoshinaga K. et al. Nat. Cell Biol. 11:1205-1211(2009) · Mapped (1) |
| Nucleotide variations in genes encoding carbonic anhydrase 8 and 10 associated with femoral bone mineral density in Japanese female with osteoporosis. Mori S., Kou I., Sato H., Emi M., Ito H., Hosoi T., Ikegawa S. J. Bone Miner. Metab. 27:213-216(2009) · Mapped (6) |
| Pre-B-cell leukemia homeobox 1 (PBX1) shows functional and possible genetic association with bone mineral density variation. Cheung C.L., Chan B.Y., Chan V., Ikegawa S., Kou I., Ngai H., Smith D., Luk K.D., Huang Q.Y., Mori S. et al. Hum. Mol. Genet. 18:679-687(2009) · Mapped (143) |
| Association of genetic variations of genes encoding thrombospondin, type 1, domain-containing 4 and 7A with low bone mineral density in Japanese women with osteoporosis. Mori S., Kou I., Sato H., Emi M., Ito H., Hosoi T., Ikegawa S. J. Hum. Genet. 53:694-697(2008) · Mapped (1) |
| Mechanisms for asporin function and regulation in articular cartilage. Nakajima M., Kizawa H., Saitoh M., Kou I., Miyazono K., Ikegawa S. J. Biol. Chem. 282:32185-32192(2007) · UniProtKB (5) · Mapped (6) |
| Expression and regulation of the osteoarthritis-associated protein asporin. Kou I., Nakajima M., Ikegawa S. J. Biol. Chem. 282:32193-32199(2007) · UniProtKB (1) · Mapped (7) |
| An aspartic acid repeat polymorphism in asporin inhibits chondrogenesis and increases susceptibility to osteoarthritis. Kizawa H., Kou I., Iida A., Sudo A., Miyamoto Y., Fukuda A., Mabuchi A., Kotani A., Kawakami A., Yamamoto S. et al. |
| The combination of SOX5, SOX6, and SOX9 (the SOX trio) provides signals sufficient for induction of permanent cartilage. Ikeda T., Kamekura S., Mabuchi A., Kou I., Seki S., Takato T., Nakamura K., Kawaguchi H., Ikegawa S., Chung U.I. Arthritis Rheum. 50:3561-3573(2004) · Mapped (29) |
| SOX9-dependent and -independent transcriptional regulation of human cartilage link protein. Kou I., Ikegawa S. J. Biol. Chem. 279:50942-50948(2004) · Mapped (3) |