1 - 25 of
156
results
for author:"Takeda J."
in Literature Citations
| A transposon-based chromosomal engineering method to survey a large cis-regulatory landscape in mice. Kokubu C., Horie K., Abe K., Ikeda R., Mizuno S., Uno Y., Ogiwara S., Ohtsuka M., Isotani A., Okabe M. et al. Nat. Genet. 41:946-952(2009) · Mapped (5) |
| Conditional inactivation of Has2 reveals a crucial role for hyaluronan in skeletal growth, patterning, chondrocyte maturation and joint formation in the developing limb. Matsumoto K., Li Y., Jakuba C., Sugiyama Y., Sayo T., Okuno M., Dealy C.N., Toole B.P., Takeda J., Yamaguchi Y. et al. Development 136:2825-2835(2009) · Mapped (2) |
| Fezf1 is required for penetration of the basal lamina by olfactory axons to promote olfactory development. Watanabe Y., Inoue K., Okuyama-Yamamoto A., Nakai N., Nakatani J., Nibu K., Sato N., Iiboshi Y., Yusa K., Kondoh G. et al. J. Comp. Neurol. 515:565-584(2009) · Mapped (1) |
| Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association. Miyake K., Yang W., Hara K., Yasuda K., Horikawa Y., Osawa H., Furuta H., Ng M.C., Hirota Y., Mori H. et al. J. Hum. Genet. 54:236-241(2009) · Mapped (74) |
| Identification of minimal promoter and genetic variants of Kruppel-like factor 11 gene and association analysis with type 2 diabetes in Japanese. Kuroda E., Horikawa Y., Enya M., Oda N., Suzuki E., Iizuka K., Takeda J. Endocr. J. 56:275-286(2009) · Mapped (5) |
| Hepatic overexpression of dominant negative Mlx improves metabolic profile in diabetes-prone C57BL/6J mice. Iizuka K., Takeda J., Horikawa Y. Biochem. Biophys. Res. Commun. 379:499-504(2009) · Mapped (7) |
| Progranulin, a secreted tumorigenesis and dementia-related factor, regulates mouse hair growth. Kato M., Hasunuma N., Nakayama R., Takeda J., Itami S., Taira M., Manabe M., Osada S. J. Dermatol. Sci. 53:234-236(2009) · Mapped (15) |
| Mutations in the small heterodimer partner gene increase morbidity risk in Japanese type 2 diabetes patients. Enya M., Horikawa Y., Kuroda E., Yonemaru K., Tonooka N., Tomura H., Oda N., Yokoi N., Yamagata K., Shihara N. et al. Hum. Mutat. 29:E271-7(2008) · Mapped (1) |
| Case report of familial Carney complex due to novel frameshift mutation c.597del C (p.Phe200LeufsX6) in PRKAR1A. Sasaki A., Horikawa Y., Suwa T., Enya M., Kawachi S., Takeda J. Mol. Genet. Metab. 95:182-187(2008) · Mapped (4) |
| Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus. Yasuda K., Miyake K., Horikawa Y., Hara K., Osawa H., Furuta H., Hirota Y., Mori H., Jonsson A., Sato Y. et al. Nat. Genet. 40:1092-1097(2008) · Mapped (6) |
| A common P2 promoter polymorphism of the hepatocyte nuclear factor-4alpha gene is associated with insulin secretion in non-obese Japanese with type 2 diabetes. Tokunaga A., Horikawa Y., Fukuda-Akita E., Okita K., Iwahashi H., Shimomura I., Takeda J., Yamagata K. Endocr. J. 55:999-1004(2008) · Mapped (8) |
| Coronary artery calcification, arterial stiffness and renal insufficiency associate with serum levels of tumor necrosis factor-alpha in Japanese type 2 diabetic patients. Hirota T., Suzuki E., Ito I., Ishiyama M., Goto S., Horikawa Y., Asano T., Kanematsu M., Hoshi H., Takeda J. Diabetes Res. Clin. Pract. 82:58-65(2008) · Mapped (6) |
| Effect of fasting on PPARgamma and AMPK activity in adipocytes. Kajita K., Mune T., Ikeda T., Matsumoto M., Uno Y., Sugiyama C., Matsubara K., Morita H., Takemura M., Seishima M. et al. Diabetes Res. Clin. Pract. 81:144-149(2008) · Mapped (1) |
| Lack of association of LRP5 and LRP6 polymorphisms with type 2 diabetes mellitus in the Japanese population. Zenibayashi M., Miyake K., Horikawa Y., Hirota Y., Teranishi T., Kouyama K., Sakaguchi K., Takeda J., Kasuga M. Endocr. J. 55:699-707(2008) · Mapped (8) |
| Replication of genome-wide association studies of type 2 diabetes susceptibility in Japan. Horikawa Y., Miyake K., Yasuda K., Enya M., Hirota Y., Yamagata K., Hinokio Y., Oka Y., Iwasaki N., Iwamoto Y. et al. J. Clin. Endocrinol. Metab. 93:3136-3141(2008) · Mapped (18) |
| T cell response mediated by myeloid cell-derived IL-12 is responsible for Porphyromonas gingivalis-induced periodontitis in IL-10-deficient mice. Sasaki H., Suzuki N., Kent R. Jr., Kawashima N., Takeda J., Stashenko P. J. Immunol. 180:6193-6198(2008) · Mapped (14) |
| Association of TCF7L2 polymorphisms with susceptibility to type 2 diabetes in 4,087 Japanese subjects. Miyake K., Horikawa Y., Hara K., Yasuda K., Osawa H., Furuta H., Hirota Y., Yamagata K., Hinokio Y., Oka Y. et al. J. Hum. Genet. 53:174-180(2008) · Mapped (26) |
| p21 provides stage specific DNA damage control to preimplantation embryos. Adiga S.K., Toyoshima M., Shiraishi K., Shimura T., Takeda J., Taga M., Nagai H., Kumar P., Niwa O. Oncogene 26:6141-6149(2007) · Mapped (3) |
| Rad54 is dispensable for the ALT pathway. Akiyama K., Yusa K., Hashimoto H., Poonepalli A., Hande M.P., Kakazu N., Takeda J., Tachibana M., Shinkai Y. Genes Cells 11:1305-1315(2006) · Mapped (4) |
| Physiologic roles of 11beta-hydroxysteroid dehydrogenase type 2 in kidney. Isomura Y., Mune T., Morita H., Suwa T., Takada N., Yamamoto Y., Takeda J. Metab. Clin. Exp. 55:1352-1357(2006) · Mapped (1) |
| Sleeping beauty transposon-based phenotypic analysis of mice: lack of Arpc3 results in defective trophoblast outgrowth. Yae K., Keng V.W., Koike M., Yusa K., Kouno M., Uno Y., Kondoh G., Gotow T., Uchiyama Y., Horie K. et al. Mol. Cell. Biol. 26:6185-6196(2006) · Mapped (1) |
| Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects. Yokoi N., Kanamori M., Horikawa Y., Takeda J., Sanke T., Furuta H., Nanjo K., Mori H., Kasuga M., Hara K. et al. Diabetes 55:2379-2386(2006) · Mapped (41) |
| Sucrase-isomaltase gene expression is inhibited by mutant hepatocyte nuclear factor (HNF)-1alpha and mutant HNF-1beta in Caco-2 cells. Gu N., Adachi T., Takeda J., Aoki N., Tsujimoto G., Ishihara A., Tsuda K., Yasuda K. J. Nutr. Sci. Vitaminol. 52:105-112(2006) · Mapped (1) |
| Mutant HNF-1alpha and mutant HNF-1beta identified in MODY3 and MODY5 downregulate DPP-IV gene expression in Caco-2 cells. Gu N., Adachi T., Matsunaga T., Takeda J., Tsujimoto G., Ishihara A., Yasuda K., Tsuda K. Biochem. Biophys. Res. Commun. 346:1016-1023(2006) · Mapped (9) |
| Bloom's syndrome gene-deficient phenotype in mouse primary cells induced by a modified tetracycline-controlled trans-silencer. Hayakawa T., Yusa K., Kouno M., Takeda J., Horie K. Gene 369:80-89(2006) · Mapped (1) |
