1 - 25 of
352
results
for author:"Kato K."
in Literature Citations
| Nitration of tyrosine residues 368 and 345 in the beta-subunit elicits FoF1-ATPase activity loss. Fujisawa Y., Kato K., Giulivi C. Biochem. J. 423:219-231(2009) · Mapped (5) |
| DNA hypomethylation at the CpG island is involved in aberrant expression of the L1 cell adhesion molecule gene in colorectal cancer. Kato K., Maesawa C., Itabashi T., Fujisawa K., Otsuka K., Kanno S., Tada H., Tatemichi Y., Kotani K., Oikawa H. et al. Int. J. Oncol. 35:467-476(2009) · Mapped (12) |
| Association of genetic variants with chronic kidney disease in individuals with different lipid profiles. Yoshida T., Kato K., Yokoi K., Oguri M., Watanabe S., Metoki N., Yoshida H., Satoh K., Aoyagi Y., Nishigaki Y. et al. Int. J. Mol. Med. 24:233-246(2009) · Mapped (774) |
| Serum hepcidin-20 is elevated during the acute phase of myocardial infarction. Suzuki H., Toba K., Kato K., Ozawa T., Tomosugi N., Higuchi M., Kusuyama T., Iso Y., Kobayashi N., Yokoyama S. et al. Tohoku J. Exp. Med. 218:93-98(2009) · Mapped (1) |
| Loss of maspin is a negative prognostic factor for invasion and metastasis in oral squamous cell carcinoma. Yoshizawa K., Nozaki S., Okamune A., Kitahara H., Ohara T., Kato K., Kawashiri S., Yamamoto E. J. Oral Pathol. Med. 38:535-539(2009) · Mapped (2) |
| Detection of a new bat gammaherpesvirus in the Philippines. Watanabe S., Ueda N., Iha K., Masangkay J.S., Fujii H., Alviola P., Mizutani T., Maeda K., Yamane D., Walid A. et al. Virus Genes 39:90-93(2009) · UniProtKB (2) |
| Association of gene polymorphisms with chronic kidney disease in high- or low-risk subjects defined by conventional risk factors. Yoshida T., Kato K., Yokoi K., Oguri M., Watanabe S., Metoki N., Yoshida H., Satoh K., Aoyagi Y., Nishigaki Y. et al. Int. J. Mol. Med. 23:785-792(2009) · Mapped (27) |
| Association of genetic variants with myocardial infarction in Japanese individuals with chronic kidney disease. Fujimaki T., Kato K., Yoshida T., Oguri M., Watanabe S., Metoki N., Yoshida H., Satoh K., Aoyagi Y., Nishigaki Y. et al. Thromb. Haemost. 101:963-968(2009) · Mapped (5) |
| Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study. Yamada Y., Fuku N., Tanaka M., Aoyagi Y., Sawabe M., Metoki N., Yoshida H., Satoh K., Kato K., Watanabe S. et al. Atherosclerosis 207:144-149(2009) · Mapped (11) |
| Role of MafA in pancreatic beta-cells. Kaneto H., Matsuoka T.A., Kawashima S., Yamamoto K., Kato K., Miyatsuka T., Katakami N., Matsuhisa M. Adv. Drug Deliv. Rev. 61:489-496(2009) · Mapped (1) |
| Human OS-9, a lectin required for glycoprotein endoplasmic reticulum-associated degradation, recognizes mannose-trimmed N-glycans. Hosokawa N., Kamiya Y., Kamiya D., Kato K., Nagata K. J. Biol. Chem. 284:17061-17068(2009) · UniProtKB (1) · Mapped (11) |
| Differential interaction and aggregation of 3-repeat and 4-repeat tau isoforms with 14-3-3zeta protein. Sadik G., Tanaka T., Kato K., Yanagi K., Kudo T., Takeda M. Biochem. Biophys. Res. Commun. 383:37-41(2009) · Mapped (5) |
| Spontaneous endometrial hyperplasia in the uteri of IL-2 receptor beta-chain transgenic mice. Kusakabe K., Kiso Y., Hondo E., Takeshita A., Kato K., Okada T., Shibata M.A., Otsuki Y. J. Reprod. Dev. 55:273-277(2009) · Mapped (5) |
| Identification and characterization of wolframin, the product of the wolfram syndrome gene (WFS1), as a novel calmodulin-binding protein. Yurimoto S., Hatano N., Tsuchiya M., Kato K., Fujimoto T., Masaki T., Kobayashi R., Tokumitsu H. Biochemistry 48:3946-3955(2009) · Mapped (1) |
| Tetrameric Orai1 is a teardrop-shaped molecule with a long, tapered cytoplasmic domain. Maruyama Y., Ogura T., Mio K., Kato K., Kaneko T., Kiyonaka S., Mori Y., Sato C. J. Biol. Chem. 284:13676-13685(2009) · Mapped (3) |
| Association of genetic variants with chronic kidney disease in Japanese individuals with type 2 diabetes mellitus. Yoshida T., Kato K., Yokoi K., Watanabe S., Metoki N., Yoshida H., Satoh K., Aoyagi Y., Nishigaki Y., Suzuki T. et al. Int. J. Mol. Med. 23:529-537(2009) · Mapped (4) |
| Association of candidate gene polymorphisms with chronic kidney disease in Japanese individuals with hypertension. Yoshida T., Kato K., Yokoi K., Watanabe S., Metoki N., Satoh K., Aoyagi Y., Nishigaki Y., Nozawa Y., Yamada Y. Hypertens. Res. 32:411-418(2009) · Mapped (112) |
| Homeobox gene HOPX is epigenetically silenced in human uterine endometrial cancer and suppresses estrogen-stimulated proliferation of cancer cells by inhibiting serum response factor. Yamaguchi S., Asanoma K., Takao T., Kato K., Wake N. Int. J. Cancer 124:2577-2588(2009) · Mapped (1) |
| Contribution of sialidase NEU1 to suppression of metastasis of human colon cancer cells through desialylation of integrin beta4. Uemura T., Shiozaki K., Yamaguchi K., Miyazaki S., Satomi S., Kato K., Sakuraba H., Miyagi T. Oncogene 28:1218-1229(2009) · Mapped (16) |
| The structure of rat liver vault at 3.5 Angstrom resolution. Tanaka H., Kato K., Yamashita E., Sumizawa T., Zhou Y., Yao M., Iwasaki K., Yoshimura M., Tsukihara T. Science 323:384-388(2009) · UniProtKB (1) |
| Defining the glycan destruction signal for endoplasmic reticulum-associated degradation. Quan E.M., Kamiya Y., Kamiya D., Denic V., Weibezahn J., Kato K., Weissman J.S. Mol. Cell 32:870-877(2008) · Mapped (4) |
| Rho-kinase contributes to sustained RhoA activation through phosphorylation of p190A RhoGAP. Mori K., Amano M., Takefuji M., Kato K., Morita Y., Nishioka T., Matsuura Y., Murohara T., Kaibuchi K. J. Biol. Chem. 284:5067-5076(2009) · Mapped (6) |
| Centrosome amplification is correlated with ploidy divergence, but not with MYCN amplification, in neuroblastoma tumors. Fukushi D., Watanabe N., Kasai F., Haruta M., Kikuchi A., Kikuta A., Kato K., Nakadate H., Tsunematsu Y., Kaneko Y. Cancer Genet. Cytogenet. 188:32-41(2009) · Mapped (7) |
| Association of a polymorphism of the apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome. Yoshida T., Kato K., Fujimaki T., Yokoi K., Oguri M., Watanabe S., Metoki N., Yoshida H., Satoh K., Aoyagi Y. et al. Genomics 93:221-226(2009) · Mapped (309) |
| Correlation of clinical features with the mutational status of GM-CSF signaling pathway-related genes in juvenile myelomonocytic leukemia. Yoshida N., Yagasaki H., Xu Y., Matsuda K., Yoshimi A., Takahashi Y., Hama A., Nishio N., Muramatsu H., Watanabe N. et al. Pediatr. Res. 65:334-340(2009) · Mapped (18) |
