Nagano, J., Kitamura, K., Hujer, K.M., Ward, C.J., Bram, R.J., Hopfer, U., Tomita, K., Huang, C., and Miller, R.T. : Fibrocystin Interacts with CAML, a protein involved in Ca2+ signaling. Biochem. Biophys. Res. Commun., 338: 880-889, 2005
Shimada, H., Kitamura, K. (equal contribution), Anraku, M., Miyoshi, T., Adachi, M., Tuyen, D.G., Wakamatsu, S., Nonoguchi, H., Tanaka, M., and Tomita, K. : Effect of telmisartan on ambulatory blood pressure monitoring, plasma brain natriuretic peptide, and oxidative status of serum albumin in hemodialysis patients. Hypertens. Res., 28: 987-994, 2005
Mera, K., Anraku, M., Kitamura, K., Nakajou, K., Maruyama, T., Tomita, K., and Otagiri, M. : Oxidation and carboxyl methyl lysine-modification of albumin: possible involvement in the progression of oxidative stress in hemodialysis patients. Hypertens. Res., 28: 973-980, 2005
Mera, K., Anraku, M., Kitamura, K., Nakajou, K., Maruyama, T., and Otagiri, M. : The structure and function of oxidized albumin in hemodialysis patients: Its role in elevated oxidative stress via neutrophil burst. Biochem. Biophys. Res. Commun., 334: 1322-1328, 2005
Wakida, N., Tuyen, D.G., Adachi, M., Miyoshi, T., Nonoguchi, H., Oka, T., Ueda, O., Tazawa, M., Kurihara, S., Yoneta, Y., Shimada, H., Oda, T., Kikuchi, Y., Matsuo, H., Hosoyamada, M., Endou, H., Otagiri, M., Tomita, K., and Kitamura, K. : Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia. J. Clin. Endocrinol. Metab., 90: 2169-2174, 2005
Furuhashi, M., Kitamura, K., Adachi, M., Miyoshi, T., Wakida, N., Ura, N., Shikano, Y., Shinshi, Y., Sakamoto, K., Hayashi, M., Satoh, N., Nishitani, T., Tomita, K., Shimamoto, K. : Liddle’s syndrome caused by a novel mutation in the proline-rich PY motif of the epithelial sodium channel β-subunit. J. Clin. Endocrinol. Metab., 90: 340-344, 2005
Tuyen, D.G., Kitamura, K., Adachi, M., Miyoshi, T., Wakida, N., Nagano, J., Nonoguchi, H., and Tomita, K. : Inhibition of prostasin expression by TGF-β1 in renal epithelial cells. Kidney Int., 67: 193-200, 2005
Kitamura, K. and Tomita, K. : Familial pseudohyperkalemia: a rare syndrome, but diverse genetic heterogeneity. Intern Med., 44: 781-782, 2005
