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1. Saito S., Ohno K., Sugawara K., Sakuraba H.: Structural and clinical implications of amino acid substitutions in N-acetylgalactosamine-4-sulfatase: Insight into mucopolysaccharidosis type VI. Mol. Genet. Metab., 93: 419-425, 2008.

2. Yoshimizu M., Tajima Y., Matsuzawa F., Aikawa S., Iwamoto K., Kobayashi T., Edmunds T., Fujishima K., Tsuji D., Itoh K., Ikekita M., Kawashima I., Sugawara K., Ohyanagi N., Suzuki T., Togawa T., Ohno K., Sakuraba H.: Binding parameters and thermodynamics of the interaction of imino sugars with a recombinant human acid -glucosidase (alglucosidase alfa): Insight into the complex formation mechanism. Clin. Chim. Acta, 391: 68-73, 2008.

3. Sugawara K., Saito S., Ohno K., Okuyama T., Sakuraba H.: Structural study on mutant -L-iduronidase: Insight into mucopolysaccharidosis type I. J. Hum. Genet., 53: 467-474, 2008.

4. Ohno K., Saito S., Sugawara K., Sakuraba H.: Structural consequences of amino acid substitutions causing Tay-Sachs disease. Mol. Genet. Metab., 94: 462-468, 2008.

5. Sugawara K., Ohno K., Saito S., Sakuraba H.: Structural characterization of mutant -galactosidases causing Fabry disease. J. Hum. Genet., 53: 812-824, 2008.

6. Tsukimura T., Tajima Y., Kawashima I., Fukushige T., Kanzaki T., Kanekura T., Ikekita M., Sugawara K., Suzuki T., Togawa T., Sakuraba H.: Uptake of a recombinant human -L-iduronidase (laronidase) by cultured fibroblasts and osteoblasts. Biol. Pharm. Bull., 31: 1691-1695, 2008.

7. Saito S., Ohno K., Sugawara K., Suzuki T., Togawa T., Sakuraba H.: Structural basis of aspartylglucosaminuria. Biochem. Biophys. Res. Commun., 377: 1168-1172, 2008.

8. Tatano Y., Fujinawa R., Kozutsumi Y., Takahashi T., Tsuji D., Takeuchi N., Tsuta K., Takada G., Sakuraba H. Itoh K.: Tropoelastin regulates chemokine expression in fibroblasts in Costello syndrome. Biochem. Biophys. Res. Commun., 372: 681-687, 2008.