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「寄付講座 臨床遺伝学研究室」の研究業績のデータです。 |
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[ 論 文 ]
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Kanzaki M., Tsukimura T., Chiba Y., Sakuraba H., Togawa T.: Surface plasmon resonance analysis of complex formation of therapeutic recombinant lysosomal enzymes with domain 9 of human cation-independent mannose 6-phosphate receptor. Mol. Genet. Metab. Reports, 25: 100639, 2020.
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Tsukimura T., Tayama Y., Shiga T., Hirai K., Togawa T., Sakuraba H.: Anti-drug antibody formation in Japanese Fabry patients following enzyme replacement therapy. Mol. Genet. Metab. Reports, 25: 100650, 2020.
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Fukuhara Y., Miura A., Yamazaki N., So T., Kosuga M., Yanagi K., Kaname T., Yamagata T., Sakuraba H., Okuyama T.: A cDNA analysis disclosed the discordance of genotype-phenotype correlation in a patient with attenuated MPS II and a 76-base deletion in the gene for iduronate-2-sulfatase. Mol. Genet. Metab. Reports, 25: 100692, 2020.
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Kami D., Yamanami M., Tsukimura T., Togawa T., Sakuraba H., Gojo S.: Cell transplantation combined with recombinant collagen peptides for the treatment of Fabry disease. Cell Transplant, 29: 963689720976362, 2020. doi: 10.1177/0963689720976362.
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