Esterification of side-chain oxysterols by lysosomal phospholipase A2 by Abe, Akira, Hiraoka, Miki, Matsuzawa, Fumiko, Aikawa, Sei-ichi, Niimura, Youichi

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Structural modeling and mutagenesis of endo-β-N-acetylglucosaminidase from Ogataea minuta identifies the importance of Trp295 for hydrolytic activity by Kitajima, Toshihiko, Jia, Yuanling, Komatsuzaki, Akiko, Cui, Juan, Matsuzawa, Fumiko, Aikawa, Sei-Ichi, Gao, Xiao-Dong, Chiba, Yasunori

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Phosphorylation-Induced Conformational Switching of CPI-17 Produces a Potent Myosin Phosphatase Inhibitor by Eto, Masumi, Kitazawa, Toshio, Matsuzawa, Fumiko, Aikawa, Sei-ichi, Kirkbride, Jason A., Isozumi, Noriyoshi, Nishimura, Yumi, Brautigan, David L., Ohki, Shin-ya

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A variant in the RP1L1 gene in a family with occult macular dystrophy in a predicted intrinsically disordered region by Hiraoka, Miki, Ishikawa, Aki, Matsuzawa, Fumiko, Aikawa, Sei-Ichi, Sakurai, Akihiro

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Clinical usefulness of multigene screening with phenotype-driven bioinformatics analysis for the diagnosis of patients with monogenic diabetes or severe insulin resistance by Hosoe, Jun, Miya, Fuyuki, Kadowaki, Hiroko, Fujiwara, Toyofumi, Suzuki, Ken, Kato, Takashi, Waki, Hironori, Sasako, Takayoshi, Aizu, Katsuya, Yamamura, Natsumi, Sasaki, Fusako, Kurano, Makoto, Hara, Kazuo, Tanaka, Masaki, Ishiura, Hiroyuki, Tsuji, Shoji, Honda, Kenjiro, Yoshimura, Jun, Morishita, Shinichi, Matsuzawa, Fumiko, Aikawa, Sei-Ichi, Boroevich, Keith A., Nangaku, Masaomi, Okada, Yukinori, Tsunoda, Tatsuhiko, Shojima, Nobuhiro, Yamauchi, Toshimasa, Kadowaki, Takashi

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Introduction of an N-Glycan Sequon Into HEXA Enhances Human β-Hexosaminidase Cellular Uptake in a Model of Sandhoff Disease by Matsuoka, Kazuhiko, Tsuji, Daisuke, Aikawa, Sei-ichi, Matsuzawa, Fumiko, Sakuraba, Hitoshi, Itoh, Kohji

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Binding parameters and thermodynamics of the interaction of imino sugars with a recombinant human acid α-glucosidase (alglucosidase alfa): Insight into the complex formation mechan... by Yoshimizu, Michiru, Tajima, Youichi, Matsuzawa, Fumiko, Aikawa, Sei-ichi, Iwamoto, Kunihiko, Kobayashi, Toshihide, Edmunds, Tim, Fujishima, Kaori, Tsuji, Daisuke, Itoh, Kohji, Ikekita, Masahiko, Kawashima, Ikuo, Sugawara, Kanako, Ohyanagi, Naho, Suzuki, Toshihiro, Togawa, Tadayasu, Ohno, Kazuki, Sakuraba, Hitoshi

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Fabry disease : correlation between structural changes in a-galactosidase, and clinical and biochemical phenotypes by MATSUZAWA, Fumiko, AIKAWA, Sei-Ichi, DOI, Hirofumi, OKUMIYA, Toshika, SAKURABA, Hitoshi

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Inhibitory effects and specificity of synthetic sialyldendrimers toward recombinant human cytosolic sialidase 2 (NEU2) by Rahman, M Motiur, Kitao, Satoshi, Tsuji, Daisuke, Suzuki, Kaori, Sakamoto, Jun-Ichi, Matsuoka, Koji, Matsuzawa, Fumiko, Aikawa, Sei-Ichi, Itoh, Kohji

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Prediction of the mechanism of action of omuralide ( clasto-lactacystin β-lactone) on human cathepsin A based on a structural model of the yeast proteasome β5/PRE2-subunit/omuralid... by Aikawa, Sei-ichi, Matsuzawa, Fumiko, Satoh, Yurie, Kadota, Yoshito, Doi, Hirofumi, Itoh, Kohji

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Bcl-2 antiapoptotic protein mediates verotoxin II-induced cell death: possible association between bcl-2 and tissue failure by E. coli O157:H7 by Suzuki, A, Doi, H, Matsuzawa, F, Aikawa, S, Takiguchi, K, Kawano, H, Hayashida, M, Ohno, S

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Introduction of an N-Glycan Sequon Into HEXA Enhances Human [beta]-Hexosaminidase Cellular Uptake in a Model of Sandhoff Disease by Matsuoka, Kazuhiko, Tsuji, Daisuke, Aikawa, Sei-ichi, Matsuzawa, Fumiko, Sakuraba, Hitoshi, Itoh, Kohji

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Diverse incidences of individual oligopeptides (dipeptidic to hexapeptidic) in proteins of human, bakers' yeast, and Escherichia coli origin registered in the Swiss-Prot data base by Doi, Hirofumi, Kitajima, Masato, Watanabe, Isamu, Kikuchi, Yasuhiro, Matsuzawa, Fumiko, Aikawa, Sei-Ichi, Takiguchi, Kyoko, Ohno, Susumu

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Structural insight into regulation of myosin phosphatase by CPI‐17 by Eto, Masumi, Kitazawa, Toshio, Matsuzawa, Fumiko, Aikawa, Sei‐ichi, Kirkbride, Jason A, Isozumi, Noriyoshi, Nishimura, Yumi, Brautigan, David L, Ohki, Shin‐ya

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Fabry disease: correlation between structural changes in alpha-galactosidase, and clinical and biochemical phenotypes by Matsuzawa, Fumiko, Aikawa, Sei-ichi, Doi, Hirofumi, Okumiya, Toshika, Sakuraba, Hitoshi

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A variant in the RP1L1 gene in a family with occult macular dystrophy in a predicted intrinsically disordered region by Hiraoka, Miki, Ishikawa, Aki, Matsuzawa, Fumiko, Aikawa, Sei-Ichi, Sakurai, Akihiro

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