Symbiotic riboflavin degradation by Microbacterium and Nocardioides bacteria
Kanazawa, Hiroshi, Ozaki, Sayoko, Doi, Yuki, Masuo, Shunsuke, Takaya, Naoki
Published in Bioscience, biotechnology, and biochemistry (03.05.2020)
Published in Bioscience, biotechnology, and biochemistry (03.05.2020)
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Idiopathic Obliterative Bronchiolitis in a Young Woman: A Rare Case of a Transbronchial Lung Biopsy Contributing to the Diagnosis
Yoshii, Naoko, Kamoi, Hiroshi, Matsui, Erika, Sato, Kanako, Nakai, Toshiyuki, Yamada, Kazuhiro, Watanabe, Tetsuya, Asai, Kazuhisa, Kanazawa, Hiroshi, Kawaguchi, Tomoya
Published in Internal Medicine (15.09.2022)
Published in Internal Medicine (15.09.2022)
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Four Na+/H+ Exchanger Isoforms Are Distributed to Golgi and Post-Golgi Compartments and Are Involved in Organelle pH Regulation
Nakamura, Norihiro, Tanaka, Shingo, Teko, Yoshinori, Mitsui, Keiji, Kanazawa, Hiroshi
Published in The Journal of biological chemistry (14.01.2005)
Published in The Journal of biological chemistry (14.01.2005)
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Two-Component Flavin-Dependent Riboflavin Monooxygenase Degrades Riboflavin in Devosia riboflavina
Kanazawa, Hiroshi, Shigemoto, Ryosuke, Kawasaki, Yukie, Oinuma, Ken-Ichi, Nakamura, Akira, Masuo, Shunsuke, Takaya, Naoki
Published in Journal of bacteriology (15.06.2018)
Published in Journal of bacteriology (15.06.2018)
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The Endosomal Na+/H+ Exchanger Contributes to Multivesicular Body Formation by Regulating the Recruitment of ESCRT-0 Vps27p to the Endosomal Membrane
Mitsui, Keiji, Koshimura, Yuri, Yoshikawa, Yuriko, Matsushita, Masafumi, Kanazawa, Hiroshi
Published in The Journal of biological chemistry (28.10.2011)
Published in The Journal of biological chemistry (28.10.2011)
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Correlation between disease activity and serum ferritin in clinically amyopathic dermatomyositis with rapidly-progressive interstitial lung disease: a case report
Yamada, Kazuhiro, Asai, Kazuhisa, Okamoto, Atsuko, Watanabe, Tetsuya, Kanazawa, Hiroshi, Ohata, Mai, Ohsawa, Masahiko, Hirata, Kazuto
Published in BMC research notes (16.01.2018)
Published in BMC research notes (16.01.2018)
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A loss-of-function mutation in the SLC9A6 gene causes X-linked mental retardation resembling Angelman syndrome
Takahashi, Yumi, Hosoki, Kana, Matsushita, Masafumi, Funatsuka, Makoto, Saito, Kayoko, Kanazawa, Hiroshi, Goto, Yu-ichi, Saitoh, Shinji
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2011)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.12.2011)
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