检索结果 - Yoshihiro Maruo

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  1. 1
    Role of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia

    Role of extrahepatic UDP-glucuronosyltransferase 1A1: Advances in understanding breast milk-induced neonatal hyperbilirubinemia 由 Ryoichi Fujiwara, Yoshihiro Maruo, Shujuan Chen, Robert H. Tukey

    出版 2015
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  2. 2
    Prolonged Unconjugated Hyperbilirubinemia Associated With Breast Milk and Mutations of the Bilirubin Uridine Diphosphate- Glucuronosyltransferase Gene

    Prolonged Unconjugated Hyperbilirubinemia Associated With Breast Milk and Mutations of the Bilirubin Uridine Diphosphate- Glucuronosyltransferase Gene 由 Yoshihiro Maruo, Kashiro Nishizawa, Hiroshi Sato, Hiroko Sawa, Morimi Shimada

    出版 2000
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  3. 3
    Six novel UDP-glucuronosyltransferase (UGT1A3) polymorphisms with varying activity

    Six novel UDP-glucuronosyltransferase (UGT1A3) polymorphisms with varying activity 由 Masaru Iwai, Yoshihiro Maruo, Masaki Ito, Kazuo Yamamoto, Hiroshi Sato, Yoshihiro Takeuchi

    出版 2004
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  4. 4
    Natural course of congenital hypothyroidism by dual oxidase 2 mutations from the neonatal period through puberty

    Natural course of congenital hypothyroidism by dual oxidase 2 mutations from the neonatal period through puberty 由 Yoshihiro Maruo, Keisuke Nagasaki, Katsuyuki Matsui, Yu Mimura, Asami Mori, Maki Fukami, Yoshihiro Takeuchi

    出版 2016
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  5. 5
    Clinical factors related to bilirubin encephalopathy in preterm infants: A case-control study

    Clinical factors related to bilirubin encephalopathy in preterm infants: A case-control study 由 Akihisa Okumura, Masahiro Hayakawa, Hiroshi Arai, Yoshihiro Maruo, Takashi Kusaka, Tetsuya Kunikata, Sota Iwatani, Yoshiaki Sato, Ichiro Morioka

    出版 2025
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  6. 6
    Transient Congenital Hypothyroidism Caused by Biallelic Mutations of the Dual Oxidase 2 Gene in Japanese Patients Detected by a Neonatal Screening Program

    Transient Congenital Hypothyroidism Caused by Biallelic Mutations of the Dual Oxidase 2 Gene in Japanese Patients Detected by a Neonatal Screening Program 由 Yoshihiro Maruo, Hiroko Takahashi, Ikumi Soeda, Noriko Nishikura, Katsuyuki Matsui, Yoriko Ota, Yu Mimura, Asami Mori, Hiroshi Satō, Yoshihiro Takeuchi

    出版 2008
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  7. 7
    Bilirubin Uridine Diphosphate-Glucuronosyltransferase Variation Is a Genetic Basis of Breast Milk Jaundice

    Bilirubin Uridine Diphosphate-Glucuronosyltransferase Variation Is a Genetic Basis of Breast Milk Jaundice 由 Yoshihiro Maruo, Yoriko Morioka, Hiroshi Fujito, Sayuri Nakahara, Takahide Yanagi, Katsuyuki Matsui, Asami Mori, Hiroshi Sato, Robert H. Tukey, Yoshihiro Takeuchi

    出版 2014
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  8. 8
    Increased intracellular stress responses and decreased KLF2 in adult patients with atopic dermatitis

    Increased intracellular stress responses and decreased KLF2 in adult patients with atopic dermatitis 由 Shuji Sugiura, Haruka Yoshida, Hisashi Sugiura, Masami Uehara, Yasuo Sugiura, Yoshihiro Maruo, Yasuhiro Hayashi, Takehiro Yamamoto, Taiki Kato, Noriki Fujimoto, Jun Udagawa

    出版 2025
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  9. 9
    Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus

    Comprehensive molecular analysis of Japanese patients with pediatric-onset MODY-type diabetes mellitus 由 Tohru Yorifuji, Rika Fujimaru, Yuki Hosokawa, Nobuyoshi Tamagawa, Momoko Shiozaki, Katsuya Aizu, K Jinno, Yoshihiro Maruo, Hironori Nagasaka, Toshihiro Tajima, Koji Kobayashi, Tatsuhiko Urakami

    出版 2011
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  10. 10
    A Novel Mechanism for the Inhibition of Hyaluronan Biosynthesis by 4-Methylumbelliferone

    A Novel Mechanism for the Inhibition of Hyaluronan Biosynthesis by 4-Methylumbelliferone 由 Ikuko Kakizaki, Kaoru Kojima, Keiichi Takagaki, Masahiko Endo, Reiji Kannagi, Masaki Ito, Yoshihiro Maruo, Hiroshi Satō, Tadashi Yasuda, Satoka Mita, Koji Kimata, Naoki Itano

    出版 2004
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  11. 11
    Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

    Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients 由 Takanobu Inoue, Akie Nakamura, Megumi Iwahashi-Odano, Kanako Tanase‐Nakao, Keiko Matsubara, Junko Nishioka, Yoshihiro Maruo, Yukihiro Hasegawa, Hiroshi Suzumura, Seiji Sato, Yoshiyuki Kobayashi, Nobuyuki Murakami, Kazuhiko Nakabayashi, Kazuki Yamazawa, Tomoko Fuke, Satoshi Narumi, Akira Oka, Tsutomu Ogata, Maki Fukami, Masayo Kagami

    出版 2020
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  12. 12
    Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities

    Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities 由 Satoshi Narumi, Keisuke Nagasaki, Mitsuo Kiriya, Erika Uehara, Kazuhisa Akiba, Kanako Tanase‐Nakao, Kazuhiro Shimura, Kiyomi Abe, Chiho Sugisawa, Tomohiro Ishii, Kenichi Miyako, Yukihiro Hasegawa, Yoshihiro Maruo, Koji Muroya, Natsuko Watanabe, Eijun Nishihara, Yuka Ito, Takahiko Kogai, Kaori Kameyama, Kazuhiko Nakabayashi, Ken‐ichiro Hata, Maki Fukami, Hirohito Shima, Atsuo Kikuchi, Jun Takayama, Gen Tamiya, Tomonobu Hasegawa

    出版 2024
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  13. 13
    Phosphatase and tensin homolog ( PTEN ) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome–like immunodeficiency

    Phosphatase and tensin homolog ( PTEN ) mutation can cause activated phosphatidylinositol 3-kinase δ syndrome–like immunodeficiency 由 Yuki Tsujita, Kanako Mitsui‐Sekinaka, Kohsuke Imai, Tzu‐Wen Yeh, Noriko Mitsuiki, Takaki Asano, Hidenori Ohnishi, Zenichiro Kato, Yujin Sekinaka, Kiyotaka Zaha, Tamaki Kato, Tsubasa Okano, Takehiro Takashima, Kaoru Kobayashi, Mitsuaki Kimura, Tomoaki Kunitsu, Yoshihiro Maruo, Hirokazu Kanegane, Masatoshi Takagi, Kenichi Yoshida, Yusuke Okuno, Hideki Muramatsu, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Seiji Kojima, Seishi Ogawa, Osamu Ohara, Satoshi Okada, Masao Kobayashi, Tomohiro Morio, Shigeaki Nonoyama

    出版 2016
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  14. 14
    Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol-3-OH kinase δ syndrome type 1

    Hematopoietic stem cell transplantation for progressive combined immunodeficiency and lymphoproliferation in patients with activated phosphatidylinositol-3-OH kinase δ syndrome typ... 由 Tsubasa Okano, Kohsuke Imai, Yuki Tsujita, Noriko Mitsuiki, Kenichi Yoshida, Chikako Kamae, Ken-Ichi Honma, Kanako Mitsui‐Sekinaka, Yujin Sekinaka, Tamaki Kato, Katsuyuki Hanabusa, Eri Endo, Takehiro Takashima, Haruka Hiroki, Tzu-Wen Yeh, Keisuke Tanaka, Masakazu Nagahori, Ikuya Tsuge, Yuki Bando, Fuminori Iwasaki, Yoshiaki Shikama, Masami Inoue, Tomiko Kimoto, Naohiko Moriguchi, Yuki Yuza, Takashi Kaneko, Kyoko Suzuki, Tomoyo Matsubara, Yoshihiro Maruo, Tomoaki Kunitsu, Tomoko Waragai, Hideki Sano, Yuko Hashimoto, Kazuhiro Tasaki, Osamu Suzuki, Toshihiko Shirakawa, Motohiro Kato, Toru Uchiyama, Masataka Ishimura, Tetsuzo Tauchi, Hiroshi Yagasaki, Shiann‐Tarng Jou, Hsin‐Hui Yu, Hirokazu Kanegane, Sven Kracker, Anne Durandy, Daiei Kojima, Hideki Muramatsu, Taizo Wada, Yuzaburo Inoue, Hidetoshi Takada, Seiji Kojima, Seishi Ogawa, Osamu Ohara, Shigeaki Nonoyama, Tomohiro Morio

    出版 2018
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