検索結果 - Mayuko Shimada

  • 検索結果 1 - 8 結果 / 8
結果の絞り込み
  1. 1
    Endogenous aldehyde-induced DNA–protein crosslinks are resolved by transcription-coupled repair

    Endogenous aldehyde-induced DNA–protein crosslinks are resolved by transcription-coupled repair 著者: Yasuyoshi Oka, Yuka Nakazawa, Mayuko Shimada, Tomoo Ogi

    出版事項 2024
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  2. 2
    Genetic background variation impacts microglial heterogeneity and disease progression in amyotrophic lateral sclerosis model mice

    Genetic background variation impacts microglial heterogeneity and disease progression in amyotrophic lateral sclerosis model mice 著者: Okiru Komine, Syuhei Ohnuma, Kunihiko Hinohara, Yuichiro Hara, Mayuko Shimada, Tomohiro Akashi, Seiji Watanabe, Akira Sobue, Noe Kawade, Tomoo Ogi, Koji Yamanaka

    出版事項 2024
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  3. 3
    PRKDC mutations in a SCID patient with profound neurological abnormalities

    PRKDC mutations in a SCID patient with profound neurological abnormalities 著者: Lisa Woodbine, Jessica A. Neal, Nanda Kumar Sasi, Mayuko Shimada, Karen Deem, Helen G. Coleman, William B. Dobyns, Tomoo Ogi, Katheryn Meek, E. Graham Davies, Penny A. Jeggo

    出版事項 2013
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  4. 4
    XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency

    XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency 著者: Chaowan Guo, Yuka Nakazawa, Lisa Woodbine, Andrea Björkman, Mayuko Shimada, Heather Fawcett, Nan Jia, Kaname Ohyama, Tao‐Sheng Li, Yuji Nagayama, Norisato Mitsutake, Qiang Pan‐Hammarström, Andrew R. Gennery, Alan R. Lehmann, Penny A. Jeggo, Tomoo Ogi

    出版事項 2015
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  5. 5
    Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair

    Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair 著者: Yuka Nakazawa, Kensaku Sasaki, Norisato Mitsutake, Michiko Matsuse, Mayuko Shimada, Tiziana Nardò, Yoshito Takahashi, Kaname Ohyama, Kosei Ito, Hiroyuki Mishima, Masayo Nomura, Akira Kinoshita, Shinji Ono, Katsuya Takenaka, Ritsuko Masuyama, Takashi Kudo, Hanoch Slor, Atsushi Utani, Satoshi Tateishi, Shunichi Yamashita, Miria Stefanini, Alan R. Lehmann, Koh-ichiro Yoshiura, Tomoo Ogi

    出版事項 2012
    全文の入手
    Artigo
    お気に入りに追加
    保存先:
  6. 6
    Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled Repair

    Ubiquitination of DNA Damage-Stalled RNAPII Promotes Transcription-Coupled Repair 著者: Yuka Nakazawa, Yuichiro Hara, Yasuyoshi Oka, Okiru Komine, Diana van den Heuvel, Chaowan Guo, Yasukazu Daigaku, Mayu Isono, Yuxi He, Mayuko Shimada, Kana Kato, Nan Jia, Satoru Hashimoto, Yuko Kotani, Yuka Miyoshi, Miyako Tanaka, Akira Sobue, Norisato Mitsutake, Takayoshi Suganami, Akio Masuda, Kinji Ohno, Shinichiro Nakada, Tomoji Mashimo, Koji Yamanaka, Martijn S. Luijsterburg, Tomoo Ogi

    出版事項 2020
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  7. 7
    Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia

    Malfunction of Nuclease ERCC1-XPF Results in Diverse Clinical Manifestations and Causes Cockayne Syndrome, Xeroderma Pigmentosum, and Fanconi Anemia 著者: Kazuya Kashiyama, Yuka Nakazawa, Daniela T. Pilz, Chaowan Guo, Mayuko Shimada, Kensaku Sasaki, Heather Fawcett, Jonathan Wing, Susan O. Lewin, Lucinda Carr, Tao‐Sheng Li, Koh-ichiro Yoshiura, Atsushi Utani, Akiyoshi Hirano, Shunichi Yamashita, Danielle Greenblatt, Tiziana Nardò, Miria Stefanini, D. McGibbon, Robert Sarkany, Hiva Fassihi, Yoshito Takahashi, Yuji Nagayama, Norisato Mitsutake, Alan R. Lehmann, Tomoo Ogi

    出版事項 2013
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:
  8. 8
    Digenic mutations in <i>ALDH2</i> and <i>ADH5</i> impair formaldehyde clearance and cause a multisystem disorder, AMeD syndrome

    Digenic mutations in <i>ALDH2</i> and <i>ADH5</i> impair formaldehyde clearance and cause a multisystem disorder, AMeD syndrome 著者: Yasuyoshi Oka, Motoharu Hamada, Yuka Nakazawa, Hideki Muramatsu, Yusuke Okuno, Koichiro Higasa, Mayuko Shimada, Honoka Takeshima, Katsuhiro Hanada, Taichi Hirano, Toshiro Kawakita, Hirotoshi Sakaguchi, Takuya Ichimura, Shuichi Ozono, Kotaro Yuge, Yoriko Watanabe, Yuko Kotani, Mutsumi Yamane, Yumiko Kasugai, Miyako Tanaka, Takayoshi Suganami, Shinichiro Nakada, Norisato Mitsutake, Yuichiro Hara, Kohji Kato, Seiji Mizuno, Noriko Miyake, Yosuke Kawai, Katsushi Tokunaga, Masao Nagasaki, Seiji Kito, Keiichi Isoyama, Masafumi Onodera, Hideo Kaneko, Naomichi Matsumoto, Fumihiko Matsuda, Keitaro Matsuo, Yoshiyuki Takahashi, Tomoji Mashimo, Seiji Kojima, Tomoo Ogi

    出版事項 2020
    全文の入手 全文の入手
    Artigo
    お気に入りに追加
    保存先:

検索ツール: