Search Results - "Yoko Katsuki"

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    Co-operation of BRCA1 and POH1 relieves the barriers posed by 53BP1 and RAP80 to resection by Kakarougkas, Andreas, Ismail, Amani, Katsuki, Yoko, Freire, Raimundo, Shibata, Atsushi, Jeggo, Penny A

    Published in Nucleic acids research (01-12-2013)
    “…In G2 phase cells, DNA double-strand break repair switches from DNA non-homologous end-joining to homologous recombination. This switch demands the promotion…”
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    Journal Article
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    Defects in homologous recombination repair behind the human diseases: FA and HBOC by Katsuki, Yoko, Takata, Minoru

    Published in Endocrine-related cancer (01-10-2016)
    “…Hereditary breast and ovarian cancer (HBOC) syndrome and a rare childhood disorder Fanconi anemia (FA) are caused by homologous recombination (HR) defects, and…”
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    FANCI-FANCD2 stabilizes the RAD51-DNA complex by binding RAD51 and protects the 5'-DNA end by Sato, Koichi, Shimomuki, Mayo, Katsuki, Yoko, Takahashi, Daisuke, Kobayashi, Wataru, Ishiai, Masamichi, Miyoshi, Hiroyuki, Takata, Minoru, Kurumizaka, Hitoshi

    Published in Nucleic acids research (15-12-2016)
    “…The FANCI-FANCD2 (I-D) complex is considered to work with RAD51 to protect the damaged DNA in the stalled replication fork. However, the means by which this…”
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    USP42 enhances homologous recombination repair by promoting R-loop resolution with a DNA–RNA helicase DHX9 by Matsui, Misaki, Sakasai, Ryo, Abe, Masako, Kimura, Yusuke, Kajita, Shoki, Torii, Wakana, Katsuki, Yoko, Ishiai, Masamichi, Iwabuchi, Kuniyoshi, Takata, Minoru, Nishi, Ryotaro

    Published in Oncogenesis (New York, NY) (15-06-2020)
    “…The nucleus of mammalian cells is compartmentalized by nuclear bodies such as nuclear speckles, however, involvement of nuclear bodies, especially nuclear…”
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    Mouse Slfn8 and Slfn9 genes complement human cells lacking SLFN11 during the replication stress response by Alvi, Erin, Mochizuki, Ayako L., Katsuki, Yoko, Ogawa, Minori, Qi, Fei, Okamoto, Yusuke, Takata, Minoru, Mu, Anfeng

    Published in Communications biology (13-10-2023)
    “…The Schlafen (SLFN)11 gene has been implicated in various biological processes such as suppression of HIV replication, replication stress response, and…”
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    Influence of intraocular lens implantation on anterior capsule contraction and posterior capsule opacification by Aose, Masamoto, MD, Matsushima, Hiroyuki, MD, PhD, Mukai, Koichiro, PhD, Katsuki, Yoko, Gotoh, Norihito, MD, PhD, Senoo, Tadashi, MD, PhD

    Published in Journal of cataract and refractive surgery (01-12-2014)
    “…Purpose To evaluate whether and how intraocular lens (IOL) implantation influences the development of anterior capsule contraction and posterior capsule…”
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    Decreased visual acuity resulting from glistening and sub-surface nano-glistening formation in intraocular lenses: A retrospective analysis of 5 cases by Matsushima, Hiroyuki, Nagata, Mayumi, Katsuki, Yoko, Ota, Ichiro, Miyake, Kensaku, Beiko, George H.H., Grzybowski, Andrzej

    Published in Saudi journal of ophthalmology (01-10-2015)
    “…To report on five patients with decreased visual acuity due to glistening and severe sub-surface nano-glistening (SSNG) formation within their intraocular…”
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    Japanese Mothers' Breastfeeding Knowledge and Attitudes Assessed by the Iowa Infant Feeding Attitudes Scale by Inoue, Madoka, Binns, Colin W, Katsuki, Yoko, Ouchi, Mikio

    Published in Asia Pacific Journal of Clinical Nutrition (01-01-2013)
    “…This study describes Japanese mothers' knowledge and attitudes towards breastfeeding using the Iowa Infant Feeding Attitudes Scale (IIFAS). A cross-sectional…”
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    Caffeine yields aneuploidy through asymmetrical cell division caused by misalignment of chromosomes by Katsuki, Yoko, Nakada, Shinichiro, Yokoyama, Tetsuji, Imoto, Issei, Inazawa, Johji, Nagasawa, Masayuki, Mizutani, Shuki

    Published in Cancer science (01-08-2008)
    “…Aneuploidy has been implicated as an important step leading to various neoplasias. Although genetic factors that block aneuploidy have been the subject of…”
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    Preventing secondary cataract and anterior capsule contraction by modification of intraocular lenses by Matsushima, Hiroyuki, Iwamoto, Hidetoshi, Mukai, Kouichiro, Katsuki, Yoko, Nagata, Mayumi, Senoo, Tadashi

    Published in Expert review of medical devices (01-03-2008)
    “…Advances in intraocular lens (IOL) design have led to the use of lenses with improved performance including tinting, asphericity, multifocality and…”
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    The role of SLFN11 in DNA replication stress response and its implications for the Fanconi anemia pathway by Mu, Anfeng, Okamoto, Yusuke, Katsuki, Yoko, Takata, Minoru

    Published in DNA repair (01-09-2024)
    “…Fanconi anemia (FA) is a hereditary disorder characterized by a deficiency in the repair of DNA interstrand crosslinks and the response to replication stress…”
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    SETDB1, HP1 and SUV39 promote repositioning of 53BP1 to extend resection during homologous recombination in G2 cells by Alagoz, Meryem, Katsuki, Yoko, Ogiwara, Hideaki, Ogi, Tomoo, Shibata, Atsushi, Kakarougkas, Andreas, Jeggo, Penny

    Published in Nucleic acids research (18-09-2015)
    “…Recent studies have shown that homologous recombination (HR) requires chromatin repression as well as relaxation at DNA double strand breaks (DSBs). HP1 and…”
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    Open-capsule intraocular lens to prevent posterior capsule opacification by Katsuki, Yoko, Matsushima, Hiroyuki, Mukai, Koichiro, Watabiki, Satoshi, Aose, Masamoto, Terauchi, Wataru, Nagamoto, Toshiyuki, Senoo, Tadashi

    Published in Journal of cataract and refractive surgery (01-07-2019)
    “…To develop a single-piece open-capsule intraocular lens (IOL) that can be inserted through a small incision and that prevents posterior capsule opacification…”
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    SLFN11 promotes stalled fork degradation that underlies the phenotype in Fanconi anemia cells by Okamoto, Yusuke, Abe, Masako, Mu, Anfeng, Tempaku, Yasuko, Rogers, Colette B., Mochizuki, Ayako L., Katsuki, Yoko, Kanemaki, Masato T., Takaori-Kondo, Akifumi, Sobeck, Alexandra, Bielinsky, Anja-Katrin, Takata, Minoru

    Published in Blood (21-01-2021)
    “…Fanconi anemia (FA) is a hereditary disorder caused by mutations in any 1 of 22 FA genes. The disease is characterized by hypersensitivity to interstrand…”
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    RNF168 E3 ligase participates in ubiquitin signaling and recruitment of SLX4 during DNA crosslink repair by Katsuki, Yoko, Abe, Masako, Park, Seon Young, Wu, Wenwen, Yabe, Hiromasa, Yabe, Miharu, van Attikum, Haico, Nakada, Shinichiro, Ohta, Tomohiko, Seidman, Michael M., Kim, Yonghwan, Takata, Minoru

    Published in Cell reports (Cambridge) (26-10-2021)
    “…SLX4/FANCP is a key Fanconi anemia (FA) protein and a DNA repair scaffold for incision around a DNA interstrand crosslink (ICL) by its partner XPF nuclease…”
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    Japanese mothers' breastfeeding knowledge and attitudes assessed by the Iowa infant feeding attitudes scale by Madoka Inoue, Colin W Binns, Yoko Katsuki, Mikio Ouchi

    Published in Asia Pacific journal of clinical nutrition (01-01-2013)
    “…This study describes Japanese mothers' knowledge and attitudes towards breastfeeding using the Iowa Infant Feeding Attitudes Scale (IIFAS). A cross-sectional…”
    Get full text
    Journal Article