檢索結果 - Yoko Aoki

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  1. 1
    Ras/MAPK syndromes and childhood hemato-oncological diseases

    Ras/MAPK syndromes and childhood hemato-oncological diseases 由 Yoko Aoki, Yoichi Matsubara

    出版 2012
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  2. 2
    The molecular genetics of <scp>RASopathies</scp>: An update on novel disease genes and new disorders

    The molecular genetics of <scp>RASopathies</scp>: An update on novel disease genes and new disorders 由 Marco Tartaglia, Yoko Aoki, Bruce D. Gelb

    出版 2022
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  3. 3
    Recent advances in RASopathies

    Recent advances in RASopathies 由 Yoko Aoki, Tetsuya Niihori, Shinichi Inoue, Yoichi Matsubara

    出版 2015
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  4. 4
    LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases

    LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases 由 Taiki Abe, Ikumi Umeki, Shin‐ichiro Kanno, Shinichi Inoue, Tetsuya Niihori, Yoko Aoki

    出版 2019
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  5. 5
    Overexpression of p27 <sup>Kip1</sup> lengthens the G <sub>1</sub> phase in a mouse model that targets inducible gene expression to central nervous system progenitor cells

    Overexpression of p27 <sup>Kip1</sup> lengthens the G <sub>1</sub> phase in a mouse model that targets inducible gene expression to central nervous system progenitor cells 由 Takayuki Mitsuhashi, Yoko Aoki, Yaman Z. Ekşioğlu, Takao Takahashi, Pradeep G. Bhide, Steven A. Reeves, Verne S. Caviness

    出版 2001
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  6. 6
    Mice with an Oncogenic HRAS Mutation are Resistant to High-Fat Diet-Induced Obesity and Exhibit Impaired Hepatic Energy Homeostasis

    Mice with an Oncogenic HRAS Mutation are Resistant to High-Fat Diet-Induced Obesity and Exhibit Impaired Hepatic Energy Homeostasis 由 Daiju Oba, Shinichi Inoue, Sachiko Miyagawa‐Tomita, Yasumi Nakashima, Tetsuya Niihori, Seiji Yamaguchi, Yoichi Matsubara, Yoko Aoki

    出版 2017
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  7. 7
    Seasonal Patterns of Respiratory Syncytial Virus, Influenza A Virus, Human Metapneumovirus, and Parainfluenza Virus Type 3 Infections on the Basis of Virus Isolation Data between 2004 and 2011 in Yamagata, Japan

    Seasonal Patterns of Respiratory Syncytial Virus, Influenza A Virus, Human Metapneumovirus, and Parainfluenza Virus Type 3 Infections on the Basis of Virus Isolation Data between 2... 由 Katsumi Mizuta, Chieko Abiko, Yoko Aoki, Tatsuya Ikeda, Yoko Matsuzaki, Tsutomu Itagaki, Fumio Katsushima, Yuriko Katsushima, Masahiro Noda, Hirokazu Kimura, Tadayuki Ahiko

    出版 2013
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  8. 8
    Detection of the Human Coronavirus 229E, HKU1, NL63, and OC43 between 2010 and 2013 in Yamagata, Japan

    Detection of the Human Coronavirus 229E, HKU1, NL63, and OC43 between 2010 and 2013 in Yamagata, Japan 由 Yohei Matoba, Chieko Abiko, Tatsuya Ikeda, Yoko Aoki, Yu Suzuki, Kazue Yahagi, Yoko Matsuzaki, Tsutomu Itagaki, Fumio Katsushima, Yuriko Katsushima, Katsumi Mizuta

    出版 2014
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  9. 9
    TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia

    TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia 由 Tsutomu Ogata, Tetsuya Niihori, Noriko Tanaka, Masahiko Kawai, Takeshi Nagashima, Ryo Funayama, Keiko Nakayama, Shinichi Nakashima, Fumiko Kato, Maki Fukami, Yoko Aoki, Yoichi Matsubara

    出版 2014
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  10. 10
    Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness

    Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness 由 Takayuki Kudo, Shigeo Kure, Katsuhisa Ikeda, An Ping Xia, Yukio Katori, Masaaki Suzuki, Kanako Kojima, Akiko Ichinohe, Yoichi Suzuki, Yoko Aoki, Toshimitsu Kobayashi, Yoichi Matsubara

    出版 2003
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  11. 11
    Detection of NRAS mutation in cell-free DNA biological fluids from patients with kaposiform lymphangiomatosis

    Detection of NRAS mutation in cell-free DNA biological fluids from patients with kaposiform lymphangiomatosis 由 Michio Ozeki, Yoko Aoki, Akifumi Nozawa, Shiho Yasue, Saori Endo, Yumiko Hori, Kentaro Matsuoka, Tetsuya Niihori, Ryo Funayama, Matsuyuki Shirota, Keiko Nakayama, Toshiyuki Fukao

    出版 2019
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  12. 12
    A two-year survey of the oseltamivir-resistant influenza A(H1N1) virus in Yamagata, Japan and the clinical effectiveness of oseltamivir and zanamivir

    A two-year survey of the oseltamivir-resistant influenza A(H1N1) virus in Yamagata, Japan and the clinical effectiveness of oseltamivir and zanamivir 由 Yoko Matsuzaki, Katsumi Mizuta, Yoko Aoki, Asuka Suto, Chieko Abiko, Kanako Sanjoh, Kanetsu Sugawara, Emi Takashita, Tsutomu Itagaki, Yuriko Katsushima, Makoto Ujike, Masatsugu Obuchi, Takato Odagiri, Masato Tashiro

    出版 2010
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  13. 13
    Epidemic Myalgia in Adults Associated with Human Parechovirus Type 3 Infection, Yamagata, Japan, 2008

    Epidemic Myalgia in Adults Associated with Human Parechovirus Type 3 Infection, Yamagata, Japan, 2008 由 Katsumi Mizuta, Makoto Kuroda, Masayuki Kurimura, Yoshikazu Yahata, Tsuyoshi Sekizuka, Yoko Aoki, Tatsuya Ikeda, Chieko Abiko, Masahiro Noda, Hirokazu Kimura, Tetsuya Mizutani, Takeo Kato, Toru Kawanami, Tadayuki Ahiko

    出版 2012
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  14. 14
    Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia

    Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia 由 Tetsuya Niihori, Meri Ouchi‐Uchiyama, Yoji Sasahara, Takashi Kaneko, Yoshiko Hashii, Masahiro Irie, Atsushi Satō, Yuka Saito‐Nanjo, Ryo Funayama, Takeshi Nagashima, Shin‐ichi Inoue, Keiko Nakayama, Keiichi Ozono, Shigeo Kure, Yoichi Matsubara, Masue Imaizumi, Yoko Aoki

    出版 2015
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  15. 15
    A genome-wide association study identifies RNF213 as the first Moyamoya disease gene

    A genome-wide association study identifies RNF213 as the first Moyamoya disease gene 由 Fumiaki Kamada, Yoko Aoki, Ayumi Narisawa, Yu Abe, Shoko Komatsuzaki, Atsuo Kikuchi, Junko Kanno, Tetsuya Niihori, Masao Ono, Naoto Ishii, Yuji Owada, Miki Fujimura, Yoichi Mashimo, Yoichi Suzuki, Akira Hata, Shigeru Tsuchiya, Teiji Tominaga, Yoichi Matsubara, Shigeo Kure

    出版 2010
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  16. 16
    Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia

    Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia 由 Tetsuya Niihori, Yoko Aoki, Hirofumi Ohashi, Kenji Kurosawa, Tatsuro Kondoh, Satoshi Ishikiriyama, Hiroshi Kawame, Hotaka Kamasaki, Tsutomu Yamanaka, Fumio Takada, Kimio Nishio, Masahiro Sakurai, Hiroshi Tamai, Tatsuro Nagashima, Yoichi Suzuki, Shigeo Kure, Kunihiro Fujii, Masue Imaizumi, Yoichi Matsubara

    出版 2005
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  17. 17
    Germline-Activating RRAS2 Mutations Cause Noonan Syndrome

    Germline-Activating RRAS2 Mutations Cause Noonan Syndrome 由 Tetsuya Niihori, Koki Nagai, Atsushi Fujita, Hirofumi Ohashi, Nobuhiko Okamoto, Satoshi Okada, Atsuko Harada, Hirotaka Kihara, Thomas Arbogast, Ryo Funayama, Matsuyuki Shirota, Keiko Nakayama, Taiki Abe, Shin‐ichi Inoue, I-Chun Tsai, Naomichi Matsumoto, Erica E. Davis, Nicholas Katsanis, Yoko Aoki

    出版 2019
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  18. 18
    Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies

    Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies 由 Shoko Komatsuzaki, Yoko Aoki, Tetsuya Niihori, Nobuhiko Okamoto, Raoul C. M. Hennekam, Saskia Hopman, Hirofumi Ohashi, Seiji Mizuno, Yoriko Watanabe, Hotaka Kamasaki, Ikuko Kondo, Nobuko Moriyama, Kenji Kurosawa, Hiroshi Kawame, Ryuhei Okuyama, Masue Imaizumi, Takeshi Rikiishi, Shigeru Tsuchiya, Shigeo Kure, Yoichi Matsubara

    出版 2010
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  19. 19
    Genomic analysis identifies masqueraders of full‐term cerebral palsy

    Genomic analysis identifies masqueraders of full‐term cerebral palsy 由 Yusuke Takezawa, Atsuo Kikuchi, Kazuhiro Haginoya, Tetsuya Niihori, Yurika Numata‐Uematsu, Takehiko Inui, Saeko Yamamura‐Suzuki, Takuya Miyabayashi, Mai Anzai, Sato Suzuki‐Muromoto, Yukimune Okubo, Wakaba Endo, Noriko Togashi, Yasuko Kobayashi, Akira Onuma, Ryo Funayama, Matsuyuki Shirota, Keiko Nakayama, Yoko Aoki, Shigeo Kure

    出版 2018
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  20. 20
    Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans

    Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans 由 Ayumi Narisawa, Shoko Komatsuzaki, Atsuo Kikuchi, Tetsuya Niihori, Yoko Aoki, Kazuko Fujiwara, Mitsuyo Tanemura, Akira Hata, Yoichi Suzuki, Caroline L. Relton, James Grinham, Kit‐yi Leung, Darren Partridge, Alexis Robinson, Victoria Stone, Peter Gustavsson, Philip Stanier, Andrew J. Copp, Nicholas D. E. Greene, Teiji Tominaga, Yoichi Matsubara, Shigeo Kure

    出版 2011
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