Search Results - Tadashi Kaname

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  1. 1
    Impact of brown rice-specific γ-oryzanol on epigenetic modulation of dopamine D2 receptors in brain striatum in high-fat-diet-induced obesity in mice

    Impact of brown rice-specific γ-oryzanol on epigenetic modulation of dopamine D2 receptors in brain striatum in high-fat-diet-induced obesity in mice by Chisayo Kozuka, Tadashi Kaname, Chigusa Shimizu‐Okabe, Chitoshi Takayama, Masato Tsutsui, Masayuki Matsushita, Keiko Abe, Hiroaki Masuzaki

    Published 2017
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  2. 2
    Definitive diagnosis of mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome caused by a recurrent <i>de novo</i> mutation in the <i>POLD1</i> gene

    Definitive diagnosis of mandibular hypoplasia, deafness, progeroid features and lipodystrophy (MDPL) syndrome caused by a recurrent <i>de novo</i> mutation in the <i... by Haruka Sasaki, Kumiko Yanagi, Satoshi Ugi, Kunihisa Kobayashi, Kumiko Ohkubo, Yuji Tajiri, Hiroshi Maegawa, Atsunori Kashiwagi, Tadashi Kaname

    Published 2017
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  3. 3
    Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism

    Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism by Yuichi Oike, Akira Hata, Takayoshi Mamiya, Tadashi Kaname, Yukihiro Noda, Misao Suzuki, Hirofumi Yasue, Toshitaka Nabeshima, Kimi Araki, K Yamamura

    Published 1999
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  4. 4
    Neointima formation in a restenosis model is suppressed in midkine-deficient mice

    Neointima formation in a restenosis model is suppressed in midkine-deficient mice by Mitsuru Horiba, Kenji Kadomatsu, Eishin Nakamura, Hisako Muramatsu, Shinya Ikematsu, Sadatoshi Sakuma, Kenji Hayashi, Yukio Yuzawa, Seiichi Matsuo, Masafumi Kuzuya, Tadashi Kaname, Makoto Hirai, Hidehiko Saito, Takashi Muramatsu

    Published 2000
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  5. 5
    Disruption of the midkine gene (<i>Mdk</i>) resulted in altered expression of a calcium binding protein in the hippocampus of infant mice and their abnormal behaviour

    Disruption of the midkine gene (<i>Mdk</i>) resulted in altered expression of a calcium binding protein in the hippocampus of infant mice and their abnormal behaviour by Eishin Nakamura, Kenji Kadomatsu, Shigeki Yuasa, Hisako Muramatsu, Takayoshi Mamiya, Toshitaka Nabeshima, Qi‐Wen Fan, Kazuhiro Ishiguro, Tadahiko Igakura, Shuichiro Matsubara, Tadashi Kaname, Mitsuru Horiba, Hidehiko Saito, Takashi Muramatsu

    Published 1998
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  6. 6
    A Null Mutation in Basigin, an Immunoglobulin Superfamily Member, Indicates Its Important Roles in Peri-implantation Development and Spermatogenesis

    A Null Mutation in Basigin, an Immunoglobulin Superfamily Member, Indicates Its Important Roles in Peri-implantation Development and Spermatogenesis by Tadahiko Igakura, Kenji Kadomatsu, Tadashi Kaname, Hisako Muramatsu, Qi‐Wen Fan, Teruo Miyauchi, Yoshiro Toyama, Naohiko Kuno, Shigeki Yuasa, Masahide Takahashi, Takao Senda, Osamu Taguchi, Ken‐Ichi Yamamura, Kimiyoshi Arimura, Takashi Muramatsu

    Published 1998
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  7. 7
    VarMeter2: An enhanced structure-based methodfmovi for predicting pathogenic missense variants through Mahalanobis distance

    VarMeter2: An enhanced structure-based methodfmovi for predicting pathogenic missense variants through Mahalanobis distance by Shiho Ohno, Chika Ogura, Akinori Yabuki, Kazuyoshi Itoh, Noriyoshi Manabe, Kiyohiko Angata, Akira Togayachi, Kiyoko F. Aoki‐Kinoshita, Jun‐ichi Furukawa, Kei‐ichiro Inamori, Jin‐ichi Inokuchi, Tadashi Kaname, Shoko Nishihara, Yoshiki Yamaguchi

    Published 2025
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  8. 8
    Loss-of-function and gain-of-function mutations in PPP3CA cause two distinct disorders

    Loss-of-function and gain-of-function mutations in PPP3CA cause two distinct disorders by Takeshi Mizuguchi, Mitsuko Nakashima, Mitsuhiro Kato, Nobuhiko Okamoto, Hirokazu Kurahashi, Nina Ekhilevitch, Masaaki Shiina, Gen Nishimura, Takashi Shibata, Muneaki Matsuo, Tae Ikeda, Kazuhiro Ogata, Naomi Tsuchida, Satomi Mitsuhashi, Satoko Miyatake, Atsushi Takata, Noriko Miyake, Kenichiro Hata, Tadashi Kaname, Yoichi Matsubara, Hirotomo Saitsu, Naomichi Matsumoto

    Published 2018
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  9. 9
    STAT6 gain-of-function variant exacerbates multiple allergic symptoms

    STAT6 gain-of-function variant exacerbates multiple allergic symptoms by Ichiro Takeuchi, Kumiko Yanagi, Shuji Takada, Toru Uchiyama, Arisa Igarashi, Kenichiro Motomura, Yuka Hayashi, Naoko Nagano, Ryo Matsuoka, Hiroki Sugiyama, Takako Yoshioka, Hirohisa Saito, Toshinao Kawai, Yumiko Miyaji, Yusuke Inuzuka, Yoichi Matsubara, Yukihiro Ohya, Toshiaki Shimizu, Kenji Matsumoto, Katsuhiro Arai, Ichiro Nomura, Tadashi Kaname, Hideaki Morita

    Published 2022
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  10. 10
    Recurrent de novo <i>MAPK8IP3</i> variants cause neurological phenotypes

    Recurrent de novo <i>MAPK8IP3</i> variants cause neurological phenotypes by Shinya Iwasawa, Kumiko Yanagi, Atsuo Kikuchi, Yasuko Kobayashi, Kazuhiro Haginoya, Hiroshi Matsumoto, Kenji Kurosawa, Masayuki Ochiai, Yasunari Sakai, Atsushi Fujita, Noriko Miyake, Tetsuya Niihori, Matsuyuki Shirota, Ryo Funayama, Shigeaki Nonoyama, Shouichi Ohga, Hiroshi Kawame, Keiko Nakayama, Yoko Aoki, Naomichi Matsumoto, Tadashi Kaname, Yoichi Matsubara, Wataru Shoji, Shigeo Kure

    Published 2019
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  11. 11
    Long-term dietary nitrite and nitrate deficiency causes the metabolic syndrome, endothelial dysfunction and cardiovascular death in mice

    Long-term dietary nitrite and nitrate deficiency causes the metabolic syndrome, endothelial dysfunction and cardiovascular death in mice by Mika Kina-Tanada, Mayuko Sakanashi, Akihide Tanimoto, Tadashi Kaname, Toshihiro Matsuzaki, Katsuhiko Noguchi, Taro Uchida, Junko Nakasone, Chisayo Kozuka, Masayoshi Ishida, Haruaki Kubota, Yuji Taira, Yuichi Totsuka, Shin-ichiro Kina, Hajime Sunakawa, Junichi Omura, Kimio Satoh, Hiroaki Shimokawa, Nobuyuki Yanagihara, Shiro Maeda, Yusuke Ohya, Masayuki Matsushita, Hiroaki Masuzaki, Akira Arasaki, Masato Tsutsui

    Published 2017
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  12. 12
    Human germline gain-of-function in STAT6: from severe allergic disease to lymphoma and beyond

    Human germline gain-of-function in STAT6: from severe allergic disease to lymphoma and beyond by Mehul Sharma, Narissara Suratannon, Daniel Leung, Safa Barış, Ichiro Takeuchi, Simran Samra, Kumiko Yanagi, Jaime S. Rosa Duque, Mehdi Benamar, Kate L. Del Bel, Mana Momenilandi, Vivien Béziat, Jean‐Laurent Casanova, P. Martin van Hagen, Katsuhiro Arai, Ichiro Nomura, Tadashi Kaname, Pantipa Chatchatee, Hideaki Morita, Talal A. Chatila, YL Lau, Stuart E. Turvey

    Published 2024
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  13. 13
    SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice

    SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice by Ippei Okada, Haruka Hamanoue, Koji Terada, Takaya Tohma, André Mégarbané, Éliane Chouery, Joelle Abou‐Ghoch, Nadine Jalkh, Özgür Çoğulu, Ferda Özkınay, Kyoji Horie, Junji Takeda, Tatsuya Furuichi, Shiro Ikegawa, Kiyomi Nishiyama, Satoko Miyatake, Akira Nishimura, Takeshi Mizuguchi, Norio Niikawa, Fumiki Hirahara, Tadashi Kaname, Koh-ichiro Yoshiura, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Takahisa Furukawa, Naomichi Matsumoto, Hirotomo Saitsu

    Published 2010
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  14. 14
    Clinical correlations of mutations affecting six components of the <scp>SWI</scp>/<scp>SNF</scp> complex: Detailed description of 21 patients and a review of the literature

    Clinical correlations of mutations affecting six components of the <scp>SWI</scp>/<scp>SNF</scp> complex: Detailed description of 21 patients and a review of the literature by Tomoki Kosho, Nobuhiko Okamoto, Hirofumi Ohashi, Yoshinori Tsurusaki, Yoko Imai, Yumiko Hibi‐Ko, Hiroshi Kawame, Tomomi Homma, Saori Tanabe, Mitsuhiro Kato, Yoko Hiraki, Takanori Yamagata, Shoji Yano, Satoru Sakazume, Takuma Ishii, Toshiro Nagai, Tohru Ohta, Norio Niikawa, Seiji Mizuno, Tadashi Kaname, Kenji Naritomi, Yoko Narumi, Keiko Wakui, Yoshimitsu Fukushima, Satoko Miyatake, Takeshi Mizuguchi, Hirotomo Saitsu, Noriko Miyake, Naomichi Matsumoto

    Published 2013
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  15. 15
    Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis

    Exploring the genetic diversity of the Japanese population: Insights from a large-scale whole genome sequencing analysis by Yosuke Kawai, Yusuke Watanabe, Yosuke Omae, Reiko Miyahara, Seik‐Soon Khor, Eisei Noiri, Koji Kitajima, Hideyuki Shimanuki, Hiroyuki Gatanaga, Kenichiro Hata, Kotaro Hattori, Aritoshi Iida, Hatsue Ishibashi-Ueda, Tadashi Kaname, Tatsuya Kanto, Ryo Matsumura, Kengo Miyo, Michio Noguchi, Kouichi Ozaki, Masaya Sugiyama, Ayako Takahashi, Haruhiko Tokuda, Tsutomu Tomita, Akihiro Umezawa, Hiroshi Watanabe, Sumiko Yoshida, Yu‐ichi Goto, Yutaka Maruoka, Yoichi Matsubara, Shumpei Niida, Masashi Mizokami, Katsushi Tokunaga

    Published 2023
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  16. 16
    Spectrum of <i>MLL2</i> (<i>ALR</i>) mutations in 110 cases of Kabuki syndrome

    Spectrum of <i>MLL2</i> (<i>ALR</i>) mutations in 110 cases of Kabuki syndrome by Mark C. Hannibal, Kati J. Buckingham, Sarah Ng, Jeffrey E. Ming, Anita Beck, Margaret J. McMillin, Heidi Gildersleeve, Abigail W. Bigham, Holly K. Tabor, Heather C. Mefford, Joseph Cook, Koh‐ichiro Yoshiura, Tadashi Matsumoto, Naomichi Matsumoto, Noriko Miyake, Hidefumi Tonoki, Kenji Naritomi, Tadashi Kaname, Toshiro Nagai, Hirofumi Ohashi, Kenji Kurosawa, Jia‐Woei Hou, Tohru Ohta, Deshung Liang, Akira Sudo, Colleen A. Morris, Siddharth Banka, Graeme Black, Jill Clayton‐Smith, Deborah A. Nickerson, Elaine H. Zackai, Tamim H. Shaikh, Dian Donnai, Norio Niikawa, Jay Shendure, Michael J. Bamshad

    Published 2011
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  17. 17
    Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities

    Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities by Fuad Chowdhury, Lei Wang, Mohammed Al‐Raqad, David J. Amor, A Baxová, Šárka Bendová, Elisa Biamino, Alfredo Brusco, Oana Caluseriu, Nancy J. Cox, Tawfiq Froukh, Meral Gunay‐Aygun, Miroslava Hančárová, Devon Haynes, Solveig Heide, George Hoganson, Tadashi Kaname, Boris Keren, Kenjiro Kosaki, Kazuo Kubota, Jennifer Lemons, Maria A. Magriñá, Paul R. Mark, Marie McDonald, Sarah Montgomery, Gina M. Morley, Hidenori Ohnishi, Nobuhiko Okamoto, David Rodriguez‐Buritica, Patrick Rump, Zdeněk Sedláček, Krista Schatz, Haley Streff, Tomoko Uehara, Jagdeep S. Walia, Patricia G. Wheeler, Antje Wiesener, Christiane Zweier, Koichi Kawakami, Ingrid M. Wentzensen, Seema R. Lalani, Victoria Mok Siu, Weimin Bi, Tuğçe B. Balcı

    Published 2021
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  18. 18
    Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes

    Assessing the efficacy of target adaptive sampling long-read sequencing through hereditary cancer patient genomes by Wataru Nakamura, Makoto Hirata, Satoyo Oda, Kenichi Chiba, Ai Okada, Raúl Nicolás Mateos, Masahiro Sugawa, Naoko Iida, Mineko Ushiama, Noriko Tanabe, Hiromi Sakamoto, Shigeki Sekine, Akira Hirasawa, Yosuke Kawai, Katsushi Tokunaga, Hatsue Ishibashi‐Ueda, Tsutomu Tomita, Michio Noguchi, Ayako Takahashi, Yu‐ichi Goto, Sumiko Yoshida, Kotaro Hattori, Ryo Matsumura, Aritoshi Iida, Yutaka Maruoka, Hiroyuki Gatanaga, Masaya Sugiyama, Satoshi Suzuki, Kengo Miyo, Yoichi Matsubara, Akihiro Umezawa, Kenichiro Hata, Tadashi Kaname, Kouichi Ozaki, Haruhiko Tokuda, Hiroshi Watanabe, Shumpei Niida, Eisei Noiri, Koji Kitajima, Yosuke Omae, Reiko Miyahara, Hideyuki Shimanuki, Shin‐ichi Tsujimoto, Norio Shiba, Shuichi Ito, Teruhiko Yoshida, Yuichi Shiraishi

    Published 2024
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  19. 19
    Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures

    Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures by Yūji Takahashi, Hidetoshi Date, Hideki Oi, Takeya Adachi, Noriaki Imanishi, En Kimura, Hotake Takizawa, Shinji Kosugi, Naomichi Matsumoto, Kenjiro Kosaki, Yoichi Matsubara, Yukio Ando, Toshihisa Anzai, Tadashi Ariga, Yoshimitsu Fukushima, Yoshihiko Furusawa, Akira Ganaha, Yu‐ichi Goto, Kenichiro Hata, Masataka Honda, Kazumoto Iijima, Tsunakuni Ikka, Issei Imoto, Tadashi Kaname, Masao Kobayashi, Seiji Kojima, Hiroki Kurahashi, Shigeo Kure, Kenji Kurosawa, Yoshihiro Maegaki, Yoshio Makita, Tomohiro Morio, Ichiei Narita, Fumio Nomura, Tsutomu Ogata, Keiichi Ozono, Akira Oka, Nobuhiko Okamoto, Shinji Saitoh, Akihiro Sakurai, Fumio Takada, Tsutomu TAKAHASHI, Akira Tamaoka, Akihiro Umezawa, Akihiro Yachie, Kouichiro Yoshiura, Yasutsugu Chinen, Mariko Eguchi, Keishi Fujio, Kiminori Hosoda, Tomohiko Ichikawa, Toshitaka Kawarai, Tomoki Kosho, Mitsuo Masuno, Akie Nakamura, Takaya Nakane, Tomoo Ogi, Satoshi Okada, Yasushi Sakata, Toshiyuki Seto, Yoshiyuki Takahashi, Tadao Takano, Mitsuharu Ueda, Hideaki Yagasaki, Toshiyuki Yamamoto, Atsushi Watanabe, Yoshihiro Hotta, Akiharu Kubo, Hirofumi Maruyama, Keiji Moriyama, Eiji Nanba, Norio Sakai, Yoshiki Sekijima, Toru Shimosegawa, Tsutomu Takeuchi, Shin‐ichi Usami, Kazuhiko Yamamoto, Hidehiro Mizusawa

    Published 2022
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