Canlyniadau Chwilio - Jun Yoshimura

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  1. 1
    siDirect 2.0: updated software for designing functional siRNA with reduced seed-dependent off-target effect

    siDirect 2.0: updated software for designing functional siRNA with reduced seed-dependent off-target effect gan Yuki Naito, Jun Yoshimura, Shinichi Morishita, Kumiko Ui‐Tei

    Cyhoeddwyd 2009
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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  2. 2
    Long-read metagenomic exploration of extrachromosomal mobile genetic elements in the human gut

    Long-read metagenomic exploration of extrachromosomal mobile genetic elements in the human gut gan Yoshihiko Suzuki, Suguru Nishijima, Yoshikazu Furuta, Jun Yoshimura, Wataru Suda, Kenshiro Oshima, Masahira Hattori, Shinichi Morishita

    Cyhoeddwyd 2019
    Cael y testun llawn Cael y testun llawn
    Artigo
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  3. 3
    Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing

    Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing gan Koichiro Doi, Taku Monjo, Pham Huy Hoang, Jun Yoshimura, Hideaki Yurino, Jun Mitsui, Hiroyuki Ishiura, Yuji Takahashi, Yaeko Ichikawa, Jun Goto, Shoji Tsuji, Shinichi Morishita

    Cyhoeddwyd 2013
    Cael y testun llawn
    Artigo
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  4. 4
    Identification of ATP1A3 Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients

    Identification of ATP1A3 Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients gan Atsushi Ishii, Yoshiaki Saito, Jun Mitsui, Hiroyuki Ishiura, Jun Yoshimura, Hidee Arai, Sumimasa Yamashita, Sadami Kimura, Hirokazu Oguni, Shinichi Morishita, Shoji Tsuji, Masayuki Sasaki, Shinichi Hirose

    Cyhoeddwyd 2013
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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  5. 5
    Recompleting the <i>Caenorhabditis elegans</i> genome

    Recompleting the <i>Caenorhabditis elegans</i> genome gan Jun Yoshimura, Kazuki Ichikawa, Massa J. Shoura, Karen L. Artiles, Idan Gabdank, Lamia Wahba, Cheryl L. Smith, Mark L. Edgley, Ann E. Rougvie, Andrew Fire, Shinichi Morishita, Erich M. Schwarz

    Cyhoeddwyd 2019
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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  6. 6
    ATF6α/β-mediated adjustment of ER chaperone levels is essential for development of the notochord in medaka fish

    ATF6α/β-mediated adjustment of ER chaperone levels is essential for development of the notochord in medaka fish gan Tokiro Ishikawa, Tetsuya Okada, Tomoko Ishikawa‐Fujiwara, Takeshi Todo, Yasuhiro Kamei, Shuji Shigenobu, Minoru Tanaka, Taro Saito, Jun Yoshimura, Shinichi Morishita, Atsushi Toyoda, Yoshiyuki Sakaki, Yoshihito Taniguchi, Shunichi Takeda, Kazutoshi Mori

    Cyhoeddwyd 2013
    Cael y testun llawn
    Artigo
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  7. 7
    Integrative analysis of genomic alterations in triple-negative breast cancer in association with homologous recombination deficiency

    Integrative analysis of genomic alterations in triple-negative breast cancer in association with homologous recombination deficiency gan Masahito Kawazu, Shinya Kojima, Toshihide Ueno, Yasushi Totoki, Hiromi Nakamura, Akiko Kunita, Wei Qü, Jun Yoshimura, Manabu Soda, Takahiko Yasuda, Natsuko Hama, Mihoko Saito-Adachi, Kazuhito Sato, Shinji Kohsaka, Eirin Sai, Masako Ikemura, Shigeru Yamamoto, Tomoko Ogawa, Masashi Fukayama, Keiichiro Tada, Yasuyuki Seto, Shinichi Morishita, Shoichi Hazama, Tatsuhiro Shibata, Yoshihiro Yamashita, Hiroyuki Mano

    Cyhoeddwyd 2017
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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  8. 8
    Human genetic variation database, a reference database of genetic variations in the Japanese population

    Human genetic variation database, a reference database of genetic variations in the Japanese population gan Koichiro Higasa, Noriko Miyake, Jun Yoshimura, K. Okamura, Tetsuya Niihori, Hirotomo Saitsu, Koichiro Doi, Masakazu Shimizu, Kazuhiko Nakabayashi, Yoko Aoki, Yoshinori Tsurusaki, Shinichi Morishita, Takahisa Kawaguchi, Osuke Migita, Keiko Nakayama, Mitsuko Nakashima, Jun Mitsui, Maiko Narahara, Keiko Hayashi, Ryo Funayama, Daisuke Yamaguchi, Hiroyuki Ishiura, Wen‐Ya Ko, Kenichiro Hata, Takeshi Nagashima, Ryo Yamada, Yoichi Matsubara, Akihiro Umezawa, Shoji Tsuji, Naomichi Matsumoto, Fumihiko Matsuda

    Cyhoeddwyd 2016
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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  9. 9
    Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy

    Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy gan Yujiro Higuchi, Ryuta Okunushi, Taichi Hara, Akihiro Hashiguchi, Jun‐Hui Yuan, Akiko Yoshimura, Kei Murayama, Akira Ohtake, Masahiro Ando, Yu Hiramatsu, Satoshi Ishihara, Hajime Tanabe, Yuji Okamoto, Eiji Matsuura, Takehiro Ueda, Tatsushi Toda, Sumimasa Yamashita, Kenichiro Yamada, Takashi Koide, Hiroaki Yaguchi, Jun Mitsui, Hiroyuki Ishiura, Jun Yoshimura, Koichiro Doi, Shinichi Morishita, Ken Sato, Masanori Nakagawa, Masamitsu Yamaguchi, Shoji Tsuji, Hiroshi Takashima

    Cyhoeddwyd 2018
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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  10. 10
    Mutations in <i>MME</i> cause an autosomal‐recessive Charcot–Marie–Tooth disease type 2

    Mutations in <i>MME</i> cause an autosomal‐recessive Charcot–Marie–Tooth disease type 2 gan Yujiro Higuchi, Akihiro Hashiguchi, Jun‐Hui Yuan, Akiko Yoshimura, Jun Mitsui, Hiroyuki Ishiura, Masaki Tanaka, Satoshi Ishihara, Hajime Tanabe, Satoshi Nozuma, Yuji Okamoto, Eiji Matsuura, Ryuichi Ohkubo, Saeko Inamizu, Wataru Shiraishi, Ryo Yamasaki, Yasumasa Ohyagi, Jun‐ichi Kira, Yasushi Oya, Hayato Yabe, Noriko Nishikawa, Shinsuke Tobisawa, Nozomu Matsuda, Masayuki Masuda, Chiharu Kugimoto, Kazuhiro Fukushima, Satoshi Yano, Jun Yoshimura, Koichiro Doi, Masanori Nakagawa, Shinichi Morishita, Shoji Tsuji, Hiroshi Takashima

    Cyhoeddwyd 2016
    Cael y testun llawn Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
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  11. 11
    ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19

    ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19 gan Yuji Takahashi, Y. Fukuda, Jun Yoshimura, Atsushi Toyoda, Kari J. Kurppa, Hiroyoko Moritoyo, Véronique Belzil, Patrick A. Dion, Koichiro Higasa, Koichiro Doi, Hiroyuki Ishiura, Jun Mitsui, Hidetoshi Date, Budrul Ahsan, Takashi Matsukawa, Yaeko Ichikawa, Takashi Moritoyo, Mayumi Ikoma, Tsukasa Hashimoto, Fumiharu Kimura, Shigeo Murayama, Osamu Onodera, Masatoyo Nishizawa, Mari Yoshida, Masashi Aoki, Gen Sobue, Jennifer A. Fifita, Kelly L. Williams, Ian P. Blair, Garth A. Nicholson, Paloma González-Pérez, Robert H. Brown, Masahiro Nomoto, Klaus Elenius, Guy A. Rouleau, Asao Fujiyama, Shinichi Morishita, Jun Goto, Shoji Tsuji

    Cyhoeddwyd 2013
    Cael y testun llawn
    Artigo
    Ychwanegu at ffefrynnau
    Wedi'i Gadw mewn:

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