Risultati della ricerca - Kenichi Chiba

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  1. 1
    Systematically developing a registry of splice-site creating variants utilizing massive publicly available transcriptome sequence data

    Systematically developing a registry of splice-site creating variants utilizing massive publicly available transcriptome sequence data di Naoko Iida, Ai Okada, Yoshihisa Kobayashi, Kenichi Chiba, Yasushi Yatabe, Yuichi Shiraishi

    Pubblicazione 2025
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  2. 2
    A comprehensive characterization of <i>cis</i>-acting splicing-associated variants in human cancer

    A comprehensive characterization of <i>cis</i>-acting splicing-associated variants in human cancer di Yuichi Shiraishi, Keisuke Kataoka, Kenichi Chiba, Ai Okada, Yasunori Kogure, Hiroko Tanaka, Seishi Ogawa, Satoru Miyano

    Pubblicazione 2018
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  3. 3
    Precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv

    Precise characterization of somatic complex structural variations from tumor/control paired long-read sequencing data with nanomonsv di Yuichi Shiraishi, Junji Koya, Kenichi Chiba, Ai Okada, Yasuhito Arai, Yuki Saito, Tatsuhiro Shibata, Keisuke Kataoka

    Pubblicazione 2023
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  4. 4
    An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data

    An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data di Yuichi Shiraishi, Yusuke Sato, Kenichi Chiba, Yusuke Okuno, Yasunobu Nagata, Kenichi Yoshida, Norio Shiba, Yasuhide Hayashi, Haruki Kume, Yukio Homma, Masashi Sanada, Seishi Ogawa, Satoru Miyano

    Pubblicazione 2013
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  5. 5
    Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients

    Variant ALDH2 is associated with accelerated progression of bone marrow failure in Japanese Fanconi anemia patients di Asuka Hira, Hiromasa Yabe, Kenichi Yoshida, Yusuke Okuno, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Jun Nakamura, Seiji Kojima, Seishi Ogawa, Keitaro Matsuo, Minoru Takata, Miharu Yabe

    Pubblicazione 2013
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  6. 6
    Mutations in the Gene Encoding the E2 Conjugating Enzyme UBE2T Cause Fanconi Anemia

    Mutations in the Gene Encoding the E2 Conjugating Enzyme UBE2T Cause Fanconi Anemia di Asuka Hira, Kenichi Yoshida, Koichi Sato, Yusuke Okuno, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Akira Shimamoto, Hidetoshi Tahara, Etsuro Ito, Seiji Kojima, Hitoshi Kurumizaka, Seishi Ogawa, Minoru Takata, Hiromasa Yabe, Miharu Yabe

    Pubblicazione 2015
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  7. 7
    <i>TERT</i> promoter mutations and chromosome 8p loss are characteristic of nonalcoholic fatty liver disease‐related hepatocellular carcinoma

    <i>TERT</i> promoter mutations and chromosome 8p loss are characteristic of nonalcoholic fatty liver disease‐related hepatocellular carcinoma di Soo Ki Kim, Yoshihide Ueda, Etsuro Hatano, Nobuyuki Kakiuchi, Haruhiko Takeda, Tomoyuki Gotō, Takahiro Shimizu, Kenichi Yoshida, Yoshihiro Ikura, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Shinji Üemoto, Tsutomu Chiba, Seishi Ogawa, Hiroyuki Marusawa

    Pubblicazione 2016
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  8. 8
    Somatic mutations in plasma cell-free DNA are diagnostic markers for esophageal squamous cell carcinoma recurrence

    Somatic mutations in plasma cell-free DNA are diagnostic markers for esophageal squamous cell carcinoma recurrence di Masami Ueda, Tomohiro Iguchi, Takaaki Masuda, Yujiro Nakahara, Hidenari Hirata, Ryutaro Uchi, Atsushi Niida, Kota Momose, Shotaro Sakimura, Kenichi Chiba, Hidetoshi Eguchi, Shuhei Ito, K Sugimachi, Makoto Yamasaki, Yutaka Suzuki, Satoru Miyano, Yuichiro� Doki, Masaki Mori, Koshi Mimori

    Pubblicazione 2016
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  9. 9
    Gene expression and risk of leukemic transformation in myelodysplasia

    Gene expression and risk of leukemic transformation in myelodysplasia di Yusuke Shiozawa, Luca Malcovati, Anna Gallì, Andrea Pellagatti, Mohsen Karimi, Aiko Sato‐Otsubo, Yusuke Sato, Hiromichi Suzuki, Tetsuichi Yoshizato, Kenichi Yoshida, Yuichi Shiraishi, Kenichi Chiba, Hideki Makishima, Jacqueline Boultwood, Eva Hellström‐Lindberg, Satoru Miyano, Mario Cazzola, Seishi Ogawa

    Pubblicazione 2017
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  10. 10
    Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia

    Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia di Yusuke Shiozawa, Luca Malcovati, Anna Gallì, Aiko Sato‐Otsubo, Keisuke Kataoka, Yusuke Sato, Yosaku Watatani, Hiromichi Suzuki, Tetsuichi Yoshizato, Kenichi Yoshida, Masashi Sanada, Hideki Makishima, Yuichi Shiraishi, Kenichi Chiba, Eva Hellström‐Lindberg, Satoru Miyano, Seishi Ogawa, Mario Cazzola

    Pubblicazione 2018
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  11. 11
    Recurrent genetic defects on chromosome 7q in myeloid neoplasms

    Recurrent genetic defects on chromosome 7q in myeloid neoplasms di Naoko Hosono, Hideki Makishima, Andrés Jerez, Kenichi Yoshida, Bartlomiej Przychodzen, Sarah McMahon, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Masashi Sanada, Inés Gómez‐Seguí, Amit Verma, Michael A. McDevitt, Mikkael A. Sekeres, Seishi Ogawa, J. Maciejewski

    Pubblicazione 2014
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  12. 12
    ACTN1 Mutations Cause Congenital Macrothrombocytopenia

    ACTN1 Mutations Cause Congenital Macrothrombocytopenia di Shinji Kunishima, Yusuke Okuno, Kenichi Yoshida, Yuichi Shiraishi, Masashi Sanada, Hideki Muramatsu, Kenichi Chiba, Hiroko Tanaka, Kôji Miyazaki, Michio Sakai, Masatoshi Ohtake, Ryōji Kobayashi, Akihiro Iguchi, Gen Niimi, Makoto Otsu, Yoshiyuki Takahashi, Satoru Miyano, Hidehiko Saito, Seiji Kojima, Seishi Ogawa

    Pubblicazione 2013
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  13. 13
    Identification of cell-type-specific mutations in nodal T-cell lymphomas

    Identification of cell-type-specific mutations in nodal T-cell lymphomas di Tran B. Nguyen, Mamiko Sakata‐Yanagimoto, Y Asabe, Daisuke Matsubara, Junko Kano, Kenichi Yoshida, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Koji Izutsu, Naoya Nakamura, Kengo Takeuchi, Hiroaki Miyoshi, Koichi Ohshima, Takashi Minowa, Seishi Ogawa, Masayuki Noguchi, Shigeru Chiba

    Pubblicazione 2017
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  14. 14
    Biallelic <i>DICER1</i> Mutations in Sporadic Pleuropulmonary Blastoma

    Biallelic <i>DICER1</i> Mutations in Sporadic Pleuropulmonary Blastoma di Masafumi Seki, Kenichi Yoshida, Yuichi Shiraishi, Teppei Shimamura, Yusuke Sato, Riki Nishimura, Yusuke Okuno, Kenichi Chiba, Hiroko Tanaka, Keisuke Kato, Motohiro Kato, Ryoji Hanada, Yuko Nomura, Hyuntae Park, Toshiaki Ishida, Akira Oka, Takashi Igarashi, Satoru Miyano, Yasuhide Hayashi, Seishi Ogawa, Junko Takita

    Pubblicazione 2014
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  15. 15
    PRPF8 defects cause missplicing in myeloid malignancies

    PRPF8 defects cause missplicing in myeloid malignancies di Amina Kurtović-Kozarić, B Przychodzen, Jagjit Singh, Maria M. Konarska, Michael J. Clemente, Zaher K. Otrock, Megan O. Nakashima, Eric D. Hsi, Kenichi Yoshida, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Seishi Ogawa, Jacqueline Boultwood, Hideki Makishima, Jaroslaw P. Maciejewski, Richard A. Padgett

    Pubblicazione 2014
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  16. 16
    Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis

    Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis di Ryunosuke Saiki, Yukihide Momozawa, Yasuhito Nannya, Masahiro Nakagawa, Yotaro Ochi, Tetsuichi Yoshizato, Chikashi Terao, Yutaka Kuroda, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Atsushi Niida, Seiya Imoto, Koichi Matsuda, Takayuki Morisaki, Yoshinori Murakami, Yoichiro Kamatani, Shuichi Matsuda, Michiaki Kubo, Satoru Miyano, Hideki Makishima, Seishi Ogawa

    Pubblicazione 2021
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  17. 17
    Unbiased Detection of Driver Mutations in Extramammary Paget Disease

    Unbiased Detection of Driver Mutations in Extramammary Paget Disease di Yoshihiro Ishida, Nobuyuki Kakiuchi, Kenichi Yoshida, Yoshikage Inoue, Hiroyuki Irie, Tatsuki R. Kataoka, Masahiro Hirata, Takeru Funakoshi, Shigeto Matsushita, Hiroo Hata, Hiroshi Uchi, Yuki Yamamoto, Yasuhiro Fujisawa, Taku Fujimura, Ryunosuke Saiki, Kengo Takeuchi, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Atsushi Otsuka, Satoru Miyano, Kenji Kabashima, Seishi Ogawa

    Pubblicazione 2020
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  18. 18
    Haploinsufficiency of TNFAIP3 ( A20 ) by germline mutation is involved in autoimmune lymphoproliferative syndrome

    Haploinsufficiency of TNFAIP3 ( A20 ) by germline mutation is involved in autoimmune lymphoproliferative syndrome di Masatoshi Takagi, Shohei Ogata, Hiroo Ueno, Kenichi Yoshida, Tzu‐Wen Yeh, Akihiro Hoshino, Jinhua Piao, Motoy Yamashita, Mai Nanya, Tsubasa Okano, Michiko Kajiwara, Hirokazu Kanegane, Hideki Muramatsu, Yusuke Okuno, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Yuki Bando, Motohiro Kato, Yasuhide Hayashi, Satoru Miyano, Kohsuke Imai, Seishi Ogawa, Seiji Kojima, Tomohiro Morio

    Pubblicazione 2016
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  19. 19
    Transcriptome analysis offers a comprehensive illustration of the genetic background of pediatric acute myeloid leukemia

    Transcriptome analysis offers a comprehensive illustration of the genetic background of pediatric acute myeloid leukemia di Norio Shiba, Kenichi Yoshida, Yusuke Hara, Genki Yamato, Yuichi Shiraishi, H. Matsuo, Yusuke Okuno, Kenichi Chiba, Hiroko Tanaka, Taeko Kaburagi, Masanobu Takeuchi, Kentaro Ohki, Masashi Sanada, Jun Okubo, Daisuke Tomizawa, Tomohiko Taki, Akira Shimada, Manabu Sotomatsu, Keizo Horibe, Takashi Taga, Souichi Adachi, Akio Tawa, Satoru Miyano, Seishi Ogawa, Yasuhide Hayashi

    Pubblicazione 2019
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  20. 20
    Integrated molecular profiling of juvenile myelomonocytic leukemia

    Integrated molecular profiling of juvenile myelomonocytic leukemia di Norihiro Murakami, Yusuke Okuno, Kenichi Yoshida, Yuichi Shiraishi, Genta Nagae, Kyogo Suzuki, Atsushi Narita, Hirotoshi Sakaguchi, Nozomu Kawashima, Xinan Wang, Yinyan Xu, Kenichi Chiba, Hiroko Tanaka, Asahito Hama, Masashi Sanada, Masafumi Ito, Masashi Hirayama, Arata Watanabe, Toshihide Ueno, Seiji Kojima, Hiroyuki Aburatani, Hiroyuki Mano, Satoru Miyano, Seishi Ogawa, Yoshiyuki Takahashi, Hideki Muramatsu

    Pubblicazione 2018
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