A comprehensive characterization of cis-acting splicing-associated variants in human cancer

Por Shiraishi, Yuichi, Kataoka, Keisuke, Chiba, Kenichi, Okada, Ai, Kogure, Yasunori, Tanaka, Hiroko, Ogawa, Seishi, Miyano, Satoru
Publicado no Genome Res (2018)

Molecular studies reveal MLL-MLLT10/AF10 and ARID5B-MLL gene fusions displaced in a case of infantile acute lymphoblastic leukemia with complex karyotype

Por Hiwatari, Mitsuteru, Seki, Masafumi, Akahoshi, Shogo, Yoshida, Kenichi, Miyano, Satoru, Shiraishi, Yuichi, Tanaka, Hiroko, Chiba, Kenichi, Ogawa, Seishi, Takita, Junko
Publicado no Oncol Lett (2017)

An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data

Por Shiraishi, Yuichi, Sato, Yusuke, Chiba, Kenichi, Okuno, Yusuke, Nagata, Yasunobu, Yoshida, Kenichi, Shiba, Norio, Hayashi, Yasuhide, Kume, Haruki, Homma, Yukio, Sanada, Masashi, Ogawa, Seishi, Miyano, Satoru
Publicado em 2013

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

Por Hira, Asuka, Yabe, Hiromasa, Yoshida, Kenichi, Okuno, Yusuke, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Miyano, Satoru, Nakamura, Jun, Kojima, Seiji, Ogawa, Seishi, Matsuo, Keitaro, Takata, Minoru, Yabe, Miharu
Publicado em 2013

Mutations in the Gene Encoding the E2 Conjugating Enzyme UBE2T Cause Fanconi Anemia

Por Hira, Asuka, Yoshida, Kenichi, Sato, Koichi, Okuno, Yusuke, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Miyano, Satoru, Shimamoto, Akira, Tahara, Hidetoshi, Ito, Etsuro, Kojima, Seiji, Kurumizaka, Hitoshi, Ogawa, Seishi, Takata, Minoru, Yabe, Hiromasa, Yabe, Miharu
Publicado no Am J Hum Genet (2015)

VAV1 mutations contribute to development of T-cell neoplasms in mice

Por Fukumoto, Kota, Sakata-Yanagimoto, Mamiko, Fujisawa, Manabu, Sakamoto, Tatsuhiro, Miyoshi, Hiroaki, Suehara, Yasuhito, Nguyen, Tran B., Suma, Sakurako, Yanagimoto, Shintaro, Shiraishi, Yuichi, Chiba, Kenichi, Bouska, Alyssa, Kataoka, Keisuke, Ogawa, Seishi, Iqbal, Javeed, Ohshima, Koichi, Chiba, Shigeru
Publicado no Blood (2020)

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

Por Ueda, Masami, Iguchi, Tomohiro, Masuda, Takaaki, Nakahara, Yujiro, Hirata, Hidenari, Uchi, Ryutaro, Niida, Atsushi, Momose, Kota, Sakimura, Shotaro, Chiba, Kenichi, Eguchi, Hidetoshi, Ito, Shuhei, Sugimachi, Keishi, Yamasaki, Makoto, Suzuki, Yutaka, Miyano, Satoru, Doki, Yuichiro, Mori, Masaki, Mimori, Koshi
Publicado no Oncotarget (2016)

Aberrant splicing and defective mRNA production induced by somatic spliceosome mutations in myelodysplasia

Por Shiozawa, Yusuke, Malcovati, Luca, Gallì, Anna, Sato-Otsubo, Aiko, Kataoka, Keisuke, Sato, Yusuke, Watatani, Yosaku, Suzuki, Hiromichi, Yoshizato, Tetsuichi, Yoshida, Kenichi, Sanada, Masashi, Makishima, Hideki, Shiraishi, Yuichi, Chiba, Kenichi, Hellström-Lindberg, Eva, Miyano, Satoru, Ogawa, Seishi, Cazzola, Mario
Publicado no Nat Commun (2018)

ACTN1 Mutations Cause Congenital Macrothrombocytopenia

Por Kunishima, Shinji, Okuno, Yusuke, Yoshida, Kenichi, Shiraishi, Yuichi, Sanada, Masashi, Muramatsu, Hideki, Chiba, Kenichi, Tanaka, Hiroko, Miyazaki, Koji, Sakai, Michio, Ohtake, Masatoshi, Kobayashi, Ryoji, Iguchi, Akihiro, Niimi, Gen, Otsu, Makoto, Takahashi, Yoshiyuki, Miyano, Satoru, Saito, Hidehiko, Kojima, Seiji, Ogawa, Seishi
Publicado em 2013

Novel neuroblastoma amplified sequence (NBAS) mutations in a Japanese boy with fever-triggered recurrent acute liver failure

Por Ono, Sahoko, Matsuda, Junko, Watanabe, Etsuko, Akaike, Hiroto, Teranishi, Hideto, Miyata, Ippei, Otomo, Takanobu, Sadahira, Yoshito, Mizuochi, Tatsuki, Kusano, Hironori, Kage, Masayoshi, Ueno, Hiroo, Yoshida, Kenichi, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Miyano, Satoru, Ogawa, Seishi, Hayashi, Yasuhide, Kanegane, Hirokazu, Ouchi, Kazunobu
Publicado no Hum Genome Var (2019)

Clonally related diffuse large B-cell lymphoma and interdigitating dendritic cell sarcoma sharing MYC translocation

Por Ochi, Yotaro, Hiramoto, Nobuhiro, Yoshizato, Tetsuichi, Ono, Yuichiro, Takeda, June, Shiozawa, Yusuke, Yoshida, Kenichi, Kakiuchi, Nobuyuki, Shiraishi, Yuichi, Tanaka, Hiroko, Chiba, Kenichi, Kazuma, Yasuhiro, Tabata, Sumie, Yonetani, Noboru, Uehara, Keiichiro, Yamashita, Daisuke, Imai, Yukihiro, Nagafuji, Koji, Yamakawa, Mitsunori, Miyano, Satoru, Takaori-Kondo, Akifumi, Ogawa, Seishi, Ishikawa, Takayuki
Publicado no Haematologica (2018)

Clonal leukemic evolution in myelodysplastic syndromes with TET2 and IDH1/2 mutations

Por Lin, Tung-Liang, Nagata, Yasunobu, Kao, Hsiao-Wen, Sanada, Masashi, Okuno, Yusuke, Huang, Chein-Fuang, Liang, Der-Cherng, Kuo, Ming-Chung, Lai, Chang-Liang, Lee, En-Hui, Shih, Yu-Shu, Tanaka, Hiroko, Shiraishi, Yuichi, Chiba, Kenichi, Lin, Tung-Huei, Wu, Jin-Hou, Miyano, Satoru, Ogawa, Seishi, Shih, Lee-Yung
Publicado em 2014

GATA2 and secondary mutations in familial myelodysplastic syndromes and pediatric myeloid malignancies

Por Wang, Xinan, Muramatsu, Hideki, Okuno, Yusuke, Sakaguchi, Hirotoshi, Yoshida, Kenichi, Kawashima, Nozomu, Xu, Yinyan, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Saito, Shoji, Nakazawa, Yozo, Masunari, Taro, Hirose, Tadashi, Elmahdi, Shaimaa, Narita, Atsushi, Doisaki, Sayoko, Ismael, Olfat, Makishima, Hideki, Hama, Asahito, Miyano, Satoru, Takahashi, Yoshiyuki, Ogawa, Seishi, Kojima, Seiji
Publicado no Haematologica (2015)

Comprehensive genetic analysis of pediatric germ cell tumors identifies potential drug targets

Por Kubota, Yasuo, Seki, Masafumi, Kawai, Tomoko, Isobe, Tomoya, Yoshida, Misa, Sekiguchi, Masahiro, Kimura, Shunsuke, Watanabe, Kentaro, Sato-Otsubo, Aiko, Yoshida, Kenichi, Suzuki, Hiromichi, Kataoka, Keisuke, Fujii, Yoichi, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Hiwatari, Mitsuteru, Oka, Akira, Hayashi, Yasuhide, Miyano, Satoru, Ogawa, Seishi, Hata, Kenichiro, Tanaka, Yukichi, Takita, Junko
Publicado no Commun Biol (2020)

Fusion partner–specific mutation profiles and KRAS mutations as adverse prognostic factors in MLL-rearranged AML

Por Matsuo, Hidemasa, Yoshida, Kenichi, Nakatani, Kana, Harata, Yutarou, Higashitani, Moe, Ito, Yuri, Kamikubo, Yasuhiko, Shiozawa, Yusuke, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Okada, Ai, Nannya, Yasuhito, Takeda, June, Ueno, Hiroo, Kiyokawa, Nobutaka, Tomizawa, Daisuke, Taga, Takashi, Tawa, Akio, Miyano, Satoru, Meggendorfer, Manja, Haferlach, Claudia, Ogawa, Seishi, Adachi, Souichi
Publicado no Blood Adv (2020)

Transcriptome analysis offers a comprehensive illustration of the genetic background of pediatric acute myeloid leukemia

Por Shiba, Norio, Yoshida, Kenichi, Hara, Yusuke, Yamato, Genki, Shiraishi, Yuichi, Matsuo, Hidemasa, Okuno, Yusuke, Chiba, Kenichi, Tanaka, Hiroko, Kaburagi, Taeko, Takeuchi, Masanobu, Ohki, Kentaro, Sanada, Masashi, Okubo, Jun, Tomizawa, Daisuke, Taki, Tomohiko, Shimada, Akira, Sotomatsu, Manabu, Horibe, Keizo, Taga, Takashi, Adachi, Souichi, Tawa, Akio, Miyano, Satoru, Ogawa, Seishi, Hayashi, Yasuhide
Publicado no Blood Adv (2019)

Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia

Por Ikeda, Fumika, Yoshida, Kenichi, Toki, Tsutomu, Uechi, Tamayo, Ishida, Shiori, Nakajima, Yukari, Sasahara, Yoji, Okuno, Yusuke, Kanezaki, Rika, Terui, Kiminori, Kamio, Takuya, Kobayashi, Akie, Fujita, Takashi, Sato-Otsubo, Aiko, Shiraishi, Yuichi, Tanaka, Hiroko, Chiba, Kenichi, Muramatsu, Hideki, Kanno, Hitoshi, Ohga, Shouichi, Ohara, Akira, Kojima, Seiji, Kenmochi, Naoya, Miyano, Satoru, Ogawa, Seishi, Ito, Etsuro
Publicado no Haematologica (2017)

Identification of the genetic and clinical characteristics of neuroblastomas using genome-wide analysis

Por Uryu, Kumiko, Nishimura, Riki, Kataoka, Keisuke, Sato, Yusuke, Nakazawa, Atsuko, Suzuki, Hiromichi, Yoshida, Kenichi, Seki, Masafumi, Hiwatari, Mitsuteru, Isobe, Tomoya, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Miyano, Satoru, Koh, Katsuyoshi, Hanada, Ryoji, Oka, Akira, Hayashi, Yasuhide, Ohira, Miki, Kamijo, Takehiko, Nagase, Hiroki, Takimoto, Tetsuya, Tajiri, Tatsuro, Nakagawara, Akira, Ogawa, Seishi, Takita, Junko
Publicado no Oncotarget (2017)

Frequent germline mutations of HAVCR2 in sporadic subcutaneous panniculitis-like T-cell lymphoma

Por Polprasert, Chantana, Takeuchi, Yasuhide, Kakiuchi, Nobuyuki, Yoshida, Kenichi, Assanasen, Thamathorn, Sitthi, Wimonmas, Bunworasate, Udomsak, Pirunsarn, Arunrat, Wudhikarn, Kitsada, Lawasut, Panisinee, Uaprasert, Noppacharn, Kongkiatkamon, Sunisa, Moonla, Chatphatai, Sanada, Masashi, Akita, Nobuhiro, Takeda, June, Fujii, Yoichi, Suzuki, Hiromichi, Nannya, Yasuhito, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Miyano, Satoru, Rojnuckarin, Ponlapat, Ogawa, Seishi, Makishima, Hideki
Publicado no Blood Adv (2019)

Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome

Por Kubota, Yasuo, Uryu, Kumiko, Ito, Tatsuya, Seki, Masafumi, Kawai, Tomoko, Isobe, Tomoya, Kumagai, Tadayuki, Toki, Tsutomu, Yoshida, Kenichi, Suzuki, Hiromichi, Kataoka, Keisuke, Shiraishi, Yuichi, Chiba, Kenichi, Tanaka, Hiroko, Ohki, Kentaro, Kiyokawa, Nobutaka, Kagawa, Jiro, Miyano, Satoru, Oka, Akira, Hayashi, Yasuhide, Ogawa, Seishi, Terui, Kiminori, Sato, Atsushi, Hata, Kenichiro, Ito, Etsuro, Takita, Junko
Publicado no Cancer Sci (2019)