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

بواسطة Shiraishi, Yuichi, Kataoka, Keisuke, Chiba, Kenichi, Okada, Ai, Kogure, Yasunori, Tanaka, Hiroko, Ogawa, Seishi, Miyano, Satoru
الحاوية / القاعدة 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

بواسطة Hiwatari, Mitsuteru, Seki, Masafumi, Akahoshi, Shogo, Yoshida, Kenichi, Miyano, Satoru, Shiraishi, Yuichi, Tanaka, Hiroko, Chiba, Kenichi, Ogawa, Seishi, Takita, Junko
الحاوية / القاعدة Oncol Lett (2017)

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

بواسطة 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
منشور في 2013

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

بواسطة 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
منشور في 2013

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

بواسطة 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
الحاوية / القاعدة Am J Hum Genet (2015)

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

بواسطة 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
الحاوية / القاعدة Blood (2020)

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

بواسطة 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
الحاوية / القاعدة Oncotarget (2016)

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

بواسطة 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
الحاوية / القاعدة Nat Commun (2018)

ACTN1 Mutations Cause Congenital Macrothrombocytopenia

بواسطة 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
منشور في 2013

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

بواسطة 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
الحاوية / القاعدة Hum Genome Var (2019)

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

بواسطة 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
الحاوية / القاعدة Haematologica (2018)

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

بواسطة 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
منشور في 2014

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

بواسطة 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
الحاوية / القاعدة Haematologica (2015)

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

بواسطة 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
الحاوية / القاعدة Commun Biol (2020)

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

بواسطة 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
الحاوية / القاعدة Blood Adv (2020)

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

بواسطة 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
الحاوية / القاعدة Blood Adv (2019)

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

بواسطة 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
الحاوية / القاعدة Haematologica (2017)

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

بواسطة 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
الحاوية / القاعدة Oncotarget (2017)

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

بواسطة 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
الحاوية / القاعدة Blood Adv (2019)

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

بواسطة 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
الحاوية / القاعدة Cancer Sci (2019)