Papers - KANEZAKI Rika
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Clinical and Molecular Cytogenetic Analysis of 15 Mosaic/Non-Down Syndrome Neonates With Transient Abnormal Myelopoiesis
Yuzawa Kentaro, Terui Kimnori, Toki Tsutomu, Kanezaki Rika, Kobayashi Akie, Sato Tomohiko, Kamio Takuya, Kudo Ko, Sasaki Shinya, Endo Mikiya, Ozono Shuichi, Ito Etsuro
PEDIATRIC BLOOD & CANCER 66 S35 2019.12
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Comprehensive genetic analyses of relapsed B-cell precursor acute lymphoblastic leukemia in children
Kubo Kaori, Kudo Ko ,Toki Tsutomu, Kanezaki Rika, Ikeda Fumika, Ito Tatsuya, Kobayashi Akie, Sato Tomohiko, Kamio Takuya, Sasaki Shinya, Terui Kiminori, Ito Etsuro
Hirosaki Medical Journal 70 ( 1 ) 13 - 23 2019.11
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小児における前駆B細胞急性リンパ芽球性白血病の再発例を対象とした網羅的遺伝子解析(Comprehensive genetic analyses of relapsed B-cell precursor acute lymphoblastic leukemia in children)
Kubo Kaori, Kudo Ko, Toki Tsutomu, Kanezaki Rika, Ikeda Fumika, Ito Tatsuya, Kobayashi Akie, Sato Tomohiko, Kamio Takuya, Sasaki Shinya, Terui Kiminori, Ito Etsuro
弘前医学 70 ( 1 ) 13 - 23 2019.11
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ダウン症関連巨核芽球性白血病発症の分子機構
金崎 里香
BIO Clinica 34 ( 13 ) 1345 - 1350 2019.10
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TAMおよびDS-AMKL発症の分子機構
金崎 里香
BIO Clinica 34 ( 6 ) 642 - 647 2019.5
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Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation.
Kudo K, Ueno H, Sato T, Kubo K, Kanezaki R, Kobayashi A, Kamio T, Sasaki S, Terui K, Kurose A, Yoshida K, Shiozawa Y, Toki T, Ogawa S, Ito E.
Genes, chromosomes & cancer 2018.12
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De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome.
Tsutomu Toki, Kenichi Yoshida, RuNan Wang, Sou Nakamura, Takanobu Maekawa, Kumiko Goi, Megumi C Katoh, Seiya Mizuno, Fumihiro Sugiyama, Rika Kanezaki, Tamayo Uechi, Yukari Nakajima, Yusuke Sato, Yusuke Okuno, Aiko Sato-Otsubo, Yusuke Shiozawa, Keisuke Kataoka, Yuichi Shiraishi, Masashi Sanada, Kenichi Chiba, Hiroko Tanaka, Kiminori Terui, Tomohiko Sato, Takuya Kamio, Hirotoshi Sakaguchi, Shouichi Ohga, Madoka Kuramitsu, Isao Hamaguchi, Akira Ohara, Hitoshi Kanno, Satoru Miyano, Seiji Kojima, Akira Ishiguro, Kanji Sugita, Naoya Kenmochi, Satoru Takahashi, Koji Eto, Seishi Ogawa, Etsuro Ito
American journal of human genetics 103 ( 3 ) 440 - 447 2018.9
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Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia.
Fumika Ikeda, Kenichi Yoshida, Tsutomu Toki, Tamayo Uechi, Shiori Ishida, Yukari Nakajima, Yoji Sasahara, Yusuke Okuno, Rika Kanezaki, Kiminori Terui, Takuya Kamio, Akie Kobayashi, Takashi Fujita, Aiko Sato-Otsubo, Yuichi Shiraishi, Hiroko Tanaka, Kenichi Chiba, Hideki Muramatsu, Hitoshi Kanno, Shouichi Ohga, Akira Ohara, Seiji Kojima, Naoya Kenmochi, Satoru Miyano, Seishi Ogawa, Etsuro Ito
Haematologica 102 ( 3 ) e93 - e96 2017.3
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ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan.
Fumika Ikeda, Tsutomu Toki, Rika Kanezaki, Kiminori Terui, Kenichi Yoshida, Hitoshi Kanno, Shouichi Ohga, Akira Ohara, Seiji Kojima, Seishi Ogawa, Etsuro Ito
International journal of hematology 103 ( 1 ) 112 - 114 2016.1
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Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.
RuNan Wang, Kenichi Yoshida, Tsutomu Toki, Takafumi Sawada, Tamayo Uechi, Yusuke Okuno, Aiko Sato-Otsubo, Kazuko Kudo, Isamu Kamimaki, Rika Kanezaki, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Kiminori Terui, Tomohiko Sato, Yuji Iribe, Shouichi Ohga, Madoka Kuramitsu, Isao Hamaguchi, Akira Ohara, Junichi Hara, Kumiko Goi, Kousaku Matsubara, Kenichi Koike, Akira Ishiguro, Yasuhiro Okamoto, Kenichiro Watanabe, Hitoshi Kanno, Seiji Kojima, Satoru Miyano, Naoya Kenmochi, Seishi Ogawa, Etsuro Ito
British journal of haematology 168 ( 6 ) 854 - 864 2015.3
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Gene alterations involving the CRLF2-JAK pathway and recurrent gene deletions in Down syndrome-associated acute lymphoblastic leukemia in Japan.
Isamu Hanada, Kiminori Terui, Fumika Ikeda, Tsutomu Toki, Rika Kanezaki, Tomohiko Sato, Takuya Kamio, Ko Kudo, Shinya Sasaki, Yoshihiro Takahashi, Yasuhide Hayashi, Takeshi Inukai, Seiji Kojima, Kenichi Koike, Yoshiyuki Kosaka, Masao Kobayashi, Masue Imaizumi, Tetsuo Mitsui, Hiroki Hori, Junichi Hara, Keizo Horibe, Jun-ichi Nagai, Hiroaki Goto, Etsuro Ito
Genes, chromosomes & cancer 53 ( 11 ) 902 - 910 2014.11
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Novel in-frame deletion of GATA1 observed in pediatric acute megakaryoblastic leukemia without Down syndrome
RuNab Wang, Rika Kanezaki, Tsutomu Toki, Kiminori Terui, Shinya Sakaki,Ko Kudo, Takuya Kamio, Tomohiko Sato, Fumika Ikeda, Ryo Araki, Hidetoshi Ochiai,Etsuro Ito
Hirosaki Medical Journal 65 ( 2-4 ) 227 - 237 2014.9
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Novel in-frame deletion of <i>GATA1</i> observed in pediatric acute megakaryoblastic leukemia without down syndrome
Wang RuNan, Kanezaki Rika, Toki Tsutomu, Terui Kiminori, Sasaki Shinya, Kudo Ko, Kamio Takuya, Sato Tomohiko, Ikeda Fumika, Araki Ryo, Ochiai Hidetoshi, Ito Etsuro
Hirosaki Medical Journal 65 ( 2-4 ) 227 - 237 2014
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The landscape of somatic mutations in Down syndrome-related myeloid disorders.
Kenichi Yoshida, Tsutomu Toki, Yusuke Okuno, Rika Kanezaki, Yuichi Shiraishi, Aiko Sato-Otsubo, Masashi Sanada, Myoung-ja Park, Kiminori Terui, Hiromichi Suzuki, Ayana Kon, Yasunobu Nagata, Yusuke Sato, RuNan Wang, Norio Shiba, Kenichi Chiba, Hiroko Tanaka, Asahito Hama, Hideki Muramatsu, Daisuke Hasegawa, Kazuhiro Nakamura, Hirokazu Kanegane, Keiko Tsukamoto, Souichi Adachi, Kiyoshi Kawakami, Koji Kato, Ryosei Nishimura, Shai Izraeli, Yasuhide Hayashi, Satoru Miyano, Seiji Kojima, Etsuro Ito, Seishi Ogawa
Nature genetics 45 ( 11 ) 1293 - 1299 2013.11
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Naturally occurring oncogenic GATA1 mutants with internal deletions in transient abnormal myelopoiesis in Down syndrome.
Tsutomu Toki, Rika Kanezaki, Eri Kobayashi, Hiroshi Kaneko, Mikiko Suzuki, Runan Wang, Kiminori Terui, Hirokazu Kanegane, Miho Maeda, Mikiya Endo, Tatsuki Mizuochi, Souichi Adachi, Yasuhide Hayashi, Masayuki Yamamoto, Ritsuko Shimizu, Etsuro Ito
Blood 121 ( 16 ) 3181 - 3184 2013.4
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Identification of TRIB1 R107L gain-of-function mutation in human acute megakaryocytic leukemia.
Takashi Yokoyama, Tsutomu Toki, Yoshihiro Aoki, Rika Kanezaki, Myoung-Ja Park, Yohei Kanno, Tomoko Takahara, Yukari Yamazaki, Etsuro Ito, Yasuhide Hayashi, Takuro Nakamura
Blood 119 ( 11 ) 2608 - 2611 2012.3
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Platelet-derived growth factor may be associated with fibrosis in a Down syndrome patient with transient myeloproliferative disorder
Jiro Ogawa, Hirokazu Kanegane, Koichi Tsuneyama, Rika Kanezaki, Takeshi Futatani, Keiko Nomura, Shin Ishizawa, Masakiyo Sasahara, Etsuro Ito, Toshio Miyawaki
EUROPEAN JOURNAL OF HAEMATOLOGY 81 ( 1 ) 58 - 64 2008.7
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Functional analysis of JAK3 mutations in transient myeloproliferative disorder and acute megakaryoblastic leukaemia accompanying Down syndrome
Tomohiko Sato, Tsutomu Toki, Rika Kanezaki, Gang Xu, Kiminori Terui, Hirokazu Kanegane, Masayoshi Miura, Souichi Adachi, Masahiro Migita, Shingo Morinaga, Takahide Nakano, Mikiya Endo, Seiji Kojima, Hitoshi Kiyoi, Hiroyuki Mano, Etsuro Ito
BRITISH JOURNAL OF HAEMATOLOGY 141 ( 5 ) 681 - 688 2008.6
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A trial of isolating the novel genes on 21q11-21 to elucidate the gene responsible for transient abnormal myelopoiesis
Ishizaki Noriko, Kanezaki Rika, Toki Tsutomu, Ito Etsuro
Hirosaki Medical Journal 55 ( 3-4 ) 83 - 94 2004
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Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients
Tomomi Uyeda, Toru Takahashi, Shuji Eto, Takumi Sato, Gang Xu, Rika Kanezaki, Tsutomu Toki, Susumu Yonesaka, Etsuro Ito
Journal of Human Genetics 49 ( 8 ) 404 - 407 2004