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Author/Creator Kanezaki, Rika

1. Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21. Issue 4 (5th February 2020)

Authors:
Yuzawa, Kentaro; Terui, Kiminori; Toki, Tsutomu; Kanezaki, Rika; Kobayashi, Akie; Sato, Tomohiko; Kamio, Takuya; Kudo, Ko; Sasaki, Shinya; Endo, Mikiya; Ozono, Shuichi; Nomura, Keiko; Ito, Etsuro
Journal:
Pediatric blood & cancer
Issue:
Volume 67:Issue 4(2020)
Page Start:
n/a
Record Type:
Journal Article
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2. Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia. Issue 1 (10th January 2022)

Authors:
Kobayashi, Akie; Ohtaka, Ryusei; Toki, Tsutomu; Hara, Junichi; Muramatsu, Hideki; Kanezaki, Rika; Takahashi, Yuka; Sato, Tomohiko; Kamio, Takuya; Kudo, Ko; Sasaki, Shinya; Yoshida, Taro; Utsugisawa, Taiju; Kanno, Hitoshi; Yoshida, Kenichi; Nannya, Yasuhito; Takahashi, Yoshiyuki; Kojima, Seiji; Mi...
Journal:
EJHaem
Issue:
Volume 3:Issue 1(2022)
Page Start:
163
Record Type:
Journal Article
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3. Gene alterations involving the CRLF2‐JAK pathway and recurrent gene deletions in Down syndrome‐associated acute lymphoblastic leukemia in Japan. Issue 11 (16th July 2014)

Authors:
Hanada, Isamu; Terui, Kiminori; Ikeda, Fumika; Toki, Tsutomu; Kanezaki, Rika; Sato, Tomohiko; Kamio, Takuya; Kudo, Ko; Sasaki, Shinya; Takahashi, Yoshihiro; Hayashi, Yasuhide; Inukai, Takeshi; Kojima, Seiji; Koike, Kenichi; Kosaka, Yoshiyuki; Kobayashi, Masao; Imaizumi, Masue; Mitsui, Tetsuo; Hor...
Journal:
Genes, chromosomes & cancer
Issue:
Volume 53:Issue 11(2014:Nov.)
Page Start:
902
Record Type:
Journal Article
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4. Highly sensitive detection of GATA1 mutations in patients with myeloid leukemia associated with Down syndrome by combining Sanger and targeted next generation sequencing. Issue 3 (21st October 2019)

Authors:
Terui, Kiminori; Toki, Tsutomu; Taga, Takashi; Iwamoto, Shotaro; Miyamura, Takako; Hasegawa, Daisuke; Moritake, Hiroshi; Hama, Asahito; Nakashima, Kentaro; Kanezaki, Rika; Kudo, Ko; Saito, Akiko M.; Horibe, Keizo; Adachi, Souichi; Tomizawa, Daisuke; Ito, Etsuro
Journal:
Genes, chromosomes & cancer
Issue:
Volume 59:Issue 3(2020)
Page Start:
160
Record Type:
Journal Article
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5. Loss of function mutations in RPL27 and RPS27 identified by whole‐exome sequencing in Diamond‐Blackfan anaemia. (25th November 2014)

Authors:
Wang, RuNan; Yoshida, Kenichi; Toki, Tsutomu; Sawada, Takafumi; Uechi, Tamayo; Okuno, Yusuke; Sato‐Otsubo, Aiko; Kudo, Kazuko; Kamimaki, Isamu; Kanezaki, Rika; Shiraishi, Yuichi; Chiba, Kenichi; Tanaka, Hiroko; Terui, Kiminori; Sato, Tomohiko; Iribe, Yuji; Ohga, Shouichi; Kuramitsu, Madoka; Hamag...
Journal:
British journal of haematology
Issue:
Volume 168:Number 6(2015:Mar.)
Page Start:
854
Record Type:
Journal Article
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6. Loss of function mutations in RPL27 and RPS27 identified by whole‐exome sequencing in Diamond‐Blackfan anaemia. (25th November 2014)

Authors:
Wang, RuNan; Yoshida, Kenichi; Toki, Tsutomu; Sawada, Takafumi; Uechi, Tamayo; Okuno, Yusuke; Sato‐Otsubo, Aiko; Kudo, Kazuko; Kamimaki, Isamu; Kanezaki, Rika; Shiraishi, Yuichi; Chiba, Kenichi; Tanaka, Hiroko; Terui, Kiminori; Sato, Tomohiko; Iribe, Yuji; Ohga, Shouichi; Kuramitsu, Madoka; Hamag...
Journal:
British journal of haematology
Issue:
Volume 168:Number 6(2015:Mar.)
Page Start:
854
Record Type:
Journal Article
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7. Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation. Issue 12 (22nd October 2018)

Authors:
Kudo, Ko; Ueno, Hiroo; Sato, Tomohiko; Kubo, Kaori; Kanezaki, Rika; Kobayashi, Akie; Kamio, Takuya; Sasaki, Shinya; Terui, Kiminori; Kurose, Akira; Yoshida, Kenichi; Shiozawa, Yusuke; Toki, Tsutomu; Ogawa, Seishi; Ito, Etsuro
Journal:
Genes, chromosomes & cancer
Issue:
Volume 57:Issue 12(2018)
Page Start:
665
Record Type:
Journal Article
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