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Purification of leukemic blast cells from blood smears using laser microdissection.
Published in:
2017
By:
- Matsuo, Hidemasa;
- Shiga, Shuichi;
- Imai, Tsuyoshi;
- Kamikubo, Yasuhiko;
- Toki, Tsutomu;
- Terui, Kiminori;
- Ito, Etsuro;
- Adachi, Souichi
Publication type:
journal article
Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing.
Published in:
2017
By:
- Ichimura, Takuya;
- Yoshida, Kenichi;
- Okuno, Yusuke;
- Yujiri, Toshiaki;
- Nagai, Kozo;
- Nishi, Masanori;
- Shiraishi, Yuichi;
- Ueno, Hiroo;
- Toki, Tsutomu;
- Chiba, Kenichi;
- Tanaka, Hiroko;
- Muramatsu, Hideki;
- Hara, Toshiro;
- Kanno, Hitoshi;
- Kojima, Seiji;
- Miyano, Satoru;
- Ito, Etsuro;
- Ogawa, Seishi;
- Ohga, Shouichi
Publication type:
journal article
ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan.
Published in:
2016
By:
- Ikeda, Fumika;
- Toki, Tsutomu;
- Kanezaki, Rika;
- Terui, Kiminori;
- Yoshida, Kenichi;
- Kanno, Hitoshi;
- Ohga, Shouichi;
- Ohara, Akira;
- Kojima, Seiji;
- Ogawa, Seishi;
- Ito, Etsuro
Publication type:
commentary
Selective KIT inhibitor KI-328 and HSP90 inhibitor show different potency against the type of KIT mutations recurrently identified in acute myeloid leukemia.
Published in:
2010
By:
- Tsujimura, Akane;
- Kiyoi, Hitoshi;
- Shiotsu, Yukimasa;
- Ishikawa, Yuichi;
- Mori, Yumiko;
- Ishida, Hiroshi;
- Toki, Tsutomu;
- Ito, Etsuro;
- Naoe, Tomoki
Publication type:
journal article
Molecular pathogenesis in Diamond-Blackfan anemia.
Published in:
2010
By:
- Ito, Etsuro;
- Konno, Yuki;
- Toki, Tsutomu;
- Terui, Kiminori
Publication type:
journal article
KCNJ2mutation in intractable ventricular arrhythmia with Andersen's syndrome.
Published in:
Pediatrics International, 2005, v. 47, n. 2, p. 220, doi. 10.1111/j.1442-200x.2005.02024.x
By:
- Takahashi, Tohru;
- Tandai, Satoshi;
- Toki, Tsutomu;
- Sato, Takumi;
- Eto, Shuji;
- Sato, Akira;
- Ueda, Tomomi;
- Sato, Sumito;
- Ichinose, Kouta;
- Ito, Etsuro;
- Yonesaka, Susumu
Publication type:
Article
Mechanism of KIT gene regulation by GATA1 lacking the N-terminal domain in Down syndrome–related myeloid disorders.
Published in:
Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-25046-z
By:
- Kanezaki, Rika;
- Toki, Tsutomu;
- Terui, Kiminori;
- Sato, Tomohiko;
- Kobayashi, Akie;
- Kudo, Ko;
- Kamio, Takuya;
- Sasaki, Shinya;
- Kawaguchi, Koji;
- Watanabe, Kenichiro;
- Ito, Etsuro
Publication type:
Article
Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients.
Published in:
Journal of Human Genetics, 2004, v. 49, n. 8, p. 404, doi. 10.1007/s10038-004-0168-x
By:
- Uyeda, Tomomi;
- Takahashi, Toru;
- Eto, Shuji;
- Sato, Takumi;
- Xu, Gang;
- Kanezaki, Rika;
- Toki, Tsutomu;
- Yonesaka, Susumu;
- Ito, Etsuro
Publication type:
Article
Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal children.
Published in:
European Journal of Pediatrics, 2015, v. 174, n. 4, p. 525, doi. 10.1007/s00431-014-2430-3
By:
- Ono, Rintaro;
- Hasegawa, Daisuke;
- Hirabayashi, Shinsuke;
- Kamiya, Takahiro;
- Yoshida, Kenichi;
- Yonekawa, Satoko;
- Ogawa, Chitose;
- Hosoya, Ryota;
- Toki, Tsutomu;
- Terui, Kiminori;
- Ito, Etsuro;
- Manabe, Atsushi
Publication type:
Article
Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.
Published in:
British Journal of Haematology, 2015, v. 168, n. 6, p. 854, doi. 10.1111/bjh.13229
By:
- 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;
- Hamaguchi, Isao;
- Ohara, Akira
Publication type:
Article
Corrigendum: The landscape of somatic mutations in Down syndrome-related myeloid disorders.
Published in:
Nature Genetics, 2013, v. 45, n. 12, p. 1516, doi. 10.1038/ng1213-1516
By:
- Yoshida, Kenichi;
- Toki, Tsutomu;
- Okuno, Yusuke;
- Kanezaki, Rika;
- Shiraishi, Yuichi;
- Sato-Otsubo, Aiko;
- Sanada, Masashi;
- Park, Myoung-ja;
- Terui, Kiminori;
- Suzuki, Hiromichi;
- Kon, Ayana;
- Nagata, Yasunobu;
- Sato, Yusuke;
- Wang, RuNan;
- Shiba, Norio;
- Chiba, Kenichi;
- Tanaka, Hiroko;
- Hama, Asahito;
- Muramatsu, Hideki;
- Hasegawa, Daisuke
Publication type:
Article
The landscape of somatic mutations in Down syndrome-related myeloid disorders.
Published in:
Nature Genetics, 2013, v. 45, n. 11, p. 1293, doi. 10.1038/ng.2759
By:
- Yoshida, Kenichi;
- Toki, Tsutomu;
- Okuno, Yusuke;
- Kanezaki, Rika;
- Shiraishi, Yuichi;
- Sato-Otsubo, Aiko;
- Sanada, Masashi;
- Park, Myoung-ja;
- Terui, Kiminori;
- Suzuki, Hiromichi;
- Kon, Ayana;
- Nagata, Yasunobu;
- Sato, Yusuke;
- Wang, RuNan;
- Shiba, Norio;
- Chiba, Kenichi;
- Tanaka, Hiroko;
- Hama, Asahito;
- Muramatsu, Hideki;
- Hasegawa, Daisuke
Publication type:
Article
Highly sensitive detection of GATA1 mutations in patients with myeloid leukemia associated with Down syndrome by combining Sanger and targeted next generation sequencing.
Published in:
Genes, Chromosomes & Cancer, 2020, v. 59, n. 3, p. 160, doi. 10.1002/gcc.22816
By:
- 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
Publication type:
Article
Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation.
Published in:
Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 665, doi. 10.1002/gcc.22676
By:
- 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
Publication type:
Article
Erythroid transcription factor GATA-1 is abundantly transcribed in mouse testis.
Published in:
Nature, 1993, v. 362, n. 6419, p. 466, doi. 10.1038/362466a0
By:
- Ito, Etsuro;
- Toki, Tsutomu
Publication type:
Article
Troglitazone and 15-deoxy-Δ12,14-prostaglandin J2 inhibit shear-induced coupling factor 6 release in endothelial cells
Published in:
Cardiovascular Research, 2005, v. 67, n. 1, p. 134, doi. 10.1016/j.cardiores.2005.02.022
By:
- Tomita, Hirofumi;
- Osanai, Tomohiro;
- Toki, Tsutomu;
- Sasaki, Satoko;
- Maeda, Naotaka;
- Murakami, Reiichi;
- Magota, Koji;
- Yasujima, Minoru;
- Okumura, Ken
Publication type:
Article
Ribosomal protein L5 facilitates rDNA-bundled condensate and nucleolar assembly.
Published in:
Life Science Alliance, 2022, v. 5, n. 7, p. 1, doi. 10.26508/lsa.202101045
By:
- Haruka Matsumori;
- Kenji Watanabe;
- Hiroaki Tachiwana;
- Tomoko Fujita;
- Yuma Ito;
- Makio Tokunaga;
- Kumiko Sakata-Sogawa;
- Hiroko Osakada;
- Tokuko Haraguchi;
- Akinori Awazu;
- Hiroshi Ochiai;
- Yuka Sakata;
- Koji Ochiai;
- Tsutomu Toki;
- Etsuro Ito;
- Goldberg, Ilya G.;
- Kazuaki Tokunaga;
- Mitsuyoshi Nakao;
- Noriko Saitoh
Publication type:
Article
Resistance of t(17;19)‐acute lymphoblastic leukemia cell lines to multiagents in induction therapy.
Published in:
Cancer Medicine, 2019, v. 8, n. 11, p. 5274, doi. 10.1002/cam4.2356
By:
- Watanabe, Atsushi;
- Inukai, Takeshi;
- Kagami, Keiko;
- Abe, Masako;
- Takagi, Masatoshi;
- Fukushima, Takashi;
- Fukushima, Hiroko;
- Nanmoku, Toru;
- Terui, Kiminori;
- Ito, Tatsuya;
- Toki, Tsutomu;
- Ito, Etsuro;
- Fujimura, Junya;
- Goto, Hiroaki;
- Endo, Mikiya;
- Look, Thomas;
- Kamps, Mark;
- Minegishi, Masayoshi;
- Takita, Junko;
- Inaba, Toshiya
Publication type:
Article
Glycogen synthase kinase-3β phosphorylates synphilin-1 in vitro.
Published in:
Neuropathology, 2003, v. 23, n. 3, p. 199, doi. 10.1046/j.1440-1789.2003.00503.x
By:
- Tanji, Kunikazu;
- Toki, Tsutomu;
- Tamo, Wakako;
- Imaizumi, Tadaatsu;
- Matsumiya, Tomoh;
- Mori, Fumiaki;
- Takahashi, Hitoshi;
- Satoh, Kei;
- Wakabayashi, Koichi
Publication type:
Article
Cloning and expression of human B cell-specific transcription factor BACH2 mapped to chromosome 6q15.
Published in:
Oncogene, 2000, v. 19, n. 33, p. 3739, doi. 10.1038/sj.onc.1203716
By:
- Sasaki, Shinya;
- Ito, Etsuro;
- Toki, Tsutomu;
- Maekawa, Taira;
- Kanezaki, Rika;
- Umenai, Takamichi;
- Muto, Akihiko;
- Nagai, Hirokazu;
- Kinoshita, Tomohiro;
- Yamamoto, Masayuki;
- Inazawa, Johji;
- Taketo, Makoto M;
- Nakahata, Tatsutoshi;
- Igarashi, Kazuhiko;
- Yokoyama, Masaru
Publication type:
Article
Human small Maf proteins form heterodimers with CNC family transcription factors and recognize the NF-E2 motif.
Published in:
Oncogene, 1997, v. 14, n. 16, p. 1901, doi. 10.1038/sj.onc.1201024
By:
- Toki, Tsutomu;
- Itoh, Jugou;
- Kitazawa, Jun'ichi;
- Arai, Koji;
- Hatakeyama, Koki;
- Akasaka, Jun-itsu;
- Igarashi, Kazuhiko;
- Nomura, Nobuo;
- Yokoyama, Masaru;
- Yamamoto, Masayuki;
- Ito, Etsuro
Publication type:
Article
Correction to: Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.
Published in:
2018
By:
- Sonoda, Motoshi;
- Ishimura, Masataka;
- Ichimiya, Yuko;
- Terashi, Eiko;
- Eguchi, Katsuhide;
- Sakai, Yasunari;
- Takada, Hidetoshi;
- Hama, Asahito;
- Kanno, Hitoshi;
- Toki, Tsutomu;
- Ito, Etsuro;
- Ohga, Shouichi
Publication type:
journal article
Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.
Published in:
2018
By:
- Sonoda, Motoshi;
- Ishimura, Masataka;
- Ichimiya, Yuko;
- Terashi, Eiko;
- Eguchi, Katsuhide;
- Sakai, Yasunari;
- Takada, Hidetoshi;
- Hama, Asahito;
- Kanno, Hitoshi;
- Toki, Tsutomu;
- Ito, Etsuro;
- Ohga, Shouichi
Publication type:
journal article
Transient erythroblastopenia due to a GATA1 variant in an infant female.
Published in:
Pediatric Blood & Cancer, 2024, v. 71, n. 3, p. 1, doi. 10.1002/pbc.30834
By:
- Yamashita, Motoi;
- Tomoda, Takahiro;
- Mizuo, Ami;
- Isoda, Takeshi;
- Egawa, Makiko;
- Yoshida, Masayuki;
- Toki, Tsutomu;
- Kudo, Ko;
- Terui, Kiminori;
- Ito, Etsuro;
- Morio, Tomohiro;
- Takagi, Masatoshi
Publication type:
Article
Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21.
Published in:
2020
By:
- 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
Publication type:
journal article
Effective response to azacitidine in a child with a second relapse of myeloid leukemia associated with Down syndrome after bone marrow transplantation.
Published in:
2018
By:
- Uemura, Suguru;
- Mori, Takeshi;
- Nagano, China;
- Takafuji, Satoru;
- Nishimura, Noriyuki;
- Toki, Tsutomu;
- Terui, Kiminori;
- Ito, Etsuro;
- Iijima, Kazumoto
Publication type:
Case Study
Preserved High Probability of Overall Survival with Significant Reduction of Chemotherapy for Myeloid Leukemia in Down Syndrome: A Nationwide Prospective Study in Japan.
Published in:
2016
By:
- Taga, Takashi;
- Watanabe, Tomoyuki;
- Tomizawa, Daisuke;
- Kudo, Kazuko;
- Terui, Kiminori;
- Moritake, Hiroshi;
- Kinoshita, Akitoshi;
- MD, Shotaro Iwamoto;
- MD, Hideki Nakayama;
- MD, Hiroyuki Takahashi;
- MD, Akira Shimada;
- Taki, Tomohiko;
- Toki, Tsutomu;
- Ito, Etsuro;
- Goto, Hiroaki;
- Koh, Katsuyoshi;
- Saito, Akiko M.;
- Horibe, Keizo;
- Nakahata, Tatsutoshi;
- Tawa, Akio
Publication type:
journal article
Transient myeloproliferative disorder with partial trisomy 21.
Published in:
2015
By:
- Takahashi, Takahide;
- Inoue, Akira;
- Yoshimoto, Junko;
- Kanamitsu, Kiichiro;
- Taki, Tomohiko;
- Imada, Masahide;
- Yamada, Mutsuko;
- Ninomiya, Shinsuke;
- Toki, Tsutomu;
- Terui, Kiminori;
- Ito, Etsuro;
- Shimada, Akira
Publication type:
journal article
Gene alterations involving the CRLF2-JAK pathway and recurrent gene deletions in Down syndrome-associated acute lymphoblastic leukemia in Japan.
Published in:
Genes, Chromosomes & Cancer, 2014, v. 53, n. 11, p. 902, doi. 10.1002/gcc.22201
By:
- 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;
- Hori, Hiroki;
- Hara, Junichi
Publication type:
Article
Down syndrome-associated haematopoiesis abnormalities created by chromosome transfer and genome editing technologies.
Published in:
Scientific Reports, 2014, p. 1, doi. 10.1038/srep06136
By:
- Kazuki, Yasuhiro;
- Yakura, Yuwna;
- Abe, Satoshi;
- Osaki, Mitsuhiko;
- Kajitani, Naoyo;
- Kazuki, Kanako;
- Takehara, Shoko;
- Honma, Kazuhisa;
- Suemori, Hirofumi;
- Yamazaki, Satoshi;
- Sakuma, Tetsushi;
- Toki, Tsutomu;
- Shimizu, Ritsuko;
- Nakauchi, Hiromitsu;
- Yamamoto, Takashi;
- Oshimura, Mitsuo
Publication type:
Article
Functional analysis of JAK3 mutations in transient myeloproliferative disorder and acute megakaryoblastic leukaemia accompanying Down syndrome.
Published in:
British Journal of Haematology, 2008, v. 141, n. 5, p. 681, doi. 10.1111/j.1365-2141.2008.07081.x
By:
- Sato, Tomohiko;
- Toki, Tsutomu;
- Kanezaki, Rika;
- Xu, Gang;
- Terui, Kiminori;
- Kanegane, Hirokazu;
- Miura, Masayoshi;
- Adachi, Souichi;
- Migita, Masahiro;
- Morinaga, Shingo;
- Nakano, Takahide;
- Endo, Mikiya;
- Kojima, Seiji;
- Kiyoi, Hitoshi;
- Mano, Hiroyuki;
- Ito, Etsuro
Publication type:
Article
Enzymatic Changes in Red Blood Cells of Diamond-Blackfan Anemia.
Published in:
Tohoku Journal of Experimental Medicine, 2021, v. 255, n. 1, p. 49, doi. 10.1620/tjem.255.49
By:
- Taiju Utsugisawa;
- Toshitaka Uchiyama;
- Tsutomu Toki;
- Keiko Shimojima-Yamamoto;
- Shouichi Ohga;
- Etsuro Ito;
- Hitoshi Kanno
Publication type:
Article
Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome.
Published in:
Cancer Science, 2019, v. 110, n. 10, p. 3358, doi. 10.1111/cas.14160
By:
- 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
Publication type:
Article
Construction of an Expression System for Aqualysin I in Escherichia coli That Gives a Markedly Improved Yield of the Enzyme Protein.
Published in:
Bioscience, Biotechnology & Biochemistry, 2008, v. 72, n. 8, p. 2012, doi. 10.1271/bbb.80132
By:
- Sakaguchi, Masayoshi;
- Niimiya, Keisuke;
- Takezawa, Makoto;
- Toki, Tsutomu;
- Sugahara, Yasusato;
- Kawakita, Masao
Publication type:
Article
Exposure to a MRI-type high-strength static magnetic field stimulates megakaryocytic/erythroid hematopoiesis in CD34+ cells from human placental and umbilical cord blood.
Published in:
Bioelectromagnetics, 2009, v. 30, n. 4, p. 280, doi. 10.1002/bem.20480
By:
- Monzen, Satoru;
- Takahashi, Kenji;
- Toki, Tsutomu;
- Ito, Etsuro;
- Sakurai, Tomonori;
- Miyakoshi, Junji;
- Kashiwakura, Ikuo
Publication type:
Article
Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia.
Published in:
EJHaem, 2022, v. 3, n. 1, p. 163, doi. 10.1002/jha2.374
By:
- 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;
- Miyano, Satoru;
- Ogawa, Seishi
Publication type:
Article
Expression of erythroid-specific genes in acute megakaryoblastic leukaemia and transient myeloproliferative disorder in Down's syndrome.
Published in:
British Journal of Haematology, 1995, v. 90, n. 3, p. 607, doi. 10.1111/j.1365-2141.1995.tb05591.x
By:
- ITO, ETSURO;
- KASAI, MIKIO;
- HAYASHI, YASOHIDE;
- TOKI, TSUTOMU;
- ARAI, KOJI;
- YOKOYAMA, SHINKICHI;
- KATO, KOJI;
- TACHIBANA, NAOKI;
- YAMAMOTO, MASAYUKI;
- YOKOYAMA, MASARU
Publication type:
Article
EXPRESSION OF A LINEAGE SPECIFIC TRANSCRIPTIONAL FACTOR GATA-1 IN LEUKAEMIC BLASTS FROM PATIENTS WITH INFANTILE LEUKAEMIA.
Published in:
British Journal of Haematology, 1992, v. 80, n. 4, p. 561, doi. 10.1111/j.1365-2141.1992.tb04577.x
By:
- Ito, Etsuro;
- Toki, Tsutomu;
- Arai, Koji;
- Kawauchi, Kyoichi;
- Tsuda, Hiroyuki;
- Yokoyama, Masaru
Publication type:
Article

Found: 38

Purification of leukemic blast cells from blood smears using laser microdissection.

Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing.

ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan.

Selective KIT inhibitor KI-328 and HSP90 inhibitor show different potency against the type of KIT mutations recurrently identified in acute myeloid leukemia.

Molecular pathogenesis in Diamond-Blackfan anemia.

KCNJ2mutation in intractable ventricular arrhythmia with Andersen's syndrome.

Mechanism of KIT gene regulation by GATA1 lacking the N-terminal domain in Down syndrome–related myeloid disorders.

Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients.

Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal children.

Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.

Corrigendum: The landscape of somatic mutations in Down syndrome-related myeloid disorders.

The landscape of somatic mutations in Down syndrome-related myeloid disorders.

Highly sensitive detection of GATA1 mutations in patients with myeloid leukemia associated with Down syndrome by combining Sanger and targeted next generation sequencing.

Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation.

Erythroid transcription factor GATA-1 is abundantly transcribed in mouse testis.

Troglitazone and 15-deoxy-Δ<sup>12,14</sup>-prostaglandin J<sub>2</sub> inhibit shear-induced coupling factor 6 release in endothelial cells

Ribosomal protein L5 facilitates rDNA-bundled condensate and nucleolar assembly.

Resistance of t(17;19)‐acute lymphoblastic leukemia cell lines to multiagents in induction therapy.

Glycogen synthase kinase-3β phosphorylates synphilin-1 in vitro.

Cloning and expression of human B cell-specific transcription factor BACH2 mapped to chromosome 6q15.

Human small Maf proteins form heterodimers with CNC family transcription factors and recognize the NF-E2 motif.

Correction to: Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.

Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.

Transient erythroblastopenia due to a GATA1 variant in an infant female.

Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21.

Effective response to azacitidine in a child with a second relapse of myeloid leukemia associated with Down syndrome after bone marrow transplantation.

Preserved High Probability of Overall Survival with Significant Reduction of Chemotherapy for Myeloid Leukemia in Down Syndrome: A Nationwide Prospective Study in Japan.

Transient myeloproliferative disorder with partial trisomy 21.

Gene alterations involving the CRLF2-JAK pathway and recurrent gene deletions in Down syndrome-associated acute lymphoblastic leukemia in Japan.

Down syndrome-associated haematopoiesis abnormalities created by chromosome transfer and genome editing technologies.

Functional analysis of JAK3 mutations in transient myeloproliferative disorder and acute megakaryoblastic leukaemia accompanying Down syndrome.

Enzymatic Changes in Red Blood Cells of Diamond-Blackfan Anemia.

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

Construction of an Expression System for Aqualysin I in Escherichia coli That Gives a Markedly Improved Yield of the Enzyme Protein.

Exposure to a MRI-type high-strength static magnetic field stimulates megakaryocytic/erythroid hematopoiesis in CD34<sup>+</sup> cells from human placental and umbilical cord blood.

Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia.

Expression of erythroid-specific genes in acute megakaryoblastic leukaemia and transient myeloproliferative disorder in Down's syndrome.

EXPRESSION OF A LINEAGE SPECIFIC TRANSCRIPTIONAL FACTOR GATA-1 IN LEUKAEMIC BLASTS FROM PATIENTS WITH INFANTILE LEUKAEMIA.