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A case of vasculogenic mesenchymal tumor in the mediastinum: whole-exome sequencing reveals origin from pre-existing germ cell tumor.
Published in:
Virchows Archiv: European Journal of Pathology, 2023, v. 482, n. 5, p. 923, doi. 10.1007/s00428-023-03529-2
By:
- Fujii, Hirotake;
- Yamada, Yosuke;
- Yamamura, Kentaro;
- Ishida, Yoshihiro;
- Tsujimura, Marina;
- Matsumoto, Kazuhisa;
- Tanaka, Satona;
- Date, Hiroshi;
- Nishikawa, Tadaaki;
- Yoshida, Yukihiro;
- Kashima, Jumpei;
- Yatabe, Yasushi;
- Ogawa, Seishi;
- Marx, Alexander;
- Ulbright, Thomas M.;
- Haga, Hironori
Publication type:
Article
Characterization of adenocarcinoma of the lung in a familial adenomatous polyposis patient.
Published in:
Pathology International, 2008, v. 58, n. 11, p. 706, doi. 10.1111/j.1440-1827.2008.02297.x
By:
- Shinmura, Kazuya;
- Suzuki, Masaya;
- Yamada, Hidetaka;
- Tao, Hong;
- Goto, Masanori;
- Kamo, Takaharu;
- Nagura, Kiyoko;
- Kageyama, Shinji;
- Kato, Motohiro;
- Ogawa, Seishi;
- Maekawa, Masato;
- Takamochi, Kazuya;
- Suzuki, Kazuya;
- Nakamura, Toshio;
- Sugimura, Haruhiko
Publication type:
Article
Coincidence of cutaneous blastic plasmacytoid dendritic cell neoplasm and myelodysplastic syndrome derived from clonal hematopoiesis.
Published in:
Blood Cancer Journal, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41408-023-00893-9
By:
- Yamada, Tomohiko;
- Hiramoto, Nobuhiro;
- Mori, Takuto;
- Yamashita, Daisuke;
- Tai, Yukimasa;
- Yamamoto, Ryusuke;
- Nishikubo, Masashi;
- Maruoka, Hayato;
- Sakamoto, Kana;
- Takeuchi, Kengo;
- Nannya, Yasuhito;
- Ogawa, Seishi;
- Ishikawa, Takayuki
Publication type:
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
BCL6 locus is hypermethylated in angioimmunoblastic T-cell lymphoma.
Published in:
2017
By:
- Nishizawa, Shoko;
- Sakata-Yanagimoto, Mamiko;
- Hattori, Keiichiro;
- Muto, Hideharu;
- Nguyen, Tran;
- Izutsu, Koji;
- Yoshida, Kenichi;
- Ogawa, Seishi;
- Nakamura, Naoya;
- Chiba, Shigeru
Publication type:
journal article
PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.
Published in:
2016
By:
- Imashuku, Shinsaku;
- Muramatsu, Hideki;
- Sugihara, Takashi;
- Okuno, Yusuke;
- Wang, Xinan;
- Yoshida, Kenichi;
- Kato, Ayako;
- Kato, Koichi;
- Tatsumi, Yasuaki;
- Hattori, Ai;
- Kita, Shinya;
- Oe, Keishi;
- Sueyoshi, Atsushi;
- Usui, Takeshi;
- Shiraishi, Yuichi;
- Chiba, Kenichi;
- Tanaka, Hiroko;
- Miyano, Satoru;
- Ogawa, Seishi;
- Kojima, Seiji
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
Clinical and genetic features of dyskeratosis congenita, cryptic dyskeratosis congenita, and Hoyeraal-Hreidarsson syndrome in Japan.
Published in:
2015
By:
- Yamaguchi, Hiroki;
- Sakaguchi, Hirotoshi;
- Yoshida, Kenichi;
- Yabe, Miharu;
- Yabe, Hiromasa;
- Okuno, Yusuke;
- Muramatsu, Hideki;
- Takahashi, Yoshiyuki;
- Yui, Shunsuke;
- Shiraishi, Yuichi;
- Chiba, Kenichi;
- Tanaka, Hiroko;
- Miyano, Satoru;
- Inokuchi, Koiti;
- Ito, Etsuro;
- Ogawa, Seishi;
- Kojima, Seiji
Publication type:
journal article
Identification of a homozygous JAK3 V674A mutation caused by acquired uniparental disomy in a relapsed early T-cell precursor ALL patient.
Published in:
2015
By:
- Kawashima-Goto, Sachiko;
- Imamura, Toshihiko;
- Seki, Masafumi;
- Kato, Motohiro;
- Yoshida, Kenichi;
- Sugimoto, Atsuya;
- Kaneda, Daisuke;
- Fujiki, Atsushi;
- Miyachi, Mitsuru;
- Nakatani, Takuya;
- Osone, Shinya;
- Ishida, Hiroyuki;
- Taki, Tomohiko;
- Takita, Junko;
- Shiraishi, Yuichi;
- Chiba, Kenichi;
- Tanaka, Hiroko;
- Miyano, Satoru;
- Ogawa, Seishi;
- Hosoi, Hajime
Publication type:
Report
Aggressive transformation of anaplastic large cell lymphoma with increased number of ALK-translocated chromosomes.
Published in:
2015
By:
- Hoshino, Akihiro;
- Nomura, Keiko;
- Hamashima, Takeru;
- Isobe, Tomoya;
- Seki, Masafumi;
- Hiwatari, Mitsuteru;
- Yoshida, Kenichi;
- Shiraishi, Yuichi;
- Chiba, Kenichi;
- Tanaka, Hiroko;
- Miyano, Satoru;
- Ogawa, Seishi;
- Takita, Junko;
- Kanegane, Hirokazu
Publication type:
Report
Expressional changes of genes and miRNA in common megakaryocyte-erythroid progenitors from lower-risk myelodysplastic syndrome.
Published in:
International Journal of Hematology, 2014, v. 100, n. 4, p. 361, doi. 10.1007/s12185-014-1639-2
By:
- Maki, Kazuhiro;
- Sasaki, Ko;
- Nagata, Yasunobu;
- Nagasawa, Fusako;
- Nakamura, Yuka;
- Ogawa, Seishi;
- Mitani, Kinuko
Publication type:
Article
Identification of unbalanced genome copy number abnormalities in patients with multiple myeloma by single-nucleotide polymorphism genotyping microarray analysis.
Published in:
International Journal of Hematology, 2012, v. 96, n. 4, p. 492, doi. 10.1007/s12185-012-1171-1
By:
- Kamada, Yuhei;
- Sakata-Yanagimoto, Mamiko;
- Sanada, Masashi;
- Sato-Otsubo, Aiko;
- Enami, Terukazu;
- Suzukawa, Kazumi;
- Kurita, Naoki;
- Nishikii, Hidekazu;
- Yokoyama, Yasuhisa;
- Okoshi, Yasushi;
- Hasegawa, Yuichi;
- Ogawa, Seishi;
- Chiba, Shigeru
Publication type:
Article
Splicing factor mutations in myelodysplasia.
Published in:
International Journal of Hematology, 2012, v. 96, n. 4, p. 438, doi. 10.1007/s12185-012-1182-y
By:
- Ogawa, Seishi
Publication type:
Article
Assessment of the international prognostic scoring system for determining chemotherapeutic indications in myelodysplastic syndrome: Japanese retrospective multicenter study.
Published in:
2005
By:
- Ito, Yoshikazu;
- Ohyashiki, Kazuma;
- Hirai, Hisamaru;
- Ogawa, Seishi;
- Mitani, Kinuko;
- Hotta, Tomomitsu;
- Bessho, Masami;
- Naoe, Tomoki;
- Mizoguchi, Hideaki;
- Uchiyama, Takashi;
- Omine, Mitsuhiro
Publication type:
journal article
Molecular cytogenetic analyses of HIG, a novel human cell line carrying t(1;3)(p36.3;q25.3) established from a patient with chronic myelogenous leukemia in blastic crisis.
Published in:
2003
By:
- Hosoya, Noriko;
- Ogawa, Seishi;
- Motokura, Tohru;
- Hangaishi, Akira;
- Wang, Lili;
- Qiao, Ying;
- Nannya, Yasuhito;
- Kogi, Mieko;
- Hirai, Hisamaru
Publication type:
journal article
On the origin of gastric tumours: analysis of a case with intramucosal gastric carcinoma and oxyntic gland adenoma.
Published in:
Journal of Pathology, 2023, v. 259, n. 4, p. 362, doi. 10.1002/path.6050
By:
- Kumagai, Ken;
- Shimizu, Takahiro;
- Nikaido, Mitsuhiro;
- Hirano, Tomonori;
- Kakiuchi, Nobuyuki;
- Takeuchi, Yasuhide;
- Minamiguchi, Sachiko;
- Sakurai, Takaki;
- Teramura, Mari;
- Utsumi, Takahiro;
- Hiramatsu, Yukiko;
- Nakanishi, Yuki;
- Takai, Atsushi;
- Miyamoto, Shin'ichi;
- Ogawa, Seishi;
- Seno, Hiroshi
Publication type:
Article
Significance of perivascular tumour cells defined by CD109 expression in progression of glioma.
Published in:
Journal of Pathology, 2017, v. 243, p. 468, doi. 10.1002/path.4981
By:
- Shiraki, Yukihiro;
- Mii, Shinji;
- Enomoto, Atsushi;
- Momota, Hiroyuki;
- Han, Yi‐Peng;
- Kato, Takuya;
- Ushida, Kaori;
- Kato, Akira;
- Asai, Naoya;
- Murakumo, Yoshiki;
- Aoki, Kosuke;
- Suzuki, Hiromichi;
- Ohka, Fumiharu;
- Wakabayashi, Toshihiko;
- Todo, Tomoki;
- Ogawa, Seishi;
- Natsume, Atsushi;
- Takahashi, Masahide
Publication type:
Article
Significance of perivascular tumour cells defined by CD109 expression in progression of glioma.
Published in:
Journal of Pathology, 2017, v. 243, n. 4, p. 468, doi. 10.1002/path.4981
By:
- Shiraki, Yukihiro;
- Mii, Shinji;
- Enomoto, Atsushi;
- Momota, Hiroyuki;
- Han, Yi-Peng;
- Kato, Takuya;
- Ushida, Kaori;
- Kato, Akira;
- Asai, Naoya;
- Murakumo, Yoshiki;
- Aoki, Kosuke;
- Suzuki, Hiromichi;
- Ohka, Fumiharu;
- Wakabayashi, Toshihiko;
- Todo, Tomoki;
- Ogawa, Seishi;
- Natsume, Atsushi;
- Takahashi, Masahide
Publication type:
Article
The Evi-1 oncoprotein inhibits c-Jun N-terminal kinase and prevents stress-induced cell death.
Published in:
EMBO Journal, 2000, v. 19, n. 12, p. 2958, doi. 10.1093/emboj/19.12.2958
By:
- Kurokawa, Mineo;
- Mitani, Kinuko;
- Yamagata, Tetsuya;
- Takahashi, Tokiharu;
- Izutsu, Koji;
- Ogawa, Seishi;
- Moriguchi, Tetsuo;
- Nishida, Eisuke;
- Yazaki, Yoshio;
- Hirai, Hisamaru
Publication type:
Article
Genetic Analysis of Pheochromocytoma and Paraganglioma Complicating Cyanotic Congenital Heart Disease.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 9, p. 2545, doi. 10.1210/clinem/dgac362
By:
- Tatsuki Ogasawara;
- Yoichi Fujii;
- Nobuyuki Kakiuchi;
- Yusuke Shiozawa;
- Ryuichi Sakamoto;
- Yoshihiro Ogawa;
- Katsuki Ootani;
- Etsuro Ito;
- Tomoaki Tanaka;
- Kenichiro Watanabe;
- Yusaku Yoshida;
- Noriko Kimura;
- Yuichi Shiraishi;
- Kenichi Chiba;
- Hiroko Tanaka;
- Satoru Miyano;
- Seishi Ogawa
Publication type:
Article
Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.
Published in:
Journal of Clinical Investigation, 2014, v. 124, n. 10, p. 4529, doi. 10.1172/JCI74747
By:
- Wenyi Shen;
- Clemente, Michael J.;
- Naoko Hosono;
- Kenichi Yoshida;
- Przychodzen, Bartlomiej;
- Tetsuichi Yoshizato;
- Yuichi Shiraishi;
- Satoru Miyano;
- Seishi Ogawa;
- Maciejewski, Jaroslaw P.;
- Hideki Makishima
Publication type:
Article
Smap1 deficiency perturbs receptor trafficking and predisposes mice to myelodysplasia.
Published in:
2013
By:
- Kon, Shunsuke;
- Minegishi, Naoko;
- Tanabe, Kenji;
- Watanabe, Toshio;
- Funaki, Tomo;
- Wong, Won Fen;
- Sakamoto, Daisuke;
- Higuchi, Yudai;
- Kiyonari, Hiroshi;
- Asano, Katsutoshi;
- Iwakura, Yoichiro;
- Fukumoto, Manabu;
- Osato, Motomi;
- Sanada, Masashi;
- Ogawa, Seishi;
- Nakamura, Takuro;
- Satake, Masanobu
Publication type:
journal article
Smap 1 deficiency perturbs receptor trafficking and predisposes mice to myelodysplasia.
Published in:
Journal of Clinical Investigation, 2013, v. 123, n. 3, p. 1123, doi. 10.1172/JCI63711
By:
- Kon, Shunsuke;
- Minegishi, Naoko;
- Tanabe, Kenji;
- Watanabe, Toshio;
- Funaki, Tomo;
- Won Fen Wong;
- Sakamoto, Daisuke;
- Higuchi, Yudai;
- Kiyonari, Hiroshi;
- Asano, Katsutoshi;
- Iwakura, Yoichiro;
- Fukumoto, Manabu;
- Osato, Motomi;
- Sanada, Masashi;
- Ogawa, Seishi;
- Nakamura, Takuro;
- Satake, Masanobu
Publication type:
Article
Genetic features of B‐cell lymphoblastic lymphoma with TCF3‐PBX1.
Published in:
Cancer Reports, 2022, v. 5, n. 9, p. 1, doi. 10.1002/cnr2.1559
By:
- Shirai, Ryota;
- Osumi, Tomoo;
- Sato‐Otsubo, Aiko;
- Nakabayashi, Kazuhiko;
- Mori, Takeshi;
- Yoshida, Masanori;
- Yoshida, Kaoru;
- Kohri, Mika;
- Ishihara, Takashi;
- Yasue, Shiho;
- Imamura, Toshihiko;
- Endo, Mikiya;
- Miyamoto, Satoshi;
- Ohki, Kentaro;
- Sanada, Masashi;
- Kiyokawa, Nobutaka;
- Ogawa, Seishi;
- Yoshioka, Takako;
- Hata, Kenichiro;
- Takagi, Masatoshi
Publication type:
Article
Noonan syndrome‐associated biallelic LZTR1 mutations cause cardiac hypertrophy and vascular malformations in zebrafish.
Published in:
Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 3, p. 1, doi. 10.1002/mgg3.1107
By:
- Nakagama, Yu;
- Takeda, Norihiko;
- Ogawa, Seishi;
- Takeda, Hiroyuki;
- Furutani, Yoshiyuki;
- Nakanishi, Toshio;
- Sato, Tatsuyuki;
- Hirata, Yoichiro;
- Oka, Akira;
- Inuzuka, Ryo
Publication type:
Article
Atypical dyskeratosis congenita diagnosed using whole-exome sequencing.
Published in:
Pediatrics International, 2017, v. 59, n. 8, p. 933, doi. 10.1111/ped.13314
By:
- Monoi, Ayaka;
- Sugawa, Masahiro;
- Kato, Motohiro;
- Seki, Masafumi;
- Yoshida, Kenichi;
- Shiraishi, Yuichi;
- Sakaguchi, Hirotoshi;
- Ogawa, Seishi;
- Takita, Junko
Publication type:
Article
Partial monosomy of 10p and duplication of another chromosome in two patients.
Published in:
Pediatrics International, 2017, v. 59, n. 1, p. 99, doi. 10.1111/ped.13181
By:
- Ohta, Sayaka;
- Isojima, Tsuyoshi;
- Mizuno, Yoko;
- Kato, Motohiro;
- Mimaki, Masakazu;
- Seki, Masafumi;
- Sato, Yusuke;
- Ogawa, Seishi;
- Takita, Junko;
- Kitanaka, Sachiko;
- Oka, Akira
Publication type:
Article
Bernard- Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion.
Published in:
2013
By:
- Kunishima, Shinji;
- Imai, Tsuyoshi;
- Kobayashi, Ryoji;
- Kato, Motohiro;
- Ogawa, Seishi;
- Saito, Hidehiko
Publication type:
Journal Article
Bernard- Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion.
Published in:
Pediatrics International, 2013, v. 55, n. 4, p. 434, doi. 10.1111/ped.12105
By:
- Kunishima, Shinji;
- Imai, Tsuyoshi;
- Kobayashi, Ryoji;
- Kato, Motohiro;
- Ogawa, Seishi;
- Saito, Hidehiko
Publication type:
Article
An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data.
Published in:
Nucleic Acids Research, 2013, v. 41, n. 7, p. e89, doi. 10.1093/nar/gkt126
By:
- 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
Publication type:
Article
Profiling the inhibitory receptors LAG-3, TIM-3, and TIGIT in renal cell carcinoma reveals malignancy.
Published in:
Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-25865-0
By:
- Takamatsu, Kimiharu;
- Tanaka, Nobuyuki;
- Hakozaki, Kyohei;
- Takahashi, Ryohei;
- Teranishi, Yu;
- Murakami, Tetsushi;
- Kufukihara, Ryohei;
- Niwa, Naoya;
- Mikami, Shuji;
- Shinojima, Toshiaki;
- Sasaki, Takashi;
- Sato, Yusuke;
- Kume, Haruki;
- Ogawa, Seishi;
- Kakimi, Kazuhiro;
- Kamatani, Takashi;
- Miya, Fuyuki;
- Tsunoda, Tatsuhiko;
- Aimono, Eriko;
- Nishihara, Hiroshi
Publication type:
Article
Complete Bone Marrow Necrosis with Charcot-Leyden Crystals Caused by Myeloid Neoplasm with Mutated NPM1 and TET2.
Published in:
Internal Medicine, 2022, v. 61, n. 21, p. 3265, doi. 10.2169/internalmedicine.8859-21
By:
- Kenki Saito;
- Takayuki Sato;
- Kenji Notohara;
- Yasuhito Nannya;
- Seishi Ogawa;
- Yasunori Ueda
Publication type:
Article
Clonal Cytopenia of Undetermined Significance in a Patient with Congenital Wilms' Tumor 1 and Acquired DNMT3A Gene Mutations.
Published in:
Internal Medicine, 2021, v. 60, n. 23, p. 3785, doi. 10.2169/internalmedicine.7571-21
By:
- Ken Murakami;
- Yuuta Yamaguchi;
- Yuko Kida;
- Yoichiro Morikawa;
- Hidetoshi Ujiie;
- Hiroyuki Sugahara;
- Yasuhito Nannya;
- Seishi Ogawa;
- Yuzuru Kanakura
Publication type:
Article
Highly Efficient Ex Vivo Expansion of Human Hematopoietic Stem Cells Using Delta1-Fc Chimeric Protein.
Published in:
Stem Cells, 2006, v. 24, n. 11, p. 2456, doi. 10.1634/stemcells.2006-0258
By:
- Suzuki, Takahiro;
- Yokoyama, Yasuhisa;
- Kumano, Keiki;
- Takanashi, Minoko;
- Kozuma, Shiro;
- Takato, Tsuyoshi;
- Nakahata, Tatsutoshi;
- Nishikawa, Mitsuo;
- Sakano, Seiji;
- Kurokawa, Mineo;
- Ogawa, Seishi;
- Chiba, Shigeru
Publication type:
Article
AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not for maintenance of hematopoietic stem cells in adult hematopoiesis.
Published in:
Nature Medicine, 2004, v. 10, n. 3, p. 299, doi. 10.1038/nm997
By:
- Ichikawa, Motoshi;
- Asai, Takashi;
- Saito, Toshiki;
- Yamamoto, Go;
- Seo, Sachiko;
- Yamazaki, Ieharu;
- Yamagata, Tetsuya;
- Mitani, Kinuko;
- Chiba, Shigeru;
- Hirai, Hisamaru;
- Ogawa, Seishi;
- Kurokawa, Mineo
Publication type:
Article
Modelling and drug targeting of a myeloid neoplasm with atypical 3q26/MECOM rearrangement using patient‐specific iPSCs.
Published in:
British Journal of Haematology, 2024, v. 205, n. 4, p. 1430, doi. 10.1111/bjh.19720
By:
- Nakamura, Momoko;
- Chonabayashi, Kazuhisa;
- Narita, Megumi;
- Matsumura, Yasuko;
- Nishikawa, Misato;
- Ochi, Yotaro;
- Nannya, Yasuhito;
- Hishizawa, Masakatsu;
- Inoue, Daichi;
- Delwel, Ruud;
- Ogawa, Seishi;
- Takaori‐Kondo, Akifumi;
- Yoshida, Yoshinori
Publication type:
Article
A rare homozygous variant in TERT gene causing variable bone marrow failure, fragility fractures, rib anomalies and extremely short telomere lengths with high serum IgE.
Published in:
British Journal of Haematology, 2024, v. 204, n. 3, p. 1086, doi. 10.1111/bjh.19176
By:
- Elbadry, Mahmoud I.;
- Tawfeek, Ahmed;
- Hirano, Tomonori;
- El‐Mokhtar, Mohamed A.;
- Kenawey, Mohamed;
- Helmy, Ahmed M.;
- Ogawa, Seishi;
- Mughal, M. Zulf;
- Nannya, Yasuhito
Publication type:
Article
A case of hepatitis‐associated aplastic anaemia following living‐donor liver transplantation for fulminant hepatitis showing loss of heterozygosity in the 6p chromosome in the affected liver.
Published in:
British Journal of Haematology, 2024, v. 204, n. 2, p. 623, doi. 10.1111/bjh.19219
By:
- Katagiri, Takamasa;
- Iwasaki, Hiroka;
- Fujieda, Atsushi;
- Kasashima, Satomi;
- Ozaki, Satoru;
- Uemori, Mizuho;
- Ogawa, Seishi;
- Nakao, Shinji
Publication type:
Article
An eltrombopag‐induced remission of bone‐marrow aplasia accompanied by marked leukoerythroblastosis and splenomegaly.
Published in:
British Journal of Haematology, 2022, v. 198, n. 5, p. e75, doi. 10.1111/bjh.18342
By:
- Arita, Kotaro;
- Murakami, Jun;
- Iwaki, Noriko;
- Hosono, Naoko;
- Tasaki, Toshiki;
- Tsujikawa, Tetsuya;
- Okazawa, Hidehiko;
- Imi, Tatsuya;
- Nannya, Yasuhito;
- Ogawa, Seishi;
- Nakao, Shinji
Publication type:
Article
The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype.
Published in:
British Journal of Haematology, 2016, v. 175, n. 3, p. 457, doi. 10.1111/bjh.14243
By:
- Yabe, Miharu;
- Yabe, Hiromasa;
- Morimoto, Tsuyoshi;
- Fukumura, Akiko;
- Ohtsubo, Keisuke;
- Koike, Takashi;
- Yoshida, Kenichi;
- Ogawa, Seishi;
- Ito, Etsuro;
- Okuno, Yusuke;
- Muramatsu, Hideki;
- Kojima, Seiji;
- Matsuo, Keitaro;
- Hira, Asuka;
- Takata, Minoru
Publication type:
Article
Genomic analysis of clonal origin of Langerhans cell histiocytosis following acute lymphoblastic leukaemia.
Published in:
British Journal of Haematology, 2016, v. 175, n. 1, p. 169, doi. 10.1111/bjh.13841
By:
- Kato, Motohiro;
- Seki, Masafumi;
- Yoshida, Kenichi;
- Sato, Yusuke;
- Oyama, Ryo;
- Arakawa, Yuki;
- Kishimoto, Hiroshi;
- Taki, Tomohiko;
- Akiyama, Masaharu;
- Shiraishi, Yuichi;
- Chiba, Kenichi;
- Tanaka, Hiroko;
- Mitsuiki, Noriko;
- Kajiwara, Michiko;
- Mizutani, Shuki;
- Sanada, Masashi;
- Miyano, Satoru;
- Ogawa, Seishi;
- Koh, Katsuyoshi;
- Takita, Junko
Publication type:
Article
Induction of HLA-B*40:02-restricted T cells possessing cytotoxic and suppressive functions against haematopoietic progenitor cells from a patient with severe aplastic anaemia.
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British Journal of Haematology, 2016, v. 172, n. 1, p. 131, doi. 10.1111/bjh.13464
By:
- Inaguma, Yoko;
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- Hosokawa, Kohei;
- Maruyama, Hiroyuki;
- Okamoto, Akinao;
- Katagiri, Takamasa;
- Shiraishi, Keiko;
- Murayama, Yuko;
- Tsuzuki‐Iba, Sachiko;
- Mizutani, Yuuki;
- Nishii, Chikako;
- Yamamoto, Naoki;
- Demachi‐Okamura, Ayako;
- Kuzushima, Kiyotaka;
- Ogawa, Seishi;
- Emi, Nobuhiko;
- Nakao, Shinji
Publication type:
Article
A robust molecular pattern for myelodysplastic syndromes in two independent cohorts investigated by next-generation sequencing can be revealed by comparative bioinformatic analyses.
Published in:
British Journal of Haematology, 2014, v. 167, n. 2, p. 278, doi. 10.1111/bjh.12971
By:
- Rose, Dominic;
- Kohlmann, Alexander;
- Nagata, Yasunobu;
- Ogawa, Seishi;
- Haferlach, Claudia;
- Kern, Wolfgang;
- Schnittger, Susanne;
- Haferlach, Torsten
Publication type:
Article
A robust molecular pattern for myelodysplastic syndromes in two independent cohorts investigated by next-generation sequencing can be revealed by comparative bioinformatic analyses.
Published in:
British Journal of Haematology, 2014, v. 165, n. 5, p. 1, doi. 10.1111/bjh.12971
By:
- Rose, Dominic;
- Kohlmann, Alexander;
- Yasunobu Nagata;
- Seishi Ogawa;
- Haferlach, Claudia;
- Kern, Wolfgang;
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- Haferlach, Torsten
Publication type:
Article
Integrated molecular analysis of adult T cell leukemia/lymphoma.
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Nature Genetics, 2015, v. 47, n. 11, p. 1304, doi. 10.1038/ng.3415
By:
- Sanada, Masashi;
- Shibata, Tatsuhiro;
- Kataoka, Keisuke;
- Nagata, Yasunobu;
- Sato-Otsubo, Aiko;
- Kotani, Shinichi;
- Watatani, Yosaku;
- Takeda, June;
- Suzuki, Hiromichi;
- Sato, Yusuke;
- Shiozawa, Yusuke;
- Yoshizato, Tetsuichi;
- Yoshida, Kenichi;
- Makishima, Hideki;
- Ogawa, Seishi;
- Iwanaga, Masako;
- Nosaka, Kisato;
- Hishizawa, Masakatsu;
- Takaori-Kondo, Akifumi;
- Itonaga, Hidehiro
Publication type:
Article
Mutational landscape and clonal architecture in grade II and III gliomas.
Published in:
Nature Genetics, 2015, v. 47, n. 5, p. 458, doi. 10.1038/ng.3273
By:
- Suzuki, Hiromichi;
- Aoki, Kosuke;
- Abe, Tatsuya;
- Muragaki, Yoshihiro;
- Watanabe, Reiko;
- Ito, Ichiro;
- Chiba, Kenichi;
- Shiraishi, Yuichi;
- Niida, Atsushi;
- Tanaka, Hiroko;
- Miyano, Satoru;
- Sato, Yusuke;
- Shiozawa, Yusuke;
- Yoshizato, Tetsuichi;
- Kataoka, Keisuke;
- Yoshida, Kenichi;
- Nagata, Yasunobu;
- Sato-Otsubo, Aiko;
- Sanada, Masashi;
- Ogawa, Seishi
Publication type:
Article
The genomic landscape of nasopharyngeal carcinoma.
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Nature Genetics, 2014, v. 46, n. 8, p. 866, doi. 10.1038/ng.3006
By:
- Lin, De-Chen;
- Meng, Xuan;
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- Nagata, Yasunobu;
- Varela, Ana Maria;
- Xu, Liang;
- Sato, Yusuke;
- Liu, Li-Zhen;
- Ding, Ling-Wen;
- Sharma, Arjun;
- Goh, Boon Cher;
- Lee, Soo Chin;
- Petersson, Bengt Fredrik;
- Yu, Feng Gang;
- Macary, Paul;
- Oo, Min Zin;
- Ha, Chan Soh;
- Yang, Henry;
- Ogawa, Seishi;
- Loh, Kwok Seng
Publication type:
Article
Establishment and characterization of novel human primary and metastatic anaplastic thyroid cancer cell lines and their genomic evolution over a year as a primagraft.
Published in:
2015
By:
- Garg, Manoj;
- Okamoto, Ryoko;
- Nagata, Yasunobu;
- Kanojia, Deepika;
- Venkatesan, Subhashree;
- M T, Anand;
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- Ho, Quoc;
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- Gery, Sigal;
- Liu, Li-Zhen;
- Tan, Kar Tong;
- Chng, Wee Joo;
- Yang, Henry;
- Ogawa, Seishi;
- Koeffler, H Phillip
Publication type:
journal article
UBTF‐internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia.
Published in:
Genes, Chromosomes & Cancer, 2023, v. 62, n. 4, p. 202, doi. 10.1002/gcc.23110
By:
- Kaburagi, Taeko;
- Shiba, Norio;
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- Ishikita, Etsuko;
- Hara, Yusuke;
- Shiraishi, Yuichi;
- Kawasaki, Hirohide;
- Sotomatsu, Manabu;
- Takizawa, Takumi;
- Taki, Tomohiko;
- Kiyokawa, Nobutaka;
- Tomizawa, Daisuke;
- Horibe, Keizo;
- Miyano, Satoru;
- Taga, Takashi;
- Adachi, Souichi;
- Ogawa, Seishi
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;
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- Kobayashi, Akie;
- Kamio, Takuya;
- Sasaki, Shinya;
- Terui, Kiminori;
- Kurose, Akira;
- Yoshida, Kenichi;
- Shiozawa, Yusuke;
- Toki, Tsutomu;
- Ogawa, Seishi;
- Ito, Etsuro
Publication type:
Article

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