Genetic basis of myelodysplastic syndromes

por OGAWA, Seishi
Publicado 2020

Genetic biomarkers for PD-1/PD-L1 blockade therapy

por Kataoka, Keisuke, Ogawa, Seishi
Publicado 2016

Chromatin-Spliceosome Mutations in Acute Myeloid Leukemia

por Ochi, Yotaro, Ogawa, Seishi
Publicado 2021

Cutaneous Adnexal Adenocarcinoma: Genomic Analysis and Successful HER2-targeted Therapy of Metastatic Disease

por HIRANO-LOTMAN, Yui, ISHIDA, Yoshihiro, ENDO, Yuichiro, OGAWA, Seishi, KABASHIMA, Kenji
Publicado 2023

Frequent Loss of the Cyclin‐dependent Kinase‐4 Inhibitor Gene in Human Gliomas

por Gomi, Akira, Sakai, Ryuichi, Ogawa, Seishi, Shinoda, Souji, Hirai, Hisamaru, Masuzawa, Toshio
Publicado 1995

Complete Bone Marrow Necrosis with Charcot-Leyden Crystals Caused by Myeloid Neoplasm with Mutated NPM1 and TET2

por Saito, Kenki, Sato, Takayuki, Notohara, Kenji, Nannya, Yasuhito, Ogawa, Seishi, Ueda, Yasunori
Publicado 2022

Frameshift Mutations of the hMSH6 Gene in Human Leukemia Cell Lines

por Hosoya, Noriko, Hangaishi, Akira, Ogawa, Seishi, Miyagawa, Kiyoshi, Mitani, Kinuko, Yazaki, Yoshio, Hirai, Hisamaru
Publicado 1998

HapMuC: somatic mutation calling using heterozygous germ line variants near candidate mutations

por Usuyama, Naoto, Shiraishi, Yuichi, Sato, Yusuke, Kume, Haruki, Homma, Yukio, Ogawa, Seishi, Miyano, Satoru, Imoto, Seiya
Publicado 2014

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

por Shiraishi, Yuichi, Kataoka, Keisuke, Chiba, Kenichi, Okada, Ai, Kogure, Yasunori, Tanaka, Hiroko, Ogawa, Seishi, Miyano, Satoru
Publicado 2018

A Case of Tyrosine Kinase Inhibitor-Resistant Chronic Myeloid Leukemia, Chronic Phase with ASXL1 Mutation

por Imataki, Osamu, Ishida, Tomoya, Kubo, Hiroyuki, Uemura, Makiko, Nanya, Yasuhito, Kawakami, Kimihiro, Ogawa, Seishi, Kadowaki, Norimitsu
Publicado 2020

Clinical significance of the increased expression of the WT1 gene in peripheral blood of patients with acquired aplastic anemia

por Ishiyama, Ken, Dung, Tran Cao, Imi, Tatsuya, Hosokawa, Kohei, Nannya, Yasuhito, Yamazaki, Hirohito, Ogawa, Seishi, Nakao, Shinji
Publicado 2022

Clonal Cytopenia of Undetermined Significance in a Patient with Congenital Wilms' Tumor 1 and Acquired DNMT3A Gene Mutations

por Murakami, Ken, Yamaguchi, Yuuta, Kida, Yuko, Morikawa, Yoichiro, Ujiie, Hidetoshi, Sugahara, Hiroyuki, Nannya, Yasuhito, Ogawa, Seishi, Kanakura, Yuzuru
Publicado 2021

T‐cell lymphoma, B‐cell lymphoma, and myelodysplastic syndrome harboring common mutations: Trilineage tumorigenesis from a common founder clone

por Yoshihara, Kyoko, Nannya, Yasuhito, Matsuda, Ikuo, Samori, Mami, Utsunomiya, Nobuto, Okada, Masaya, Hirota, Seiichi, Ogawa, Seishi, Yoshihara, Satoshi
Publicado 2021

Molecular studies reveal MLL-MLLT10/AF10 and ARID5B-MLL gene fusions displaced in a case of infantile acute lymphoblastic leukemia with complex karyotype

por Hiwatari, Mitsuteru, Seki, Masafumi, Akahoshi, Shogo, Yoshida, Kenichi, Miyano, Satoru, Shiraishi, Yuichi, Tanaka, Hiroko, Chiba, Kenichi, Ogawa, Seishi, Takita, Junko
Publicado 2017

Noonan syndrome‐associated biallelic LZTR1 mutations cause cardiac hypertrophy and vascular malformations in zebrafish

por Nakagama, Yu, Takeda, Norihiko, Ogawa, Seishi, Takeda, Hiroyuki, Furutani, Yoshiyuki, Nakanishi, Toshio, Sato, Tatsuyuki, Hirata, Yoichiro, Oka, Akira, Inuzuka, Ryo
Publicado 2019

Oncogenic FGFR1 mutation and amplification in common cellular origin in a composite tumor with neuroblastoma and pheochromocytoma

por Tasaka, Keiji, Ueno, Hiroo, Yamasaki, Kai, Okuno, Takahiro, Isobe, Tomoya, Kimura, Shunsuke, Umeda, Katsutsugu, Hara, Junichi, Ogawa, Seishi, Takita, Junko
Publicado 2022

A role for SETD2 loss in tumorigenesis through DNA methylation dysregulation

por Javaid, Hira, Barberis, Alessandro, Chervova, Olga, Nassiri, Isar, Voloshin, Vitaly, Sato, Yusuke, Ogawa, Seishi, Fairfax, Benjamin, Buffa, Francesca, Humphrey, Timothy C.
Publicado 2023

Genetic differences between Asian and Caucasian chronic lymphocytic leukemia

por KAWAMATA, NORIHIKO, MOREILHON, CHIMENE, SAITOH, TAKAYUKI, KARASAWA, MASAMITSU, BERNSTEIN, BRIAN K., SATO-OTSUBO, AIKO, OGAWA, SEISHI, RAYNAUD, SOPHIE, KOEFFLER, H. PHILLIP
Publicado 2013

Myelodysplastic Syndrome-Associated SRSF2 Mutations Cause Splicing Changes by Altering Binding Motif Sequences

por Masaki, So, Ikeda, Shun, Hata, Asuka, Shiozawa, Yusuke, Kon, Ayana, Ogawa, Seishi, Suzuki, Kenji, Hakuno, Fumihiko, Takahashi, Shin-Ichiro, Kataoka, Naoyuki
Publicado 2019

Next‐generation sequencing in two cases of de novo acute basophilic leukaemia

por Shimizu, Takuya, Kondo, Tadakazu, Nannya, Yasuhito, Watanabe, Mizuki, Kitawaki, Toshio, Shindo, Takero, Hishizawa, Masakatsu, Yamashita, Kouhei, Ogawa, Seishi, Takaori‐Kondo, Akifumi
Publicado 2021