Gain-of-function c-CBL mutations associated with uniparental disomy of 11q in myeloid neoplasms

Por Ogawa, Seishi, Sanada, Masashi, Shih, Lee-Young, Suzuki, Takahiro, Otsu, Makoto, Nakauchi, Hiromitsu, Koeffler, H. Philip
Publicado no Cell Cycle (2010)

Favorable outcome of patients who have 13q deletion: a suggestion for revision of the WHO ‘MDS-U’ designation

Por Hosokawa, Kohei, Katagiri, Takamasa, Sugimori, Naomi, Ishiyama, Ken, Sasaki, Yumi, Seiki, Yu, Sato-Otsubo, Aiko, Sanada, Masashi, Ogawa, Seishi, Nakao, Shinji
Publicado em 2012

Hidden abnormalities and novel classification of t(15;17) acute promyelocytic leukemia (APL) based on genomic alterations

Por Akagi, Tadayuki, Shih, Lee-Yung, Kato, Motohiro, Kawamata, Norihiko, Yamamoto, Go, Sanada, Masashi, Okamoto, Ryoko, Miller, Carl W., Liang, Der-Cherng, Ogawa, Seishi, Koeffler, H. Phillip
Publicado em 2009

Allelotypes of lung adenocarcinomas featuring ALK fusion demonstrate fewer onco- and suppressor gene changes

Por Ninomiya, Hironori, Kato, Motohiro, Sanada, Masashi, Takeuchi, Kengo, Inamura, Kentaro, Motoi, Noriko, Nagano, Hiroko, Nomura, Kimie, Sakao, Yukinori, Okumura, Sakae, Mano, Hiroyuki, Ogawa, Seishi, Ishikawa, Yuichi
Publicado em 2013

An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data

Por 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
Publicado em 2013

GE-34 THE MUTATIONAL LANDSCAPE AND TEMPORAL AND SPATIAL CLONAL EVOLUTION TO PROGRESSION IN 351 LOW-GRADE GLIOMAS

Por Suzuki, Hiromichi, Aoki, Kosuke, Ohka, Fumiharu, Motomura, Kazuya, Fujii, Masazumi, Sanada, Masashi, Nakamura, Hideo, Mizoguchi, Masahiro, Abe, Tatsuya, Muragaki, Yoshihiro, Wakabayashi, Toshihiko, Ogawa, Seishi, Natsume, Atsushi
Publicado em 2014

Genetic Profiling of Myeloproliferative Disorders by Single Nucleotide Polymorphism Oligonucleotide Micorarray

Por Kawamata, Norihiko, Ogawa, Seishi, Yamamoto, Go, Lehmann, Soren, Levine, Ross L., Pikman, Yana, Nannya, Toshiki, Sanada, Masashi, Miller, Carl W., Gilliland, D. Gary, Koeffler, H. Phillip
Publicado no Exp Hematol (2008)

Highly Sensitive Method for Genomewide Detection of Allelic Composition in Nonpaired, Primary Tumor Specimens by Use of Affymetrix Single-Nucleotide–Polymorphism Genotyping Microar...

Por Yamamoto, Go , Nannya, Yasuhito , Kato, Motohiro , Sanada, Masashi , Levine, Ross L. , Kawamata, Norihiko , Hangaishi, Akira , Kurokawa, Mineo , Chiba, Shigeru , Gilliland, D. Gary , Koeffler, H. Phillip , Ogawa, Seishi 
Publicado em 2007

Genomic profiling of adult acute lymphoblastic leukemia by single nucleotide polymorphism oligonucleotide microarray and comparison to pediatric acute lymphoblastic leukemia

Por Okamoto, Ryoko, Ogawa, Seishi, Nowak, Daniel, Kawamata, Norihiko, Akagi, Tadayuki, Kato, Motohiro, Sanada, Masashi, Weiss, Tamara, Haferlach, Claudia, Dugas, Martin, Ruckert, Christian, Haferlach, Torsten, Koeffler, H. Phillip
Publicado em 2010

Frequent genomic abnormalities in acute myeloid leukemia/myelodysplastic syndrome with normal karyotype

Por Akagi, Tadayuki, Ogawa, Seishi, Dugas, Martin, Kawamata, Norihiko, Yamamoto, Go, Nannya, Yasuhito, Sanada, Masashi, Miller, Carl W., Yung, Amanda, Schnittger, Susanne, Haferlach, Torsten, Haferlach, Claudia, Koeffler, H. Phillip
Publicado em 2009

Genome-wide approach to identify second gene targets for malignant rhabdoid tumors using high-density oligonucleotide microarrays

Por Takita, Junko, Chen, Yuyan, Kato, Motohiro, Ohki, Kentaro, Sato, Yusuke, Ohta, Shigeru, Sugita, Kanji, Nishimura, Riki, Hoshino, Noriko, Seki, Masafumi, Sanada, Masashi, Oka, Akira, Hayashi, Yasuhide, Ogawa, Seishi
Publicado no Cancer Sci (2014)

Structural Determinants of the Gain-of-Function Phenotype of Human Leukemia-associated Mutant CBL Oncogene

Por Nadeau, Scott A., An, Wei, Mohapatra, Bhopal C., Mushtaq, Insha, Bielecki, Timothy A., Luan, Haitao, Zutshi, Neha, Ahmad, Gulzar, Storck, Matthew D., Sanada, Masashi, Ogawa, Seishi, Band, Vimla, Band, Hamid
Publicado no J Biol Chem (2017)

Cbl-family ubiquitin ligases and their recruitment of CIN85 are largely dispensable for epidermal growth factor receptor endocytosis

Por Ahmad, Gulzar, Mohapatra, Bhopal, Schulte, Nancy A., Nadeau, Scott, Luan, Haitao, Zutshi, Neha, Tom, Eric, Ortega-Cava, Cesar, Tu, Chun, Sanada, Masashi, Ogawa, Seishi, Toews, Myron L., Band, Vimla, Band, Hamid
Publicado no Int J Biochem Cell Biol (2014)

Internal deletion of BCOR reveals a tumor suppressor function for BCOR in T lymphocyte malignancies

Por Tanaka, Tomoyuki, Nakajima-Takagi, Yaeko, Aoyama, Kazumasa, Tara, Shiro, Oshima, Motohiko, Saraya, Atsunori, Koide, Shuhei, Si, Sha, Manabe, Ichiro, Sanada, Masashi, Nakayama, Manabu, Masuko, Masayoshi, Sone, Hirohito, Koseki, Haruhiko, Iwama, Atsushi
Publicado no J Exp Med (2017)

Physiological Srsf2 P95H expression causes impaired hematopoietic stem cell functions and aberrant RNA splicing in mice

Por Kon, Ayana, Yamazaki, Satoshi, Nannya, Yasuhito, Kataoka, Keisuke, Ota, Yasunori, Nakagawa, Masahiro Marshall, Yoshida, Kenichi, Shiozawa, Yusuke, Morita, Maiko, Yoshizato, Tetsuichi, Sanada, Masashi, Nakayama, Manabu, Koseki, Haruhiko, Nakauchi, Hiromitsu, Ogawa, Seishi
Publicado no Blood (2018)

A High Occurrence of Acquisition and/or Expansion of C-CBL Mutant Clones in the Progression of High-Risk Myelodysplastic Syndrome to Acute Myeloid Leukemia

Por Kao, Hsiao-Wen, Sanada, Masashi, Liang, Der-Cherng, Lai, Chang-Liang, Lee, En-Hui, Kuo, Ming-Chung, Lin, Tung-Liang, Shih, Yu-Shu, Wu, Jin-Hou, Huang, Chein-Fuang, Ogawa, Seishi, Shih, Lee-Yung
Publicado em 2011

Deletion of the TNFAIP3/A20 gene detected by FICTION analysis in classical Hodgkin lymphoma

Por Nomoto, Junko, Hiramoto, Nobuhiro, Kato, Motohiro, Sanada, Masashi, Maeshima, Akiko Miyagi, Taniguchi, Hirokazu, Hosoda, Fumie, Asakura, Yoshitaka, Munakata, Wataru, Sekiguchi, Naohiro, Maruyama, Dai, Watanabe, Takashi, Nakagama, Hitoshi, Takeuchi, Kengo, Tobinai, Kensei, Ogawa, Seishi, Kobayashi, Yukio
Publicado em 2012

Smap1 deficiency perturbs receptor trafficking and predisposes mice to myelodysplasia

Por 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
Publicado em 2013

Aberrant splicing of U12-type introns is the hallmark of ZRSR2 mutant myelodysplastic syndrome

Por Madan, Vikas, Kanojia, Deepika, Li, Jia, Okamoto, Ryoko, Sato-Otsubo, Aiko, Kohlmann, Alexander, Sanada, Masashi, Grossmann, Vera, Sundaresan, Janani, Shiraishi, Yuichi, Miyano, Satoru, Thol, Felicitas, Ganser, Arnold, Yang, Henry, Haferlach, Torsten, Ogawa, Seishi, Koeffler, H. Phillip
Publicado no Nat Commun (2015)

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

Por Kawamata, Norihiko, Ogawa, Seishi, Zimmermann, Martin, Kato, Motohiro, Sanada, Masashi, Hemminki, Kari, Yamatomo, Go, Nannya, Yasuhito, Koehler, Rolf, Flohr, Thomas, Miller, Carl W., Harbott, Jochen, Ludwig, Wolf-Dieter, Stanulla, Martin, Schrappe, Martin, Bartram, Claus R., Koeffler, H. Phillip
Publicado em 2008