Development of an osteosarcoma model with MYCN amplification and TP53 mutation in hiPS cell‐derived neural crest cells von Mukae, Kyosuke, Takenobu, Hisanori, Endo, Yuki, Haruta, Masayuki, Shi, Tianyuan, Satoh, Shunpei, Ohira, Miki, Funato, Michinori, Toguchida, Junya, Osafune, Kenji, Nakahata, Tatsutoshi, Kanda, Hiroaki, Kamijo, Takehiko

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ATM depletion induces proteasomal degradation of FANCD2 and sensitizes neuroblastoma cells to PARP inhibitors von Parvin, Sultana, Akter, Jesmin, Takenobu, Hisanori, Katai, Yutaka, Satoh, Shunpei, Okada, Ryu, Haruta, Masayuki, Mukae, Kyosuke, Wada, Tomoko, Ohira, Miki, Ando, Kiyohiro, Kamijo, Takehiko

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Loss of p53 suppresses replication stress-induced DNA damage in ATRX-deficient neuroblastoma von Akter, Jesmin, Katai, Yutaka, Sultana, Parvin, Takenobu, Hisanori, Haruta, Masayuki, Sugino, Ryuichi P., Mukae, Kyosuke, Satoh, Shunpei, Wada, Tomoko, Ohira, Miki, Ando, Kiyohiro, Kamijo, Takehiko

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Polycomb EZH1 regulates cell cycle/5‐fluorouracil sensitivity of neuroblastoma cells in concert with MYCN von Shinno, Yoshitaka, Takenobu, Hisanori, Sugino, Ryuichi P., Endo, Yuki, Okada, Ryu, Haruta, Masayuki, Satoh, Shunpei, Mukae, Kyosuke, Shaliman, Dilibaerguli, Wada, Tomoko, Akter, Jesmin, Ando, Kiyohiro, Nakazawa, Atsuko, Yoshida, Hideo, Ohira, Miki, Hishiki, Tomoro, Kamijo, Takehiko

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Outcome of renal tumors registered in Japan Wilms Tumor Study‐2 (JWiTS‐2): A report from the Japan Children's Cancer Group (JCCG) von Koshinaga, Tsugumichi, Takimoto, Tetsuya, Oue, Takaharu, Okita, Hajime, Tanaka, Yukichi, Nozaki, Miwako, Tsuchiya, Kunihiko, Inoue, Eisuke, Haruta, Masayuki, Kaneko, Yasuhiko, Fukuzawa, Masahiro

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Clinical prognostic value of DNA methylation in hepatoblastoma: Four novel tumor suppressor candidates von Honda, Shohei, Minato, Masashi, Suzuki, Hiromu, Fujiyoshi, Masato, Miyagi, Hisayuki, Haruta, Masayuki, Kaneko, Yasuhiko, Hatanaka, Kanako C., Hiyama, Eiso, Kamijo, Takehiko, Okada, Tadao, Taketomi, Akinobu

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Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney von Haruta, Masayuki, Arai, Yasuhito, Okita, Hajime, Tanaka, Yukichi, Takimoto, Tetsuya, Kamijo, Takehiko, Oue, Takaharu, Souzaki, Ryota, Taguchi, Tomoaki, Kuwahara, Yasumichi, Chin, Motoaki, Nakadate, Hisaya, Hiyama, Eiso, Ishida, Yasushi, Koshinaga, Tsugumichi, Kaneko, Yasuhiko

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Blastemal predominant type Wilms tumor in Japan: Japan Children's Cancer Group von Koshinaga, Tsugumichi, Takimoto, Tetsuya, Okita, Hajime, Tanaka, Yukichi, Inoue, Eisuke, Oue, Takaharu, Nozaki, Miwako, Tsuchiya, Kunihiko, Haruta, Masayuki, Kaneko, Yasuhiko, Fukuzawa, Masahiro

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RASSF1A methylation may have two biological roles in neuroblastoma tumorigenesis depending on the ploidy status and age of patients von Haruta, Masayuki, Kamijo, Takehiko, Nakagawara, Akira, Kaneko, Yasuhiko

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Establishment and characterization of a novel MDM2/MYCN-co-amplified neuroblastoma cell line, NBN-SHIM, established from a late recurrent stage MS tumor von Kato, Keisuke, Nagai, Jun-ichi, Goto, Hiroaki, Shinkai, Masato, Kitagawa, Norihiko, Toyoda, Yasunori, Nishi, Toshiji, Kigasawa, Hisato, Tanaka, Mio, Kurosawa, Kenji, Ito, Yumi, Haruta, Masayuki, Kamijo, Takehiko, Yoshimi, Ai, Tsuchida, Masahiro, Nagahara, Noriyuki, Tanaka, Yukichi

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Combined Genetic and Chromosomal Characterization of Wilms Tumors Identifies Chromosome 12 Gain as a Potential New Marker Predicting a Favorable Outcome von Haruta, Masayuki, Arai, Yasuhito, Okita, Hajime, Tanaka, Yukichi, Takimoto, Tetsuya, Sugino, Ryuichi P., Yamada, Yasuhiro, Kamijo, Takehiko, Oue, Takaharu, Fukuzawa, Masahiro, Koshinaga, Tsugumichi, Kaneko, Yasuhiko

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Management of pediatric renal tumor: Past and future trials of the Japan Wilms Tumor Study Group von Oue, Takaharu, Fukuzawa, Masahiro, Koshinaga, Tsugumichi, Okita, Hajime, Nozaki, Miwako, Chin, Motoki, Kaneko, Yasuhiko, Tanaka, Yukichi, Haruta, Masayuki, Tsuchiya, Kunihiko, Kuwajima, Shigeko, Takimoto, Tetsuya

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Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor von Ichikawa, Mizuho, Arai, Yasuhito, Haruta, Masayuki, Furukawa, Shinsuke, Ariga, Tadashi, Kajii, Tadashi, Kaneko, Yasuhiko

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Different incidences of epigenetic but not genetic abnormalities between Wilms tumors in Japanese and Caucasian children von Haruta, Masayuki, Arai, Yasuhito, Watanabe, Naoki, Fujiwara, Yuiko, Honda, Shohei, Ohshima, Junjiro, Kasai, Fumio, Nakadate, Hisaya, Horie, Hiroshi, Okita, Hajime, Hata, Jun‐Ichi, Fukuzawa, Masahiro, Kaneko, Yasuhiko

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Yolk sac tumor but not seminoma or teratoma is associated with abnormal epigenetic reprogramming pathway and shows frequent hypermethylation of various tumor suppressor genes von Furukawa, Shinsuke, Haruta, Masayuki, Arai, Yasuhito, Honda, Shohei, Ohshima, Junjiro, Sugawara, Waka, Kageyama, Yukio, Higashi, Yotsuo, Nishida, Kazunori, Tsunematsu, Yukiko, Nakadate, Hisaya, Ishii, Masahiro, Kaneko, Yasuhiko

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The methylation status of RASSF1A promoter predicts responsiveness to chemotherapy and eventual cure in hepatoblastoma patients von Honda, Shohei, Haruta, Masayuki, Sugawara, Waka, Sasaki, Fumiaki, Ohira, Miki, Matsunaga, Tadashi, Yamaoka, Hiroaki, Horie, Hiroshi, Ohnuma, Naomi, Nakagawara, Akira, Hiyama, Eiso, Todo, Satoru, Kaneko, Yasuhiko

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Genome-wide analysis of allelic imbalances reveals 4q deletions as a poor prognostic factor and MDM4 amplification at 1q32.1 in hepatoblastoma von Arai, Yasuhito, Honda, Shohei, Haruta, Masayuki, Kasai, Fumio, Fujiwara, Yuiko, Ohshima, Junjiro, Sasaki, Fumiaki, Nakagawara, Akira, Horie, Hiroshi, Yamaoka, Hiroyuki, Hiyama, Eiso, Kaneko, Yasuhiko

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RASSF1A methylation indicates a poor prognosis in hepatoblastoma patients von Honda, Shohei, Miyagi, Hisayuki, Suzuki, Hiromu, Minato, Masashi, Haruta, Masayuki, Kaneko, Yasuhiko, Hatanaka, Kanako C., Hiyama, Eiso, Kamijo, Takehiko, Okada, Tadao, Taketomi, Akinobu

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Experience-Driven Axon Retraction without Binocular Imbalance in Developing Visual Cortex von Haruta, Masayuki, Hata, Yoshio

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A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids von Okita, Chiga, Meguro, Makiko, Hoshiya, Hidetoshi, Haruta, Masayuki, Sakamoto, Yu-ki, Oshimura, Mitsuo

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