Evaluation of ATM heterozygous mutations underlying individual differences in radiosensitivity using genome editing in human cultured cells von Royba, Ekaterina, Miyamoto, Tatsuo, Natsuko Akutsu, Silvia, Hosoba, Kosuke, Tauchi, Hiroshi, Kudo, Yoshiki, Tashiro, Satoshi, Yamamoto, Takashi, Matsuura, Shinya

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Updated summary of genome editing technology in human cultured cells linked to human genetics studies von Miyamoto, Tatsuo, Akutsu, Silvia Natsuko, Matsuura, Shinya

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iPSC reprogramming-mediated aneuploidy correction in autosomal trisomy syndromes von Akutsu, Silvia Natsuko, Miyamoto, Tatsuo, Oba, Daiju, Tomioka, Keita, Ochiai, Hiroshi, Ohashi, Hirofumi, Matsuura, Shinya

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Imaging of the Ciliary Cholesterol Underlying the Sonic Hedgehog Signal Transduction von Miyamoto, Tatsuo, Hosoba, Kosuke, Akutsu, Silvia Natsuko, Matsuura, Shinya

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Insufficiency of ciliary cholesterol in hereditary Zellweger syndrome von Miyamoto, Tatsuo, Hosoba, Kosuke, Itabashi, Takeshi, Iwane, Atsuko H, Akutsu, Silvia Natsuko, Ochiai, Hiroshi, Saito, Yumiko, Yamamoto, Takashi, Matsuura, Shinya

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PLK1-mediated phosphorylation of WDR62/MCPH2 ensures proper mitotic spindle orientation von Miyamoto, Tatsuo, Akutsu, Silvia Natsuko, Fukumitsu, Akihiro, Morino, Hiroyuki, Masatsuna, Yoshinori, Hosoba, Kosuke, Kawakami, Hideshi, Yamamoto, Takashi, Shimizu, Kenji, Ohashi, Hirofumi, Matsuura, Shinya

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NBS1 I171V variant underlies individual differences in chromosomal radiosensitivity within human populations von Tomioka, Keita, Miyamoto, Tatsuo, Akutsu, Silvia Natsuko, Yanagihara, Hiromi, Fujita, Kazumasa, Royba, Ekaterina, Tauchi, Hiroshi, Yamamoto, Takashi, Koh, Iemasa, Hirata, Eiji, Kudo, Yoshiki, Kobayashi, Masao, Okada, Satoshi, Matsuura, Shinya

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Exploration of genetic basis underlying individual differences in radiosensitivity within human populations using genome editing technology von Miyamoto, Tatsuo, Akutsu, Silvia Natsuko, Tauchi, Hiroshi, Kudo, Yoshiki, Tashiro, Satoshi, Yamamoto, Takashi, Matsuura, Shinya

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Applications of Genome Editing Technology in Research on Chromosome Aneuploidy Disorders von Akutsu, Silvia Natsuko, Fujita, Kazumasa, Tomioka, Keita, Miyamoto, Tatsuo, Matsuura, Shinya

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CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis von Kume, Kodai, Kurashige, Takashi, Muguruma, Keiko, Morino, Hiroyuki, Tada, Yui, Kikumoto, Mai, Miyamoto, Tatsuo, Akutsu, Silvia Natsuko, Matsuda, Yukiko, Matsuura, Shinya, Nakamori, Masahiro, Nishiyama, Ayumi, Izumi, Rumiko, Niihori, Tetsuya, Ogasawara, Masashi, Eura, Nobuyuki, Kato, Tamaki, Yokomura, Mamoru, Nakayama, Yoshiaki, Ito, Hidefumi, Nakamura, Masataka, Saito, Kayoko, Riku, Yuichi, Iwasaki, Yasushi, Maruyama, Hirofumi, Aoki, Yoko, Nishino, Ichizo, Izumi, Yuishin, Aoki, Masashi, Kawakami, Hideshi

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Premature aging syndrome showing random chromosome number instabilities with CDC20 mutation von Fujita, Harumi, Sasaki, Takashi, Miyamoto, Tatsuo, Akutsu, Silvia Natsuko, Sato, Showbu, Mori, Takehiko, Nakabayashi, Kazuhiko, Hata, Kenichiro, Suzuki, Hisato, Kosaki, Kenjiro, Matsuura, Shinya, Matsubara, Yoichi, Amagai, Masayuki, Kubo, Akiharu

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iPSC reprogramming-mediated aneuploidy correction in autosomal trisomy syndromes von Silvia Natsuko Akutsu, Tatsuo Miyamoto, Daiju Oba, Keita Tomioka, Hiroshi Ochiai, Hirofumi Ohashi, Shinya Matsuura

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