Αποτελέσματα αναζήτησης - Nishi, Eriko

Chiasmata and the kinetochore component Dam1 are crucial for elimination of erroneous chromosome attachments and centromere oscillation at meiosis I από Wakiya, Misuzu, Nishi, Eriko, Kawai, Shinnosuke, Yamada, Kohei, Katsumata, Kazuhiro, Hirayasu, Ami, Itabashi, Yuta, Yamamoto, Ayumu

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Exome Sequencing Identification of EP300 Mutation in a Proband with Coloboma and Imperforate Anus: Possible Expansion of the Phenotypic Spectrum of Rubinstein-Taybi Syndrome από Masuda, Koji, Akiyama, Kazuhiro, Arakawa, Michiko, Nishi, Eriko, Kitazawa, Noritaka, Higuchi, Tsukasa, Katou, Yuki, Shirahige, Katsuhiko, Izumi, Kosuke

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A Taz1- and Microtubule-Dependent Regulatory Relationship between Telomere and Centromere Positions in Bouquet Formation Secures Proper Meiotic Divisions από Katsumata, Kazuhiro, Hirayasu, Ami, Miyoshi, Junpei, Nishi, Eriko, Ichikawa, Kento, Tateho, Kazuki, Wakuda, Airi, Matsuhara, Hirotada, Yamamoto, Ayumu

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Loss-of-function mutations and global rearrangements in GPC3 in patients with Simpson–Golabi–Behmel syndrome από Shimojima, Keiko, Ondo, Yumiko, Nishi, Eriko, Mizuno, Seiji, Ito, Miharu, Ioi, Aya, Shimizu, Mariko, Sato, Maho, Inoue, Masami, Okamoto, Nobuhiko, Yamamoto, Toshiyuki

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Trimodal therapy with high-dose-rate brachytherapy and hypofractionated external beam radiation combined with long-term androgen deprivation for unfavorable-risk prostate cancer από Mori, Keiichiro, Sasaki, Hiroshi, Tsutsumi, Yuki, Sato, Shun, Takiguchi, Yuki, Saito, Shun, Nishi, Eriko, Ishii, Gen, Yamamoto, Toshihiro, Koike, Yusuke, Miki, Jun, Shimomura, Tatsuya, Kimura, Takahiro, Miki, Kenta, Shariat, Shahrokh F., Takahashi, Hiroyuki, Aoki, Manabu, Egawa, Shin

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ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects από Izumi, Kosuke, Brett, Maggie, Nishi, Eriko, Drunat, Séverine, Tan, Ee-Shien, Fujiki, Katsunori, Lebon, Sophie, Cham, Breana, Masuda, Koji, Arakawa, Michiko, Jacquinet, Adeline, Yamazumi, Yusuke, Chen, Shu-Ting, Verloes, Alain, Okada, Yuki, Katou, Yuki, Nakamura, Tomohiko, Akiyama, Tetsu, Gressens, Pierre, Foo, Roger, Passemard, Sandrine, Tan, Ene-Choo, El Ghouzzi, Vincent, Shirahige, Katsuhiko

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Clinical and molecular spectrum of CHOPS syndrome από Raible, Sarah E., Mehta, Devanshi, Bettale, Chiara, Fiordaliso, Sarah, Kaur, Maninder, Medne, Livija, Rio, Marlene, Haan, Eric, White, Susan M., Cusmano-Ozog, Kristina, Nishi, Eriko, Guo, Yiran, Wu, Honglin, Shi, Xiaoqing, Zhao, Qingjie, Zhang, Xueqin, Lei, Qi, Lu, Aimei, He, Xiyu, Okamoto, Nobuhiko, Miyake, Noriko, Piccione, Joseph, Allen, Julian, Matsumoto, Naomichi, Pipan, Mary, Krantz, Ian D., Izumi, Kosuke

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Missense Mutations in NKAP Cause a Disorder of Transcriptional Regulation Characterized by Marfanoid Habitus and Cognitive Impairment από Fiordaliso, Sarah K., Iwata-Otsubo, Aiko, Ritter, Alyssa L., Quesnel-Vallières, Mathieu, Fujiki, Katsunori, Nishi, Eriko, Hancarova, Miroslava, Miyake, Noriko, Morton, Jenny E.V., Lee, Sangmoon, Hackmann, Karl, Bando, Masashige, Masuda, Koji, Nakato, Ryuichiro, Arakawa, Michiko, Bhoj, Elizabeth, Li, Dong, Hakonarson, Hakon, Takeda, Ryojun, Harr, Margaret, Keena, Beth, Zackai, Elaine H., Okamoto, Nobuhiko, Mizuno, Seiji, Ko, Jung Min, Valachova, Alica, Prchalova, Darina, Vlckova, Marketa, Pippucci, Tommaso, Seiler, Christoph, Choi, Murim, Matsumoto, Naomichi, Di Donato, Nataliya, Barash, Yoseph, Sedlacek, Zdenek, Shirahige, Katsuhiko, Izumi, Kosuke

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