Resultados da pesquisa - Fukuzawa, Ryuji
- A mostrar 1 - 17 resultados de 17
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Sequential WT1 and CTNNB1 mutations and alterations of β‐catenin localisation in intralobar nephrogenic rests and associated Wilms tumours: two case studies Por Fukuzawa, Ryuji, Heathcott, Rosemary W, More, Helen E, Reeve, Anthony E
Publicado em 2007Text -
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Novel heterozygous mutation in the extracellular domain of FGFR1 associated with Hartsfield syndrome Por Takagi, Masaki, Miyoshi, Tatsuya, Nagashima, Yuka, Shibata, Nao, Yagi, Hiroko, Fukuzawa, Ryuji, Hasegawa, Tomonobu
Publicado em 2016Text -
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A Novel Case of Somatic KCNJ5 Mutation in Pediatric-Onset Aldosterone-Producing Adenoma Por Uchida, Noboru, Amano, Naoko, Yamaoka, Yui, Uematsu, Ayumi, Sekine, Yuji, Suzuki, Makoto, Watanabe, Jun, Nishimoto, Koshiro, Mukai, Kuniaki, Fukuzawa, Ryuji, Hasegawa, Tomonobu, Ishii, Tomohiro
Publicado em 2017Text -
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A Novel Mutation in LEPRE1 That Eliminates Only the KDEL ER- Retrieval Sequence Causes Non-Lethal Osteogenesis Imperfecta Por Takagi, Masaki, Ishii, Tomohiro, Barnes, Aileen M., Weis, MaryAnn, Amano, Naoko, Tanaka, Mamoru, Fukuzawa, Ryuji, Nishimura, Gen, Eyre, David R., Marini, Joan C., Hasegawa, Tomonobu
Publicado em 2012Text -
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MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency Por Shima, Hirohito, Hayashi, Mie, Tachibana, Takashi, Oshiro, Makoto, Amano, Naoko, Ishii, Tomohiro, Haruna, Hidenori, Igarashi, Maki, Kon, Masafumi, Fukuzawa, Ryuji, Tanaka, Yukichi, Fukami, Maki, Hasegawa, Tomonobu, Narumi, Satoshi
Publicado em 2018Text -
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Human Papillomavirus E6/E7 Expression in Preeclampsia-Affected Placentae Por Reily-Bell, Ashley L., Fisher, Amanda, Harrison, Bryony, Bowie, Sara, Ray, Sankalita, Hawkes, Mary, Wise, Lyn M., Fukuzawa, Ryuji, Macaulay, Erin C., Devenish, Celia J., Hung, Noelyn A., Slatter, Tania L.
Publicado em 2020Text -
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Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome Por Higashimoto, Ken, Maeda, Toshiyuki, Okada, Junichiro, Ohtsuka, Yasufumi, Sasaki, Kensaku, Hirose, Akiko, Nomiyama, Makoto, Takayanagi, Toshimitsu, Fukuzawa, Ryuji, Yatsuki, Hitomi, Koide, Kayoko, Nishioka, Kenichi, Joh, Keiichiro, Watanabe, Yoriko, Yoshiura, Koh-ichiro, Soejima, Hidenobu
Publicado em 2013Text -
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Selective Ablation of Tumorigenic Cells Following Human Induced Pluripotent Stem Cell‐Derived Neural Stem/Progenitor Cell Transplantation in Spinal Cord Injury Por Kojima, Kota, Miyoshi, Hiroyuki, Nagoshi, Narihito, Kohyama, Jun, Itakura, Go, Kawabata, Soya, Ozaki, Masahiro, Iida, Tsuyoshi, Sugai, Keiko, Ito, Shuhei, Fukuzawa, Ryuji, Yasutake, Kaori, Renault‐Mihara, Francois, Shibata, Shinsuke, Matsumoto, Morio, Nakamura, Masaya, Okano, Hideyuki
Publicado em 2018Text -
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Germline mutations and somatic inactivation of TRIM28 in Wilms tumour Por Halliday, Benjamin J., Fukuzawa, Ryuji, Markie, David M., Grundy, Richard G., Ludgate, Jackie L., Black, Michael A., Skeen, Jane E., Weeks, Robert J., Catchpoole, Daniel R., Roberts, Aedan G. K., Reeve, Anthony E., Morison, Ian M.
Publicado em 2018Text -
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Pathological classification of human iPSC-derived neural stem/progenitor cells towards safety assessment of transplantation therapy for CNS diseases Por Sugai, Keiko, Fukuzawa, Ryuji, Shofuda, Tomoko, Fukusumi, Hayato, Kawabata, Soya, Nishiyama, Yuichiro, Higuchi, Yuichiro, Kawai, Kenji, Isoda, Miho, Kanematsu, Daisuke, Hashimoto-Tamaoki, Tomoko, Kohyama, Jun, Iwanami, Akio, Suemizu, Hiroshi, Ikeda, Eiji, Matsumoto, Morio, Kanemura, Yonehiro, Nakamura, Masaya, Okano, Hideyuki
Publicado em 2016Text