Hakutulokset - Shigeo Kure

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  1. 1
    A syngeneic monoclonal antibody to murine Meth-A sarcoma (HepSS-1) recognizes heparan sulfate glycosaminoglycan (HS-GAG): cell density and transformation dependent alteration in cell surface HS-GAG defined by HepSS-1.

    A syngeneic monoclonal antibody to murine Meth-A sarcoma (HepSS-1) recognizes heparan sulfate glycosaminoglycan (HS-GAG): cell density and transformation dependent alteration in ce... Tekijä Shigeo Kure, Osamu Yoshie

    Julkaistu 1986
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  2. 2
    Structure, turnover, and heme-mediated suppression of the level of mRNA encoding rat liver delta-aminolevulinate synthase.

    Structure, turnover, and heme-mediated suppression of the level of mRNA encoding rat liver delta-aminolevulinate synthase. Tekijä Masayuki Yamamoto, Shigeo Kure, J D Engel, K. Hiraga

    Julkaistu 1988
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  3. 3
    Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia.

    Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia. Tekijä Shigeo Kure, M. Takayanagi, K. Narisawa, K. Tada, J Leisti

    Julkaistu 1992
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  4. 4
    Genetics and Biomarkers of Moyamoya Disease: Significance of<i>RNF213</i>as a Susceptibility Gene

    Genetics and Biomarkers of Moyamoya Disease: Significance of<i>RNF213</i>as a Susceptibility Gene Tekijä Miki Fujimura, Shinya Sonobe, Yasuo Nishijima, Kuniyasu Niizuma, Hiroyuki Sakata, Shigeo Kure, Teiji Tominaga

    Julkaistu 2014
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  5. 5
    GATA2 haploinsufficiency accelerates EVI1-driven leukemogenesis

    GATA2 haploinsufficiency accelerates EVI1-driven leukemogenesis Tekijä S. Katayama, Mikiko Suzuki, Ayaka Yamaoka, Nadine Keleku-Lukwete, Fumiki Katsuoka, Akihito Otsuki, Shigeo Kure, James Douglas Engel, Masayuki Yamamoto

    Julkaistu 2017
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  6. 6
    Beneficial Effects of Systemically Administered Human Muse Cells in Adriamycin Nephropathy

    Beneficial Effects of Systemically Administered Human Muse Cells in Adriamycin Nephropathy Tekijä Nao Uchida, Yoshihiro Kushida, Masaaki Kitada, Shohei Wakao, Naonori Kumagai, Yasumasa Kuroda, Yoshiaki Kondo, Yukari Hirohara, Shigeo Kure, Gregorio D. Chazenbalk, Mari Dezawa

    Julkaistu 2017
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  7. 7
    Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness

    Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness Tekijä Takayuki Kudo, Shigeo Kure, Katsuhisa Ikeda, An Ping Xia, Yukio Katori, Masaaki Suzuki, Kanako Kojima, Akiko Ichinohe, Yoichi Suzuki, Yoko Aoki, Toshimitsu Kobayashi, Yoichi Matsubara

    Julkaistu 2003
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  8. 8
    Long-Term Treatment and Diagnosis of Tetrahydrobiopterin-Responsive Hyperphenylalaninemia with a Mutant Phenylalanine Hydroxylase Gene

    Long-Term Treatment and Diagnosis of Tetrahydrobiopterin-Responsive Hyperphenylalaninemia with a Mutant Phenylalanine Hydroxylase Gene Tekijä Haruo Shintaku, Shigeo Kure, Toshihiro Ohura, Yoshiyuki Okano, Misao Ohwada, Naruji Sugiyama, Nobuo Sakura, Ichiro Yoshida, Makoto Yoshino, Yoichi Matsubara, Ken Suzuki, Kikumaro Aoki, Teruo Kitagawa

    Julkaistu 2003
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  9. 9
    Successful use of an artificial placenta to support extremely preterm ovine fetuses at the border of viability

    Successful use of an artificial placenta to support extremely preterm ovine fetuses at the border of viability Tekijä Haruo Usuda, Shimpei Watanabe, Masatoshi Saito, Shinichi Sato, Gabrielle C. Musk, Ms Erin Fee, Sean Carter, Yusaku Kumagai, Tsukasa Takahashi, Mr Shinichi Kawamura, Takushi Hanita, Shigeo Kure, Nobuo Yaegashi, John P. Newnham, Matthew W. Kemp

    Julkaistu 2019
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  10. 10
    Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia

    Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia Tekijä Tetsuya Niihori, Meri Ouchi‐Uchiyama, Yoji Sasahara, Takashi Kaneko, Yoshiko Hashii, Masahiro Irie, Atsushi Satō, Yuka Saito‐Nanjo, Ryo Funayama, Takeshi Nagashima, Shin‐ichi Inoue, Keiko Nakayama, Keiichi Ozono, Shigeo Kure, Yoichi Matsubara, Masue Imaizumi, Yoko Aoki

    Julkaistu 2015
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  11. 11
    Construction and integration of three de novo Japanese human genome assemblies toward a population-specific reference

    Construction and integration of three de novo Japanese human genome assemblies toward a population-specific reference Tekijä Jun Takayama, Shu Tadaka, Kenji Yano, Fumiki Katsuoka, Chinatsu Gocho, Takamitsu Funayama, Satoshi Makino, Yasunobu Okamura, Atsuo Kikuchi, Sachiyo Sugimoto, Junko Kawashima, Akihito Otsuki, Mika Sakurai‐Yageta, Jun Yasuda, Shigeo Kure, Kengo Kinoshita, Masayuki Yamamoto, Gen Tamiya

    Julkaistu 2021
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  12. 12
    A genome-wide association study identifies RNF213 as the first Moyamoya disease gene

    A genome-wide association study identifies RNF213 as the first Moyamoya disease gene Tekijä Fumiaki Kamada, Yoko Aoki, Ayumi Narisawa, Yu Abe, Shoko Komatsuzaki, Atsuo Kikuchi, Junko Kanno, Tetsuya Niihori, Masao Ono, Naoto Ishii, Yuji Owada, Miki Fujimura, Yoichi Mashimo, Yoichi Suzuki, Akira Hata, Shigeru Tsuchiya, Teiji Tominaga, Yoichi Matsubara, Shigeo Kure

    Julkaistu 2010
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  13. 13
    Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia

    Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia Tekijä Tetsuya Niihori, Yoko Aoki, Hirofumi Ohashi, Kenji Kurosawa, Tatsuro Kondoh, Satoshi Ishikiriyama, Hiroshi Kawame, Hotaka Kamasaki, Tsutomu Yamanaka, Fumio Takada, Kimio Nishio, Masahiro Sakurai, Hiroshi Tamai, Tatsuro Nagashima, Yoichi Suzuki, Shigeo Kure, Kunihiro Fujii, Masue Imaizumi, Yoichi Matsubara

    Julkaistu 2005
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  14. 14
    Microchromosomal deletions involving <i>SCN1A</i> and adjacent genes in severe myoclonic epilepsy in infancy

    Microchromosomal deletions involving <i>SCN1A</i> and adjacent genes in severe myoclonic epilepsy in infancy Tekijä Ji‐wen Wang, Hirokazu Kurahashi, Atsushi Ishii, Toshio Kojima, Masaharu Ohfu, Takahito Inoue, Atsushi Ogawa, Sawa Yasumoto, Hirokazu Oguni, Shigeo Kure, Tatsuya Fujii, Masatoshi Ito, Takehiko Okuno, Yukiyoshi Shirasaka, Jun Natsume, Aki Hasegawa, Akihiko Konagaya, Sunao Kaneko, Shinichi Hirose

    Julkaistu 2008
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  15. 15
    Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies

    Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies Tekijä Shoko Komatsuzaki, Yoko Aoki, Tetsuya Niihori, Nobuhiko Okamoto, Raoul C. M. Hennekam, Saskia Hopman, Hirofumi Ohashi, Seiji Mizuno, Yoriko Watanabe, Hotaka Kamasaki, Ikuko Kondo, Nobuko Moriyama, Kenji Kurosawa, Hiroshi Kawame, Ryuhei Okuyama, Masue Imaizumi, Takeshi Rikiishi, Shigeru Tsuchiya, Shigeo Kure, Yoichi Matsubara

    Julkaistu 2010
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  16. 16
    Genomic analysis identifies masqueraders of full‐term cerebral palsy

    Genomic analysis identifies masqueraders of full‐term cerebral palsy Tekijä Yusuke Takezawa, Atsuo Kikuchi, Kazuhiro Haginoya, Tetsuya Niihori, Yurika Numata‐Uematsu, Takehiko Inui, Saeko Yamamura‐Suzuki, Takuya Miyabayashi, Mai Anzai, Sato Suzuki‐Muromoto, Yukimune Okubo, Wakaba Endo, Noriko Togashi, Yasuko Kobayashi, Akira Onuma, Ryo Funayama, Matsuyuki Shirota, Keiko Nakayama, Yoko Aoki, Shigeo Kure

    Julkaistu 2018
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  17. 17
    Omics research project on prospective cohort studies from the Tohoku Medical Megabank Project

    Omics research project on prospective cohort studies from the Tohoku Medical Megabank Project Tekijä S. Koshiba, Ikuko N. Motoike, Daisuke Saigusa, Jin Inoue, Matsuyuki Shirota, Yasutake Katoh, Fumiki Katsuoka, Inaho Danjoh, Atsushi Hozawa, Shinichi Kuriyama, Naoko Minegishi, Masao Nagasaki, Takako Takai‐Igarashi, Soichi Ogishima, Nobuo Fuse, Shigeo Kure, Gen Tamiya, Osamu Tanabe, Jun Yasuda, Kengo Kinoshita, Masayuki Yamamoto

    Julkaistu 2018
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  18. 18
    De novo <i>GABRA1</i> mutations in Ohtahara and West syndromes

    De novo <i>GABRA1</i> mutations in Ohtahara and West syndromes Tekijä Hirofumi Kodera, Chihiro Ohba, Mitsuhiro Kato, Toshiyuki Maeda, Kaoru Araki, Daisuke Tajima, Muneaki Matsuo, Naomi Hino‐Fukuyo, Kosuke Kohashi, Akihiko Ishiyama, Saoko Takeshita, Hirotaka Motoi, Taro Kitamura, Atsuo Kikuchi, Yoshinori Tsurusaki, Mitsuko Nakashima, Noriko Miyake, Masayuki Sasaki, Shigeo Kure, Kazuhiro Haginoya, Hirotomo Saitsu, Naomichi Matsumoto

    Julkaistu 2016
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  19. 19
    The guanylate cyclase C agonist linaclotide ameliorates the gut–cardio–renal axis in an adenine-induced mouse model of chronic kidney disease

    The guanylate cyclase C agonist linaclotide ameliorates the gut–cardio–renal axis in an adenine-induced mouse model of chronic kidney disease Tekijä Fumika Nanto-Hara, Yoshitomi Kanemitsu, Shinji Fukuda, Kôichi Kikuchi, Kei Asaji, Daisuke Saigusa, Tomoyuki Iwasaki, Hsin‐Jung Ho, Eikan Mishima, Takehiro Suzuki, Chitose Suzuki, Tomoya Tsukimi, Tetsuro Matsuhashi, Yoshitsugu Oikawa, Yukako Akiyama, Shigeo Kure, Yuji Owada, Yoshihisa Tomioka, Tomoyoshi Soga, Sadayoshi Ito, Takaaki Abe

    Julkaistu 2019
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  20. 20
    A sublethal ATP11A mutation associated with neurological deterioration causes aberrant phosphatidylcholine flipping in plasma membranes

    A sublethal ATP11A mutation associated with neurological deterioration causes aberrant phosphatidylcholine flipping in plasma membranes Tekijä Katsumori Segawa, Atsuo Kikuchi, Tomoyasu Noji, Yuki Sugiura, Keita Hiraga, Chigure Suzuki, Kazuhiro Haginoya, Yasuko Kobayashi, Mitsuhiro Matsunaga, Yuki Ochiai, Kyoko Yamada, Takuo Nishimura, Shinya Iwasawa, Wataru Shoji, Fuminori Sugihara, Kohei Nishino, Hidetaka Kosako, Masahito Ikawa, Yasuo Uchiyama, Makoto Suematsu, Hiroshi Ishikita, Shigeo Kure, Shigekazu Nagata

    Julkaistu 2021
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