Rezultati pretrage - Hatasu Kobayashi

Detaljiziraj rezultate
  1. 1
    Polyphenols with Anti-Amyloid β Aggregation Show Potential Risk of Toxicity Via Pro-Oxidant Properties

    Polyphenols with Anti-Amyloid β Aggregation Show Potential Risk of Toxicity Via Pro-Oxidant Properties od Hatasu Kobayashi, Mariko Murata, Shosuke Kawanishi, Shinji Oikawa

    Izdano 2020
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  2. 2
    Distribution of Moyamoya Disease Susceptibility Polymorphism p.R4810K in RNF213 in East and Southeast Asian Populations

    Distribution of Moyamoya Disease Susceptibility Polymorphism p.R4810K in RNF213 in East and Southeast Asian Populations od Wanyang Liu, Toshiaki Hitomi, Hatasu Kobayashi, Kouji H. Harada, Akio Koizumi

    Izdano 2012
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  3. 3
    A new horizon of moyamoya disease and associated health risks explored through RNF213

    A new horizon of moyamoya disease and associated health risks explored through RNF213 od Akio Koizumi, Hatasu Kobayashi, Toshiaki Hitomi, Kouji H. Harada, Toshiyuki Habu, Shohab Youssefian

    Izdano 2015
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  4. 4
    Taurine reduces microglia activation in the brain of aged senescence-accelerated mice by increasing the level of TREM2

    Taurine reduces microglia activation in the brain of aged senescence-accelerated mice by increasing the level of TREM2 od Ahmed Sharif, Ning Ma, Jun Kawanokuchi, Keiya Matsuoka, Shinji Oikawa, Hatasu Kobayashi, Yusuke Hiraku, Mariko Murata

    Izdano 2024
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  5. 5
    Genetic Study of Intracranial Aneurysms

    Genetic Study of Intracranial Aneurysms od Junxia Yan, Toshiaki Hitomi, Katsunobu Takenaka, Masayasu Kato, Hatasu Kobayashi, Hiroko Okuda, Kouji H. Harada, Akio Koizumi

    Izdano 2015
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  6. 6
    Knockdown of TFRC suppressed the progression of nasopharyngeal carcinoma by downregulating the PI3K/Akt/mTOR pathway

    Knockdown of TFRC suppressed the progression of nasopharyngeal carcinoma by downregulating the PI3K/Akt/mTOR pathway od Guofei Feng, Yasushi Arima, Kaoru Midorikawa, Hatasu Kobayashi, Shinji Oikawa, Weilin Zhao, Zhe Zhang, Kazuhiko Takeuchi, Mariko Murata

    Izdano 2023
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  7. 7
    Expansion of Intronic GGCCTG Hexanucleotide Repeat in NOP56 Causes SCA36, a Type of Spinocerebellar Ataxia Accompanied by Motor Neuron Involvement

    Expansion of Intronic GGCCTG Hexanucleotide Repeat in NOP56 Causes SCA36, a Type of Spinocerebellar Ataxia Accompanied by Motor Neuron Involvement od Hatasu Kobayashi, Kōji Abe, Tohru Matsuura, Yoshio Ikeda, Toshiaki Hitomi, Yuji Akechi, Toshiyuki Habu, Wanyang Liu, Hiroko Okuda, Akio Koizumi

    Izdano 2011
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  8. 8
    Moyamoya disease patient mutations in the RING domain of RNF213 reduce its ubiquitin ligase activity and enhance NFκB activation and apoptosis in an AAA+ domain-dependent manner

    Moyamoya disease patient mutations in the RING domain of RNF213 reduce its ubiquitin ligase activity and enhance NFκB activation and apoptosis in an AAA+ domain-dependent manner od Midori Takeda, Tohru Tezuka, Minsoo Kim, Jung-Mi Choi, Yuki Oichi, Hatasu Kobayashi, Kouji H. Harada, Tsunehiro Mizushima, Shigeru Taketani, Akio Koizumi, Shohab Youssefian

    Izdano 2020
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  9. 9
    P.R4810K, a polymorphism of RNF213, the susceptibility gene for moyamoya disease, is associated with blood pressure

    P.R4810K, a polymorphism of RNF213, the susceptibility gene for moyamoya disease, is associated with blood pressure od Akio Koizumi, Hatasu Kobayashi, Wanyang Liu, Yukiko Fujii, Lalantha Senevirathna, Shanika Nanayakkara, Hiroko Okuda, Toshiaki Hitomi, Kouji H. Harada, Katsunobu Takenaka, Takao Watanabe, Shinichiro Shimbo

    Izdano 2012
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  10. 10
    RNF213 Acts as a Molecular Switch for Cav-1 Ubiquitination and Phosphorylation in Human Cells

    RNF213 Acts as a Molecular Switch for Cav-1 Ubiquitination and Phosphorylation in Human Cells od Jungmi Choi, Ryoichi Inoue, Yuki Masuo, Yukiko Shimizu, Kazuhiro Sonomura, Minsoo Kim, Hatasu Kobayashi, Kouji H. Harada, Yohei Mineharu, Akio Koizumi, Tohru Tezuka, Shohab Youssefian

    Izdano 2025
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  11. 11
    Rare variants in <i>RNF213</i> , a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia‐induced pulmonary hypertension in mice

    Rare variants in <i>RNF213</i> , a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia‐induced pulmonary hypertension... od Hatasu Kobayashi, Risako Kabata, Hideyuki Kinoshita, Takaaki Morimoto, Koh Ono, Midori Takeda, Jung-Mi Choi, Hiroko Okuda, Wanyang Liu, Kouji H. Harada, Takeshi Kimura, Shohab Youssefian, Akio Koizumi

    Izdano 2018
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  12. 12
    Biochemical and Functional Characterization of RNF213 (Mysterin) R4810K, a Susceptibility Mutation of Moyamoya Disease, in Angiogenesis In Vitro and In Vivo

    Biochemical and Functional Characterization of RNF213 (Mysterin) R4810K, a Susceptibility Mutation of Moyamoya Disease, in Angiogenesis In Vitro and In Vivo od Hatasu Kobayashi, Yoshiko Matsuda, Toshiaki Hitomi, Hiroko Okuda, Hirotomo Shioi, Tetsuya Matsuda, Hirohiko Imai, Masakatsu Sone, Daisuke Taura, Kouji H. Harada, Toshiyuki Habu, Yasushi Takagi, Susumu Miyamoto, Akio Koizumi

    Izdano 2015
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  13. 13
    Prevalence of <i>RNF213</i> p.R4810K Variant in Early-Onset Stroke With Intracranial Arterial Stenosis

    Prevalence of <i>RNF213</i> p.R4810K Variant in Early-Onset Stroke With Intracranial Arterial Stenosis od Teppei Kamimura, Shuhei Okazaki, Takaaki Morimoto, Hatasu Kobayashi, Kouji H. Harada, Tsutomu Tomita, Aya Higashiyama, Takeshi Yoshimoto, Jun Takahashi, Jyoji Nakagawara, Masatoshi Koga, Ḱazunori Toyoda, Hirofumi Maruyama, Akio Koizumi, Masafumi Ihara

    Izdano 2019
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  14. 14
    Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families

    Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families od Hiroko Okuda, Atsuko Noguchi, Hatasu Kobayashi, Daiki Kondo, Kouji H. Harada, Shohab Youssefian, Hirotomo Shioi, Risako Kabata, Yuki Domon, Kazufumi Kubota, Yutaka Kitano, Yasunori Takayama, Toshiaki Hitomi, Kousaku Ohno, Yoshiaki Saito, Takeshi Asano, Makoto Tominaga, Tsutomu Takahashi, Akio Koizumi

    Izdano 2016
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  15. 15
    RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients

    RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients od Hatasu Kobayashi, M Brozman, Kateřina Kyselová, Daša Viszlayová, Takaaki Morimoto, Martin Roubec, David Školoudík, Andrea Petrovičová, Dominik Juskanič, Jozef Strauss, Marián Halaj, Peter Kurray, Marián Hranai, Kouji H. Harada, Sumiko Inoue, Yukako Yoshida, Toshiyuki Habu, Roman Herzig, Shohab Youssefian, Akio Koizumi

    Izdano 2016
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  16. 16
    Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease

    Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease od Takaaki Morimoto, Yohei Mineharu, Koh Ono, Masahiro Nakatochi, Sahoko Ichihara, Risako Kabata, Yasushi Takagi, Yang Cao, Lanying Zhao, Hatasu Kobayashi, Kouji H. Harada, Katsunobu Takenaka, Takeshi Funaki, Mitsuhiro Yokota, Tatsuaki Matsubara, Ken Yamamoto, Hideo Izawa, Takeshi Kimura, Susumu Miyamoto, Akio Koizumi

    Izdano 2017
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  17. 17
    A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians

    A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians od Wanyang Liu, Hirokuni Hashikata, Kayoko Inoue, Norio Matsuura, Yohei Mineharu, Hatasu Kobayashi, Ken‐ichiro Kikuta, Yasushi Takagi, Toshiaki Hitomi, Boris Krischek, Li‐Ping Zou, Fang Fang, Roman Herzig, Jeongeun Kim, Hyun‐Seung Kang, Chang Wan Oh, David‐Alexandre Trégouët, Nobuo Hashimoto, Akio Koizumi

    Izdano 2009
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  18. 18
    RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population

    RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population od Sirui Zhou, Amirthagowri Ambalavanan, Daniel Rochefort, Pingxing Xie, Cynthia V. Bourassa, Pascale Hince, Alexandre Dionne‐Laporte, Dan Spiegelman, Ziv Gan‐Or, Cathy Mirarchi, Vesséla Zaharieva, Nicolas Dupré, Hatasu Kobayashi, Toshiaki Hitomi, Kouji H. Harada, Akio Koizumi, Lan Xiong, Patrick A. Dion, Guy A. Rouleau

    Izdano 2016
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  19. 19
    Identification of RNF213 as a Susceptibility Gene for Moyamoya Disease and Its Possible Role in Vascular Development

    Identification of RNF213 as a Susceptibility Gene for Moyamoya Disease and Its Possible Role in Vascular Development od Wanyang Liu, Daisuke Morito, Seiji Takashima, Yohei Mineharu, Hatasu Kobayashi, Toshiaki Hitomi, Hirokuni Hashikata, Norio Matsuura, Satoru Yamazaki, Atsushi Toyoda, Ken‐ichiro Kikuta, Yasushi Takagi, Kouji H. Harada, Asao Fujiyama, Roman Herzig, Boris Krischek, Li‐Ping Zou, Jeong Eun Kim, Masafumi Kitakaze, Susumu Miyamoto, Kazuhiro Nagata, Nobuo Hashimoto, Akio Koizumi

    Izdano 2011
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  20. 20
    Moyamoya Disease Susceptibility Variant <i>RNF213</i> p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis

    Moyamoya Disease Susceptibility Variant <i>RNF213</i> p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis od Shuhei Okazaki, Takaaki Morimoto, Yoichiro Kamatani, Teppei Kamimura, Hatasu Kobayashi, Kouji H. Harada, Tsutomu Tomita, Aya Higashiyama, Jun Takahashi, Jyoji Nakagawara, Masatoshi Koga, Ḱazunori Toyoda, Kazuo Washida, Satoshi Saitô, Atsushi Takahashi, Makoto Hirata, Koichi Matsuda, Hideki Mochizuki, Michael Chong, Guillaume Paré, Martin O’Donnell, Tetsuro Ago, Jun Hata, Toshiharu Ninomiya, Martin Dichgans, Stéphanie Debette, Michiaki Kubo, Akio Koizumi, Masafumi Ihara

    Izdano 2019
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