Hasil Pencarian - Shohab Youssefian

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  1. 1
    Reduced pain sensitivity of episodic pain syndrome model mice carrying a Nav1.9 mutation by ANP-230, a novel sodium channel blocker

    Reduced pain sensitivity of episodic pain syndrome model mice carrying a Nav1.9 mutation by ANP-230, a novel sodium channel blocker oleh Hiroko Okuda, Sumiko Inoue, Yoshihiro Oyamada, Akio Koizumi, Shohab Youssefian

    Diterbitkan 2023-04-01
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  2. 2
    Deletion of 2 amino acids in IHH in a Japanese family with brachydactyly type A1

    Deletion of 2 amino acids in IHH in a Japanese family with brachydactyly type A1 oleh Nozomu Ozaki, Hiroko Okuda, Hatasu Kobayashi, Kouji H. Harada, Sumiko Inoue, Shohab Youssefian, Akio Koizumi

    Diterbitkan 2021-07-01
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  3. 3
    β-cell-specific overexpression of adiponectin receptor 1 does not improve diabetes mellitus in Akita mice.

    β-cell-specific overexpression of adiponectin receptor 1 does not improve diabetes mellitus in Akita mice. oleh Jungmi Choi, Hatasu Kobayashi, Hiroko Okuda, Kouji H Harada, Midori Takeda, Hiroyuki Fujimoto, Shunsuke Yamane, Daisuke Tanaka, Shohab Youssefian, Nobuya Inagaki, Akio Koizumi

    Diterbitkan 2018-01-01
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  4. 4
    Rare variants in , a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia-induced pulmonary hypertension in mice

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

    Diterbitkan 2018-05-01
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  5. 5
    Dysregulation of RNF213 promotes cerebral hypoperfusion

    Dysregulation of RNF213 promotes cerebral hypoperfusion oleh Takaaki Morimoto, Jun-ichiro Enmi, Yorito Hattori, Satoshi Iguchi, Satoshi Saito, Kouji H. Harada, Hiroko Okuda, Yohei Mineharu, Yasushi Takagi, Shohab Youssefian, Hidehiro Iida, Susumu Miyamoto, Masafumi Ihara, Hatasu Kobayashi, Akio Koizumi

    Diterbitkan 2018-02-01
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  6. 6
    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. oleh 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

    Diterbitkan 2016-01-01
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  7. 7
    RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients.

    RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients. oleh Hatasu Kobayashi, Miroslav 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

    Diterbitkan 2016-01-01
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  8. 8
    Genetic Analysis of <i>SCN11A</i>, <i>SCN10A</i>, and <i>SCN9A</i> in Familial Episodic Pain Syndrome (FEPS) in Japan and Proposal of Clinical Diagnostic Criteria

    Genetic Analysis of <i>SCN11A</i>, <i>SCN10A</i>, and <i>SCN9A</i> in Familial Episodic Pain Syndrome (FEPS) in Japan and Proposal of Clinical Diagnostic Criteria oleh Atsuko Noguchi, Tohru Tezuka, Hiroko Okuda, Hatasu Kobayashi, Kouji H. Harada, Takeshi Yoshida, Shinji Akioka, Keiko Wada, Aya Takeya, Risako Kabata-Murasawa, Daiki Kondo, Ken Ishikawa, Takeshi Asano, Michimasa Fujiwara, Nozomi Hishikawa, Tomoyuki Mizukami, Toshiaki Hitomi, Shohab Youssefian, Yoshihiro Nagai, Manabu Tanaka, Kaoru Eto, Hideaki Shiraishi, Fumimasa Amaya, Akio Koizumi, Tsutomu Takahashi

    Diterbitkan 2024-06-01
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  9. 9
    Familial episodic limb pain in kindreds with novel Nav1.9 mutations.

    Familial episodic limb pain in kindreds with novel Nav1.9 mutations. oleh Risako Kabata, Hiroko Okuda, Atsuko Noguchi, Daiki Kondo, Michimasa Fujiwara, Kenichiro Hata, Yoshifumi Kato, Ken Ishikawa, Manabu Tanaka, Yuji Sekine, Nozomi Hishikawa, Tomoyuki Mizukami, Junichi Ito, Manami Akasaka, Ken Sakurai, Takeshi Yoshida, Hironori Minoura, Takashi Hayashi, Kohei Inoshita, Misayo Matsuyama, Noriko Kinjo, Yang Cao, Sumiko Inoue, Hatasu Kobayashi, Kouji H Harada, Shohab Youssefian, Tsutomu Takahashi, Akio Koizumi

    Diterbitkan 2018-01-01
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