Zobrazeno 1 - 10
of 478
pro vyhledávání: '"Akio Koizumi"'
Autor:
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
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 13, p 6832 (2024)
Familial episodic pain syndrome (FEPS) is an early childhood onset disorder of severe episodic limb pain caused mainly by pathogenic variants of SCN11A, SCN10A, and SCN9A, which encode three voltage-gated sodium channels (VGSCs) expressed as key dete
Externí odkaz:
https://doaj.org/article/8ecf42c31d3f41a98eac36f023956cb5
Autor:
Kazuyoshi Furukawa, Kahori Okamoto-Matsuda, Kouji H. Harada, Mutsuko Minata, Toshiaki Hitomi, Hatasu Kobayashi, Akio Koizumi
Publikováno v:
Environmental Health and Preventive Medicine, Vol 29, Pp 21-21 (2024)
Background: Perfluorooctanoic acid (PFOA) is one of the major per- and polyfluoroalkyl substances. The role of ATP-binding cassette (ABC) transporters in PFOA toxicokinetics is unknown. Methods: In this study, two ABC transporters, ABCB1 and ABCB4, w
Externí odkaz:
https://doaj.org/article/6a296a2c154f4485b0607379ad84edc1
Autor:
Yohei Mineharu, Yasuhisa Nakamura, Noriaki Sato, Takahiko Kamata, Yuki Oichi, Tomoko Fujitani, Takeshi Funaki, Yasushi Okuno, Susumu Miyamoto, Akio Koizumi, Kouji H. Harada
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-15 (2022)
Abstract Moyamoya disease (MMD) is a rare cerebrovascular disease endemic in East Asia. The p.R4810K mutation in RNF213 gene confers a risk of MMD, but other factors remain largely unknown. We tested the association of gut microbiota with MMD. Fecal
Externí odkaz:
https://doaj.org/article/64f5bbac517244d8ae716a8bd36e886e
Publikováno v:
Heliyon, Vol 9, Iss 4, Pp e15423- (2023)
The sodium channel Nav1.9 is expressed in the sensory neurons of small diameter dorsal root ganglia that transmit pain signals, and gain-of-function Nav1.9 mutations have been associated with both painful and painless disorders. We initially determin
Externí odkaz:
https://doaj.org/article/82426671ec4a4a4290cc25e577c21d7f
Autor:
Nozomu Ozaki, Hiroko Okuda, Hatasu Kobayashi, Kouji H. Harada, Sumiko Inoue, Shohab Youssefian, Akio Koizumi
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-8 (2021)
Abstract Background Brachydactyly type A1 (BDA1) is an autosomal dominant disorder characterized by uniform shortening of the middle phalanges in all digits. It is associated with variants in the Indian Hedgehog (IHH) gene, which plays a key role in
Externí odkaz:
https://doaj.org/article/ff359c3e9a0949ae8577323a034cb113
Publikováno v:
Environmental Health and Preventive Medicine, Vol 25, Iss 1, Pp 1-10 (2020)
Abstract Objectives After the Fukushima Daiichi nuclear power plant disaster in 2011, residents of Kawauchi village who experienced evacuation had a high risk of suffering from diabetes and metabolic syndrome compared with non-evacuees. In addition t
Externí odkaz:
https://doaj.org/article/506ac8130a354ec086a69491f6e1e30c
Autor:
Futoshi Eto, Takeshi Yoshimoto, Shuhei Okazaki, Kunihiro Nishimura, Shiori Ogura, Eriko Yamaguchi, Kazuki Fukuma, Satoshi Saito, Kazuo Washida, Masatoshi Koga, Kazunori Toyoda, Takaaki Morimoto, Hirofumi Maruyama, Akio Koizumi, Masafumi Ihara
Publikováno v:
Frontiers in Aging Neuroscience, Vol 13 (2021)
IntroductionDysregulation of the RING finger protein 213 (RNF213) gene impairs vascular formation in experimental animal models. In addition, vascular abnormalities in the circle of Willis are associated with cerebrovascular disease. Here, we evaluat
Externí odkaz:
https://doaj.org/article/f60456a69efd4c98bad0322534d09e50
Autor:
Kiichi Takahashi, Takayoshi Ohba, Yosuke Okamoto, Atsuko Noguchi, Hiroko Okuda, Hatasu Kobayashi, Kouji H. Harada, Akio Koizumi, Kyoichi Ono, Tsutomu Takahashi
Publikováno v:
Heliyon, Vol 7, Iss 6, Pp e07396- (2021)
Gain-of-function mutations in voltage-gated sodium channels (NaV1.7, NaV1.8, and NaV1.9) are known causes of inherited pain disorders. Identification and functional assessment of new NaV1.7 mutations could help elucidate the phenotypic spectrum of Na
Externí odkaz:
https://doaj.org/article/48c5388dbd0a40fc9ca837a09f833e6b
Autor:
Kyoko Nomura, Kanae Karita, Atsuko Araki, Emiko Nishioka, Go Muto, Miyuki Iwai-Shimada, Mariko Nishikitani, Mariko Inoue, Shinobu Tsurugano, Naomi Kitano, Mayumi Tsuji, Sachiko Iijima, Kayo Ueda, Michihiro Kamijima, Zentaro Yamagata, Kiyomi Sakata, Masayuki Iki, Hiroyuki Yanagisawa, Masashi Kato, Hidekuni Inadera, Yoshihiro Kokubo, Kazuhito Yokoyama, Akio Koizumi, Takemi Otsuki
Publikováno v:
Environmental Health and Preventive Medicine, Vol 24, Iss 1, Pp 1-6 (2019)
Abstract In 1952, the Japanese Society for Hygiene had once passed a resolution at its 22nd symposium on population control, recommending the suppression of population growth based on the idea of cultivating a healthier population in the area of euge
Externí odkaz:
https://doaj.org/article/f8d7efe6f1f8415f83ed1dc2b24db4fb
Autor:
Yukihiro Koretsune, Koichi Kusakawa, Kouji H. Harada, Akio Koizumi, Shinichiro Uchiyama, Hirotsugu Atarashi, Ken Okumura, Masahiro Yasaka, Takeshi Yamashita, Atsushi Taniguchi, Taku Fukaya, Hiroshi Inoue, for J-dabigatran surveillance and JAPAF study investigators
Publikováno v:
Cardiology and Therapy, Vol 8, Iss 1, Pp 43-54 (2019)
Abstract Introduction Following approval of dabigatran and other antithrombotics in Japan, few studies have specifically evaluated the clinical characteristics of patients prescribed these antithrombotics for nonvalvular atrial fibrillation (NVAF) in
Externí odkaz:
https://doaj.org/article/43ca58f89c1b409d9a71c36096dfc509