Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Masahiro Takahashi"'
Autor:
Takashi Ishino, Daisuke Kikuchi, Toshinori Kubota, Noriko Ogasawara, Misako Hyogo, Chiharu Kihara, Tomoko Esaki, Satoshi Iwasaki, Jun Nakayama, Masahiro Takahashi, Yumiko Kobayashi, Yoh ichiro Iwasa, Masako Nakai, Yuika Sakurai, Mayuri Okami, Hidehiko Takeda, Sakiko Furutate, Nana Tsuchihashi, Yukihide Maeda, Marina Kobayashi, Hiroshi Yoshihashi, Tomoko Shintani, Tadao Yoshida, Tetsuo Ikezono, Hidekane Yoishimura, Shin-ichi Usami, Han Matsuda, Yasuhiro Arai, Yuko Kataoka, Kozo Kumakawa, Taisuke Kobayashi, Risa Tona, Kyoko Nagai, Shinya Morita, Akiko Sugaya, Yohei Honkura, Remi Motegi, Shuji Izumi, Hiroshi Yamazaki, Yasushi Naito, Shin-ya Nishio, Yuzuru Ninoyu, Hideaki Sakata, Yukihiko Kanda, Shinichiro Oka, Mayumi Suematsu
Publikováno v:
Human Genetics. 141:865-875
Mutations in the OTOF gene are a common cause of hereditary hearing loss and the main cause of auditory neuropathy spectrum disorder (ANSD). Although it is reported that most of the patients with OTOF mutations have stable, congenital or prelingual o
Autor:
Masahiro Takahashi, Jun Nakayama, Yuika Sakurai, Tetsuo Ikezono, Mayuri Okami, Mayumi Suematsu, Shin-ichi Usami, Sakiko Furutate, Masako Nakai, Hiroshi Yoshihashi, Yoh-ichiro Iwasa, Shinichiro Oka, Misako Hyogo, Tomoko Shintani, Hideaki Sakata, Noriko Ogasawara, Yuko Kataoka, Daisuke Kikuchi, Marina Kobayashi, Yumiko Kobayashi, Yohei Honkura, Shuji Izumi, Toshinori Kubota, Hidekane Yoshimura, Kyoko Nagai, Yuzuru Ninoyu, Chiharu Kihara, Risa Tona, Satoshi Iwasaki, Hiroshi Yamazaki, Yasushi Naito, Yasuhiro Arai, Shin-ya Nishio, Yukihiko Kanda, Taisuke Kobayashi, Akiko Sugaya, Kozo Kumakawa, Hidehiko Takeda, Yukihide Maeda, Tadao Yoshida, Han Matsuda, Shinya Morita, Takashi Ishino, Tomoko Esaki, Remi Motegi, Nana Tsuchihashi
Publikováno v:
Human Genetics. 141:993-995
Autor:
Shingo Fukuma, Eiichiro Uchino, Shigenori Yamamoto, Yuki Sato, Shinya Yamamoto, Akiko Mii, Keiichi Kaneko, Michiyuki Matsuda, Masamichi Yamamoto, Hiromi Imamura, Masahiro Takahashi, Motoko Yanagita, Jin Nakamura
Publikováno v:
J Am Soc Nephrol
Background Depletion of ATP in renal tubular cells plays the central role in the pathogenesis of kidney diseases. Nevertheless, inability to visualize spatiotemporal in vivo ATP distribution and dynamics has hindered further analysis. Methods A novel
Autor:
Masakatsu Itose, Reiko Takimoto, Ruytaro Kamijo, Tetsuo Suzawa, Yuji Sasama, Motohiro Tanaka, Hiroshi Yoshida, Masahiro Takahashi, Koutaro Maki, Kaori Ikezaki, Tatsuo Shirora
Publikováno v:
Oral Science International. 17:115-125
Autor:
Tetsuo Ikezono, Hidehiko Takeda, Yukihiko Kanda, Timothy F. Day, Satoshi Iwasaki, Shin-ichiro Kitajiri, Shin-ya Nishio, Masahiro Takahashi, Satoko Abe, Hiroshi Yamazaki, Shin-ichi Usami, Hiroki Miyajima, Takaaki Murata, Yasushi Naito, Hideaki Moteki
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific Reports
Scientific Reports
Human ACTG1 mutations are associated with high-frequency hearing loss, and patients with mutations in this gene are good candidates for electric acoustic stimulation. To better understand the genetic etiology of hearing loss cases, massively parallel
Autor:
Masahiro Takahashi, Tomomi Yamamoto-Fukuda, Hiromi Kojima, Naotaro Akiyama, Yasuhiro Tanaka, Masaomi Motegi, Yutaka Yamamoto, Kazuhisa Yamamoto
Publikováno v:
Otology & Neurotology. 40:e803-e811
INTRODUCTION Partial epithelial-mesenchymal transition (p-EMT) is a process by which epithelial cells partially lose their intercellular adhesion and change to obtain migration ability. The transcription factor p63 regulates the expression of cadheri
Autor:
Hirofumi Sakaguchi, Yuika Sakurai, Chie Oshikawa, Kenji Ohyama, Shin-ya Nishio, Yasuhiro Arai, Hideaki Moteki, Jun Shinagawa, Takashi Ishino, Shin-ichi Usami, Satoshi Iwasaki, Masahiro Takahashi, Natsumi Uehara, Koshi Otsuki, Yumi Ohta, Shin Masuda, Satoko Abe, Naoko Sakuma
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Variants in the EYA4 gene are known to lead to autosomal dominant non-syndromic hereditary hearing loss, DFNA10. To date, 30 variants have been shown to be responsible for hearing loss in a diverse set of nationalities. To better understand the clini
Autor:
Tatsutoshi Honda, Noritoshi Kawate, Masahiro Takahashi, Hiromichi Tamada, Shingo Hatoya, Toshio Inaba
Publikováno v:
Journal of Veterinary Medical Science. 80:532-535
It is currently unclear how mechanical micro-vibration affects the in vitro culture of embryos in Japanese Black cow. In the experimental groups, immature oocytes and fertilized embryos were cultured using the micro-vibration culture system with the
Autor:
Mohamed Adel, Hajime Ishida, Soo-Byung Park, Yong-Il Kim, Mutsumi Isa, Yu Hikita, Tetsutaro Yamaguchi, Masahiro Takahashi, Koutaro Maki, Daisuke Tomita, Takatoshi Nakawaki, Ryosuke Kimura, Akira Kawaguchi, Shugo Haga
Publikováno v:
Archives of Oral Biology. 85:142-147
Objective The interferon regulatory factor 6 gene (IRF6) is one of the most conspicuous genes among a large number of candidate risk genes for non-syndromic cleft lip with or without cleft palate, which is considered to be a multifactorial defect. Va
Autor:
T Shinohara, Noritoshi Kawate, Toshio Inaba, Nobutada Sakagami, Masahiro Takahashi, Hiromichi Tamada, Y. Ohta
Publikováno v:
Reproduction in Domestic Animals. 53:270-273
This study examined the effects of treatment with U0126, which inhibits MAPK by inhibiting MAPK kinase, during the first 2 hr of in vitro maturation on bovine developmental competence and on gap junction (GAPJ) communication between the oocyte and cu