Zobrazeno 1 - 10
of 233
pro vyhledávání: '"Yasuhiro Arai"'
Autor:
Naoko Sakuma, Shin-ya Nishio, Shin-ichi Goto, Yohei Honkura, Kiyoshi Oda, Hidehiko Takeda, Marina Kobayashi, Kozo Kumakawa, Satoshi Iwasaki, Masahiro Takahashi, Taku Ito, Yasuhiro Arai, Yasuhiro Isono, Natsuko Obara, Takeshi Matsunobu, Kimihiro Okubo, Shin-ichi Usami
Publikováno v:
Genes, Vol 15, Iss 4, p 489 (2024)
The PTPRQ gene has been identified as one of the genes responsible for non-syndromic sensorineural hearing loss (SNHL), and assigned as DFNA73 and DFNB84. To date, about 30 causative PTPRQ variants have been reported to cause SNHL. However, the detai
Externí odkaz:
https://doaj.org/article/b0c01e38a5644460a5ff2f20c0e6e309
Autor:
Goshi Nishimura, Daisuke Sano, Yasuhiro Arai, Takashi Hatano, Hideaki Takahashi, Teruhiko Tanabe, Takashi Wada, Daiki Morishita, Nobuhiko Oridate
Publikováno v:
Cancer Medicine, Vol 8, Iss 17, Pp 7197-7206 (2019)
Abstract Background Transoral surgery (TOS) has been widely applied for early T‐stage head and neck cancer (HNC). The resection is performed with a minimum safety margin for function preservation under a limited surgical field; therefore, it is dif
Externí odkaz:
https://doaj.org/article/6f086c5140a24a27a48c40f2c5d6a6c6
Autor:
Yasuhiro Arai, Masahiro Takahashi, Naoko Sakuma, Shin-Ya Nisio, Nobuhiko Oridate, Shin-Ichi Usami
Publikováno v:
Acta Oto-Laryngologica Case Reports, Vol 2, Iss 1, Pp 137-140 (2017)
GJB2 gene mutation is the most common cause of congenital sensorineural hearing loss worldwide. Most GJB2 gene mutations have been associated with autosomal recessive non-syndromic hearing loss (DFNB1), but some are also associated with autosomal dom
Externí odkaz:
https://doaj.org/article/cdf9bb0ce1e145bebd692cfe0dd24350
Autor:
Yoh-Ichiro Iwasa, Shin-Ya Nishio, Akiko Sugaya, Yuko Kataoka, Yukihiko Kanda, Mirei Taniguchi, Kyoko Nagai, Yasushi Naito, Tetsuo Ikezono, Rie Horie, Yuika Sakurai, Rina Matsuoka, Hidehiko Takeda, Satoko Abe, Chiharu Kihara, Takashi Ishino, Shin-Ya Morita, Satoshi Iwasaki, Masahiro Takahashi, Tsukasa Ito, Yasuhiro Arai, Shin-Ichi Usami
Publikováno v:
PLoS ONE, Vol 14, Iss 5, p e0215932 (2019)
The OTOF gene (Locus: DFNB9), encoding otoferlin, is reported to be one of the major causes of non-syndromic recessive sensorineural hearing loss, and is also reported to be the most common cause of non-syndromic recessive auditory neuropathy spectru
Externí odkaz:
https://doaj.org/article/5b4d97771f374fe9b4900e835e3a8700
Autor:
KANAME SATO, DAISUKE SANO, HIDEAKI TAKAHASHI, TATSU KUWAHARA, YOSHIHIRO AIZAWA, JUN AOYAMA, YUSUKE NOJIMA, TAKASHI HATANO, YASUHIRO ARAI, GOSHI NISHIMURA, HIROMITSU HATAKEYAMA, NOBUHIKO ORIDATE
Publikováno v:
Anticancer Research. 43:2571-2582
Autor:
Yasuhiro Arai, Noriaki Matsushima
Publikováno v:
Canadian Journal of Economics/Revue canadienne d'économique. 56:114-132
Publikováno v:
Nihon Bika Gakkai Kaishi (Japanese Journal of Rhinology). 62:153-158
Publikováno v:
Journal of Society of Cosmetic Chemists of Japan. 56:33-40
Publikováno v:
IEEJ Transactions on Electronics, Information and Systems. 142:64-73
Publikováno v:
IEICE Communications Society Magazine. 16:131-136