Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Rina Matsuoka"'
Autor:
Rina Matsuoka, Shinsuke Akagi, Tomohiro Konishi, Masashi Kondo, Hideki Matsubara, Shohei Yamamoto, Keiji Izushi, Yuichi Tasaka
Publikováno v:
Journal of Pharmaceutical Health Care and Sciences, Vol 10, Iss 1, Pp 1-8 (2024)
Abstract Background Drug-drug interactions (DDIs) increase the incidence of adverse drug reactions (ADRs). In a previous report, we revealed that the incidence of potential DDIs due to the same CYP molecular species in one prescription exceeds 90% am
Externí odkaz:
https://doaj.org/article/041504f2fb574a8d904f7826fa719a5b
Autor:
Ichiro Fukunaga, Yoko Oe, Keiko Danzaki, Sayaka Ohta, Cheng Chen, Madoka Iizumi, Takahiro Shiga, Rina Matsuoka, Takashi Anzai, Remi Hibiya-Motegi, Shori Tajima, Katsuhisa Ikeda, Wado Akamatsu, Kazusaku Kamiya
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102290- (2021)
The gap junction beta-2 (GJB2) gene is the most common genetic cause of hereditary deafness worldwide. Among them, the G45E/Y136X mutation in GJB2 is the third most prevalent in Japan. In this study, we generated two induced pluripotent stem cell (iP
Externí odkaz:
https://doaj.org/article/3f4ede43415d429eac1f2147b38eb85c
Autor:
Ichiro Fukunaga, Takahiro Shiga, Cheng Chen, Yoko Oe, Keiko Danzaki, Sayaka Ohta, Rina Matsuoka, Takashi Anzai, Remi Hibiya-Motegi, Shori Tajima, Katsuhisa Ikeda, Wado Akamatsu, Kazusaku Kamiya
Publikováno v:
Stem Cell Research, Vol 43, Iss , Pp - (2020)
The gap junction beta-2 (GJB2) gene is the most common genetic cause of hereditary deafness worldwide. Especially, V37I mutation in GJB2 is most prevalent in Southeast Asia including Thailand, Malaysia, and Indonesia. Furthermore, it is the second mo
Externí odkaz:
https://doaj.org/article/daa88550283048028768a456886f5b9c
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:
Shori Tajima, Takashi Anzai, Rina Matsuoka, Hiroko Okada, Takuma Ide, Mitsuhisa Fujimaki, Shota Kaya, Shin Ito, Katsuhisa Ikeda
Publikováno v:
Case Reports in Otolaryngology, Vol 2018 (2018)
Deep neck abscess is a life-threatening infection that causes laryngeal edema and upper airway occlusion. The predominant bacterial species involved in this disorder is group A streptococcus. Group G streptococcus (GGS) constitutes the normal commens
Externí odkaz:
https://doaj.org/article/72c1dfaf5e284c74803e2bb3c33fcd6c
Autor:
Tomohiro Kitano, Maiko Miyagawa, Shin-Ya Nishio, Hideaki Moteki, Kiyoshi Oda, Kenji Ohyama, Hiromitsu Miyazaki, Hiroshi Hidaka, Ken-Ichi Nakamura, Takaaki Murata, Rina Matsuoka, Yoko Ohta, Nobuhiro Nishiyama, Kozo Kumakawa, Sakiko Furutate, Satoshi Iwasaki, Takechiyo Yamada, Yumi Ohta, Natsumi Uehara, Yoshihiro Noguchi, Shin-Ichi Usami
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0177636 (2017)
A variant in a transcription factor gene, POU4F3, is responsible for autosomal dominant nonsyndromic hereditary hearing loss, DFNA15. To date, 14 variants, including a whole deletion of POU4F3, have been reported to cause HL in various ethnic groups.
Externí odkaz:
https://doaj.org/article/1f0880387c96479eac09fb7838185e0b
Autor:
Satoshi Hara, Ayako Inoshita, Nobukazu Miyamoto, Yusuke Takata, Rina Matsuoka, Takashi Anzai, Masahiro Nakamura, Katsuhisa Ikeda, Fumihiko Matsumoto
Publikováno v:
Auris Nasus Larynx. 50:458-462
Autor:
Nanako Shiroshita, Shinichi Ohba, Yo Suzuki, Shin Ito, Hiroko Koiwai, Fumihiko Matsumoto, Ayako Inoshita, Takatoshi Kasai, Naoko Sata, Katsuhisa Ikeda, Rina Matsuoka
Publikováno v:
Auris Nasus Larynx. 49:1078-1082
Concurrent chemoradiotherapy (CCRT) is one of the most promising treatments for advanced head and neck cancer (HNC). On the other hand, CCRT may induce severe edema in laryngo-pharyngeal structures in association with radiation. This is a report of a
Autor:
Keiko Wakui, Hiromitsu Miyazaki, Yumiko Kobayashi, Shin-ichi Usami, Hirofumi Sakaguchi, Kozo Kumakawa, Natsumi Uehara, Tomomi Yamaguchi, Yoshimitsu Fukushima, Tomoki Kosho, Takashi Ishino, Kenji Ohyama, Satoko Abe, Hideaki Moteki, Shin-ya Nishio, Masahiro Takahashi, Rina Matsuoka, Yoh Yokota
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Scientific Reports
Scientific Reports
Sensorineural hearing loss is a common deficit and mainly occurs due to genetic factors. Recently, copy number variants (CNVs) in the STRC gene have also been recognized as a major cause of genetic hearing loss. We investigated the frequency of STRC
Autor:
Ayako Inoshita, Rina Matsuoka, Takatoshi Kasai, Fusae Kawana, Nanako Shiroshita, Mitsue Kato, Naoko Sata, Katsuhisa Ikeda
Publikováno v:
Journal of Thoracic Disease. 10:6702-6710
Background: Childhood obstructive sleep apnea (OSA) has important implications for growth, learning, behavior, cognition and cardiovascular health as well as snoring and OSA in adulthood. In this study, we elucidated the sex differences in polysomnog