Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Sawako Masuda"'
Autor:
Koichi Tsunoda, Toyota Ishii, Hiroyuki Kuroda, Hiroaki Nakatani, Masaru Tateda, Sawako Masuda, Tetsuya Takiguchi, Fujinobu Tanaka, Hayato Misawa, Masamitsu Senarita, Mihiro Takazawa, Kenji Itoh, Thomas Baer
Publikováno v:
Heliyon, Vol 10, Iss 4, Pp e25751- (2024)
We speculated that increased blood-plasma levels of Substance P may serve as an indicator of glottal incompetence, which is usually indicated by reduced maximum phonation time. We performed an initial study to test the plausibility of this hypothesis
Externí odkaz:
https://doaj.org/article/ecddf9d57fb84fec8093bcebfc502327
Autor:
Yifei Xu, Yuki Tsurinaga, Tsubasa Matsumoto, Ryuji Muta, Taichi Yano, Hiroshi Sakaida, Sawako Masuda, Koki Ueda, Guofei Feng, Shimpei Gotoh, Satoru Ogawa, Makoto Ikejiri, Kaname Nakatani, Mizuho Nagao, Masaki Tanabe, Kazuhiko Takeuchi
Publikováno v:
Case Reports in Genetics, Vol 2024 (2024)
Primary ciliary dyskinesia (PCD) is a hereditary disease caused by genes related to motile cilia. We report two male pediatric cases of PCD caused by hemizygous pathogenic variants in the OFD1 centriole and centriolar satellite protein (OFD1) gene. T
Externí odkaz:
https://doaj.org/article/3b6aec926727480589126864b134efcb
Autor:
Masatsugu Masuda, Ayako Kanno, Kiyomitsu Nara, Hideki Mutai, Naoya Morisada, Kazumoto Iijima, Noriko Morimoto, Atsuko Nakano, Tomoko Sugiuchi, Yasuhide Okamoto, Sawako Masuda, Sayaka Katsunuma, Kaoru Ogawa, Tatsuo Matsunaga
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-10 (2022)
Abstract Some patients have an atypical form of branchio-oto-renal (BOR) syndrome, which does not satisfy the diagnostic criteria, despite carrying a pathogenic variant (P variant) or a likely pathogenic variant (LP variant) of a causative gene. P/LP
Externí odkaz:
https://doaj.org/article/4493ac24dd0e4f55b506ef65f709bc2f
Autor:
Asa Kitamura, Kuniaki Toriyabe, Miki Hagimoto-Akasaka, Makoto Ikejiri, Toshio Minematsu, Shigeru Suga, Masako Kitano, Kazuhiko Takeuchi, Satoko Usui, Sawako Masuda, Eiji Kondo, Masamichi Kihira, Fumihiro Morikawa, Tomoaki Ikeda
Publikováno v:
Clinical and Experimental Obstetrics & Gynecology, Vol 49, Iss 12, p 259 (2022)
Background: There are no detailed reports in the literature on maternal cytomegalovirus antibody screening for universal newborn hearing screening (UNHS) referral patients. We examined maternal cytomegalovirus antibody screening results and estimated
Externí odkaz:
https://doaj.org/article/e22070e665054ebb906738a4f13fc637
Autor:
Kazuhiko Takeuchi, Yifei Xu, Satoru Ogawa, Makoto Ikejiri, Kaname Nakatani, Shimpei Gotoh, Satoko Usui, Sawako Masuda, Mizuho Nagao, Takao Fujisawa
Publikováno v:
Human Genome Variation, Vol 8, Iss 1, Pp 1-3 (2021)
Abstract We report the first Japanese case of primary ciliary dyskinesia caused by DNAH9 variations. The patient, a 5-year-old girl, had repeated episodes of productive cough after contracting the common cold at the age of 1 year and 6 months. She di
Externí odkaz:
https://doaj.org/article/694c8e7bf4d2482db6f3d3c519609cf4
Autor:
Satoshi Nakamura, Sachiko Tsunoda, Hiroshi Sakaida, Sawako Masuda, Ahamad Shah Said, Kazuhiko Takeuchi
Publikováno v:
Allergology International, Vol 68, Iss 1, Pp 39-45 (2019)
Background: Genetic and environmental factors are proposed to be involved in cedar pollen allergy sensitization and onset. The impact of these factors will provide key information for the prevention of cedar pollen sensitization and allergy onset, wh
Externí odkaz:
https://doaj.org/article/b9d12ae1f10940e4a4d2a13b73686138
Autor:
Hideki Mutai, Koichiro Wasano, Yukihide Momozawa, Yoichiro Kamatani, Fuyuki Miya, Sawako Masuda, Noriko Morimoto, Kiyomitsu Nara, Satoe Takahashi, Tatsuhiko Tsunoda, Kazuaki Homma, Michiaki Kubo, Tatsuo Matsunaga
Publikováno v:
PLoS Genetics, Vol 16, Iss 4, p e1008643 (2020)
Hereditary hearing loss is challenging to diagnose because of the heterogeneity of the causative genes. Further, some genes involved in hereditary hearing loss have yet to be identified. Using whole-exome analysis of three families with congenital, s
Externí odkaz:
https://doaj.org/article/a1fd6ee65284460e8b9ac7c9e5a2b959
Autor:
Nobuko Yamamoto, Hideki Mutai, Kazunori Namba, Noriko Morita, Shin Masuda, Yasuyuki Nishi, Atsuko Nakano, Sawako Masuda, Masato Fujioka, Kimitaka Kaga, Kaoru Ogawa, Tatsuo Matsunaga
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-11 (2017)
Abstract Background To date, 102 genes have been reported as responsible for non-syndromic hearing loss, some of which are associated with specific audiogram features. Four genes have been reported as causative for mid-frequency sensorineural hearing
Externí odkaz:
https://doaj.org/article/3d0d09fe9c84481f8aa8c51778a0377f
Autor:
Kei-ichi Yamanaka, Said Ahmad Shah, Hiroshi Sakaida, Akisa Yamagiwa, Sawako Masuda, Hitoshi Mizutani, Kazuhiko Takeuchi
Publikováno v:
Allergology International, Vol 64, Iss 1, Pp 54-59 (2015)
Background: This study aims to examine the immunological parameters, focusing IL-10 productivity, in prophylactic sublingual immunotherapy (SLIT) in asymptomatic subjects sensitized to Japanese cedar pollen (JCP). Methods: This study was conducted as
Externí odkaz:
https://doaj.org/article/84f47d19de5a427395cf03213461cd14
Publikováno v:
Allergology International, Vol 63, Iss 2, Pp 211-217 (2014)
Background: Methylated catechin, one of the active ingredients in green tea, has been reported to ameliorate allergic reactions. We evaluated the efficacy of 'Benifuuki' green tea, which contains O-methylated epigallocatechin-3-O-[3-O-methyl] gallate
Externí odkaz:
https://doaj.org/article/2a86d52a261e4ccd9803edfc5b094d75