Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Ryuji Nakagawa"'
Autor:
Hiroki Sato, Kenichi Suga, Masashi Suzue, Yukako Honma, Yasunobu Hayabuchi, Shunsuke Miyai, Hiroki Kurahashi, Ryuji Nakagawa
Publikováno v:
Human Genome Variation, Vol 9, Iss 1, Pp 1-4 (2022)
Abstract Ellis–van Creveld syndrome is an autosomal recessive skeletal dysplasia that is characterized by thoracic hypoplasia, polydactyly, oral abnormalities, and congenital heart disease. It is caused by pathogenic variants in the EVC or EVC2 gen
Externí odkaz:
https://doaj.org/article/06d179584d8d44769e55574d0d6d39e5
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background Betamimetics have been used for tocolysis extensively in the past, and one of them, ritodrine is widely used in Japan. Various adverse events have been reported for this agent, including newborn hypoglycemia and hypokalemia, as we
Externí odkaz:
https://doaj.org/article/61efb76dae5d4cdc9cfe941b86ad8ed4
Autor:
Issei Imoto, Masako Saito, Kenichi Suga, Tomohiro Kohmoto, Masanobu Otsu, Keisuke Horiuchi, Hironao Nakayama, Shigeki Higashiyama, Mayumi Sugimoto, Ayumi Sasaki, Yukako Homma, Miki Shono, Ryuji Nakagawa, Yasunobu Hayabuchi, Shoichiro Tange, Shoji Kagami, Kiyoshi Masuda
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract A disintegrin and metalloprotease 17 (ADAM17) is the major sheddase that processes more than 80 substrates, including tumour necrosis factor-α (TNFα). The homozygous genetic deficiency of ADAM17 causing a complete loss of ADAM17 expression
Externí odkaz:
https://doaj.org/article/f54d298d87a549a0b4eef6bb10764fdc
Autor:
Akinori Miyashita, Asako Koike, Gyungah Jun, Li-San Wang, Satoshi Takahashi, Etsuro Matsubara, Takeshi Kawarabayashi, Mikio Shoji, Naoki Tomita, Hiroyuki Arai, Takashi Asada, Yasuo Harigaya, Masaki Ikeda, Masakuni Amari, Haruo Hanyu, Susumu Higuchi, Takeshi Ikeuchi, Masatoyo Nishizawa, Masaichi Suga, Yasuhiro Kawase, Hiroyasu Akatsu, Kenji Kosaka, Takayuki Yamamoto, Masaki Imagawa, Tsuyoshi Hamaguchi, Masahito Yamada, Takashi Morihara, Masatoshi Takeda, Takeo Takao, Kenji Nakata, Yoshikatsu Fujisawa, Ken Sasaki, Ken Watanabe, Kenji Nakashima, Katsuya Urakami, Terumi Ooya, Mitsuo Takahashi, Takefumi Yuzuriha, Kayoko Serikawa, Seishi Yoshimoto, Ryuji Nakagawa, Jong-Won Kim, Chang-Seok Ki, Hong-Hee Won, Duk L. Na, Sang Won Seo, Inhee Mook-Jung, Peter St. George-Hyslop, Richard Mayeux, Jonathan L. Haines, Margaret A. Pericak-Vance, Makiko Yoshida, Nao Nishida, Katsushi Tokunaga, Ken Yamamoto, Shoji Tsuji, Ichiro Kanazawa, Yasuo Ihara, Gerard D. Schellenberg, Lindsay A. Farrer, Ryozo Kuwano
Publikováno v:
PLoS ONE, Vol 8, Iss 7 (2013)
Externí odkaz:
https://doaj.org/article/0289c56476fd4079895cf6a184cb4a86
Autor:
Akinori Miyashita, Asako Koike, Gyungah Jun, Li-San Wang, Satoshi Takahashi, Etsuro Matsubara, Takeshi Kawarabayashi, Mikio Shoji, Naoki Tomita, Hiroyuki Arai, Takashi Asada, Yasuo Harigaya, Masaki Ikeda, Masakuni Amari, Haruo Hanyu, Susumu Higuchi, Takeshi Ikeuchi, Masatoyo Nishizawa, Masaichi Suga, Yasuhiro Kawase, Hiroyasu Akatsu, Kenji Kosaka, Takayuki Yamamoto, Masaki Imagawa, Tsuyoshi Hamaguchi, Masahito Yamada, Takashi Morihara, Masatoshi Takeda, Takeo Takao, Kenji Nakata, Yoshikatsu Fujisawa, Ken Sasaki, Ken Watanabe, Kenji Nakashima, Katsuya Urakami, Terumi Ooya, Mitsuo Takahashi, Takefumi Yuzuriha, Kayoko Serikawa, Seishi Yoshimoto, Ryuji Nakagawa, Jong-Won Kim, Chang-Seok Ki, Hong-Hee Won, Duk L Na, Sang Won Seo, Inhee Mook-Jung, Alzheimer Disease Genetics Consortium, Peter St George-Hyslop, Richard Mayeux, Jonathan L Haines, Margaret A Pericak-Vance, Makiko Yoshida, Nao Nishida, Katsushi Tokunaga, Ken Yamamoto, Shoji Tsuji, Ichiro Kanazawa, Yasuo Ihara, Gerard D Schellenberg, Lindsay A Farrer, Ryozo Kuwano
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e58618 (2013)
To discover susceptibility genes of late-onset Alzheimer's disease (LOAD), we conducted a 3-stage genome-wide association study (GWAS) using three populations: Japanese from the Japanese Genetic Consortium for Alzheimer Disease (JGSCAD), Koreans, and
Externí odkaz:
https://doaj.org/article/0e666a618e5646909cf4e46bb2598bac
Autor:
Atsuko Yoshida, Takashi Kaji, Junki Imaizumi, Aya Shirakawa, Kenichi Suga, Ryuji Nakagawa, Kazuhisa Maeda, Minoru Irahara, Takeshi Iwasa
Publikováno v:
The Journal of Obstetrics and Gynaecology Research. 48(3):866-868
Many transgender men receive testosterone therapy to achieve virilization. The therapy is often mistaken for having a contraceptive effect because it causes amenorrhea. However, some treated patients become pregnant, which is not well known. A 25-yea
Autor:
Noriko Yokota, Hiroki Ishibashi, Kenichi Suga, Hiroki Mori, Akiko Kitamura, Ryuji Nakagawa, Mitsuo Shimada
Publikováno v:
The journal of medical investigation : JMI. 69(1.2)
The patient was a 15 months-old boy who had been diagnosed CHARGE syndrome, which is a multiple congenital anomaly syndrome caused by mutations in the CHD7 gene. Mechanical ventilation management was initiated 2 hours after birth for dysphagia and re
Autor:
Kenichi Suga, Yoshifumi Wakata, Chihiro Kubo, Manami Tanaka, Shunsuke Takeuchi, Keita Osumi, Masashi Suzue, Maki Urushihara, Ryuji Nakagawa, Shoji Kagami
Background We recently reported on a late preterm infant born at 36 gestational weeks with serious arrhythmia due to hyperkalemia associated with long term maternal ritodrine administration. In a previous nation-wide surveillance, maternal combined a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e0e639ed6a47f71cc10764dbdb2c085
https://doi.org/10.21203/rs.3.rs-1313318/v1
https://doi.org/10.21203/rs.3.rs-1313318/v1
Autor:
Kenichi Suga, Eishi Sogawa, Atsuko Yoshida, Ryuji Nakagawa, Takashi Kaji, Naoto Yonetani, Takeshi Iwasa
Publikováno v:
Twin Research and Human Genetics. 24(3):184-186
We report a very rare case of monochorionic dizygotic twins conceived spontaneously. The fetuses were sex-discordant in ultrasonography despite being monochorionic twins. After birth, the girl and boy showed normal phenotypes but they showed blood ch
Autor:
Shoji Kagami, Miki Shono, Maika Fukui, Kenichi Suga, Naoto Yonetani, Ryuji Nakagawa, Yuko Ichihara
Publikováno v:
The Journal of Medical Investigation. 67:170-173
Background : Biotin is a water-soluble vitamin that plays various biological roles through histone modification, such as immune functions and fetal growth. Mammalian maternal biotin deficiency during gestation induces fetal growth restriction. Preter