Zobrazeno 1 - 10
of 397
pro vyhledávání: '"Hajime, Ishida"'
Autor:
Yoko Uchida-Fukuhara, Shigeru Shimamura, Rikai Sawafuji, Takumi Nishiuchi, Minoru Yoneda, Hajime Ishida, Hirofumi Matsumura, Takumi Tsutaya
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Detailed investigation of extremely severe pathological conditions in ancient human skeletons is important as it could shed light on the breadth of potential interactions between humans and disease etiologies in the past. Here, we applied pa
Externí odkaz:
https://doaj.org/article/b82f840e52d54c6694f27bbb21d6d330
Autor:
Tsugumi Uema, Jasmine F. Millman, Shiki Okamoto, Takehiro Nakamura, Kiyoto Yamashiro, Moriyuki Uehara, Ken-ichiro Honma, Minoru Miyazato, Asuka Ashikari, Seiichi Saito, Shiro Maeda, Minako Imamura, Hajime Ishida, Masayuki Matsushita, Koshi Nakamura, Hiroaki Masuzaki
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-13 (2022)
Abstract Numerous studies have revealed distinct differences in the profiles of gut microbiota between non-obese and obese individuals. To date, however, little is known if any disparities in the community of gut microbiota exist between metabolicall
Externí odkaz:
https://doaj.org/article/2cb2ca72aafa46b8b0c54e11f7370604
Autor:
Shimpei Goto, Keiichi Kataoka, Mutsumi Isa, Kenji Nakamori, Makoto Yoshida, Sadayuki Murayama, Akira Arasaki, Hajime Ishida, Ryosuke Kimura
Publikováno v:
PLoS ONE, Vol 18, Iss 3, p e0283636 (2023)
Cortical bone thickness is important for the mechanical function of bone. Ontogeny, aging, sex, body size, hormone levels, diet, behavior, and genetics potentially cause variations in postcranial cortical robusticity. However, the factors associated
Externí odkaz:
https://doaj.org/article/2a0ca12db0104af08342a53332820e62
Autor:
Keiichi Kataoka, Hironori Fujita, Mutsumi Isa, Shimpei Gotoh, Akira Arasaki, Hajime Ishida, Ryosuke Kimura
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Morphological variations in human teeth have long been recognized and, in particular, the spatial and temporal distribution of two patterns of dental features in Asia, i.e., Sinodonty and Sundadonty, have contributed to our understanding of
Externí odkaz:
https://doaj.org/article/f56ab95d996d4e4ea798457e5c7339f4
Autor:
Asuka Ashikari, Minoru Miyazato, Koshi Nakamura, Kiyoto Yamashiro, Takehiro Nakamura, Tsugumi Uema, Moriyuki Uehara, Hiroaki Masuzaki, Seiichi Saito, Shiro Maeda, Hajime Ishida, Masayuki Matsushita
Publikováno v:
Metabolites, Vol 12, Iss 5, p 468 (2022)
(1) Background: Evidence has accumulated regarding the etiology of lower urinary tract symptoms associated with obesity and metabolic syndrome. Therefore, the present study aimed to identify which subjectively and objectively measured voiding paramet
Externí odkaz:
https://doaj.org/article/1b322302d12f4c199fedcefccf83ad6a
Autor:
MUHAMMAD SHOAIB AKHTAR, RYUICHI ASHINO, HIROKI OOTA, HAJIME ISHIDA, YOSHIHITO NIIMURA, KAZUSHIGE TOUHARA, AMANDA D. MELIN, SHOJI KAWAMURA
Publikováno v:
Anthropological Science. 130:93-106
Publikováno v:
Anthropological Science (Japanese Series). 130:55-74
Autor:
Minoru Yoneda, Angela R. Lieverse, Hajime Ishida, Daisuke Kubo, Hirofumi Matsumura, Rebecca L. Bourgeois
Publikováno v:
Anthropological Science. 130:47-57
Autor:
Toshihiro Kumabe, Kimitoshi Sato, Takashi Toma, Kae Koganebuchi, Shuhei Mano, Kiyotaka Fujii, Keiichiro Joh, Motoyuki Ogawa, Hidenobu Soejima, Hiroki Oota, Kuniaki Haneji, Hajime Ishida
Publikováno v:
Annals of Human Genetics
Background:Ring finger protein 213 (RNF213) is a susceptibility gene of moyamoya disease (MMD). A previous case–control study and a family analysis demonstrated a strong association of the East Asian-specific variant, R4810K (rs112735431), with MMD
Autor:
Mohamed Adel, Tetsutaro Yamaguchi, Daisuke Tomita, Takatoshi Nakawaki, Yong-Il Kim, Yu Hikita, Shugo Haga, Masahiro Takahashi, Mohamed A Nadim, Akira Kawaguchi, Mutsumi Isa, Walid H El-Kenany, Abbadi A El-Kadi, Soo-Byung Park, Hajime Ishida, Koutaro Maki, Ryosuke Kimura
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0170645 (2017)
FGFR1 plays an important role in the development of the nervous system as well as the regulation of the skeletal development and bone homeostasis. Mutations in FGFR1 genes affect skull development, specifically suture and synchondrosis, resulting in
Externí odkaz:
https://doaj.org/article/0d13319be5f34b7f8e1793bf04258ed0