Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Eishin Ogawa"'
Autor:
Takahiro Matsuki, Kana Yahagi, Hiroshi Mori, Hoshitaka Matsumoto, Taeko Hara, Saya Tajima, Eishin Ogawa, Hiroko Kodama, Kazuya Yamamoto, Takuji Yamada, Satoshi Matsumoto, Ken Kurokawa
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
The factors shaping the development of infants' gut microbiota are poorly understood. Here, the authors show that alterations in gut microbiota development in infants are associated with the presence of bifidobacteria having a gene for utilisation of
Externí odkaz:
https://doaj.org/article/6bc1bcb4578842b29ebd9ba9c24ac85e
Autor:
Yuriko Katsushima, Takeya Sato, Chika Yamada, Moe Ito, Yuki Suzuki, Eishin Ogawa, Izumi Sukegawa, Jun Sukegawa, Kohji Fukunaga, Teruyuki Yanagisawa
Publikováno v:
Journal of Pharmacological Sciences, Vol 122, Iss 3, Pp 193-204 (2013)
Release of growth hormone (GH) from the somatotroph is regulated by binding GH-releasing hormone (GHRH) to its cognate receptor (GHRHR), one of the members of the G protein–coupled receptor (GPCR) superfamily. Proteins bound to the carboxy (C)-term
Externí odkaz:
https://doaj.org/article/6ad180a5ad724bcda7d2bc7556fd70c0
Autor:
Eishin Ogawa, Kahoko Motoyama, Kiyomi Takamiya, Hiroko Kodama, Tohru Yorifuji, Tsuyoshi Isojima, Masakazu Mimaki, Shigehiro Enkai, Yasuhiro Sato
Publikováno v:
Hormone Research in Paediatrics. 94:229-234
Introduction: Transient neonatal diabetes mellitus (TNDM) is a rare condition that is characterized by the presence of diabetes mellitus during the first 6 months of life and remission by 18 months of age. It usually relapses at a median age of 14 ye
Autor:
Kazuhiro Katayama, Izumi Hamada, Atsushi Hosui, Minoru Itou, Tetsuo Takehara, Yasushi Matsuzaki, Katsunori Miyoshi, Hiroko Kodama, Keiko Hosho, Yoriyuki Takamori, Yoshiyuki Sakai, Yasuhiro Takikawa, Yoko Miyoshi, Tomomi Tsuru, Toshifumi Ito, Shinobu Ida, Kojiro Michitaka, Eishin Ogawa
Publikováno v:
Biological Trace Element Research
The essential trace element zinc maintains liver functions. Liver diseases can alter overall zinc concentrations, and hypozincemia is associated with various hepatic pathologies. Modulating systemic zinc through dietary supplementation is potentially
Publikováno v:
Beneficial Microbes. 7:453-461
The objective of the study was to investigate whether an infant formula supplemented with galacto-oligosaccharides (GOS; OM55N) was able to stimulate the growth of indigenous bifidobacteria and to establish microbiota similar to that of breastfed inf
Autor:
Mitsuyoshi Suzuki, Hiroko Kodama, Yasuhiro Sato, Kenji Wakabayashi, Eishin Ogawa, Kahoko Motoyama
Publikováno v:
Pediatrics International. 58:872-876
Background Biotin deficiency has been reported in Japanese infants fed special formulas for medical reasons, including those with milk allergy and congenital metabolic diseases, because these formulas contain little biotin. Serum biotin measurement i
Publikováno v:
Pediatrics International. 58:867-871
BACKGROUND Given that nutritional biotin deficiency in Japanese infants has been reported, a straightforward method for estimating biotin level is needed. The biotin content in infant formula, breast milk, and the sera of infants fed with various typ
Autor:
Toshihiro Ohura, Osamu Sakamoto, Mitsugu Uematsu, Kazuhiro Haginoya, Yoichi Matsubara, Eishin Ogawa, Yuki Hasegawa, Shoko Komatsuzaki, Nobuyuki Shimozawa
Publikováno v:
Pediatrics International. 57:1189-1192
Zellweger syndrome, one of the peroxisome biogenesis disorders, is an autosomal recessive disease caused by mutations in PEX genes. It is characterized by severe hypotonia, failure to thrive, psychomotor retardation, liver dysfunction, and sensorineu
Autor:
Toshiaki Hitomi, Hatasu Kobayashi, Akio Koizumi, Kouji H. Harada, Hiroko Okuda, Eishin Ogawa, Hiroyuki Adachi, Wanyang Liu, Junxia Yan, Tsutomu Takahashi, Toshihiro Ohura, Ikuko Takahashi
Publikováno v:
Journal of Human Genetics. 58:366-377
Familial goiter is a genetic disease showing heterogeneous expression. To identify causative genes, we investigated three multigenerational goiter families with an autosomal dominant inheritance pattern. We performed genome-wide linkage analysis on a
Autor:
Eishin Ogawa, Teruyuki Yanagisawa, Moe Ito, Kohji Fukunaga, Yuki Suzuki, Jun Sukegawa, Chika Yamada, Yuriko Katsushima, Izumi Sukegawa, Takeya Sato
Publikováno v:
Journal of Pharmacological Sciences, Vol 122, Iss 3, Pp 193-204 (2013)
Release of growth hormone (GH) from the somatotroph is regulated by binding GH-releasing hormone (GHRH) to its cognate receptor (GHRHR), one of the members of the G protein–coupled receptor (GPCR) superfamily. Proteins bound to the carboxy (C)-term