Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Teruo Sugawara"'
Autor:
Katsuhiko Warita, Takanori Miki, Yoshiki Matsumoto, Teruo Sugawara, Takashi Nanmori, Hideto Yamada, Yoshiaki Tabuchi, Tomoko Mitsuhashi, Yasuhiko Ebina, Jeffrey A. Kant, Noriaki Sakuragi, Ichiro Takasaki, Toshifumi Yokoyama, Takashi Kondo, Nobuhiko Hoshi, Hiroshi Kitagawa, Yoshiki Takeuchi, Fumio Hayashi, Zhi-Yu Wang
Publikováno v:
Congenital Anomalies. 50:40-51
XY females are rare individuals who carry a Y chromosome but are phenotypically female. In approximately 80-90% of these cases, there are no mutations in the SRY gene, a testis-determining gene on the short arm of the Y chromosome, and the pathophysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bf87e66c49190881aa2ac0b6f10b46c
https://doi.org/10.1111/j.1741-4520.2009.00254.x
https://doi.org/10.1111/j.1741-4520.2009.00254.x
Autor:
Yoshiaki Tabuchi, Noriaki Sakuragi, Tomoko Mitsuhashi, Yoshiki Takeuchi, Ichiro Takasaki, Nobuhiko Hoshi, Takanori Miki, Yoshiki Matsumoto, Jeffrey A. Kant, Fumio Hayashi, Hiroshi Kitagawa, Katsuhiko Warita, Takashi Nanmori, Zhi-Yu Wang, Teruo Sugawara, Toshifumi Yokoyama, Hideto Yamada, Yasuhiko Ebina, Takashi Kondo
Publikováno v:
Congenital Anomalies. 50:85-94
In normal ontogenetic development, the expression of the sex-determining region of the Y chromosome (SRY) gene, involved in the first step of male sex differentiation, is spatiotemporally regulated in an elaborate fashion. SRY is expressed in germ ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f2a3cc18de560fe9ae72d9d26276a68
https://doi.org/10.1111/j.1741-4520.2010.00274.x
https://doi.org/10.1111/j.1741-4520.2010.00274.x
Autor:
Shiho Fukui, Takashi Tanida, Nobuhiko Hoshi, Kana Ishihara, Katsuhiko Warita, Tomoko Mitsuhashi, Hiroshi Kitagawa, Tetsurou Inamoto, Takashi Nanmori, Toshifumi Yokoyama, Wang-Mei Qi, Yoshiaki Tabuchi, Teruo Sugawara
Publikováno v:
Toxicology Letters. 189:40-47
A major question is whether exposure to mixtures of low-dose endocrine disruptors (EDs) having different action mechanisms affects neurodevelopment differently than exposure to EDs individually. We therefore investigated the effects of fetal and neon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e42b17d823e284d423af73cd81f9af3
https://doi.org/10.1016/j.toxlet.2009.04.005
https://doi.org/10.1016/j.toxlet.2009.04.005
Autor:
Zhan-Peng Yue, Yoshiki Matsumoto, Yoshiki Takeuchi, Toshifumi Yokoyama, Hiroshi Kitagawa, Kazutaka Okamoto, Ken-ichiro Mutoh, Takanori Miki, Teruo Sugawara, Nobuhiko Hoshi, Yoshihisa Hasegawa, Katsuhiko Warita
Publikováno v:
Biology of Reproduction. 78:59-67
We aimed to elucidate the mechanism of action of estrogenic endocrine disruptors and the rescue of reproductive function, particularly the responsiveness of testes to eCG and/or activin A (ACT) after establishing reproductive disorders. Newborn male
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::614eadbb3825fb5586e30d480945d7df
https://doi.org/10.1095/biolreprod.106.059857
https://doi.org/10.1095/biolreprod.106.059857
Autor:
Takashi Tanida, Kana Ishihara, Teruo Sugawara, Hiroshi Kitagawa, Katsuhiko Warita, Nobuhiko Hoshi
Publikováno v:
Journal of Veterinary Medical Science. 69:347-352
In 1976, men who were exposed to the highest concentrations of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) after an explosion at a chemical plant near Seveso, Italy, produced more girls than boys. However, few studies have examined the possibility tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dc593b0d56fdddd4dfd2e9599509c22
https://doi.org/10.1292/jvms.69.347
https://doi.org/10.1292/jvms.69.347
Autor:
Teruo Sugawara, E. Nomura
Publikováno v:
Toxicology Mechanisms and Methods. 16:287-294
Endocrine systems of humans and animals are disturbed by dioxin-like compounds, which are ligands of the aryl hydrocarbon receptor (AhR). It is important to determine the accumulation of dioxin-like compounds in the environment for maintenance of hum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46dc126d3c7674b2f96626b995e3a791
https://doi.org/10.1080/15376520600616875
https://doi.org/10.1080/15376520600616875
Autor:
Teruo Sugawara, Seiichiro Fujimoto
Publikováno v:
Biochemical Journal. 380:153-160
The first step in the biosynthesis of steroid hormones is conversion of cholesterol into pregnenolone. StAR (steroidogenic acute regulatory) protein plays a crucial role in the intra-mitochondrial movement of cholesterol. STS (steroid sulphatase), wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08f5724abaa47eeed88cde8bfcbb5928
https://doi.org/10.1042/bj20031379
https://doi.org/10.1042/bj20031379
Publikováno v:
Journal of Endocrinology. 180:135-144
Endometrial carcinoma is a common malignancy of the genital tract. In the present study, we examined the expression of human steroidogenic acute regulatory (StAR) protein, P450 side-chain cleavage enzyme (P450 scc), 17alpha-hydroxylase/17,20-desmolas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::448d4a6556dc87d35ea72450b6573045
https://doi.org/10.1677/joe.0.1800135
https://doi.org/10.1677/joe.0.1800135
Autor:
Syuji Abe, Yuko Fujimoto, Seiichiro Fujimoto, Kenji Fujieda, Eiji Nomura, Masaki Saito, Teruo Sugawara, Noriaki Sakuragi
Publikováno v:
Endocrinology. 142:3570-3577
Coregulators have been suggested to act as a bridging apparatus between nuclear receptors and the transcriptional machinery. The orphan receptor SF-1 plays a role in controlling the basal and cAMP-stimulated expression of the human steroidogenic acut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3df3412bf1f667bbcbed735bfcaf745a
https://doi.org/10.1210/endo.142.8.8309
https://doi.org/10.1210/endo.142.8.8309
Publikováno v:
Hormone Research in Paediatrics. 56:182-187
Background: X-linked ichthyosis (XLI) is an inherited skin disorder caused by a deficiency of steroid sulfatase (STS). The gene and protein of STS were examined in 19 Japanese patients with XLI. Results: In Western blotting analysis, no cross-reactin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f75776524e29872a52e3d0bd28568bbd
https://doi.org/10.1159/000048116
https://doi.org/10.1159/000048116