検索結果 146 件
フルテキストURL | Int_J_Med_Microbiol_306_8_657.pdf |
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著者 | Chourashi, Rhishita| Mondal, Moumita| Sinha, Ritam| Debnath, Anusuya| Das, Suman| Koley, Hemanta| Sekhar Chatterjeea, Nabendu| |
キーワード | ChiS Mucin Vibrio cholerae Virulence |
備考 | This is an Accepted Manuscript of an article published by Elsevier GmbH| |
発行日 | 2016-12 |
出版物タイトル | International Journal of Medical Microbiology |
巻 | 306巻 |
号 | 8号 |
出版者 | ELSEVIER GMBH |
開始ページ | 657 |
終了ページ | 665 |
ISSN | 14384221 |
NCID | AA11427330 |
資料タイプ | 学術雑誌論文 |
言語 | 英語 |
OAI-PMH Set | 岡山大学 |
論文のバージョン | author |
PubMed ID | 27670078 |
DOI | 10.1016/j.ijmm.2016.09.003 |
Web of Science KeyUT | 000390824600008 |
関連URL | isVersionf https://doi.org/10.1016/j.ijmm.2016.09.003 |
タイトル(別表記) | Transcription factor Runx3 in the mouse hypothalamo-pituitary-gonadal system |
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フルテキストURL | poalas_034_002.pdf |
著者 | 高橋 純夫| |
抄録 | Runx3 is a transcription factor that belongs to the Runx family. Female Runx3 knockout (Runx3−⁄−) mouse was anovulatory and infertile. Ovarian transplantation experiment suggested that lack of ovulation in Runx3−⁄− mice was caused by alteration of gonadotropin secretion in Runx3−⁄− mice. Cyp11a1 mRNA expression was less in Runx3−⁄− mouse ovaries than in wt ones. Hypothalamic Gnrh1 mRNA was increased, and Kiss1 mRNA expression in the anteroventral periventricular nucleus was decreased, but Kisspeptin mRNA in the arcuate nucleus was increased in Runx3-/- mice. Pituitary Fshb mRNA levels were increased in Runx3−⁄− mice. Cholesterol side-chain cleavage enzyme gene (Cyp11a1) expression was decreased in ovaries of Runx3−⁄− mice. These findings suggest that anovulation in Runx3−⁄− mice was partly due to the alterations in hypothalamus-pituitary-ovary system. Runx3 plays a key role in female reproduction through alteration of gonadotropin secretion. |
出版物タイトル | 岡山実験動物研究会報 |
発行日 | 2018-04 |
巻 | 34巻 |
開始ページ | 2 |
終了ページ | 4 |
言語 | 日本語 |
論文のバージョン | publisher |
フルテキストURL | Reprod_Fertil_Dev_29_7_1280.pdf fig.pdf |
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著者 | Horihata, Kei| Yoshioka, Shin| Sano, Masahiro| Yamamoto, Yuki| Kimura, Koji| Skarzynski, Dariusz J.| Okuda, Kiyoshi| |
キーワード | luteal phase ovary progesterone prostaglandin reproduction |
備考 | This is an Accepted Manuscript of an article published by CSIRO Publishing| |
発行日 | 2016-05-17 |
出版物タイトル | Reproduction, Fertility and Development |
巻 | 29巻 |
号 | 7号 |
出版者 | CSIRO Publishing |
開始ページ | 1280 |
終了ページ | 1286 |
ISSN | 10313613 |
NCID | AA10718189 |
資料タイプ | 学術雑誌論文 |
言語 | 英語 |
OAI-PMH Set | 岡山大学 |
著作権者 | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja |
論文のバージョン | author |
PubMed ID | 27185011 |
DOI | 10.1071/RD15538 |
Web of Science KeyUT | 000403550200002 |
関連URL | https://doi.org/10.1071/RD15538 |
フルテキストURL | Reprod_Fertil_Dev_28_6_673.pdf |
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著者 | Yamamoto, Yuki| Kohka, Misa| Kobayashi, Yoshihiko| Woclawek-Potocka, Izabela| Okuda, Kiyoshi| |
キーワード | endothelin converting enzyme endothelin receptor epithelial cell ovarian steroids oviductal contraction and relaxation |
備考 | This is an Accepted Manuscript of an article published by CSIRO Publishing| |
発行日 | 2014-11 |
出版物タイトル | Reproduction, Fertility and Development |
巻 | 28巻 |
号 | 6号 |
出版者 | CSIRO Publishing |
開始ページ | 673 |
終了ページ | 681 |
ISSN | 1031-3613 |
NCID | AA10718189 |
資料タイプ | 学術雑誌論文 |
言語 | 英語 |
OAI-PMH Set | 岡山大学 |
著作権者 | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja |
論文のバージョン | author |
PubMed ID | 25370848 |
DOI | 10.1071/RD14076 |
Web of Science KeyUT | 000374546100003 |
関連URL | isVersionOf https://doi.org/10.1071/RD14076 |
フルテキストURL | Reprod_Fertil_Dev_29_10_1902.pdf |
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著者 | Bui, Tra M. T.| Nguyễn, Khánh X.| Karata, Asako| Ferré, Pilar| Trần, Minh T.| Wakai, Takuya| Funahashi, Hiroaki| |
キーワード | pig |
備考 | This is an Accepted Manuscript of an article published by CSIRO Publishing| |
発行日 | 2016-12-12 |
出版物タイトル | Reproduction, Fertility and Development |
巻 | 29巻 |
号 | 10号 |
出版者 | CSIRO Publishing |
開始ページ | 1902 |
終了ページ | 1909 |
ISSN | 1031-3613 |
NCID | AA10718189 |
資料タイプ | 学術雑誌論文 |
言語 | 英語 |
OAI-PMH Set | 岡山大学 |
著作権者 | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja |
論文のバージョン | author |
PubMed ID | 27938625 |
DOI | 10.1071/RD16321 |
Web of Science KeyUT | 000409376900003 |
関連URL | https://doi.org/10.1071/RD16321 |
フルテキストURL | K0005439_other2.pdf |
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著者 | Onoda, Satoshi| Kimata, Yoshihiro| Matsumoto, Kumiko| Yamada, Kiyoshi| |
備考 | 学位審査副論文| |
発行日 | 2016-01 |
出版物タイトル | Plastic and Reconstructive Surgery |
巻 | 137巻 |
号 | 1号 |
出版者 | Lippincott Williams & Wilkins |
開始ページ | 83e |
終了ページ | 91e |
ISSN | 00321052 |
NCID | AA00775696 |
資料タイプ | 学術雑誌論文 |
言語 | 英語 |
OAI-PMH Set | 岡山大学 |
著作権者 | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.ja |
論文のバージョン | author |
PubMed ID | 26710064 |
DOI | 10.1097/PRS.0000000000001884 |
Web of Science KeyUT | 000367333300001 |
関連URL | https://doi.org/10.1097/PRS.0000000000001884 |
タイトル(別表記) | Dissecting the hierarchy and lineage of mesenchymal stem cells by mouse genetics |
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フルテキストURL | poalas_033_015_017.pdf |
著者 | 宝田 剛志| |
抄録 | Determination of stem cell hierarchy/lineage is indispensable for a better understanding and augmentation of many aspects of medical sciences, including the mechanisms of tissue development and maintenance of tissue homeostasis, as well as disease development. It also has implications in the field of tissue regeneration for medical treatments and disease modeling for drug discovery using iPS technology. Mesenchymal stem cells are multipotent stem cell that can differentiate into various type of cells including osteoblasts, adipocytes, myocytes and chondrocytes. Runt-related transcription factor 2 (Runx2) is an essential transcriptional regulator of osteoblast differentiation. Runx2 deficiency in Prx1+-derived cells (Runx2prx1−/− mice) resulted in defective intramembranous ossification. Double-positive cells for Prx1-GFP and stem cell antigen-1 (Sca1) (Prx1+Sca1+ cells) in the calvaria expressed Runx2 at lower levels and were more homogeneous and primitive as compared with Prx1+Sca1− cells. Our results suggest that osteoblast differentiation in vivo may begin at the Prx1+Sca1+ MSC stage with sequential progression to Prx1+Sca1−cells, then Osx+Prx1−Sca1− osteoblast precursors, which eventually form mature α1(I)-collagen+ osteoblasts. |
出版物タイトル | 岡山実験動物研究会報 |
発行日 | 2017-04 |
巻 | 33巻 |
開始ページ | 15 |
終了ページ | 17 |
言語 | 日本語 |
論文のバージョン | publisher |
JaLCDOI | 10.18926/AMO/54499 |
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フルテキストURL | 70_4_243.pdf |
著者 | Osawa, Masahiro| Ohashi, Kadoaki| Kubo, Toshio| Ichihara, Eiki| Takata, Saburo| Takigawa, Nagio| Takata , Minoru| Tanimoto, Mitsune| Kiura, Katsuyuki| |
抄録 | Vandetanib (ZactimaTM) is a novel, orally available inhibitor of both vascular endothelial growth factor receptor-2 (VEGFR-2) and epidermal growth factor receptor (EGFR) tyrosine kinase. In the present study, a line of transgenic mice with a mouse Egfr gene mutation (delE748-A752) corresponding to a human EGFR mutation (delE746-A750) was established. The transgenic mice developed atypical adenomatous hyperplasia to adenocarcinoma of the lung at around 5 weeks of age and died of lung tumors at approximately 17 weeks of age. In the mice treated with vandetanib (6mg/kg/day), these lung tumors disappeared and the phosphorylations of EGFR and VEGFR-2 were reduced in lung tissues to levels comparable to those of non-transgenic control mice. The median overall survival time of the transgenic mice was 28 weeks in the vandetanib-treated group and 17 weeks in the vehicle-treated group. Vandetanib significantly prolonged the survival of the transgenic mice (log-rank test, p<0.01); resistance to vandetanib occurred at 20 weeks of age and the animals died from their lung tumors at about 28 weeks of age. These data suggest that vandetanib could suppress the progression of tumors harboring an activating EGFR mutation. |
キーワード | vandetanib VEGFR EGFR nonsmall cell lung cancer transgenic mouse |
Amo Type | Original Article |
出版物タイトル | Acta Medica Okayama |
発行日 | 2016-08 |
巻 | 70巻 |
号 | 4号 |
出版者 | Okayama University Medical School |
開始ページ | 243 |
終了ページ | 253 |
ISSN | 0386-300X |
NCID | AA00508441 |
資料タイプ | 学術雑誌論文 |
言語 | 英語 |
著作権者 | CopyrightⒸ 2016 by Okayama University Medical School |
論文のバージョン | publisher |
査読 | 有り |
PubMed ID | 27549668 |
Web of Science KeyUT | 000384748600003 |
著者 | 山本 ゆき| |
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発行日 | 2016-02-01 |
出版物タイトル | 岡山大学農学部学術報告 |
巻 | 105巻 |
資料タイプ | 紀要論文 |
著者 | 坂口 英| |
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発行日 | 2015-02-01 |
出版物タイトル | 岡山大学農学部学術報告 |
巻 | 104巻 |
資料タイプ | 紀要論文 |
著者 | Takayama, Hiroki| Miyake, Yasuhiro| Nouso, Kazuhiro| Ikeda, Fusao| Shiraha, Hidenori| Takaki, Akinobu| Kobashi, Haruhiko| Yamamoto, Kazuhide| |
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発行日 | 2011-01 |
出版物タイトル | Journal of Gastroenterology and Hepatology |
巻 | 26巻 |
号 | 1号 |
資料タイプ | 学術雑誌論文 |
著者 | 成田 裕一| Kajari Karmakar| Sébastien Ducret| Filippo M. Rijli| |
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発行日 | 2014-04 |
出版物タイトル | 岡山実験動物研究会報 |
巻 | 30巻 |
資料タイプ | その他 |
著者 | Kosaka, Junko| Morimatsu, Hiroshi| Takahashi, Toru| Shimizu, Hiroko| Kawanishi, Susumu| Omori, Emiko| Endo, Yasumasa| Tamaki, Naofumi| Morita, Manabu| Morita, Kiyoshi| |
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発行日 | 2013-05-07 |
出版物タイトル | PLoS ONE |
巻 | 8巻 |
号 | 5号 |
資料タイプ | 学術雑誌論文 |
著者 | 大内 淑代| |
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発行日 | 2013-12-02 |
出版物タイトル | 岡山医学会雑誌 |
巻 | 125巻 |
号 | 3号 |
資料タイプ | 学術雑誌論文 |
著者 | Nishikawa, Toshio| Takaoka, Munenori| Ohara, Toshiaki| Tomono, Yasuko| Hao, Huifang| Bao, Xiaohong| Fukazawa, Takuya| Wang, Zhigang| Sakurama, Kazufumi| Fujiwara, Yasuhiro| Motoki, Takayuki| Shirakawa, Yasuhiro| Yamatsuji, Tomoki| Tanaka, Noriaki| Fujiwara, Toshiyoshi| Naomoto, Yoshio| |
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発行日 | 2013-03 |
出版物タイトル | Cancer Biology & Therapy |
巻 | 14巻 |
号 | 3号 |
資料タイプ | 学術雑誌論文 |
著者 | Shimzu, K.| Takahashi, T.| Iwasaki, T.| Shimizu, H.| Inoue, K.| Morimatsu, H.| Omori, E.| Matsumi, M.| Akagi, R.| Morita, K.| |
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発行日 | 2008-11 |
出版物タイトル | Medicinal Chemistry |
巻 | 4巻 |
号 | 6号 |
資料タイプ | 学術雑誌論文 |
著者 | Endo, Yasumasa| Tomofuji, Takaaki| Ekuni, Daisuke| Azuma, Tetsuji| Irie, Koichiro| Kasuyama, Kenta| Morita, Manabu| |
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発行日 | 2013-01 |
出版物タイトル | Journal of Clinical Periodontology |
巻 | 40巻 |
号 | 1号 |
資料タイプ | 学術雑誌論文 |
著者 | Yashiro, Masato| Tsukahara, Hirokazu| Matsukawa, Akihiro| Yamada, Mutsuko| Fujii, Yosuke| Nagaoka, Yoshiharu| Tsuge, Mitsuru| Yamashita, Nobuko| Ito, Toshihiro| Yamada, Masao| Masutani, Hiroshi| |
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発行日 | 2013-01 |
出版物タイトル | Critical Care Medicine |
巻 | 41巻 |
号 | 1号 |
資料タイプ | 学術雑誌論文 |
著者 | 近藤 康博| |
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発行日 | 2013-02-01 |
出版物タイトル | 岡山大学農学部学術報告 |
巻 | 102巻 |
資料タイプ | 紀要論文 |
JaLCDOI | 10.18926/AMO/48686 |
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フルテキストURL | 66_4_317.pdf |
著者 | Pak, Wing| Takayama, Fusako| Hasegawa, Azusa| Mankura, Mitsumasa| Egashira, Toru| Ueki, Keiji| Nakamoto, Kazuo| Kawasaki, Hiromu| Mori, Akitane| |
抄録 | This study aimed to investigate the therapeutic effects of the water extract of leaves of Vitis coignetiae Pulliat (VCPL) on nonalcoholic steatohepatitis (NASH) with advanced fibrosis, as our previous study exhibited its preventive effect on NASH. The NASH animal model [PCT/JP2007/52477] was prepared by loading recurrent and intermittent hypoxemia stress to a rat with fatty liver, which resembled the condition occurring in patients with obstructive sleep apnea (OSA) and fatty liver, who have a high incidence of NASH. Intermittent hypoxemia stress is regarded as a condition similar to warm ischemia followed by re-oxygenation, which induces oxidative stress (OS). The daily 100 or 300mg/kg VCPL administrations were performed for 3 weeks perorally beginning at the time of detection of advanced liver fibrosis. The therapeutic efficacy of VCPL on NASH was demonstrated by the reduction of the leakage of hepato-biliary enzymes and the amelioration of liver fibrosis. The OS elevation in NASH rats was measured based on the derivation of reactive oxygen species from liver mitochondrial energy metabolism and on the decrease in plasma SOD-like activity. The aggravation of inflammatory responses was demonstrated by the neutrophil infiltration (elevated myeloperoxidase activity) and the progression of fibrosis in the livers of NASH rats. In addition, the NASH rats without VCPL treatment also exhibited activation of nuclear factor-κB, a key factor in the link between oxidative stress and inflammation. All of these changes were reduced dose-dependently by the VCPL administration. These findings indicate that VCPL may improve hepatic fibrosis or at least suppress the progression of NASH, by breaking the crosstalk between OS and inflammation. |
キーワード | non-alcoholic steatohepatitis antioxidative oxidative stress anti-inflammation Vitis coignetiae Pulliat |
Amo Type | Original Article |
出版物タイトル | Acta Medica Okayama |
発行日 | 2012-08 |
巻 | 66巻 |
号 | 4号 |
出版者 | Okayama University Medical School |
開始ページ | 317 |
終了ページ | 327 |
ISSN | 0386-300X |
NCID | AA00508441 |
資料タイプ | 学術雑誌論文 |
言語 | 英語 |
著作権者 | CopyrightⒸ 2012 by Okayama University Medical School |
論文のバージョン | publisher |
査読 | 有り |
PubMed ID | 22918204 |
Web of Science KeyUT | 000307918900004 |