検索結果 150 件
フルテキストURL | ApplEntomolZool_2019_00643.pdf |
---|---|
著者 | Terada, Kenji| Matsumura, Kentarou| Miyatake, Takahisa| |
キーワード | Temperature Experimental evolution Hatching rate Seed beetle Callosobruchus chinensis |
備考 | This is an Accepted Manuscript of an article published by Springer Japan| |
発行日 | 2019-09-13 |
出版物タイトル | Applied Entomology and Zoology |
巻 | 54巻 |
出版者 | Springer Japan |
開始ページ | 459 |
終了ページ | 464 |
ISSN | 00036862 |
NCID | AA00543238 |
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 |
DOI | 10.1007/s13355-019-00643-z |
NAID | 40022061862 |
Web of Science KeyUT | 000503219100014 |
関連URL | isVersionOf https://doi.org/10.1007/s13355-019-00643-z |
JaLCDOI | 10.18926/AMO/56930 |
---|---|
フルテキストURL | 73_4_285.pdf |
著者 | Otani, Yoshihiro| Ichikawa, Tomotsugu| Kurozumi, Kazuhiko| Date, Isao| |
抄録 | Gliomas are characterized as highly diffuse infiltrating tumors, and currently available treatments such as surgery, radiation and chemotherapy are unfeasible or show limited efficacy against these tumors. Recent genetic and epigenetic analyses of glioma have revealed increasing evidence of the role of driver genetic alterations in glioma development and led to the identification of prognostic factors. Despite these findings, the survival rates of glioma patients remain low, and alternative treatments and novel targets are needed. Recent studies identified neural stem cells as the possible origin of gliomas, and some evidence has revealed shared functions and mechanisms between glioma cells and neurons, also supporting their similarity. The cytoskeleton plays important roles in the migration of normal cells as well as cancer cells. Recent reports have described a role for microtubules, a component of the cytoskeleton, in glioma invasion. Notably, several factors that regulate microtubule functions, such as microtubule-associated proteins, plus-end tracking proteins, or motor proteins, are upregulated in glioma tissues compared with normal tissue, and upregulation of these factors is associated with high invasiveness of glioma cells. In this review, we describe the mechanism of microtubules in glioma invasion and discuss the possibility of microtubule-targeted therapy to inhibit glioma invasion. |
キーワード | glioma cytoskeletons invasion microtubules |
Amo Type | Review |
出版物タイトル | Acta Medica Okayama |
発行日 | 2019-08 |
巻 | 73巻 |
号 | 4号 |
出版者 | Okayama University Medical School |
開始ページ | 285 |
終了ページ | 297 |
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Ⓒ 2019 by Okayama University Medical School |
論文のバージョン | publisher |
査読 | 有り |
PubMed ID | 31439951 |
JaLCDOI | 10.18926/AMO/56860 |
---|---|
フルテキストURL | 73_3_189.pdf |
著者 | Sakamoto, Shinji| Kawai, Hiroki| Okahisa, Yuko| Tsutsui, Ko| Kanbayashi, Takashi| Tanaka, Keiko| Mizuki, Yutaka| Takaki, Manabu| Yamada, Norihito| |
抄録 | Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a recently-discovered autoimmune disorder in which antibodies target NMDAR in the brain. The number of reported cases of anti-NMDAR encephalitis has increased rapidly. Anti-NMDAR encephalitis can be mistakenly diagnosed as psychiatric disorders because many patients present with prominent psychiatric symptoms and visit psychiatric institutions first. Thus, psychiatrists should cultivate a better understanding of anti-NMDAR encephalitis. In this review, we present the mechanisms, epidemiology, symptoms and clinical course, diagnostic tests, treatment and outcomes of patients with anti-NMDAR encephalitis. Furthermore, we discuss the diversity of clinical spectra of anti-NMDAR encephalitis, and demonstrate a differential diagnosis of psychiatric disease from the perspective of psychiatry. |
キーワード | NMDAR encephalitis psychiatric symptom schizophrenia mood disorder |
Amo Type | Review |
出版物タイトル | Acta Medica Okayama |
発行日 | 2019-06 |
巻 | 73巻 |
号 | 3号 |
出版者 | Okayama University Medical School |
開始ページ | 189 |
終了ページ | 195 |
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Ⓒ 2019 by Okayama University Medical School |
論文のバージョン | publisher |
査読 | 有り |
PubMed ID | 31235965 |
フルテキストURL | InfectGenetEvol_54_47.pdf |
---|---|
著者 | Ghosh, Priyanka| Kumar, Dhirendra| Chowdhury, Goutam| Singh, Puneeta| Samanta, Prosenjit| Dutta, Shanta| Ramamurthy, T.| Sharma, N. C.| Sinha, Preety| Prasad, Yogendra| Shinoda, Sumio| Mukhopadhyay, Asish K.| |
キーワード | Cholera Vibrio cholerae ctxAB promoter ctxB gyrA rstB rtxA tcpA |
発行日 | 2017-10 |
出版物タイトル | Infection, Genetics and Evolution |
巻 | 54巻 |
出版者 | Elsevier Science |
開始ページ | 47 |
終了ページ | 53 |
ISSN | 15671348 |
NCID | AA11697619 |
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 | 28625543 |
DOI | 10.1016/j.meegid.2017.06.015 |
Web of Science KeyUT | 000411461400006 |
関連URL | isVersionOf https://doi.org/10.1016/j.meegid.2017.06.015 |
フルテキストURL | Int_J_Med_Microbiol_306_8_657.pdf |
---|---|
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 |
---|---|
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 |
---|---|
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 |
---|---|
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 |
---|---|
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 |
---|---|
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 |
---|---|
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 |
---|---|
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| |
---|---|
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| |
---|---|
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| |
---|---|
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| |
---|---|
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| |
---|---|
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| |
---|---|
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| |
---|---|
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.| |
---|---|
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 |