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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
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
73巻
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
73巻
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
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
306巻
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
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
29巻
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
28巻
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
29巻
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
137巻
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
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
70巻
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
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
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
26巻
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
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
8巻
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
125巻
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
14巻
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
4巻
6号
資料タイプ 学術雑誌論文