10 research outputs found
桑田佳祐と夏目漱石の「鎌倉物語」、駆け込み巡礼歌 : 縁切尼寺・「東慶寺」という磁場、〈縁〉を〈無縁〉で結ぶ原理
application/pdf論文(Article)departmental bulletin pape
The State of Skiing in Physical Education in Primary Schools in Iwate Prefecture
岩手県内の学校体育において,冬期になると実施されている代表的な学習内容の一つに,スキーを挙げることができる。そこで県内の小学校体育におけるスキー授業の実態を明らかにし,諸問題を検討するためのアンケート調査を行った。調査対象は,県内11ヶ所の教育事務所を通して,全県下小学校総数496校より,スキー実施校273校を抽出,アンケート用紙を郵送し,207校より回答を得た。回収率は75.8%であった。アンケートにより基礎的な資料を得ることができた。しかし,岩手県を一つの地域として捉えてしまうと,地理的,気候的な要素,学校の立地条件などにより実施状況が一様ではなく,様々な観点から継続的研究が必要と思われる。県内学校スキーは,寒冷・積雪地の冬の自然を生かしたスポーツとして,地域環境に相応したスキー形態をより取り入れるべきと思われる。しかしながら,スキーを体育の教材として行う場合,用具の問題,経済的な問題,実習場所と時間的問題,指導者,指導内容,指導法などの問題が少なくない。この状況において現場教師は,学校スキー研究の必要性を感じており,研究会の設立を期待し,その成果を待ち望んでいることがうかがえた。departmental bulletin pape
Brain research and clinical psychiatry : establishment of a psychiatry brain bank in Japan
2018-08The Japan Agency of Medical Research and Development (AMED) has approved the budget for the 5-year project called Establishment of the JAPAN Brain Bank Network, which commenced in 2016. This project was established with the aim of storing brain tissue samples to enable research on the etiologies and mechanisms of psychiatric diseases, which would eventually improve standards of clinical treatment for these diseases. Japanese researchers in the field of biological psychiatry have historically depended on Western brain banks, particularly from Europe and the United States, which is regrettable. To remedy this situation and improve the Japanese research standards, attempts for establishing an autonomous Japanese brain bank are ongoing. Reviews of the previous attempts on elucidating the etiopathology of neuropsychiatric diseases reveal that rapid advances result from studies on tissue samples from diseased brains. For example, in the Kraepelin era, i.e. in 1900 years before and after, long-term, resolute research on diseased brain specimens ultimately led to the discoveries of entities such as Alzheimer disease and Lewy body disease. The recent advances in techniques of neuroimaging and molecular biology have resulted in a shift of interest from brain tissue analysis. However, the integration of findings of all these techniques is recommended going forward, with a shift in focus back to brain tissue analysis. The JAPAN Brain Bank Network project was launched under this setting. The success of this project largely depends on the will of patients and family members (for donating samples) as well as cooperation among many clinicians. In this paper, we provide a brief overview of the history of biological psychiatric research and related perspectives, which will hopefully encourage further studies that will help bridge the gap between clinical and biological research on psychiatric diseases.departmental bulletin pape
Comparison of the developmental potential of 2-week-old preantral follicles derived from vitrified ovarian tissue slices, vitrified whole ovaries and vitrified/transplanted newborn mouse ovaries using the metal surface method-3
Ovaries were collected from newborn mice and immediately frozen-thawed with the vitrification method and then transplanted to the renal capsule of recipient mice for 14 days. The fresh ovaries were collected from newborn mice and only transplanted without freezing. No significant difference was found in the diameter of the granulosa cell outgrowth of follicles after 10 day of culture.<p><b>Copyright information:</b></p><p>Taken from "Comparison of the developmental potential of 2-week-old preantral follicles derived from vitrified ovarian tissue slices, vitrified whole ovaries and vitrified/transplanted newborn mouse ovaries using the metal surface method"</p><p>http://www.biomedcentral.com/1472-6750/8/38</p><p>BMC Biotechnology 2008;8():38-38.</p><p>Published online 4 Apr 2008</p><p>PMCID:PMC2364622.</p><p></p
Comparison of the developmental potential of 2-week-old preantral follicles derived from vitrified ovarian tissue slices, vitrified whole ovaries and vitrified/transplanted newborn mouse ovaries using the metal surface method-1
(C) (bar = 100 um). Antral-like cavity formation (D-H) (bar = 100 um) with different antral stages and ovulated oocyte (I) with nearby granulosa cells were observed.<p><b>Copyright information:</b></p><p>Taken from "Comparison of the developmental potential of 2-week-old preantral follicles derived from vitrified ovarian tissue slices, vitrified whole ovaries and vitrified/transplanted newborn mouse ovaries using the metal surface method"</p><p>http://www.biomedcentral.com/1472-6750/8/38</p><p>BMC Biotechnology 2008;8():38-38.</p><p>Published online 4 Apr 2008</p><p>PMCID:PMC2364622.</p><p></p
Comparison of the developmental potential of 2-week-old preantral follicles derived from vitrified ovarian tissue slices, vitrified whole ovaries and vitrified/transplanted newborn mouse ovaries using the metal surface method-4
15), 6 μl droplets (n = 114), and unfrozen control group (n = 127). The preantral follicles were derived by isolation from 14-day-old mouse ovaries. Means with different letters for each end points were significantly different (P < 0.05).<p><b>Copyright information:</b></p><p>Taken from "Comparison of the developmental potential of 2-week-old preantral follicles derived from vitrified ovarian tissue slices, vitrified whole ovaries and vitrified/transplanted newborn mouse ovaries using the metal surface method"</p><p>http://www.biomedcentral.com/1472-6750/8/38</p><p>BMC Biotechnology 2008;8():38-38.</p><p>Published online 4 Apr 2008</p><p>PMCID:PMC2364622.</p><p></p
Comparison of the developmental potential of 2-week-old preantral follicles derived from vitrified ovarian tissue slices, vitrified whole ovaries and vitrified/transplanted newborn mouse ovaries using the metal surface method-0
) (bar = 100 um). Dead (C) and survival ovary (D) after transplantation under the renal capsule for 14 days (bar = 100 um).<p><b>Copyright information:</b></p><p>Taken from "Comparison of the developmental potential of 2-week-old preantral follicles derived from vitrified ovarian tissue slices, vitrified whole ovaries and vitrified/transplanted newborn mouse ovaries using the metal surface method"</p><p>http://www.biomedcentral.com/1472-6750/8/38</p><p>BMC Biotechnology 2008;8():38-38.</p><p>Published online 4 Apr 2008</p><p>PMCID:PMC2364622.</p><p></p
Comparison of the developmental potential of 2-week-old preantral follicles derived from vitrified ovarian tissue slices, vitrified whole ovaries and vitrified/transplanted newborn mouse ovaries using the metal surface method-2
D preantral follicles derived from frozen-thawed transplanted ovaries of newborn mice (circle, vitrified in 6 μl volume, n = 31). No significant difference was found in the diameter of the granulosa cell outgrowth of follicles after 8 day of culture between in 2 μl and 6 μl vitrification groups. The comparison of granulosa outgrowth was not demonstrated at day 10 and day 12, because the overgrowth of the antral cavity and hatched oocyte from antral cavity were frequently found in preantral follicles from 14-day old mice.<p><b>Copyright information:</b></p><p>Taken from "Comparison of the developmental potential of 2-week-old preantral follicles derived from vitrified ovarian tissue slices, vitrified whole ovaries and vitrified/transplanted newborn mouse ovaries using the metal surface method"</p><p>http://www.biomedcentral.com/1472-6750/8/38</p><p>BMC Biotechnology 2008;8():38-38.</p><p>Published online 4 Apr 2008</p><p>PMCID:PMC2364622.</p><p></p
