検索結果 10646 件
フルテキストURL | K0006030_abstract_review.pdf K0006030_fulltext.pdf K0006030_other_1 supplemantary Information.pdf |
---|---|
著者 | 森廣 俊昭| |
発行日 | 2019-09-25 |
資料タイプ | 学位論文 |
学位授与番号 | 甲第6030号 |
学位授与年月日 | 2019-09-25 |
学位・専攻分野 | 博士(医学) |
授与大学 | 岡山大学 |
言語 | 英語 |
フルテキストURL | K0006029_abstract_review.pdf K0006029_fulltext.pdf |
---|---|
著者 | 桒田 和也| |
発行日 | 2019-09-25 |
資料タイプ | 学位論文 |
学位授与番号 | 甲第6029号 |
学位授与年月日 | 2019-09-25 |
学位・専攻分野 | 博士(医学) |
授与大学 | 岡山大学 |
言語 | 英語 |
フルテキストURL | K0006028_abstract_review.pdf K0006028_fulltext_org.pdf K0006028_summary.pdf |
---|---|
著者 | 大西 章史| |
発行日 | 2019-09-25 |
資料タイプ | 学位論文 |
学位授与番号 | 甲第6028号 |
学位授与年月日 | 2019-09-25 |
学位・専攻分野 | 博士(医学) |
授与大学 | 岡山大学 |
言語 | 英語 |
著作権者 | © 2019 Akifumi Onishi et al. |
フルテキストURL | K0006026_abstract_review.pdf K0006026_fulltext.pdf |
---|---|
著者 | 西村 慎吾| |
発行日 | 2019-09-25 |
資料タイプ | 学位論文 |
学位授与番号 | 甲第6026号 |
学位授与年月日 | 2019-09-25 |
学位・専攻分野 | 博士(医学) |
授与大学 | 岡山大学 |
言語 | 英語 |
フルテキストURL | K0006025_abstract_review.pdf K0006025_fulltext.pdf |
---|---|
著者 | 清水 俊彦| |
発行日 | 2019-09-25 |
資料タイプ | 学位論文 |
学位授与番号 | 甲第6025号 |
学位授与年月日 | 2019-09-25 |
学位・専攻分野 | 博士(医学) |
授与大学 | 岡山大学 |
言語 | 英語 |
フルテキストURL | K0006024_abstract_review.pdf K0006024_fulltext.pdf K0006024_other_1 figure.pdf K0006024_other_2 Supplementary figures and legends.pdf |
---|---|
著者 | 渡邉 伸一郎| |
発行日 | 2019-09-25 |
資料タイプ | 学位論文 |
学位授与番号 | 甲第6024号 |
学位授与年月日 | 2019-09-25 |
学位・専攻分野 | 博士(医学) |
授与大学 | 岡山大学 |
言語 | 英語 |
フルテキストURL | fcell_2019_00160_p.pdf fcell_2019_00160_a.pdf |
---|---|
著者 | Satoh, Ayano| Hayashi-Nishino, Mitsuko| Shakuno, Takuto| Masuda, Junko| Koreishi, Mayuko| Murakami, Runa| Nakamura, Yoshimasa| Nakamura, Toshiyuki| Abe-Kanoh, Naomi| Honjo, Yasuko| Malsam, Joerg| Yu, Sidney| ishino, Kunihiko | |
キーワード | Golgi golgins glycosylation endoplasmic reticulum electron tomography |
発行日 | 2019-08-27 |
出版物タイトル | Frontiers in Cell and Developmental Biology |
巻 | 7巻 |
開始ページ | 160 |
ISSN | 2296634X |
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 | publisher |
PubMed ID | 31544102 |
DOI | 10.3389/fcell.2019.00160 |
関連URL | isVersionOf https://doi.org/10.3389/fcell.2019.00160 |
フルテキストURL | Biochemistry_58_26_2934.pdf |
---|---|
著者 | Shibukawa, Atsushi| Kojima, Keiichi| Nakajima, Yu| Nishimura, Yosuke| Yoshizawa, Susumu| Sudo, Yuki| |
備考 | This fulltext will be available in Jun 2020| |
発行日 | 2019-05-31 |
出版物タイトル | Biochemistry |
巻 | 58巻 |
号 | 26号 |
出版者 | American Chemical Society |
開始ページ | 2934 |
終了ページ | 2943 |
ISSN | 00062960 |
NCID | AA00564599 |
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 | 31150215 |
DOI | 10.1021/acs.biochem.9b00257 |
関連URL | isVersionOf https://doi.org/10.1021/acs.biochem.9b00257 |
フルテキストURL | SciRep_9_7863.pdf |
---|---|
著者 | Yamanashi, Taro| Maki, Misayo| Kojima, Keiichi| Shibukawa, Atsushi| Tsukamoto, Takashi| Chowdhury, Srikanta| Yamanaka, Akihiro| Takagi, Shin| Sudo, Yuki| |
発行日 | 2019-05-27 |
出版物タイトル | Scientific reports |
巻 | 9巻 |
号 | 1号 |
出版者 | Nature Publishing Group |
開始ページ | 7863 |
ISSN | 20452322 |
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 | publisher |
PubMed ID | 31133660 |
DOI | 10.1038/s41598-019-44308-x |
関連URL | isVersionOf https://doi.org/10.1038/s41598-019-44308-x |
フルテキストURL | RSocOpenSci_6_5_190293_p.pdf |
---|---|
著者 | Tani, Yumeki| Kaneta, Takashi| |
キーワード | gold nanoparticle optical force vesicles |
発行日 | 2019-05-15 |
出版物タイトル | Royal Society Open Science |
巻 | 6巻 |
号 | 5号 |
出版者 | Royal Society Publishing |
開始ページ | 190293 |
ISSN | 20545703 |
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 | publisher |
PubMed ID | 31218066 |
DOI | 10.1098/rsos.190293 |
関連URL | isVersionOf https://doi.org/10.1098/rsos.190293 |
フルテキストURL | ChemRec_19_2_3_452.pdf |
---|---|
著者 | Kaneta, Takashi| |
キーワード | DNA sequencing capillary electrophoresis laser-induced fluorescence micellar electrokinetic chromatography |
発行日 | 2018-08-06 |
出版物タイトル | Chemical Record |
巻 | 19巻 |
号 | 2-3号 |
出版者 | Wiley |
開始ページ | 452 |
終了ページ | 461 |
ISSN | 15278999 |
NCID | AA11515019 |
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 | 30079538 |
DOI | 10.1002/tcr.201800051 |
関連URL | isVersionOf https://doi.org/10.1002/tcr.201800051 |
フルテキストURL | VirusRes_177_1_75.pdf Table 1-revised.pdf FigS-revised.pdf Figs_revised.pdf Table S.pdf |
---|---|
著者 | Kondo, Hideki| Hirano, Shuichi| Chiba, Sotaro| Andika, Ida Bagus| Hirai, Makoto| Maeda, Takanori| Tamada, Tetsuo| |
キーワード | AlkB Benyvirus Burdock mottle virus Endogenous viral element Paleovirology Transcriptome shotgun assembly |
発行日 | 2013-10 |
出版物タイトル | Virus Research |
巻 | 177巻 |
号 | 1号 |
出版者 | Elsevier Science |
開始ページ | 75 |
終了ページ | 86 |
ISSN | 01681702 |
NCID | AA10642076 |
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 | 23911632 |
DOI | 10.1016/j.virusres.2013.07.015 |
Web of Science KeyUT | 000324974100009 |
関連URL | isVersionOf https://doi.org/10.1016/j.virusres.2013.07.015 |
フルテキストURL | VirusRes_213_353.pdf tables_revised.pdf Fig S.pdf Supplementary_tables_revised.pdf |
---|---|
著者 | Kondo, Hideki| Hisano, Sakae| Chiba, Sotaro| Maruyama, Kazuyuki| Andika, Ida Bagus| Toyoda, Kazuhiro| Fujimori, Fumihiro| Suzuki, Nobuhiro| |
キーワード | Deep sequencing Double stranded RNA virus Powdery mildew Saccharomyces cerevisiae virus L-A Totivirus Ustilago maydis virus H1 |
発行日 | 2016-02 |
出版物タイトル | Virus Research |
巻 | 213巻 |
出版者 | Elsevier Science |
開始ページ | 353 |
終了ページ | 364 |
ISSN | 01681702 |
NCID | AA10642076 |
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 | 26592174 |
DOI | 10.1016/j.virusres.2015.11.015 |
Web of Science KeyUT | 000371840600042 |
関連URL | isVersionOf https://doi.org/10.1016/j.virusres.2015.11.015 |
JaLCDOI | 10.18926/AMO/57379 |
---|---|
フルテキストURL | 73_5_469.pdf |
著者 | Yamasaki, Satoshi| Kada, Akiko| Nagai, Hirokazu| Yoshida, Isao| Choi, Ilseung| Saito, Akiko M.| Iwasakia, Hiromi| |
抄録 | Romidepsin is an important therapeutic option for patients with peripheral T-cell lymphoma (PTCL). However, the timing of romidepsin administration remains controversial. Romidepsin was launched in Japan as a consolidation therapy agent after conventional salvage chemotherapy with gemcitabine, dexamethasone, and cisplatin (GDP). GDP therapy will be administered every 3 weeks. If complete response, partial response, or stable disease is confirmed after 2-4 GDP cycles, romidepsin will be administered every 4 weeks. The primary endpoint is a 2-year progression-free survival rate. Patients participating in this study and undergoing treatment can expect results similar to or better than those of conventional therapies. |
キーワード | peripheral T-cell lymphoma not otherwise specified angioimmunoblastic T-cell lymphoma gemcitabine cisplatin, romidepsin |
Amo Type | Clinical Study Protocol |
出版物タイトル | Acta Medica Okayama |
発行日 | 2019-10 |
巻 | 73巻 |
号 | 5号 |
出版者 | Okayama University Medical School |
開始ページ | 469 |
終了ページ | 474 |
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 | 31649375 |
Web of Science KeyUT | 000491886600014 |
JaLCDOI | 10.18926/AMO/57377 |
---|---|
フルテキストURL | 73_5_457.pdf |
著者 | Iwamuro, Masaya| Takahara, Masahiro| Yamazaki, Tatsuhiro| Tanaka, Takehiro| Kondo, Yoshitaka| Hiraoka, Sakiko| Okada, Hiroyuki| |
抄録 | A 60-year-old Caucasian male was diagnosed with lung adenocarcinoma and multiple metastases to the bone, spleen, and brain. He underwent radiotherapy for the brain and lumbar spine metastases, plus chemotherapy (cisplatin and pemetrexed). The chemotherapy was discontinued due to vomiting and hyponatremia, and nivolumab was then administered. Eight months later, 18F-fluorodeoxyglucose positron emission tomography showed tracer uptake in the colon. Colonoscopy revealed a reddish multinodular polyp in the sigmoid colon. The polyp showed irregular microvessels. No colonic mucosal surface structures were observed. Colonic metastasis of the lung carcinoma was highly suspected; the polyp was therefore surgically removed. The histological analysis revealed granulation tissue and suppurative inflammation without neoplastic changes. We diagnosed the lesion as a granulation polyp. Despite the difficulty in diagnosing these lesions due to their rarity and similarity to metastatic colon tumors, we suggest that recognizing the endoscopic features of the polyp surface may allow a preoperative diagnosis. |
キーワード | colonoscopy colonic neoplasms granulation polyp |
Amo Type | Case Report |
出版物タイトル | Acta Medica Okayama |
発行日 | 2019-10 |
巻 | 73巻 |
号 | 5号 |
出版者 | Okayama University Medical School |
開始ページ | 457 |
終了ページ | 461 |
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 | 31649373 |
Web of Science KeyUT | 000491886600012 |
JaLCDOI | 10.18926/AMO/57376 |
---|---|
フルテキストURL | 73_5_449.pdf |
著者 | Matsunaga, Kazuyuki| Takemaru, Makoto| Yamashiro, Keisuke| Yoshihara-Hirata, Chiaki| Inohara, Ken| Shimoe, Yutaka| Tanaka, Akio| Kuriyama, Masaru| Takashiba, Shogo| |
抄録 | We report a case of acute prevertebral abscess caused by traumatic tooth fractures in a 77-year-old Japanese man. After being transferred to our hospital the patient was initially diagnosed with a neck hematoma; however, blood culture showed Streptococcus parasanguinis, an oral bacterium, and an MRI examination suggested prevertebral abscesses. Tooth fractures, severe periodontitis, and peri-implantitis with Streptococcus parasanguinis were observed. Antibiotics were administered and fractured teeth were extracted. The patient's condition then gradually improved. We concluded that bacteremia caused by traumatic tooth fractures induced the acute prevertebral abscesses. |
キーワード | prevertebral abscess deep neck infection periodontal disease peri-implantitis Streptococcus parasanguinis |
Amo Type | Case Report |
出版物タイトル | Acta Medica Okayama |
発行日 | 2019-10 |
巻 | 73巻 |
号 | 5号 |
出版者 | Okayama University Medical School |
開始ページ | 449 |
終了ページ | 456 |
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 | 31649372 |
Web of Science KeyUT | 000491886600011 |
JaLCDOI | 10.18926/AMO/57374 |
---|---|
フルテキストURL | 73_5_433.pdf |
著者 | Tamada, Shoko| Mitsui, Takashi| Ohira, Akiko| Tani, Kazumasa| Maki, Jota| Eguchi, Takeshi| Eto, Eriko| Hayata, Kei| Masuyama, Hisashi| |
抄録 | An association between preeclampsia and (pro)renin was recently reported. Intracellular signaling of the (pro) renin receptor [(P)RR] increases the expressions of TGF-β and PAI-1. In this study we sought to clarify the involvement of (pro)renin in the pathogenesis of preeclampsia via the intracellular signaling of (P)RR on preeclampsia placentas. Activated (pro)renin plasma concentrations were compared between pregnant women with (n=15) and without (n=28) preeclampsia. The placentas were immunohistochemically evaluated with anti-HIF-1α and anti-(P)RR antibodies. HTR-8/SVneo cells were cultured under hypoxic conditions and treated with human recombinant (pro)renin. The mRNA expressions of HIF-1α, (P)RR, PAI-1, TGF-β, and ET-1 were also examined by real-time RCR. The activated (pro)renin plasma concentration was significantly higher in the third vs. the second trimester in the preeclampsia patients. HIF-1α and (P)RR expressions were significantly increased in the preeclampsia placentas. The mRNA expressions of PAI-1, TGF-β, and ET-1 were significantly increased in the experiments using recombinant (pro)renin vs. hypoxic conditions. (P)RR expression in preeclampsia placentas is increased by persistent hypoxia through the second and third trimesters, and PAI-1, TGF-β, and ET-1 production is increased via (P)RR. Our results suggest that ET-1 production via the intracellular signaling of (P)RR is important in the pathogenesis of preeclampsia. |
キーワード | preeclampsia (pro)renin (pro)renin receptor endothelin-1 HTR-8/SVneo |
Amo Type | Original Article |
出版物タイトル | Acta Medica Okayama |
発行日 | 2019-10 |
巻 | 73巻 |
号 | 5号 |
出版者 | Okayama University Medical School |
開始ページ | 433 |
終了ページ | 440 |
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 | 31649370 |
Web of Science KeyUT | 000491886600009 |
JaLCDOI | 10.18926/AMO/57370 |
---|---|
フルテキストURL | 73_5_403.pdf |
著者 | Ando, Akemi| Mitsuhashi, Toshiharu| Honda, Mitsugi| Hanayama, Yoshihisa| Hasegawa, Kou| Obika, Mikako| Kataoka, Hitomi| Otsuka, Fumio| |
抄録 | Osteoporosis increases the risk of bone fractures. It is diagnosed based on an individual’s bone mineral density (BMD) or a fracture without trauma. BMD is usually measured by the dual energy X-ray absorptiometry (DXA) method. Here we investigated factors for the earliest possible prediction of decreased BMD by examining the relationships between patients’ BMD values and changes in the patients’ physical and laboratory values. We retrospectively reviewed the medical records of 149 patients who visited our department in 2014-2015 for a variety of reasons and underwent an area BMD examination by DXA. We analyzed the relationships between decreasing BMD and the patients’ gender, age, body mass index (BMI), medical background, hemoglobin, electrolytes, and thyroid function. Thirty-nine of the patients were diagnosed with osteoporosis based on their T-scores. An adjusted analysis showed that female gender, aging, and increased serum calcium level were significantly related to decreasing femoral BMD, whereas high BMI was associated with an increase in femoral BMD. Collectively the results indicate that for the early detection of low BMD, it is important for general-practice physicians to consider conducting a BMD checkup when treating female and elderly patients with a low BMI and/or elevated serum calcium level. |
キーワード | bone mineral density (BMD) body mass index (BMI) female gender hypercalcemia osteoporosis |
Amo Type | Original Article |
出版物タイトル | Acta Medica Okayama |
発行日 | 2019-10 |
巻 | 73巻 |
号 | 5号 |
出版者 | Okayama University Medical School |
開始ページ | 403 |
終了ページ | 411 |
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 | 31649366 |
Web of Science KeyUT | 000491886600005 |
JaLCDOI | 10.18926/AMO/57369 |
---|---|
フルテキストURL | 73_5_393.pdf |
著者 | Yi Yi Cho Thein| Win, Myitzu| Thuzara, Moe| Matsumoto, Hiroshi| Yamada, Kiyoshi| Kimata, Yoshihiro| Leung, Michael| |
抄録 | Although many surgical centers perform microsurgery routinely in developed countries, performing microsurgery is challenging in resource-poor developing countries, such as Myanmar. With the establishment of educational training programs and the assistance of volunteer plastic surgical teams, local plastic surgeons can learn the techniques of microsurgery and apply them clinically. The purpose of this study was to establish baseline data and define the challenges of performing microsurgery in Yangon General Hospital, Myanmar. Sixty-four patients underwent reconstruction with free flaps from January 2015 to January 2018. All clinical records of these cases were assessed. The number of free flap reconstructions performed increased from 11 in the first year to 24 in the third year. The anterolateral thigh flap was the most commonly used (42%). The most common sites of reconstruction were mandible and intraoral defects. Total flap survival occurred in 58 of 64 patients (89%). The total salvageable flap rate for revision surgery was 66.6%; the successful revision rate was highest in 2017, with fewer complications. The flap salvage rates increased and the operative duration decreased as clinical experience improved. Establishing a microsurgical center requires a strong multidisciplinary team, clinical experience, continuous learning, sensible clinical application, and effective interdepartmental and intradepartmental cooperation. |
キーワード | microsurgery educational programs challenges of microsurgical free flaps reoperation flap salvageable rate |
Amo Type | Original Article |
出版物タイトル | Acta Medica Okayama |
発行日 | 2019-10 |
巻 | 73巻 |
号 | 5号 |
出版者 | Okayama University Medical School |
開始ページ | 393 |
終了ページ | 401 |
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 | 31649365 |
Web of Science KeyUT | 000491886600004 |
JaLCDOI | 10.18926/AMO/57367 |
---|---|
フルテキストURL | 73_5_383.pdf |
著者 | Fu, Li| Nishibori, Masahiro| |
抄録 | High mobility group box-1 (HMGB1) is a non-histone, DNA-binding nuclear protein belonging to the family of damage-associated molecular patterns (DAMPs). HMGB1 has been reported to play an important role during epileptogenesis although the mechanisms of its actions are still not clear. Many hypotheses have been suggested especially about the relationship between HMGB1 and inflammation responses and blood-brain barrier disruption during epileptogenesis. In this review, we will mainly discuss the role of HMGB1 in epileptogenesis. |
キーワード | HMGB1 epileptogenesis inflammation blood-brain barrier |
Amo Type | Review |
出版物タイトル | Acta Medica Okayama |
発行日 | 2019-10 |
巻 | 73巻 |
号 | 5号 |
出版者 | Okayama University Medical School |
開始ページ | 383 |
終了ページ | 386 |
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 | 31649363 |
Web of Science KeyUT | 000491886600002 |