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FullText URL OncoImmunol_8_12_1671760.pdf
Author Sakamoto, Shuichi| Kagawa, Shunsuke| Kuwada, Kazuya| Ito, Atene| Kajioka, Hiroki| Kakiuchi, Yoshihiko| Watanabe, Megumi| Kagawa, Tetsuya| Yoshida, Ryuichi| Kikuchi, Satoru| Kuroda, Shinji| Tazawa, Hiroshi| Fujiwara, Toshiyoshi|
Keywords Gastric cancer tumor-associated macrophages tumor microenvironment peritoneal dissemination
Published Date 2019-10-22
Publication Title OncoImmunology
Volume volume8
Issue issue12
Publisher TAYLOR & FRANCIS
Start Page e1671760
ISSN 2162402X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2019 The Author(s).
File Version publisher
DOI 10.1080/2162402X.2019.1671760
Web of Science KeyUT 000494085400001
Related Url isVersionOf https://doi.org/10.1080/2162402X.2019.1671760
FullText URL EBioMedicine_2017_154.pdf
Author Kunisada, Yuki| Eikawa, Shingo| Tomonobu, Nahoko| Domae, Shohei| Uehara, Takenori| Hori, Shohei| Furusawa, Yukihiro| Hase, Koji| Sasaki, Akira| Udono, Heiichiro|
Keywords Glycolysis Regulatory T cell (Treg) Tumor immunity Tumor microenvironment mTOR
Published Date 2017-10-16
Publication Title EBioMedicine
Volume volume25
Publisher Elsevier Science
Start Page 154
End Page 164
ISSN 23523964
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2017 The Authors.
File Version publisher
PubMed ID 29066174
DOI 10.1016/j.ebiom.2017.10.009
Web of Science KeyUT 000417440500026
Related Url isVersionOf https://doi.org/10.1016/j.ebiom.2017.10.009
FullText URL PlosOne14_1_211505.pdf
Author Miyoshi, Yuichi| Ohtsuki, Takashi| Kashida, Hiromu| Asanuma, Hiroyuki| Watanabe, Kazunori|
Published Date 2019-01-29
Publication Title PLoS One
Volume volume14
Issue issue1
Publisher PUBLIC LIBRARY SCIENCE
Start Page e0211505
ISSN 1932-6203
Content Type Journal Article
language French
OAI-PMH Set 岡山大学
Copyright Holders © 2019 Miyoshi et al.
File Version publisher
PubMed ID 30695081
DOI 10.1371/journal.pone.0211505
Web of Science KeyUT 000457046400041
Related Url isVersionOf https://doi.org/10.1371/journal.pone.0211505
FullText URL IntJMolSci_20_8_1973.pdf
Author Nakano, Keisuke| Takabatake, Kiyofumi| Kawai, Hotaka| Yoshida, Saori| Maeda, Hatsuhiko| Kawakami, Toshiyuki| Nagatsuka, Hitoshi|
Keywords cell differentiation epithelial-mesenchymal interaction immunohistochemistry malignant transformation notch signaling odontogenic tumor pleomorphic adenoma
Published Date 2019-04-23
Publication Title International Journal of Molecular Sciences
Volume volume20
Issue issue8
Publisher MDPI
Start Page 1973
ISSN 14220067
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2019 by the authors.
File Version publisher
PubMed ID 31018488
DOI 10.3390/ijms20081973
Web of Science KeyUT 000467648700171
Related Url isVersionOf https://doi.org/10.3390/ijms20081973
FullText URL Epilepsia_49_3_521.pdf
Author Ohmori, Iori| Ouchida, Mamoru| Kobayashi, Katsuhiro| Jitsumori, Yoshimi| Inoue, Takushi| Shimizu, Kenji| Matsui, Hideki| Ohtsuka, Yoko| Maegaki, Yoshihiro|
Keywords Rasmussen encephalitis SCN1A genetic-environmental interaction
Published Date 2007-11-21
Publication Title Epilepsia
Volume volume49
Issue issue3
Publisher Blackwell
Start Page 521
End Page 526
ISSN 0013-9580
NCID AA00180597
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version author
PubMed ID 18031552
DOI 10.1111/j.1528-1167.2007.01411.x
Web of Science KeyUT 000253477800020
Related Url isVersionOf https://doi.org/10.1111/j.1528-1167.2007.01411.x
FullText URL AnnGastroenterolSurg_3_4_396.pdf
Author Fujiwara, Toshiyoshi|
Keywords adenovirus clinical trial esophageal cancer radiotherapy telomerase
Published Date 2019-07-05
Publication Title Annals of gastroenterological surgery
Volume volume3
Issue issue4
Publisher John Wiley & Sons
Start Page 396
End Page 404
ISSN 24750328
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
Copyright Holders © 2019 The Authors
File Version publisher
PubMed ID 31346579
DOI 10.1002/ags3.12270
Web of Science KeyUT 000475745100009
Related Url isVersionOf https://doi.org/10.1002/ags3.12270
FullText URL CellRep_28_5_1362.pdf
Author Abe, Fumitaka| Haque, Emdadul| Hisano, Hiroshi| Tanaka, Tsuyoshi| Kamiya, Yoko| Mikami, Masafumi| Kawaura, Kanako| Endo, Masaki| Onishi, Kazumitsu| Hayashi, Takeshi| Sato, Kazuhiro|
Keywords CRISPR/Cas9 Qsd1 multiple mutation seed dormancy wheat
Published Date 2019-07-30
Publication Title Cell Reports
Volume volume28
Issue issue5
Publisher Cell Press
Start Page 1362
End Page 1369
ISSN 22111247
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version publisher
PubMed ID 31365876
DOI 10.1016/j.celrep.2019.06.090
Related Url isVersionOf https://doi.org/10.1016/j.celrep.2019.06.090
FullText URL K0006059_abstract_review.pdf K0006059_fulltext.pdf
Author SAID MOHAMED ABDELSABOUR AFIFY|
Published Date 2019-09-25
Content Type Thesis or Dissertation
Grant Number 甲第6059号
Granted Date 2019-09-25
Thesis Type Doctor of Philosophy
Grantor 岡山大学
language English
FullText URL K0006044_abstract_review.pdf.pdf summary.pdf.pdf fulltext.pdf.pdf
Author Kunitomo, Yuri|
Published Date 2019-09-25
Content Type Thesis or Dissertation
Grant Number 甲第6044号
Granted Date 2019-09-25
Thesis Type Doctor of Philosophy in Dental Science
Grantor 岡山大学
language English
FullText URL K0006040_abstract_review.pdf K0006040_fulltext.pdf K0006040_Other2(Suppl Figure).pdf
Author Mitsui, Yosuke|
Published Date 2019-09-25
Content Type Thesis or Dissertation
Grant Number 甲第6040号
Granted Date 2019-09-25
Thesis Type Doctor of Philosophy in Medical Science
Grantor 岡山大学
language English
FullText URL K0006037_abstract_review.pdf K0006037_fulltext.pdf K0006037_other_1 supplementary figure.pdf K0006037_other_2 supplementary material.pdf
Author Katsura, Yuki|
Published Date 2019-09-25
Content Type Thesis or Dissertation
Grant Number 甲第6037号
Granted Date 2019-09-25
Thesis Type Doctor of Philosophy in Medical Science
Grantor 岡山大学
language English
FullText URL K0006034_abstract_review.pdf K0006034_fulltext.pdf
Author Nishimura, Yoshito|
Published Date 2019-09-25
Content Type Thesis or Dissertation
Grant Number 甲第6034号
Granted Date 2019-09-25
Thesis Type Doctor of Philosophy in Medical Science
Grantor 岡山大学
language English
FullText URL K0006031_abstract_review.pdf K0006031_fulltext.pdf
Author Iwata, Nahoko|
Published Date 2019-09-25
Content Type Thesis or Dissertation
Grant Number 甲第6031号
Granted Date 2019-09-25
Thesis Type Doctor of Philosophy in Medical Science
Grantor 岡山大学
language English
FullText URL K0006024_abstract_review.pdf K0006024_fulltext.pdf K0006024_other_1 figure.pdf K0006024_other_2 Supplementary figures and legends.pdf
Author Watanabe, Shin-ichiro|
Published Date 2019-09-25
Content Type Thesis or Dissertation
Grant Number 甲第6024号
Granted Date 2019-09-25
Thesis Type Doctor of Philosophy in Medical Science
Grantor 岡山大学
language English
FullText URL fcell_2019_00160_p.pdf fcell_2019_00160_a.pdf
Author 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 |
Keywords Golgi golgins glycosylation endoplasmic reticulum electron tomography
Published Date 2019-08-27
Publication Title Frontiers in Cell and Developmental Biology
Volume volume7
Start Page 160
ISSN 2296634X
Content Type Journal Article
language English
OAI-PMH Set 岡山大学
File Version publisher
PubMed ID 31544102
DOI 10.3389/fcell.2019.00160
Related Url isVersionOf https://doi.org/10.3389/fcell.2019.00160
JaLCDOI 10.18926/AMO/57379
FullText URL 73_5_469.pdf
Author Yamasaki, Satoshi| Kada, Akiko| Nagai, Hirokazu| Yoshida, Isao| Choi, Ilseung| Saito, Akiko M.| Iwasakia, Hiromi|
Abstract 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.
Keywords peripheral T-cell lymphoma not otherwise specified angioimmunoblastic T-cell lymphoma gemcitabine cisplatin, romidepsin
Amo Type Clinical Study Protocol
Publication Title Acta Medica Okayama
Published Date 2019-10
Volume volume73
Issue issue5
Publisher Okayama University Medical School
Start Page 469
End Page 474
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31649375
Web of Science KeyUT 000491886600014
JaLCDOI 10.18926/AMO/57377
FullText URL 73_5_457.pdf
Author Iwamuro, Masaya| Takahara, Masahiro| Yamazaki, Tatsuhiro| Tanaka, Takehiro| Kondo, Yoshitaka| Hiraoka, Sakiko| Okada, Hiroyuki|
Abstract 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.
Keywords colonoscopy colonic neoplasms granulation polyp
Amo Type Case Report
Publication Title Acta Medica Okayama
Published Date 2019-10
Volume volume73
Issue issue5
Publisher Okayama University Medical School
Start Page 457
End Page 461
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31649373
Web of Science KeyUT 000491886600012
JaLCDOI 10.18926/AMO/57374
FullText URL 73_5_433.pdf
Author Tamada, Shoko| Mitsui, Takashi| Ohira, Akiko| Tani, Kazumasa| Maki, Jota| Eguchi, Takeshi| Eto, Eriko| Hayata, Kei| Masuyama, Hisashi|
Abstract 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.
Keywords preeclampsia (pro)renin (pro)renin receptor endothelin-1 HTR-8/SVneo
Amo Type Original Article
Publication Title Acta Medica Okayama
Published Date 2019-10
Volume volume73
Issue issue5
Publisher Okayama University Medical School
Start Page 433
End Page 440
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31649370
Web of Science KeyUT 000491886600009
JaLCDOI 10.18926/AMO/57367
FullText URL 73_5_383.pdf
Author Fu, Li| Nishibori, Masahiro|
Abstract 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.
Keywords HMGB1 epileptogenesis inflammation blood-brain barrier
Amo Type Review
Publication Title Acta Medica Okayama
Published Date 2019-10
Volume volume73
Issue issue5
Publisher Okayama University Medical School
Start Page 383
End Page 386
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31649363
Web of Science KeyUT 000491886600002
JaLCDOI 10.18926/AMO/57366
FullText URL 73_5_379.pdf
Author Wake, Hidenori|
Abstract Histidine-rich glycoprotein (HRG) is a 75 kDa glycoprotein synthesized in the liver whose plasma concentration is 100-150 μg/ml. HRG has been shown to modulate sepsis-related biological reactions by binding to several substances and cells, including heparin, factor XII, fibrinogen, thrombospondin, plasminogen, C1q, IgG, heme, LPS, dead cells, bacteria, and fungi. Therefore, reduction of plasma HRG levels in sepsis leads to dysregulation of coagulation, fibrinolysis, and immune response, resulting in disseminated intravascular coagulation and multiple organ failure. This review summarizes the binding and functional properties of HRG in sepsis.
Keywords htidine-rich glycoprotein septic pathogenesis immunothrombosis
Amo Type Review
Publication Title Acta Medica Okayama
Published Date 2019-10
Volume volume73
Issue issue5
Publisher Okayama University Medical School
Start Page 379
End Page 382
ISSN 0386-300X
NCID AA00508441
Content Type Journal Article
language English
Copyright Holders CopyrightⒸ 2019 by Okayama University Medical School
File Version publisher
Refereed True
PubMed ID 31649362
Web of Science KeyUT 000491886600001