検索結果 - 岡山大学学術成果リポジトリ

The Genotypic and Phenotypic Characteristics Contributing to Flomoxef Sensitivity in Clinical Isolates of ESBL-Producing E. coli Strains from Urinary Tract Infections

フルテキストURL	fulltext.pdf
著者	Sakaeda, Kazuma\| Sadahira, Takuya\| Maruyama, Yuki\| Iwata, Takehiro\| Watanabe, Masami\| Wada, Koichiro\| Araki, Motoo\|
キーワード	antimicrobial resistance Escherichia coli urinary tract infections flomoxef ST131
発行日	2023-03-06
出版物タイトル	Antibiotics
巻	12巻
号	3号
出版者	MDPI
開始ページ	522
ISSN	2079-6382
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	© 2023 by the authors.
論文のバージョン	publisher
PubMed ID	36978389
DOI	10.3390/antibiotics12030522
Web of Science KeyUT	000952995400001
関連URL	isVersionOf https://doi.org/10.3390/antibiotics12030522

SPRED2: A Novel Regulator of Epithelial-Mesenchymal Transition and Stemness in Hepatocellular Carcinoma Cells

フルテキストURL	fulltext.pdf
著者	Gao, Tong\| Yang, Xu\| Fujisawa, Masayoshi\| Ohara, Toshiaki\| Wang, Tianyi\| Tomonobu, Nahoko\| Sakaguchi, Masakiyo\| Yoshimura, Teizo\| Matsukawa, Akihiro\|
キーワード	cancer stem cells epithelial-mesenchymal transition ERK1/2-MAPK tumorigenesis
発行日	2023-03-05
出版物タイトル	International Journal of Molecular Sciences
巻	24巻
号	5号
出版者	MDPI
開始ページ	4996
ISSN	1422-0067
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	© 2023 by the authors.
論文のバージョン	publisher
PubMed ID	36902429
DOI	10.3390/ijms24054996
Web of Science KeyUT	000947675000001
関連URL	isVersionOf https://doi.org/10.3390/ijms24054996

Autophagy as a potential mechanism underlying the biological effect of 1,25-Dihydroxyvitamin D3 on periodontitis: a narrative review

フルテキストURL	fulltext.pdf
著者	Chen, Xiaoting\| Arias, Zulema\| Omori, Kazuhiro\| Yamamoto, Tadashi\| Shinoda-Ito, Yuki\| Takashiba, Shogo\|
キーワード	Vitamin D Autophagy Periodontitis Epithelial barrier Immunity Inflammation Alveolar bone loss
発行日	2023-02-13
出版物タイトル	BMC Oral Health
巻	23巻
号	1号
出版者	BMC
開始ページ	90
ISSN	1472-6831
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	© The Author(s) 2023.
論文のバージョン	publisher
PubMed ID	36782172
DOI	10.1186/s12903-023-02802-9
Web of Science KeyUT	000937967900001
関連URL	isVersionOf https://doi.org/10.1186/s12903-023-02802-9

Effect of a Cyclooxygenase-2 Inhibitor in Combination with (−)-Epigallocatechin Gallate or Polyphenon E on Cisplatin-Induced Lung Tumorigenesis in A/J Mice

JaLCDOI	10.18926/AMO/64363
フルテキストURL	77_1_65.pdf
著者	Sato, Ken\| Takigawa, Nagio\| Kubo, Toshio\| Katayama, Hideki\| Kishino, Daizo\| Okada, Toshiaki\| Hisamoto, Akiko\| Mimoto, Junko\| Ochi, Nobuaki\| Yoshino, Tadashi\| Ueoka, Hiroshi\| Tanimoto, Mitsune\| Maeda, Yoshionobu\| Kiura, Katsuyuki\|
抄録	We investigated the effects of celecoxib combined with (−)-epigallocatechin-3-gallate (EGCG) or polyphenon E in a cisplatin-induced lung tumorigenesis model. Four-week-old female A/J mice were divided into seven groups: (i) Control, (ii) 150 mg/kg celecoxib (150Cel), (iii) 1,500 mg/kg celecoxib (1500Cel), (iv) EGCG+150 mg/kg celecoxib (EGCG+150Cel), (v) EGCG+1,500 mg/kg celecoxib (EGCG+1500Cel), (vi) polyphenon E+150 mg/kg celecoxib (PolyE+150Cel), and (vii) polyphenon E+1,500 mg/kg celecoxib (PolyE+1500Cel). All mice were administered cisplatin (1.62 mg/kg of body weight, i.p.) 1×/week for 10 weeks and sacrificed at week 30; the numbers of tumors on the lung surface were then determined. The tumor incidence and multiplicity (no. of tumors/mouse, mean±SD) were respectively 95% and 2.15±1.50 in Control, 95% and 2.10±1.29 in 150Cel, 86% and 1.67±1.20 in 1500Cel, 71% and 1.38±1.24 in EGCG+150Cel, 67% and 1.29±1.38 in EGCG+1500Cel, 80% and 1.95±1.36 in PolyE+150Cel, and 65% and 1.05±0.10 in PolyE+1500Cel. The combination of high-dose celecoxib with EGCG or polyphenon E significantly reduced multiplicity in cisplatin-induced lung tumors.
キーワード	celecoxib cisplatin EGCG lung tumor polyphenon E
Amo Type	Original Article
出版物タイトル	Acta Medica Okayama
発行日	2023-02
巻	77巻
号	1号
出版者	Okayama University Medical School
開始ページ	65
終了ページ	70
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 Ⓒ 2023 by Okayama University Medical School
論文のバージョン	publisher
査読	有り
PubMed ID	36849147
Web of Science KeyUT	000952992100004

Extracellular Vesicles: New Classification and Tumor Immunosuppression

フルテキストURL	fulltext.pdf
著者	Sheta, Mona\| Taha, Eman A.\| Lu, Yanyin\| Eguchi, Takanori\|
キーワード	extracellular vesicle exosome autophagy amphisome matrix vesicle cellular communication tumor microenvironment immunosuppression immune evasion therapy resistance
発行日	2023-01-10
出版物タイトル	Biology
巻	12巻
号	1号
出版者	MDPI
開始ページ	110
ISSN	2079-7737
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	© 2023 by the authors.
論文のバージョン	publisher
PubMed ID	36671802
DOI	10.3390/biology12010110
Web of Science KeyUT	000914496600001
関連URL	isVersionOf https://doi.org/10.3390/biology12010110

Cycloartenyl Ferulate Is the Predominant Compound in Brown Rice Conferring Cytoprotective Potential against Oxidative Stress-Induced Cytotoxicity

フルテキストURL	fulltext.pdf
著者	Wu, Hongyan\| Nakamura, Toshiyuki\| Guo, Yingnan\| Matsumoto, Riho\| Munemasa, Shintaro\| Murata, Yoshiyuki\| Nakamura, Yoshimasa\|
キーワード	cycloartenyl ferulate antioxidative effect cytoprotective potential heme oxygenase-1 nuclear factor erythroid 2-related factor 2
発行日	2023-01-03
出版物タイトル	International Journal Of Molecular Sciences
巻	24巻
号	1号
出版者	MDPI
開始ページ	822
ISSN	1422-0067
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	© 2023 by the authors.
論文のバージョン	publisher
PubMed ID	36614263
DOI	10.3390/ijms24010822
Web of Science KeyUT	000910246300001
関連URL	isVersionOf https://doi.org/10.3390/ijms24010822

Oligoarginine-Conjugated Peptide Foldamers Inhibiting Vitamin D Receptor-Mediated Transcription

フルテキストURL	fulltext.pdf
著者	Takyo, Mami\| Sato, Yumi\| Hirata, Naoya\| Tsuchiya, Keisuke\| Ishida, Hiroaki\| Kurohara, Takashi\| Yanase, Yuta\| Ito, Takahito\| Kanda, Yasunari\| Yamamoto, Keiko\| Misawa, Takashi\| Demizu, Yosuke\|
発行日	2022-12-20
出版物タイトル	ACS Omega
巻	7巻
号	50号
出版者	American Chemical Society
開始ページ	46573
終了ページ	46582
ISSN	2470-1343
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	© 2022 The Authors.
論文のバージョン	publisher
PubMed ID	36570290
DOI	10.1021/acsomega.2c05409
Web of Science KeyUT	000904000700001
関連URL	isVersionOf https://doi.org/10.1021/acsomega.2c05409

Crystal structures of photosystem II from a cyanobacterium expressing psbA2 in comparison to psbA3 reveal differences in the D1 subunit

フルテキストURL	fulltext.pdf
著者	Nakajima, Yoshiki\| Ugai-Amo, Natsumi\| Tone, Naoki\| Nakagawa, Akiko\| Iwai, Masako\| Ikeuchi, Masahiko\| Sugiura, Miwa\| Suga, Michihiro\| Jian-Ren, Shen\|
発行日	2022-12
出版物タイトル	Journal Of Biological Chemistry
巻	298巻
号	12号
出版者	Elsevier
開始ページ	102668
ISSN	1083-351X
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	© 2022 THE AUTHORS.
論文のバージョン	publisher
PubMed ID	36334624
DOI	10.1016/j.jbc.2022.102668
Web of Science KeyUT	000897992300012
関連URL	isVersionOf https://doi.org/10.1016/j.jbc.2022.102668

Chemopreventive effects and anti-tumorigenic mechanisms of Actinidia arguta, known as sarunashi in Japan toward 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)- induced lung tumorigenesis in a/J mouse

フルテキストURL	fulltext20221227-2.pdf
著者	Takata, Jun\| Miyake, Naoko\| Saiki, Yusuke\| Tada, Misako\| Sasaki, Kensuke\| Kubo, Toshio\| Kiura, Katsuyuki\| Arimoto-Kobayashi, Sakae\|
キーワード	Akt signal transduction Lung tumorigenesis Anti-mutagenesis DNA methylation Tobacco-specific nitrosamine Isoquercetin
発行日	2022-12-09
出版物タイトル	Genes and Environment
巻	44巻
号	1号
出版者	Springer Science and Business Media LLC
開始ページ	26
ISSN	1880-7062
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	© The Author(s) 2022.
論文のバージョン	publisher
PubMed ID	36494703
DOI	10.1186/s41021-022-00255-0
Web of Science KeyUT	000896571200001
関連URL	isVersionOf https://doi.org/10.1186/s41021-022-00255-0

Defect-free and crystallinity-preserving ductile deformation in semiconducting Ag2S

フルテキストURL	fulltext.pdf
著者	Misawa, Masaaki\| Hokyo, Hinata\| Fukushima, Shogo\| Shimamura, Kohei\| Koura, Akihide\| Shimojo, Fuyuki\| Kalia, Rajiv K.\| Nakano, Aiichiro\| Vashishta, Priya\|
発行日	2022-11-14
出版物タイトル	Scientific Reports
巻	12巻
号	1号
出版者	Nature Portfolio
開始ページ	19458
ISSN	2045-2322
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	© The Author(s) 2022
論文のバージョン	publisher
PubMed ID	36376359
DOI	10.1038/s41598-022-24004-z
Web of Science KeyUT	000883823800060
関連URL	isVersionOf https://doi.org/10.1038/s41598-022-24004-z

Optical collection of extracellular vesicles in a culture medium enhanced by interactions with gold nanoparticles

フルテキストURL	fulltext20221122-2.pdf
著者	Tani, Yumeki\| Ochiai, Kenta\| Kaneta, Takashi\|
キーワード	Optical force Extracellular vesicle exosome Gold nanoparticle Optical trapping
備考	This version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature’s AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: http://dx.doi.org/10.1007/s44211-022-00207-2\| This full-text will be available in November 2023.\|
発行日	2022-11-05
出版物タイトル	Analytical Sciences
巻	39巻
号	5号
出版者	Springer Science and Business Media LLC
開始ページ	643
終了ページ	651
ISSN	0910-6340
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	© 2022, The Author(s), under exclusive licence to The Japan Society for Analytical Chemistry
論文のバージョン	author
PubMed ID	36334243
DOI	10.1007/s44211-022-00207-2
Web of Science KeyUT	000879131000001
関連URL	isVersionOf https://doi.org/10.1007/s44211-022-00207-2

Footedness for scratching itchy eyes in rodents

フルテキストURL	fulltext20221117-1.pdf
著者	Katayama, Yukitoshi\| Miura, Ayane\| Sakamoto, Tatsuya\| Takanami, Keiko\| Sakamoto, Hirotaka\|
キーワード	itchy eyes histamine gastrin-releasing peptide receptor footedness
発行日	2022-10-19
出版物タイトル	Proceedings of the Royal Society B: Biological Sciences
巻	289巻
号	1985号
出版者	The Royal Society
開始ページ	20221126
ISSN	0962-8452
NCID	AA00786976
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	© 2022 The Author(s)
論文のバージョン	author
PubMed ID	36259204
DOI	10.1098/rspb.2022.1126
Web of Science KeyUT	000872392900003
関連URL	isVersionOf https://doi.org/10.1098/rspb.2022.1126

Graphene Oxide-based Endodontic Sealer: An in Vitro Study

JaLCDOI	10.18926/AMO/64122
フルテキストURL	76_6_715.pdf
著者	Mohammed Zahedul Islam Nizami\| Gorduysus, Melahat\| Shinoda-Ito, Yuki\| Yamamoto, Tadashi\| Nishina, Yuta\| Takashiba, Shogo\| Arias, Zulema\|
抄録	The failure of endodontic treatment is directly associated with microbial infection in the root canal or periapical areas. An endodontic sealer that is both bactericidal and biocompatible is essential for the success of root canal treatments. This is one of the vital issues yet to be solved in clinical dental practice. This in vitro study assessed the effectiveness of graphene oxide (GO) composites GO-CaF2 and GO-Ag-CaF2 as endodontic sealer materials. Dentin slices were coated with either the GO-based composites or commonly used root canal sealers (non-eugenol zinc oxide sealer). The coated slices were treated in 0.9% NaCl, phosphate-buffered saline (PBS), and simulated body fluid (SBF) at 37˚C for 24 hours to compare their sealing effect on the dentin surface. In addition, the radiopacity of these composites was examined to assess whether they complied with the requirements of a sealer for good radiographic visualization. Scanning electron microscopy showed the significant sealing capability of the composites as coating materials. Radiographic images confirmed their radiopacity. Mineral deposition indicated their bioactivity, especially of GO-Ag-CaF2, and thus it is potential for regenerative application. They were both previously shown to be bactericidal to oral microbes and cytocompatible with host cells. With such a unique assemblage of critical properties, these GO-based composites show promise as endodontic sealers for protection against reinfection in root canal treatment and enhanced success in endodontic treatment overall.
キーワード	bioactive sealer graphene oxide mineral deposition antimicrobial activity radiopacity
Amo Type	Original Article
出版物タイトル	Acta Medica Okayama
発行日	2022-12
巻	76巻
号	6号
出版者	Okayama University Medical School
開始ページ	715
終了ページ	721
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 Ⓒ 2022 by Okayama University Medical School
論文のバージョン	publisher
査読	有り
PubMed ID	36549774
Web of Science KeyUT	000905195100012

Fetal Cerebellar Growth Curves Based on Biomathematics in Normally Developing Japanese Fetuses and Fetuses with Trisomy 18

JaLCDOI	10.18926/AMO/64114
フルテキストURL	76_6_645.pdf
著者	Tada, Katsuhiko\| Miyagi, Yasunari\| Komatsu, Reina\| Okimoto, Naoki\| Tsukahara, Saya\| Tateishi, Yoko\| Ooka, Naomi\| Yoshida, Mizuho\| Kumazawa, Kazumasa\|
抄録	We used biomathematics to describe and compare cerebellar growth in normally developing and trisomy 18 Japanese fetuses. This retrospective study included 407 singleton pregnancies with fetuses at 14-39 weeks of gestation and 33 fetuses with trisomy 18 at 17-35 weeks. We used ultrasonography to measure fetal transverse cerebellar diameter (TCD) and anteroposterior cerebellar diameter (APCD). We hypothesized that cerebellar growth is proportional to cerebellar length at any given time point. We determined the formula L(t) ≒Keat+r, where e is Napier’s number, t is time, L is cerebellar length, and a, K, and r are constants. We then obtained regression functions for each TCD and APCD in all fetuses. The regression equations for TCD and APCD values in normal fetuses, expressed as exponential functions, were TCD(t)=27.85e0.02788t−28.62 (mm) (adjusted R2=0.997), and APCD(t)=324.29e0.00286t−322.62 (mm) (adjusted R2=0.995). These functions indicated that TCD and APCD grew at constant rates of 2.788%/week and 0.286%/week, respectively, throughout gestation. TCD (0.0153%/week) and APCD (0.000430%/week) grew more slowly in trisomy 18 fetuses. This study demonstrates the potential of biomathematics in clinical research and may aid in biological understanding of fetal cerebellar growth.
キーワード	biomathematics cerebellum fetus trisomy 18 syndrome ultrasonography
Amo Type	Original Article
出版物タイトル	Acta Medica Okayama
発行日	2022-12
巻	76巻
号	6号
出版者	Okayama University Medical School
開始ページ	645
終了ページ	650
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 Ⓒ 2022 by Okayama University Medical School
論文のバージョン	publisher
査読	有り
PubMed ID	36549766
Web of Science KeyUT	000905195100004

MiR-338-3p Is a Biomarker in Neonatal Acute Respiratory Distress Syndrome (ARDS) and Has Roles in the Inflammatory Response of ARDS Cell Models

JaLCDOI	10.18926/AMO/64113
フルテキストURL	76_6_635.pdf
著者	Zhang, Cuicui\| Ji, Yanan\| Wang, Qin\| Ruan, Lianying\|
抄録	To investigate the association between serum miR-338-3p levels and neonatal acute respiratory distress syndrome (ARDS) and its mechanism. The relative miR-338-3p expression in serum was detected by quantitative real-time RT-PCR. Interleukin-1beta (IL-1β), IL-6, and tumor necrosis factor-alpha (TNF-α) levels were detected by ELISAs. A receiver operating characteristic (ROC) curve analysis of serum miR-338-3p evaluated the diagnosis of miR-338-3p in neonatal ARDS. Pearson’s correlation analysis evaluated the correlation between serum miR-338-3p and neonatal ARDS clinical factors. Flow cytometry evaluated apoptosis, and a CCK-8 assay assessed cell viability. A luciferase assay evaluated the miR-338-3p/AKT3 relationship. The miR- 338-3p expression was decreased in neonatal ARDS patients and in lipopolysaccharide (LPS)-treated cells. The ROC curve showed the accuracy of miR-338-3p for evaluating neonatal ARDS patients. The correlation analysis demonstrated that miR-338-3p was related to PRISM-III, PaO2/FiO2, oxygenation index, IL-1β, IL-6, and TNF-α in neonatal ARDS patients. MiR-338-3p overexpression inhibited the secretion of inflammatory components, stifled cell apoptosis, and LPS-induced advanced cell viability. The double-luciferase reporter gene experiment confirmed that miR-338-3p negatively regulates AKT3 mRNA expression. Serum miR-338-3p levels were related to the diagnosis and severity of neonatal ARDS, which may be attributed to its regulatory effect on inflammatory response in ARDS.
キーワード	miR-338-3p AKT3 neonatal ARDS inflammation diagnosis
Amo Type	Original Article
出版物タイトル	Acta Medica Okayama
発行日	2022-12
巻	76巻
号	6号
出版者	Okayama University Medical School
開始ページ	635
終了ページ	643
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 Ⓒ 2022 by Okayama University Medical School
論文のバージョン	publisher
査読	有り
PubMed ID	36549765
Web of Science KeyUT	000905195100003

Current Insights into Mesenchymal Signatures in Glioblastoma

JaLCDOI	10.18926/AMO/64024
フルテキストURL	76_5_489.pdf
著者	Matsumoto, Yuji\| Ichikawa, Tomotsugu\| Kurozumi, Kazuhiko\| Date, Isao\|
抄録	Glioblastoma (GBM) is a fatal primary malignant brain tumor in adults. Despite decades of research, the prognosis for GBM patients is still disappointing. One major reason for the intense therapeutic resistance of GBM is inter- and intra-tumor heterogeneity. GBM-intrinsic transcriptional profiling has suggested the presence of at least three subtypes of GBM: the proneural, classic, and mesenchymal subtypes. The mesenchymal subtype is the most aggressive, and patients with the mesenchymal subtype of primary and recurrent tumors tend to have a worse prognosis compared with patients with the other subtypes. Furthermore, GBM can shift from other subtypes to the mesenchymal subtype over the course of disease progression or recurrence. This phenotypic transition is driven by diverse tumor-intrinsic molecular mechanisms or microenvironmental factors. Thus, better understanding of the plastic nature of mesenchymal transition in GBM is pivotal to developing new therapeutic strategies. In this review, we provide a comprehensive overview of the current understanding of the elements involved in the mesenchymal transition of GBM and discuss future perspectives.
キーワード	glioma glioblastoma mesenchymal subtype mesenchymal transition heterogeneity
Amo Type	Review
出版物タイトル	Acta Medica Okayama
発行日	2022-10
巻	76巻
号	5号
出版者	Okayama University Medical School
開始ページ	489
終了ページ	502
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 Ⓒ 2022 by Okayama University Medical School
論文のバージョン	publisher
査読	有り
PubMed ID	36352795
Web of Science KeyUT	000884907100001

Novel Self-Forming Nanosized DDS Particles for BNCT: Utilizing A Hydrophobic Boron Cluster and Its Molecular Glue Effect

フルテキストURL	fulltext.pdf
著者	Fithroni, Abdul Basith\| Kobayashi, Kazuko\| Uji, Hirotaka\| Ishimoto, Manabu\| Akehi, Masaru\| Ohtsuki, Takashi\| Matsuura, Eiji\|
キーワード	boron neutron capture therapy (BNCT) biologically self-degradable amphipathic polymer (Lactosome) hydrophobic boron cluster carborane isomers or o-carborane alkylated derivatives molecular glue effect
発行日	2022-10-21
出版物タイトル	CELLS
巻	11巻
号	20号
出版者	MDPI
開始ページ	3307
ISSN	2073-4409
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	© 2022 by the authors.
論文のバージョン	publisher
PubMed ID	36291173
DOI	10.3390/cells11203307
Web of Science KeyUT	000872497500001
関連URL	isVersionOf https://doi.org/10.3390/cells11203307

Time-series transcriptome of Brachypodium distachyon during bacterial flagellin-induced pattern-triggered immunity

フルテキストURL	fulltext.pdf
著者	Ogasahara, Tsubasa\| Kouzai, Yusuke\| Watanabe, Megumi\| Takahashi, Akihiro\| Takahagi, Kotaro\| Kim, June-Sik\| Matsui, Hidenori\| Yamamoto, Mikihiro\| Toyoda, Kazuhiro\| Ichinose, Yuki\| Mochida, Keiichi\| Noutoshi, Yoshiteru\|
キーワード	Brachypodium distachyon monocotyledonous plant microbe-associated molecular pattern time-series transcriptome analysis reactive oxygen species pattern-triggered immunity
発行日	2022-09-15
出版物タイトル	Frontiers In Plant Science
巻	13巻
出版者	Frontiers Media S.A.
開始ページ	1004184
ISSN	1664-462X
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	© 2022 Ogasahara, Kouzai, Watanabe, Takahashi, Takahagi, Kim, Matsui, Yamamoto, Toyoda, Ichinose, Mochida and Noutoshi.
論文のバージョン	publisher
PubMed ID	36186055
DOI	10.3389/fpls.2022.1004184
Web of Science KeyUT	000863600900001
関連URL	isVersionOf https://doi.org/10.3389/fpls.2022.1004184

Cnm of Streptococcus mutans is important for cell surface structure and membrane permeability

フルテキストURL	fulltext.pdf
著者	Naka, Shuhei\| Matsuoka, Daiki\| Goto, Kana\| Misaki, Taro\| Nagasawa, Yasuyuki\| Ito, Seigo\| Nomura, Ryota\| Nakano, Kazuhiko\| Matsumoto-Nakano, Michiyo\|
キーワード	Streptococcus mutans collagen-binding protein membrane permeability cell structure RNA-seq
発行日	2022-09-13
出版物タイトル	Frontiers In Cellular And Infection Microbiology
巻	12巻
出版者	Frontiers Media S.A.
開始ページ	994014
ISSN	2235-2988
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	© 2022 Naka, Matsuoka, Goto, Misaki, Nagasawa, Ito, Nomura, Nakano and Matsumoto-Nakano.
論文のバージョン	publisher
PubMed ID	36176579
DOI	10.3389/fcimb.2022.994014
Web of Science KeyUT	000861324100001
関連URL	isVersionOf https://doi.org/10.3389/fcimb.2022.994014

Effects of Wnt-β-Catenin Signaling and Sclerostin on the Phenotypes of Rat Pheochromocytoma PC12 Cells

フルテキストURL	fulltext20220921-2.pdf
著者	Morimoto, Eisaku\| Inagaki, Kenichi\| Komatsubara, Motoshi\| Terasaka, Tomohiro\| Itoh, Yoshihiko\| Fujisawa, Satoshi\| Sasaki, Erika\| Nishiyama, Yuki\| Hara, Takayuki\| Wada, Jun\|
キーワード	Wnt-β-catenin signaling sclerostin catecholamine PPGL PC12
発行日	2022-8-5
出版物タイトル	Journal of the Endocrine Society
巻	6巻
号	10号
出版者	The Endocrine Society
開始ページ	1
終了ページ	8
ISSN	2472-1972
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	© The Author(s) 2022.
論文のバージョン	publisher
PubMed ID	36042979
DOI	10.1210/jendso/bvac121
Web of Science KeyUT	000845523100003
関連URL	isVersionOf https://doi.org/10.1210/jendso/bvac121