result 2923 件
FullText URL | fulltext.pdf |
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Author | Kataoka, Takahiro| Naoe, Shota| Murakami, Kaito| Fujimoto, Yuki| Yukimine, Ryohei| Tanaka, Ayumi| Yamaoka, Kiyonori| |
Keywords | autoimmune diseases cytokine antioxidant function lipopolysaccharide radon inhalation |
Published Date | 2022-08-26 |
Publication Title | International Journal Of Environmental Research And Public Health |
Volume | volume19 |
Issue | issue17 |
Publisher | MDPI |
Start Page | 10632 |
ISSN | 1660-4601 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 by the authors. |
File Version | publisher |
PubMed ID | 36078348 |
DOI | 10.3390/ijerph191710632 |
Web of Science KeyUT | 000851073300001 |
Related Url | isVersionOf https://doi.org/10.3390/ijerph191710632 |
JaLCDOI | 10.18926/AMO/63906 |
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FullText URL | 76_4_465.pdf |
Author | Bekku, Kensuke| Tsugawa, Takuji| Tsuboi, Kazuma| Noda, Gaku| Inoue, Yousuke| Murao, Wataru| Ebara, Shin| |
Abstract | We aimed to identify the role of first-line monotherapy with vascular endothelial growth factor receptor tyrosine kinase inhibitors (VEGFR-TKI) in patients with metastatic RCC. Eligible patients were categorized into three groups (favorable, intermediate, and poor risk) according to the International Metastatic RCC Database Consortium risk criteria. Overall survival (OS) was the primary endpoint. Survival was compared using the log-rank test. A total of 108 patients were retrospectively analyzed. The numbers of patients in the favorable-, intermediate-, and poor-risk groups were 32 (30%), 66 (61%), and 10 (9%), repestively. The median OS values in the entire cohort was 36 months (95% confidence interval [CI] 29-53). The median OS in the favorable, intermediate, and poor risk groups were 94 months (95% CI: 43-Not reached), 30 months (95% CI: 20-38), and 8 months (95% CI: 0-Not reached), respectively (p<0.05). Prior nephrectomy, clear cell histology, clinical T stage ≤2, no metastasis at the time of diagnosis, nivolumab beyond first-line therapy, and objective response to VEGFR-TKIs were factors significantly prolonging OS on univariate analysis. VEGFR-TKI monotherapy as first-line therapy was an effective treatment option for patients with metastatic clear cell RCC with favorable risk. |
Keywords | metastatic renal cell carcinoma molecular-targeted therapy immuno-checkpoint inhibitor real-world setting |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2022-08 |
Volume | volume76 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 465 |
End Page | 472 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
Copyright Holders | Copyright Ⓒ 2022 by Okayama University Medical School |
File Version | publisher |
Refereed | True |
PubMed ID | 36123162 |
JaLCDOI | 10.18926/AMO/63905 |
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FullText URL | 76_4_457.pdf |
Author | Sun, Weiying| Hasebe, Satoshi| |
Abstract | To clarify the preventive effects of 0.01% atropine eye drops against myopia progression and axial elongation in children, a meta-analysis was carried out based on data obtained from PubMed and Web of Science as of August 1, 2021. Randomized controlled trials (RCTs) that enrolled myopic children who had received atropine for at least one year were included in this study, Key search terms included myopia, children, and 0.01% or low-dose atropine. Heterogeneity was quantified by I2 statistics, and meta-analyses were performed using the fixed-effect model. Five RCTs involving 809 unique children were analyzed. One trial was excluded because of a poor Jadad score and markedly rapid myopia progression in controls. The mean effect sizes for 12 months in myopia progression and axial elongation synthesized from the remaining 4 RCTs were 0.20 (95% CI: 0.13 to 0.27) D and −0.08 (−0.11 to −0.04) mm, respectively (p<0.0001). The corresponding inhibition ratios were 28% and 19%. I2 statistics were 6% or less. Sensitivity analysis and funnel plots demonstrated the robustness of the estimation. The 0.01% atropine-induced inhibition ratio for myopia progression in Asian children was roughly half of that originally reported and did not reach the minimum requirement for clinical treatment. |
Keywords | myopia 0.01% atropine low-dose atropine axial length myopia progression |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2022-08 |
Volume | volume76 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 457 |
End Page | 463 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
Copyright Holders | Copyright Ⓒ 2022 by Okayama University Medical School |
File Version | publisher |
Refereed | True |
PubMed ID | 36123161 |
Web of Science KeyUT | 000882167300011 |
JaLCDOI | 10.18926/AMO/63903 |
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FullText URL | 76_4_439.pdf |
Author | Miyaji, Chikara| Takao, Soshi| Noguchi, Masayuki| Okazaki, Tsubasa| Sato, Shunsuke| Yorifuji, Takashi| |
Abstract | This study examined the relationship between cognitive/structural social capital and post-traumatic stress disorder (PTSD) among victims of heavy rain and flood. Participants were individuals aged≥18 years affected by the July 2018 heavy rainfall in the cities of Kurashiki and Soja, Japan, and living in temporary housing. We distributed five copies of a questionnaire to 1,991 households and received responses from 1,927 individuals (907 men, 1,008 women, 12 respondents of unspecified sex) in 1,029 households (51.7%). We estimated odds ratios (ORs) and 95% confidence intervals (CIs) for associations between high (vs. low) social capital and PTSD or other outcomes. After covariate adjustment, the odds of having PTSD were lower in participants with high cognitive social capital than those with low cognitive social capital (OR=0.346, 95%CI: 0.263-0.456). Elderly women with higher structural social capital tended to have lower PTSD odds than those with lower structural social capital (OR=0.671, 95%CI: 0.431-1.046). The opposite pattern was observed for elderly men (OR=1.315, 95%CI: 0.792-2.183). Cognitive social capital is a protective factor that may reduce PTSD or promote a favorable PTSD prognosis after heavy rainfall and flood events. The associations between structural social capital and PTSD differ by age and sex. |
Keywords | social capital post-traumatic stress disorder disaster flooding |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2022-08 |
Volume | volume76 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 439 |
End Page | 446 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
Copyright Holders | Copyright Ⓒ 2022 by Okayama University Medical School |
File Version | publisher |
Refereed | True |
PubMed ID | 36123159 |
Web of Science KeyUT | 000882167300010 |
JaLCDOI | 10.18926/AMO/63902 |
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FullText URL | 76_4_429.pdf |
Author | Yamadori, Yusuke| Hirao, Tomohiro| Nlandu R. Ngatu| Kanda, Kanae| Syed Mahfuz Al Hasan| Murakami, Akitsu| Mashima, Yukinori| Shirakami, Gotaro| |
Abstract | Blood pressure (BP) often rises before surgery. This study investigated whether BP elevation immediately before surgery was associated with adverse outcomes. Medical records of 11,732 patients (average age: 61 years; male: 47.4%) who underwent non-cardiac elective inpatient surgery under general anesthesia at Kagawa University Hospital between January 2011 and June 2019 were reviewed. Differences between the first BP values measured on the day before surgery and the first BP values in the operating room were defined as Δ systolic BP (ΔSBP) and Δ diastolic BP (ΔDBP). The relationships between ΔSBP/ΔDBP and 30-day mortality, 30-day readmission, and over-the-standard length of hospital stay (OSLOS) were assessed. OSLOS was defined as a hospital stay longer than mean+2 standard deviations and was calculated using the Japanese Diagnosis Procedure Combination data. In univariate analysis, the differences in ΔSBP and ΔDBP between the OSLOS and standard LOS groups were both 2 mmHg. In multivariate logistic regression analysis, only ΔDBP was associated with OSLOS. The adjusted odds ratio (95% confidence interval) for the largest quartile was 1.31 (1.02-1.69) (p<0.05). ΔDBP was associated with OSLOS; however, there may be little need to worry about large ΔSBPs and ΔDBPs in clinical practice. |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2022-08 |
Volume | volume76 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 429 |
End Page | 437 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
Copyright Holders | Copyright Ⓒ 2022 by Okayama University Medical School |
File Version | publisher |
Refereed | True |
PubMed ID | 36123158 |
Web of Science KeyUT | 000882167300009 |
FullText URL | fulltext.pdf |
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Author | Sumi, Tomonari| Harada, Kouji| |
Published Date | 2022-08-19 |
Publication Title | ISCIENCE |
Volume | volume25 |
Issue | issue8 |
Publisher | CELL PRESS |
Start Page | 104723 |
ISSN | 2589-0042 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 The Author(s). |
File Version | publisher |
PubMed ID | 35813874 |
DOI | 10.1016/j.isci.2022.104723 |
Web of Science KeyUT | 000843628600010 |
Related Url | isVersionOf https://doi.org/10.1016/j.isci.2022.104723 |
FullText URL | fulltext.pdf |
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Author | Kajiwara, Tsuyoshi| Sasaki, Toru| Otani, Yoji| |
Keywords | global stability two routes of infection two compartments type reproduction number lyapunov functional |
Published Date | 2022-08-02 |
Publication Title | Mathematical Biosciences And Engineering |
Volume | volume19 |
Issue | issue11 |
Publisher | American Institute of Mathematical Sciences |
Start Page | 11047 |
End Page | 11070 |
ISSN | 1547-1063 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 the Author(s), licensee AIMS Press. |
File Version | publisher |
DOI | 10.3934/mbe.2022515 |
Web of Science KeyUT | 000850188600006 |
Related Url | isVersionOf https://doi.org/10.3934/mbe.2022515 |
JaLCDOI | 10.18926/AMO/63896 |
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FullText URL | 76_4_415.pdf |
Author | Kang, Haijun| Huang, Dongmei| Kang, Gangjin| Yang, Xu| Li, Heng| Liu, Siyuan| Gou, Wenjun| Liu, Linglin| Qiu, Yuyan| |
Abstract | Posterior capsule opacification (PCO) is a post-surgery complication of cataract surgery, and lens epithelial cells (LECs) are involved in its development. A suppressive effect on LECs is exerted by the non specific chloride channel inhibitor 5-nitro-2-(3-phenylpropylamino) benzoic acid (NPPB) exerts. Herein, the growth and migration inhibitory effects of NPPB on LECs were assessed, and the mechanism underlying the effects were investigated by focusing on Ca2+/CaMKII signaling. LECs were treated with different concentrations of NPPB, and the changes in cell viability, cell-cycle distribution, anchorage-dependent growth, migration, Ca2+ level, and CaMKII expression were evaluated. NPPB inhibited LECs’ proliferation and induced G1 cell-cycle arrest in the cells. Regarding LECs’ mobility, NPPB suppressed the cells’ anchorage-dependent growth ability and inhibited their migration. Changes in cell phenotypes were associated with an increased intracellular Ca2+ level and down-regulation of CaMKII. Together these results confirmed the inhibitory effect of NPPB on the proliferation and migration of LECs, and the effect was shown to be associated with the induced level of Ca2+ and the inhibition of CaMKII signaling transduction. |
Keywords | 5-nitro-2-(3-phenylpropylamino) benzoic acid CaMKII lens epithelial cell migration proliferation |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2022-08 |
Volume | volume76 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 415 |
End Page | 421 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
Copyright Holders | Copyright Ⓒ 2022 by Okayama University Medical School |
File Version | publisher |
Refereed | True |
PubMed ID | 36123156 |
Web of Science KeyUT | 000882167300007 |
JaLCDOI | 10.18926/AMO/63894 |
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FullText URL | 76_4_399.pdf |
Author | Kajiwara, Yukiko| Iwamoto, Takayuki| Zhu, Yidan| Kochi, Mariko| Shien, Tadahiko| Taira, Naruto| Doihara, Hiroyoshi| Toyooka, Shinichi| |
Abstract | According to a recent report, a low Ki67 level after short-term preoperative hormone therapy (post-Ki67) might suggest a more favorable prognosis compared with a high post-Ki67 level in patients with hormone receptorpositive/human epidermal growth factor 2-negative (HR+/HER2−) breast cancer with high levels of Ki67. This study aimed to evaluate the pre-treatment genetic differences between these two patient groups. Forty-five luminal B-like patients were stratified into two groups, namely, a group with high (H→H) and one with low (H→L) Ki67 levels after short-term preoperative aromatase inhibitor (AI) treatment. We compared pre-treatmentgene expression profiles between the two groups. In gene level analysis, there was no significant difference between the two groups by the class comparison test. In pathway analysis, five metabolism-related gene sets were significantly upregulated in the H→L group (p≤0.05). In the search for novel targets, five genes (PARP, BRCA2, FLT4, CDK6, and PDCD1LG2) showed significantly higher expression in the H→H group (p≤0.05). Several metabolism-related pathways were associated with sensitivity to AI. In the future, it will be necessary to seek out new therapeutic strategies for the poor prognostic group with high post-Ki67. |
Keywords | breast cancer short-term hormone therapy gene expression profiling Ki-67 targeted therapy |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2022-08 |
Volume | volume76 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 399 |
End Page | 408 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
Copyright Holders | Copyright Ⓒ 2022 by Okayama University Medical School |
File Version | publisher |
Refereed | True |
PubMed ID | 36123154 |
Web of Science KeyUT | 000882167300005 |
FullText URL | fulltext.pdf |
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Author | Nara, Shigetoshi| Fujii, Hiroshi| Tsukada, Hiromichi| Tsuda, Ichiro| |
Published Date | 2022-08-19 |
Publication Title | Scientific Reports |
Volume | volume12 |
Issue | issue1 |
Publisher | Nature Portfolio |
Start Page | 14172 |
ISSN | 2045-2322 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © The Author(s) 2022 |
File Version | publisher |
PubMed ID | 35986200 |
DOI | 10.1038/s41598-022-18313-6 |
Web of Science KeyUT | 000842561700031 |
Related Url | isVersionOf https://doi.org/10.1038/s41598-022-18313-6 |
JaLCDOI | 10.18926/AMO/63887 |
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FullText URL | 76_4_359.pdf |
Author | Hiramatsu-Asano, Sumie| Wada, Jun| |
Abstract | Systemic lupus erythematosus (SLE) is a potentially fatal systemic autoimmune disease, and its etiology involves both genetic and environmental factors such as sex hormone imbalance, genetic predisposition, epigenetic regulation, and immunological factors. Dysregulation of microRNA (miRNA) is suggested to be one of the epigenetic factors in SLE. miRNA is a 22-nucleotide single-stranded noncoding RNA that contributes to post-transcriptional modulation of gene expression. miRNA targeting therapy has been suggested to be useful for the treatment of cancers and other diseases. Gene knockout and miRNA targeting therapy have been demonstrated to improve SLE disease activity in mice. However, these approaches have not yet reached the level of clinical application. miRNA targeting therapy is limited by the fact that each miRNA has multiple targets. In addition, the expression of certain miRNAs may differ among cell tissues within a single SLE patient. This limitation can be overcome by targeted delivery and chemical modifications. In the future, further research into miRNA chemical modifications and delivery systems will help us develop novel therapeutic agents for SLE. |
Keywords | systemic lupus erythematosus miRNA miRNA targeting therapy |
Amo Type | Review |
Publication Title | Acta Medica Okayama |
Published Date | 2022-08 |
Volume | volume76 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 359 |
End Page | 371 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
Copyright Holders | Copyright Ⓒ 2022 by Okayama University Medical School |
File Version | publisher |
Refereed | True |
PubMed ID | 36123150 |
Web of Science KeyUT | 000882167300002 |
FullText URL | fulltext.pdf |
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Author | Tsuge, Mitsuru| Ikeda, Masanori| Tsukahara, Hirokazu| |
Keywords | bronchial asthma chronic obstructive pulmonary disease lung function trajectory type 2 inflammation airway remodeling omalizumab mepolizumab benralizumab dupilumab |
Published Date | 2022-08-19 |
Publication Title | Children - Basel |
Volume | volume9 |
Issue | issue8 |
Publisher | MDPI |
Start Page | 1253 |
ISSN | 2227-9067 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 by the authors. |
File Version | publisher |
PubMed ID | 36010143 |
DOI | 10.3390/children9081253 |
Web of Science KeyUT | 000846009500001 |
Related Url | isVersionOf https://doi.org/10.3390/children9081253 |
FullText URL | fulltext20220906-1.pdf |
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Author | Kakehi, Ayaka| Hagiya, Hideharu| Iio, Koji| Nakano, Yasuhiro| Ihoriya, Hiromi| Taira, Yuki| Nakamoto, Kenta| Hasegawa, Kou| Higashikage, Akihito| Otsuka, Fumio| |
Keywords | Candida dubliniensis Candidemia COVID-19 Sequencing analysis |
Note | © 2022 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. This manuscript version is made available under the CC-BY-NC-ND 4.0 License. http://creativecommons.org/licenses/by-nc-nd/4.0/. This is the accepted manuscript version. The formal published version is available at [https://doi.org/10.1016/j.jiac.2022.07.007] . | |
Published Date | 2022-10 |
Publication Title | Journal of Infection and Chemotherapy |
Volume | volume28 |
Issue | issue10 |
Publisher | Elsevier BV |
Start Page | 1433 |
End Page | 1435 |
ISSN | 1341-321X |
NCID | AA11057978 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. |
File Version | author |
PubMed ID | 35863730 |
DOI | 10.1016/j.jiac.2022.07.007 |
Web of Science KeyUT | 000843880400016 |
Related Url | isVersionOf https://doi.org/10.1016/j.jiac.2022.07.007 |
FullText URL | fulltext20220830-3.pdf |
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Author | Amioka, Naofumi| Takaishi, Atsushi| Nakamura, Kazufumi| Endo, Toyohiro| Iida, Toshihiro| Yamaji, Tatsuya| Mori, Hisatoshi| Kishinoue, Takao| Yasuhara, Kentaro| Matsuo, Naoaki| Tanimoto, Masafumi| Nakano, Yukari| Onishi, Nobuhiko| Ueeda, Masayuki| Ito, Hiroshi| |
Keywords | Clinical pathway Acute decompensated heart failure Tolvaptan Cardiac rehabilitation Prognosis |
Note | © 2022 Elsevier B.V. This manuscript version is made available under the CC-BY-NC-ND 4.0 License. http://creativecommons.org/licenses/by-nc-nd/4.0/. This is the accepted manuscript version. The formal published version is available at [https://doi.org/10.1016/j.jjcc.2022.03.014] . | |
Published Date | 2022-09 |
Publication Title | Journal of Cardiology |
Volume | volume80 |
Issue | issue3 |
Publisher | Elsevier BV |
Start Page | 232 |
End Page | 239 |
ISSN | 0914-5087 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 Elsevier B.V. |
File Version | author |
PubMed ID | 35428556 |
DOI | 10.1016/j.jjcc.2022.03.014 |
Web of Science KeyUT | 000838175500008 |
Related Url | isVersionOf https://doi.org/10.1016/j.jjcc.2022.03.014 |
FullText URL | fulltext.pdf |
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Author | Yamamoto, Norio| Tsujimoto, Yasushi| Yokoo, Suguru| Demiya, Koji| Inoue, Madoka| Noda, Tomoyuki| Ozaki, Toshifumi| Yorifuji, Takashi| |
Keywords | trochanteric fracture intertrochanteric fracture pertrochanteric fracture reduction tip-apex distance mechanical failure fixation failure cut-out systematic review meta-analysis |
Published Date | 2022-08-19 |
Publication Title | Journal Of Clinical Medicine |
Volume | volume11 |
Issue | issue16 |
Publisher | MDPI |
Start Page | 4879 |
ISSN | 2077-0383 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 by the authors. |
File Version | publisher |
PubMed ID | 36013114 |
DOI | 10.3390/jcm11164879 |
Web of Science KeyUT | 000845562100001 |
Related Url | isVersionOf https://doi.org/10.3390/jcm11164879 |
FullText URL | fulltext.pdf |
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Author | Mitsudo, Koichi| Inoue, Haruka| Niki, Yuta| Sato, Eisuke| Suga, Seiji| |
Keywords | enone hydrogenation iridium palladium PEM reactor |
Published Date | 2022-08-19 |
Publication Title | Beilstein Journal Of Organic Chemistry |
Volume | volume18 |
Publisher | Beilstein-Institut |
Start Page | 1055 |
End Page | 1061 |
ISSN | 1860-5397 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 Mitsudo et al. |
File Version | publisher |
DOI | 10.3762/bjoc.18.107 |
Web of Science KeyUT | 000843361500001 |
Related Url | isVersionOf https://doi.org/10.3762/bjoc.18.107 |
FullText URL | fulltext.pdf |
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Author | Maruyama, Takayuki| Ekuni, Daisuke| Higuchi, Masakazu| Takayama, Eiji| Tokuno, Shinichi| Morita, Manabu| |
Keywords | periodontitis psychological stress voice analysis prospective cohort study |
Published Date | 2022-08-02 |
Publication Title | International Journal Of Environmental Research |
Volume | volume19 |
Issue | issue15 |
Publisher | MDPI |
Start Page | 9489 |
ISSN | 1660-4601 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 by the authors. |
File Version | publisher |
PubMed ID | 35954845 |
DOI | 10.3390/ijerph19159489 |
Web of Science KeyUT | 000838914100001 |
Related Url | isVersionOf https://doi.org/10.3390/ijerph19159489 |
FullText URL | fulltext.pdf |
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Author | Tokumasu, Kazuki| Honda, Hiroyuki| Sunada, Naruhiko| Sakurada, Yasue| Matsuda, Yui| Yamamoto, Koichiro| Nakano, Yasuhiro| Hasegawa, Toru| Yamamoto, Yukichika| Otsuka, Yuki| Hagiya, Hideharu| Kataoka, Hitomi| Ueda, Keigo| Otsuka, Fumio| |
Keywords | general fatigue post-exertional malaise long COVID myalgic encephalomyelitis chronic fatigue syndrome post COVID-19 condition |
Published Date | 2022-06-25 |
Publication Title | Medicina |
Volume | volume58 |
Issue | issue7 |
Publisher | MDPI |
Start Page | 850 |
ISSN | 1010-660X |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 by the authors. |
File Version | publisher |
PubMed ID | 35888568 |
DOI | 10.3390/medicina58070850 |
Web of Science KeyUT | 000834490500001 |
Related Url | isVersionOf https://doi.org/10.3390/medicina58070850 |
FullText URL | fulltext.pdf |
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Author | Ono, Kisho| Sato, Kohei| Nakamura, Tomoya| Yoshida, Yume| Murata, Shogo| Yoshida, Kunihiro| Kanemoto, Hideka| Umemori, Koki| Kawai, Hotaka| Obata, Kyoichi| Ryumon, Shoji| Hasegawa, Kazuaki| Kunisada, Yuki| Okui, Tatsuo| Ibaragi, Soichiro| Nagatsuka, Hitoshi| Sasaki, Akira| |
Keywords | oral cancer spheroid three-dimensional culture anticancer drug |
Published Date | 2022-07-18 |
Publication Title | International Journal Of Medical Sciences |
Volume | volume19 |
Issue | issue8 |
Publisher | Ivyspring International Publisher |
Start Page | 1320 |
End Page | 1333 |
ISSN | 1449-1907 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © The author(s). |
File Version | publisher |
PubMed ID | 35928727 |
DOI | 10.7150/ijms.74109 |
Web of Science KeyUT | 000830781500011 |
Related Url | isVersionOf https://doi.org/10.7150/ijms.74109 |
FullText URL | s41598-022-16279-z.pdf |
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Author | Takeuchi-Hatanaka, Kazu| Koyama, Yoshinobu| Okamoto, Kentaro| Sakaida, Kyosuke| Yamamoto, Tadashi| Takashiba, Shogo| |
Published Date | 2022-07-19 |
Publication Title | Scientific Reports |
Volume | volume12 |
Issue | issue1 |
Publisher | Nature Portfolio |
Start Page | 12353 |
ISSN | 2045-2322 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © The Author(s) 2022 |
File Version | publisher |
PubMed ID | 35854051 |
DOI | 10.1038/s41598-022-16279-z |
Web of Science KeyUT | 000827810800083 |
Related Url | isVersionOf https://doi.org/10.1038/s41598-022-16279-z |