result 1962 件
JaLCDOI | 10.18926/AMO/64362 |
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FullText URL | 77_1_57.pdf |
Author | Katsumata, Ryo| Manabe, Noriaki| Monobe, Yasumasa| Ayaki, Maki| Suehiro, Mitsuhiko| Fujita, Minoru| Kamada, Tomoari| Kawamoto, Hirofumi| Haruma, Ken| |
Abstract | Melanosis coli (MC) is an acquired colorectal disorder visualized as colonic mucosa pigmentation. Disease severity is confirmed based on MC depth, shape, and coloration, although the clinical course is not fully understood. This study sought to clarify characteristics of MC development and disappearance and to investigate its clinical course and severity. Contributors to MC grade progression were explored. This study reviewed MC cases discovered via colonoscopy at a single institution over a 10-year period. Of all 216 MC cases, 17 developing and 10 disappearing cases were detected. Anthranoid laxative use was a key factor: 29.4% of the developing cases had used such agents before the initial MC diagnosis, whereas 40% of disappearing cases had discontinued anthranoids prior to detection of MC disappearance. Among 70 grade I cases, progression to grade II occurred in 16 cases during a mean follow-up of 3.67±2.1 years (rate of progression=22.8%). Males more commonly showed progressive than stable grade I cases, and the probability of progression was higher for male than for female cases. An association between anthranoid administration and MC presence was presumed, and grade I MC was found to progress in severity over 5 years. |
Keywords | melanosis sex characteristics laxatives colorectal neoplasms colonoscopy |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2023-02 |
Volume | volume77 |
Issue | issue1 |
Publisher | Okayama University Medical School |
Start Page | 57 |
End Page | 64 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
Copyright Holders | Copyright Ⓒ 2023 by Okayama University Medical School |
File Version | publisher |
Refereed | True |
PubMed ID | 36849146 |
Web of Science KeyUT | 000952992100003 |
JaLCDOI | 10.18926/AMO/64360 |
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FullText URL | 77_1_37.pdf |
Author | Yamanouchi, Kosho| Maeda, Shigeto| |
Abstract | Systemic therapy for stage IV breast cancer is usually an initial treatment and is based on findings regarding biomarkers (e.g., hormone receptors and human epidermal growth factor receptor-2 [HER2]). However, the response to therapy and outcomes sometime differ among patients with similar prognostic factors including grade, hormone receptor, HER2, and more. We conducted retrospective analyses to evaluate the correlations between the overall survival (OS) of 46 stage IV breast cancer patients and (i) the peripheral absolute lymphocyte count (ALC) and (ii) composite blood cell markers. The peripheral blood cell markers included the neutrophil- to-lymphocyte ratio (NLR), the monocyte-to-lymphocyte ratio (MLR), the systemic immune-inflammation index (SII), the systemic inflammation response index (SIRI), and the most recently introduced indicator, the pan-immune-inflammatory value (PIV). The SIRI and PIV showed prognostic impacts on the patients: those with a low SIRI or a low PIV showed significantly better OS than those with a high SIRI (5-year, 66.0% vs. 35.0%, p<0.05) or high PIV (5-year, 68.1% vs. 38.5%, p<0.05), respectively. This is the first report indicating the possible prognostic value of the PIV for OS in patients with stage IV breast cancer. Further studies with larger numbers of patients are necessary for further clarification. |
Keywords | breast cancer pan-immune-inflammatory value prognosis |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2023-02 |
Volume | volume77 |
Issue | issue1 |
Publisher | Okayama University Medical School |
Start Page | 37 |
End Page | 43 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
Copyright Holders | Copyright Ⓒ 2023 by Okayama University Medical School |
File Version | publisher |
Refereed | True |
PubMed ID | 36849144 |
Web of Science KeyUT | 000952992100001 |
FullText URL | fulltext.pdf |
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Author | Nakajima, Yoshiki| Ugai-Amo, Natsumi| Tone, Naoki| Nakagawa, Akiko| Iwai, Masako| Ikeuchi, Masahiko| Sugiura, Miwa| Suga, Michihiro| Jian-Ren, Shen| |
Published Date | 2022-12 |
Publication Title | Journal Of Biological Chemistry |
Volume | volume298 |
Issue | issue12 |
Publisher | Elsevier |
Start Page | 102668 |
ISSN | 1083-351X |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 THE AUTHORS. |
File Version | publisher |
PubMed ID | 36334624 |
DOI | 10.1016/j.jbc.2022.102668 |
Web of Science KeyUT | 000897992300012 |
Related Url | isVersionOf https://doi.org/10.1016/j.jbc.2022.102668 |
FullText URL | fulltext20221122-4.pdf |
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Author | Yamaguchi, Kizashi| Shoji, Mitsuo| Isobe, Hiroshi| Kawakami, Takashi| Miyagawa, Koichi| Suga, Michihiro| Akita, Fusamichi| Shen, Jian-Ren| |
Keywords | Water oxidation Oxygen evolution Photosystem II HR XRD SFX XFEL QM/MM calculation DLPNO CCSD(T-0) computations, Oxyl radical character |
Note | (C) 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.ccr.2022.214742| This full-text file will be available in Aug. 2024.| |
Published Date | 2022-11 |
Publication Title | Coordination Chemistry Reviews |
Volume | volume471 |
Publisher | Elsevier BV |
Start Page | 214742 |
ISSN | 0010-8545 |
NCID | AA00619249 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 Elsevier B.V. |
File Version | author |
DOI | 10.1016/j.ccr.2022.214742 |
Web of Science KeyUT | 000879286600003 |
Related Url | isVersionOf https://doi.org/10.1016/j.ccr.2022.214742 |
FullText URL | fulltext20221114-1.pdf |
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Author | Isobe, Hiroshi| Shoji, Mitsuo| Suzuki, Takayoshi| Shen, Jian-Ren| Yamaguchi, Kizashi| |
Note | This document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Physical Chemistry B, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.jpcb.2c02596| This full-text will be available in Sep. 2023.| |
Published Date | 2022-09-15 |
Publication Title | The Journal of Physical Chemistry B |
Volume | volume126 |
Issue | issue38 |
Publisher | American Chemical Society (ACS) |
Start Page | 7212 |
End Page | 7228 |
ISSN | 1520-6106 |
NCID | AA11114073 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 American Chemical Society |
File Version | author |
PubMed ID | 36107406 |
DOI | 10.1021/acs.jpcb.2c02596 |
Web of Science KeyUT | 000863255500001 |
Related Url | isVersionOf https://doi.org/10.1021/acs.jpcb.2c02596 |
JaLCDOI | 10.18926/AMO/64125 |
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FullText URL | 76_6_737.pdf |
Author | Yamaoka, Masakazu| Yamamoto, Yumi| Minami, Eriko| |
Abstract | Paraplegia after an operation for acute aortic dissection Stanford type A (AADA) is fairly uncommon, and there is no consensus about optimal treatment. We present a case in which cerebrospinal fluid drainage (CSFD) and permissive hypertension were used for treatment of paraplegia. When the patient showed complete bilateral paraplegia after operation for AADA, we immediately began CSFD and maintained mean arterial blood pressure at over 90 mmHg. His neurological deficit gradually recovered, and he was eventually able to walk without support. The combination of CSFD and permissive hypertension could be a first-line emergent treatment for postoperative paraplegia after AADA surgery. |
Keywords | paraplegia acute aortic dissection cerebrospinal drainage permissive hypertension |
Amo Type | Case Report |
Publication Title | Acta Medica Okayama |
Published Date | 2022-12 |
Volume | volume76 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 737 |
End Page | 742 |
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 | 36549777 |
Web of Science KeyUT | 000905195100015 |
JaLCDOI | 10.18926/AMO/64120 |
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FullText URL | 76_6_695.pdf |
Author | Onishi, Hideki| Nouso, Kazuhiro| Takaki, Akinobu| Oyama, Atsushi| Adachi, Takuya| Wada, Nozomu| Takeuchi, Yasuto| Shiraha, Hidenori| Okada, Hiroyuki| |
Abstract | This study sought to identify factors that are predictive of a therapeutic response to hepatic arterial infusion chemotherapy (HAIC) by focusing on the number of prior transcatheter arterial chemoembolization (TACE) sessions. To determine the parameters predicting a good response to HAIC, we retrospectively analyzed 170 patients with hepatocellular carcinoma (HCC) who received HAIC regimens comprising low-dose cisplatin combined with 5-fluorouracil (LFP) or cisplatin (CDDP) for the first time. In both the LFP and CDDP regimens, the response rates were significantly lower in patients with three or more prior TACE sessions than in those with two or fewer prior TACE sessions (LFP 57% versus 28%; p=0.01, CDDP 27% versus 6%; p=0.01). Multivariable logistic regression analysis revealed that the number of prior TACE sessions (≥ 3) was significantly associated with non-responder status (odds ratio 4.17, 95% Confidence Interval (CI) 1.76-9.86) in addition to the HAIC regimen. Multivariable analysis using the Cox proportional hazards model revealed that a larger number of prior TACE sessions (≥ 3) was a significant risk factor for survival (hazard ratio 1.60, 95% CI 1.12-2.29) in addition to Child-Pugh class, serum alpha-fetoprotein concentration, and maximum diameter of HCC. HCC patients who receive fewer prior TACE sessions (≤ 2) were found to be better responders to HAIC. |
Keywords | hepatic arterial infusion chemotherapy hepatocellular carcinoma refractory transcatheter arterial chemoembolization |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2022-12 |
Volume | volume76 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 695 |
End Page | 703 |
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 | 36549772 |
Web of Science KeyUT | 000905195100010 |
JaLCDOI | 10.18926/AMO/64119 |
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FullText URL | 76_6_689.pdf |
Author | Yamanouchi, Kosho| Kuba, Sayaka| Matsumoto, Megumi| Yano, Hiroshi| Morita, Michi| Sakimura, Chika| Otsubo, Ryota| Hidaka, Masaaki| Nagayasu, Takeshi| Eguchi, Susumu| |
Abstract | Taxanes are key drugs for patients with breast cancer. A major adverse effect of taxanes is peripheral neuropathy (PN). To investigate the ability of compression therapy using sleeves and stockings to prevent PN due to the taxane docetaxel, we conducted a single-center historical control trial. Patients receiving docetaxel at 75 mg/m2 every 3 weeks for 4 cycles as first-line chemotherapy for breast cancer were eligible. PN was evaluated using the common terminology criteria for adverse events version 4.0. The primary endpoint was the incidence of allgrade PN until 3 weeks after the fourth docetaxel administration. We evaluated 26 patients in the intervention group and compared their data to those collected retrospectively from 52 patients treated with docetaxel without compression. Neither the incidence of all-grade PN until 3 weeks after the fourth docetaxel administration (63.5% in the control group vs. 76.9% in the intervention group, p=0.31) nor that of PN grade ≥ 2 (13.5% vs. 15.4%, p=0.99) differed between the groups. In this study, the efficacy of compression therapy using sleeves and stockings to prevent PN induced by docetaxel was not demonstrated. Further clinical studies including medications or intervention are needed to reduce the incidence and severity of PN induced by chemotherapy. |
Keywords | breast cancer docetaxel neuropathy compression |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2022-12 |
Volume | volume76 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 689 |
End Page | 694 |
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 | 36549771 |
Web of Science KeyUT | 000905195100009 |
JaLCDOI | 10.18926/AMO/64116 |
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FullText URL | 76_6_661.pdf |
Author | Abe, Yuko| Taira, Naruto| Kashiwabara, Kosuke| Tsurutani, Junji| Kitada, Masahiro| Takahashi, Masato| Kato, Hiroaki| Kikawa, Yuichiro| Sakata, Eiko| Naito, Yoichi| Hasegawa, Yoshie| Saito, Tsuyoshi| Iwasa, Tsutomu| Takashima, Tsutomu| Aihara, Tomohiko| Mukai, Hirofumi| Hara, Fumikata| Shien, Tadahiko| Doihara, Hiroyoshi| Toyooka, Shinichi| |
Abstract | Chemotherapy-induced peripheral neuropathy (CIPN) is an important clinical challenge that threatens patients’ quality of life. This sub-study of the ABROAD trial investigated the influence of single nucleotide polymorphisms (SNPs) on CIPN, using genotype data from a randomized study to determine the optimal dose of a 3-week-cycle regimen of nab-paclitaxel (q3w nab-PTX) in patients with metastatic breast cancer (MBC). Patients with HER2-negative MBC were randomly assigned to three doses of q3w nab-PTX (SD: 260 mg/m2 vs. MD: 220 mg/m2 vs. LD: 180 mg/m2). Five SNPs (EPHA4-rs17348202, EPHA5-rs7349683, EPHA6-rs301927, LIMK2-rs5749248, and XKR4-rs4737264) were analyzed based on the results of a previous genome-wide association study. Per-allele SNP associations were assessed by a Cox regression to model the cumulative dose of nab-PTX up to the onset of severe or worsening sensory neuropathy. A total of 141 patients were enrolled in the parent study; 91(65%) were included in this sub-study. Worsening of CIPN was significantly greater in the cases with XKR4 AC compared to those with a homozygote AA (HR 1.86, 95%CI: 1.00001−3.46, p=0.049). There was no significant correlation of CIPN with any other SNP. A multivariate analysis showed that the cumulative dose of nab-PTX was most strongly correlated with CIPN (p<0.01). |
Keywords | metastatic breast cancer taxane-induced peripheral neuropathy chemotherapy-induced peripheral neuropathy nab-paclitaxel single nucleotide polymorphism |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2022-12 |
Volume | volume76 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 661 |
End Page | 671 |
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 | 36549768 |
Web of Science KeyUT | 000905195100006 |
JaLCDOI | 10.18926/AMO/64111 |
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FullText URL | 76_6_617.pdf |
Author | Kobayashi, Katsuhiro| Shibata, Takashi| Tsuchiya, Hiroki| Akiyama, Tomoyuki| |
Abstract | We developed an artificial intelligence (AI) technique to identify epileptic discharges (spikes) in pediatric scalp electroencephalograms (EEGs). We built a convolutional neural network (CNN) model to automatically classify steep potential images into spikes and background activity. For the CNN model’ training and validation, we examined 100 children with spikes in EEGs and another 100 without spikes. A different group of 20 children with spikes and 20 without spikes were the actual test subjects. All subjects were ≥ 3 to < 18 years old. The accuracy, sensitivity, and specificity of the analysis were >0.97 when referential and combination EEG montages were used, and < 0.97 with a bipolar montage. The correct classification of background activity in individual patients was significantly better with a referential montage than with a bipolar montage (p=0.0107). Receiver operating characteristic curves yielded an area under the curve > 0.99, indicating high performance of the classification method. EEG patterns that interfered with correct classification included vertex sharp transients, sleep spindles, alpha rhythm, and low-amplitude ill-formed spikes in a run. Our results demonstrate that AI is a promising tool for automatically interpreting pediatric EEGs. Some avenues for improving the technique were also indicated by our findings. |
Keywords | neural network deep learning electroencephalogram children spike |
Amo Type | Original Article |
Publication Title | Acta Medica Okayama |
Published Date | 2022-12 |
Volume | volume76 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 617 |
End Page | 624 |
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 | 36549763 |
Web of Science KeyUT | 000905195100001 |
FullText URL | K0006688_abstract_review.pdf K0006688_fulltext.pdf K0006688_summary.pdf |
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Author | ABE, Yuko| |
Published Date | 2022-09-22 |
Content Type | Thesis or Dissertation |
Grant Number | 甲第6688号 |
Granted Date | 2022-09-22 |
Thesis Type | Doctor of Philosophy in Medical Science |
Grantor | 岡山大学 |
language | English |
Copyright Holders | © 2022 by Okayama University Medical School. |
FullText URL | fulltext.pdf |
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Author | Hayibor, Kennedy Mawunya| Sunatsuki, Yukinari| Suzuki, Takayoshi| |
Keywords | (pyridyl)(imidazolyl)azines aldazines kryptoracemate crystal structure |
Published Date | 2022-10-11 |
Publication Title | Molecules |
Volume | volume27 |
Issue | issue20 |
Publisher | MDPI |
Start Page | 6788 |
ISSN | 1420-3049 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 by the authors. |
File Version | publisher |
PubMed ID | 36296383 |
DOI | 10.3390/molecules27206788 |
Web of Science KeyUT | 000873383100001 |
Related Url | isVersionOf https://doi.org/10.3390/molecules27206788 |
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 |
FullText URL | fulltext20220830-1.pdf |
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Author | Hagiya, Hideharu| Takase, Ryosuke| Sazumi, Yosuke| Nishimura, Yoshito| Honda, Hiroyuki| Otsuka, Fumio| |
Note | This is an Accepted Manuscript of an article published by SAGE Publications.| |
Published Date | 2022-05-05 |
Publication Title | Journal of Infection Prevention |
Volume | volume23 |
Issue | issue5 |
Publisher | SAGE Publications |
Start Page | 239 |
End Page | 242 |
ISSN | 1757-1774 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | Copyright © 2022 by Infection Prevention Society |
File Version | author |
PubMed ID | 36003134 |
DOI | 10.1177/17571774221094160 |
Web of Science KeyUT | 000843414400007 |
Related Url | isVersionOf https://doi.org/10.1177/17571774221094160 |
FullText URL | fulltext.pdf |
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Author | Uchida, Haruhito A.| Takatsuka, Tetsuharu| Hada, Yoshiko| Umebayashi, Ryoko| Takeuchi, Hidemi| Shikata, Kenichi| Subramanian, Venkateswaran| Daugherty, Alan| Wada, Jun| |
Keywords | edaravone angiotensin II abdominal aortic aneurysm atherosclerosis |
Published Date | 2022-08-14 |
Publication Title | Biomolecules |
Volume | volume12 |
Issue | issue8 |
Publisher | MDPI |
Start Page | 1117 |
ISSN | 2218-273X |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 by the authors. |
File Version | publisher |
PubMed ID | 36009011 |
DOI | 10.3390/biom12081117 |
Web of Science KeyUT | 000846165000001 |
Related Url | isVersionOf https://doi.org/10.3390/biom12081117 |
FullText URL | fulltext.pdf |
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Author | Hada, Yoshiko| Uchida, Haruhito A.| Umebayashi, Ryoko| Yoshida, Masashi| Wada, Jun| |
Keywords | cilostazol angiotensin II fibrosis osteopontin cAMP-PKA |
Published Date | 2022-08-13 |
Publication Title | International Journal Of Molecular Sciences |
Volume | volume23 |
Issue | issue16 |
Publisher | MDPI |
Start Page | 9065 |
ISSN | 1422-0067 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 by the authors. |
File Version | publisher |
PubMed ID | 36012328 |
DOI | 10.3390/ijms23169065 |
Web of Science KeyUT | 000845679000001 |
Related Url | isVersionOf https://doi.org/10.3390/ijms23169065 |
FullText URL | fulltext.pdf |
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Author | Muzembo, Basilua Andre| Kitahara, Kei| Ohno, Ayumu| Debnath, Anusuya| Okamoto, Keinosuke| Miyoshi, Shin-Ichi| |
Keywords | rapid test cholera Vibrio cholera O1 sensitivity specificity accuracy update |
Published Date | 2021-11-13 |
Publication Title | Diagnostics |
Volume | volume11 |
Issue | issue11 |
Publisher | MDPI |
Start Page | 2095 |
ISSN | 2075-4418 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2021 by the authors. |
File Version | publisher |
PubMed ID | 34829444 |
DOI | 10.3390/diagnostics11112095 |
Web of Science KeyUT | 000832340400001 |
Related Url | isVersionOf https://doi.org/10.3390/diagnostics11112095 |
FullText URL | fulltext.pdf |
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Author | Mitalo, Oscar W.| Asiche, William O.| Kang, Seung W.| Ezura, Hiroshi| Akagi, Takashi| Kubo, Yasutaka| Ushijima, Koichiro| |
Keywords | chlorophyll citrus degreening ethylene RNA-Seq on-tree storage |
Published Date | 2022-07-13 |
Publication Title | Frontiers In Plant Science |
Volume | volume13 |
Publisher | Frontiers Media SA |
Start Page | 918226 |
ISSN | 1664-462X |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 Mitalo, Asiche, Kang, Ezura, Akagi, Kubo and Ushijima. |
File Version | publisher |
PubMed ID | 35909736 |
DOI | 10.3389/fpls.2022.918226 |
Web of Science KeyUT | 000832990000001 |
Related Url | isVersionOf https://doi.org/10.3389/fpls.2022.918226 |
FullText URL | fulltext.pdf |
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Author | Hotta, K.| Saeki, S.| Yamaguchi, M.| Harada, D.| Bessho, A.| Tanaka, K.| Inoue, K.| Gemba, K.| Shiojiri, M.| Kato, Y.| Ninomiya, T.| Kubo, T.| Kishimoto, J.| Shioyama, Y.| Katsui, K.| Sasaki, J.| Kiura, K.| Sugio, K.| |
Note | DOI of original article: https://doi.org/10.1016/j.esmoop.2021.100191 | |
Published Date | 2022-08 |
Publication Title | ESMO OPEN |
Volume | volume7 |
Issue | issue4 |
Publisher | ELSEVIER |
ISSN | 2059-7029 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © 2022 The Author(s). |
File Version | publisher |
PubMed ID | 35802950 |
DOI | 10.1016/j.esmoop.2022.100532 |
Web of Science KeyUT | 000828209200003 |
Related Url | isVersionOf https://doi.org/10.1016/j.esmoop.2022.100532 https://doi.org/10.1016/j.esmoop.2021.100191 |
FullText URL | fulltext.pdf |
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Author | Oiwa, Masahiko| Kuroda, Kosuke| Kawanoue, Naoya| Morimatsu, Hiroshi| |
Keywords | Biomarker Clavien-Dindo classification Histidine-rich glycoprotein Intensive care unit Perioperative management Postoperative complication Predictor |
Published Date | 2022-07-20 |
Publication Title | BMC Anesthesiology |
Volume | volume22 |
Issue | issue1 |
Publisher | BMC |
Start Page | 232 |
ISSN | 1471-2253 |
Content Type | Journal Article |
language | English |
OAI-PMH Set | 岡山大学 |
Copyright Holders | © The Author(s) 2022. |
File Version | publisher |
PubMed ID | 35858852 |
DOI | 10.1186/s12871-022-01774-7 |
Web of Science KeyUT | 000828247900001 |
Related Url | isVersionOf https://doi.org/10.1186/s12871-022-01774-7 |