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1,040 results on '"Kim, Sun Jung"'

12. Healthcare Big Data Analysis Using Representative National Community Health Survey of 2021: Is Income Change Due to Covid-19 Pandemic Associated with Unmet Healthcare Needs in S. Korea

Author

Lee, Yeong Jun, Myeong, Se Hyeon, Kim, Sun Jung, Angrisani, Leopoldo, Series Editor, Arteaga, Marco, Series Editor, Chakraborty, Samarjit, Series Editor, Chen, Jiming, Series Editor, Chen, Shanben, Series Editor, Chen, Tan Kay, Series Editor, Dillmann, Rüdiger, Series Editor, Duan, Haibin, Series Editor, Ferrari, Gianluigi, Series Editor, Ferre, Manuel, Series Editor, Jabbari, Faryar, Series Editor, Jia, Limin, Series Editor, Kacprzyk, Janusz, Series Editor, Khamis, Alaa, Series Editor, Kroeger, Torsten, Series Editor, Li, Yong, Series Editor, Liang, Qilian, Series Editor, Martín, Ferran, Series Editor, Ming, Tan Cher, Series Editor, Minker, Wolfgang, Series Editor, Misra, Pradeep, Series Editor, Mukhopadhyay, Subhas, Series Editor, Ning, Cun-Zheng, Series Editor, Nishida, Toyoaki, Series Editor, Oneto, Luca, Series Editor, Panigrahi, Bijaya Ketan, Series Editor, Pascucci, Federica, Series Editor, Qin, Yong, Series Editor, Seng, Gan Woon, Series Editor, Speidel, Joachim, Series Editor, Veiga, Germano, Series Editor, Wu, Haitao, Series Editor, Zamboni, Walter, Series Editor, Zhang, Junjie James, Series Editor, Park, Ji Su, editor, Yang, Laurence T., editor, Pan, Yi, editor, and Park, Jong Hyuk, editor

Published
2023
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15. Hip

Author

Kim, Sun Jung, Oh, So Won, Yang, Seoung-Oh, editor, Oh, So Won, editor, Choi, Yun Young, editor, and Ryu, Jin-Sook, editor

Published
2022
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22. Immune cell expression patterns of CD39/CD73 ectonucleotidases in rodent models of cardiac arrest and resuscitation

Author

Aoki, Tomoaki, primary, Wong, Vanessa, additional, Yin, Tai, additional, Nakamura, Eriko, additional, Endo, Yusuke, additional, Hayashida, Kei, additional, Robson, Simon C., additional, Nandurkar, Harshal, additional, Diamond, Betty, additional, Kim, Sun Jung, additional, Murao, Atsushi, additional, Wang, Ping, additional, Becker, Lance B., additional, and Shinozaki, Koichiro, additional

Published
2024
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35. Comparative transcriptional and functional profiling defines conserved programs of intestinal DC differentiation in humans and mice

Author

Watchmaker, Payal B, Lahl, Katharina, Lee, Mike, Baumjohann, Dirk, Morton, John, Kim, Sun Jung, Zeng, Ruizhu, Dent, Alexander, Ansel, K Mark, Diamond, Betty, Hadeiba, Husein, and Butcher, Eugene C

Subjects
Biomedical and Clinical Sciences, Immunology, Biodefense, Emerging Infectious Diseases, Prevention, Vaccine Related, Underpinning research, 1.1 Normal biological development and functioning, Inflammatory and immune system, Animals, Antigens, CD, Antigens, CD1, CD11b Antigen, Cell Differentiation, Cells, Cultured, Cluster Analysis, Cross-Priming, Dendritic Cells, Flow Cytometry, Glycoproteins, Humans, Integrin alpha Chains, Integrins, Intestinal Mucosa, Mice, Mice, Knockout, Mice, Transgenic, Microscopy, Confocal, Oligonucleotide Array Sequence Analysis, Receptors, Chemokine, T-Lymphocytes, Regulatory, Th17 Cells, Transcriptome, Biochemistry and cell biology
Abstract

Dendritic cells (DCs) that orchestrate mucosal immunity have been studied in mice. Here we characterized human gut DC populations and defined their relationship to previously studied human and mouse DCs. CD103(+)Sirpα(-) DCs were related to human blood CD141(+) DCs and to mouse intestinal CD103(+)CD11b(-) DCs and expressed markers of cross-presenting DCs. CD103(+)Sirpα(+) DCs aligned with human blood CD1c(+) DCs and mouse intestinal CD103(+)CD11b(+) DCs and supported the induction of regulatory T cells. Both CD103(+) DC subsets induced the TH17 subset of helper T cells, while CD103(-)Sirpα(+) DCs induced the TH1 subset of helper T cells. Comparative analysis of transcriptomes revealed conserved transcriptional programs among CD103(+) DC subsets and identified a selective role for the transcriptional repressors Bcl-6 and Blimp-1 in the specification of CD103(+)CD11b(-) DCs and intestinal CD103(+)CD11b(+) DCs, respectively. Our results highlight evolutionarily conserved and divergent programming of intestinal DCs.

Published
2014

36. Combination of [18F]FDG and [18F]PSMA-1007 PET/CT predicts tumour aggressiveness at staging and biochemical failure postoperatively in patients with prostate cancer.

Author

Kim, Jisu, Lee, Seunghwan, Kim, Dongwoo, Kim, Hyun Jeong, Oh, Kyeong Taek, Kim, Sun Jung, Choi, Young Deuk, Giesel, Frederik L., Kopka, Klaus, Hoepping, Alexander, Lee, Misu, and Yun, Mijin

Subjects
PROSTATE cancer patients, POSITRON emission tomography, PROSTATE-specific membrane antigen, ONE-way analysis of variance, PROSTATE-specific antigen, FISHER exact test
Abstract

Purpose: [18F]fluorodeoxyglucose ([18F]FDG) positron emission tomography/computed tomography (PET/CT) has limitations in prostate cancer (PCa) detection owing to low glycolysis in the primary tumour. Recently, prostate-specific membrane antigen (PSMA) PET/CT has been useful for biochemical failure detection and radioligand therapy (RLT) guidance. However, few studies have evaluated its use in primary prostate tumours using PSMA and [18F]FDG PET/CT. This study aimed to evaluate [18F]PSMA-1007 and [18F]FDG PET/CT for primary tumour detection and understand the association of metabolic heterogeneity with clinicopathological characteristics at staging and postoperatively. Method: This prospective study included 42 index tumours (27 acinar and 15 ductal-dominant) in 42 patients who underwent [18F]PSMA-1007 and [18F]FDG PET/CT and subsequent radical prostatectomy. All patients were followed for a median of 26 mo, and serum prostate-specific antigen levels were measured every 3 mo to evaluate biochemical failure. One-way analysis of variance, Tukey's multiple comparison test, and Fisher's exact test were performed. Results: All 42 index tumours were detected on [18F]PSMA-1007 PET/CT, whereas only 15 were detected on [18F]FDG PET/CT (62.3% vs. 37.7%, p < 0.0001). A high SUVmax for [18F]PSMA-1007 was observed in tumours with high Gleason scores (GS 6–7 vs. GS 8–10; 12.1 vs. 20.1, p < 0.05). Tumours with [18F]FDG uptake were mostly ductal dominant (acinar-dominant 4/27; ductal-dominant; 11/15, p < 0.001), with lower [18F]PSMA-1007 uptake than tumours without [18F]FDG uptake (SUVmax 16.58 vs. 11.19, p < 0.001). There were 16.6% (7/42) of patients with pStage IV in whom the primary tumours were [18F]FDG positive. Biochemical failure was observed in 14.8% (4/27) of patients with [18F]FDG negative tumours but in 53.3% (8/15) of patients with [18F]FDG positive tumours (p = 0.013). Conclusions: [18F]PSMA-1007 PET/CT was superior to [18F]FDG PET/CT in detecting primary PCa. In contrast, tumours with [18F]FDG uptake are associated with larger size, a ductal-dominant type, and likely to undergo metastasis at staging and biochemical failure postoperatively. [ABSTRACT FROM AUTHOR]

Published
2024
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38. Postchemoradiation magnetic resonance imaging circumferential resection margin predicts treatment failure after multidisciplinary directed sphincter preservation in low rectal cancer

Author

Kim, Sun Jung, primary, Lee, Yong Joon, additional, Park, Min Young, additional, Yang, Seung Yoon, additional, Han, Yoon Dae, additional, Cho, Min Soo, additional, Hur, Hyuk, additional, Lee, Kang Young, additional, Lim, Joon Seok, additional, and Min, Byung Soh, additional

Published
2023
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