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43 results on '"Chen, Yi-Jyun"'

3. The numbers of fungi: are the most speciose genera truly diverse?

Author

Bhunjun, Chitrabhanu S., Niskanen, Tuula, Suwannarach, Nakarin, Wannathes, Nopparat, Chen, Yi-Jyun, McKenzie, Eric H. C., Maharachchikumbura, Sajeewa S. N., Buyck, Bart, Zhao, Chang-Lin, Fan, Yu-Guang, Zhang, Jing-Yi, Dissanayake, Asha J., Marasinghe, Diana S., Jayawardena, Ruvishika S., Kumla, Jaturong, Padamsee, Mahajabeen, Chen, Ya-Ya, Liimatainen, Kare, Ammirati, Joseph F., Phukhamsakda, Chayanard, Liu, Jian-Kui, Phonrob, Wiphawanee, Randrianjohany, Émile, Hongsanan, Sinang, Cheewangkoon, Ratchadawan, Bundhun, Digvijayini, Khuna, Surapong, Yu, Wen-Jie, Deng, Lun-Sha, Lu, Yong-Zhong, Hyde, Kevin D., and Lumyong, Saisamorn

Published
2022
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4. Appressorial interactions with host and their evolution

Author

Chethana, K. W. Thilini, Jayawardena, Ruvishika S., Chen, Yi-Jyun, Konta, Sirinapa, Tibpromma, Saowaluck, Phukhamsakda, Chayanard, Abeywickrama, Pranami D., Samarakoon, Milan C., Senwanna, Chanokned, Mapook, Ausana, Tang, Xia, Gomdola, Deecksha, Marasinghe, Diana S., Padaruth, Oundhyalah D., Balasuriya, Abhaya, Xu, Jianping, Lumyong, Saisamorn, and Hyde, Kevin D.

Published
2021
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5. The numbers of fungi: is the descriptive curve flattening?

Author

Hyde, Kevin D., Jeewon, Rajesh, Chen, Yi-Jyun, Bhunjun, Chitrabhanu S., Calabon, Mark S., Jiang, Hong-Bo, Lin, Chuan-Gen, Norphanphoun, Chada, Sysouphanthong, Phongeun, Pem, Dhandevi, Tibpromma, Saowaluck, Zhang, Qian, Doilom, Mingkwan, Jayawardena, Ruvishika S., Liu, Jian-Kui, Maharachchikumbura, Sajeewa S. N., Phukhamsakda, Chayanard, Phookamsak, Rungtiwa, Al-Sadi, Abdullah M., Thongklang, Naritsada, Wang, Yong, Gafforov, Yusufjon, Gareth Jones, E. B., and Lumyong, Saisamorn

Published
2020
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6. One stop shop IV: taxonomic update with molecular phylogeny for important phytopathogenic genera: 76–100 (2020)

Author

Jayawardena, Ruvishika S., Hyde, Kevin D., Chen, Yi Jyun, Papp, Viktor, Palla, Balázs, Papp, Dávid, Bhunjun, Chitrabhanu S., Hurdeal, Vedprakash G., Senwanna, Chanokned, Manawasinghe, Ishara S., Harischandra, Dulanjalee L., Gautam, Ajay Kumar, Avasthi, Shubhi, Chuankid, Boontiya, Goonasekara, Ishani D., Hongsanan, Sinang, Zeng, XiangYu, Liyanage, Kapila K., Liu, NingGuo, Karunarathna, Anuruddha, Hapuarachchi, Kalani K., Luangharn, Thatsanee, Raspé, Olivier, Brahmanage, Rashika, Doilom, Mingkwan, Lee, Hyang B., Mei, Liu, Jeewon, Rajesh, Huanraluek, Naruemon, Chaiwan, Napalai, Stadler, Marc, and Wang, Yong

Published
2020
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7. Construct an Intelligent Yield Alert and Diagnostic Analysis System via Data Analysis: Empirical Study of a Semiconductor Foundry

Author

Chen, Yi-Jyun, Lee, Yen-Han, Chiu, Ming-Chuan, Rannenberg, Kai, Editor-in-Chief, Sakarovitch, Jacques, Series Editor, Goedicke, Michael, Series Editor, Tatnall, Arthur, Series Editor, Neuhold, Erich J., Series Editor, Pras, Aiko, Series Editor, Tröltzsch, Fredi, Series Editor, Pries-Heje, Jan, Series Editor, Whitehouse, Diane, Series Editor, Reis, Ricardo, Series Editor, Furnell, Steven, Series Editor, Furbach, Ulrich, Series Editor, Winckler, Marco, Series Editor, Rauterberg, Matthias, Series Editor, Moon, Ilkyeong, editor, Lee, Gyu M., editor, Park, Jinwoo, editor, Kiritsis, Dimitris, editor, and von Cieminski, Gregor, editor

Published
2018
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19. Diversity and Function of Appressoria

Author

Chethana, K. W. Thilini, primary, Jayawardena, Ruvishika S., additional, Chen, Yi-Jyun, additional, Konta, Sirinapa, additional, Tibpromma, Saowaluck, additional, Abeywickrama, Pranami D., additional, Gomdola, Deecksha, additional, Balasuriya, Abhaya, additional, Xu, Jianping, additional, Lumyong, Saisamorn, additional, and Hyde, Kevin D., additional

Published
2021
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24. Topical application of marine briarane-type diterpenes effectively inhibits 12-O-tetradecanoylphorbol-13-acetate-induced inflammation and dermatitis in murine skin

Author

Wei Wen-Chi, Lin Sheng-Yen, Chen Yi-Jyun, Wen Chih-Chun, Huang Chiung-Yao, Palanisamy Arulselvan, Yang Ning-Sun, and Sheu Jyh-Horng

Subjects
Briarane-type diterpene, TPA-induced mouse dermatitis, Dendritic cells, Vascular permeability, Edema, Medicine
Abstract

Abstract Background Skin is the largest organ in the body, and is directly exposed to extrinsic assaults. As such, the skin plays a central role in host defense and the cutaneous immune system is able to elicit specific local inflammatory and systemic immune responses against harmful stimuli. 12-O-tetradecanoylphorbol-13-acetate (TPA) can stimulate acute and chronic inflammation and tumor promotion in skin. TPA-induced dermatitis is thus a useful in vivo pharmacological platform for drug discovery. In this study, the inhibitory effect of briarane-type diterpenes (BrDs) from marine coral Briareum excavatum on TPA-induced dermatitis and dendritic cell (DC) function was explored. Methods Evans blue dye exudation was used to determine vascular permeability. H&E-stained skin section was used to determine the formation of edema in mouse abdominal skin. We also used immunohistochemistry staining and western blot assays to evaluate the activation of specific inflammation makers and key mediators of signaling pathway in the mouse skin. Furthermore, mouse bone marrow DCs were used to determine the relationship between the chemical structure of BrDs and their regulation of DC function. Results BrD1 remarkably suppressed TPA-induced vascular permeability and edema in skin. At the biochemical level, BrD1 inhibited TPA-induced expression of cyclooxygenase-2, inducible nitric oxide synthase and matrix metalloproteinase-9, the key indicators of cutaneous inflammation. This inhibition was apparently mediated by interference with the Akt/NF-κB-mediated signaling network. BrD1 also inhibited TNF-α and IL-6 expression in LPS-stimulated BMDCs. The 8, 17-epoxide of BrDs played a crucial role in the inhibition of IL-6 expression, and replacement of the C-12 hydroxyl group with longer esters in BrDs gradually decreased this inhibitory activity. Conclusions Our results suggest that BrDs warrant further investigation as natural immunomodulatory agents for control of inflammatory skin diseases.

Published
2011
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28. Activation of gas bubble emissions indicated by the upward decreasing Lead-210 activity at a submarine mud volcano (TY1) offshore southwestern Taiwan

Author

Hiruta, Akihiro, primary, Yang, Tsanyao Frank, additional, Lin, Saulwood, additional, Su, Chih-Chieh, additional, Chen, Nai-Chen, additional, Chen, Yi-Jyun, additional, Chen, Hsuan-Wen, additional, Yang, Tsung-Han, additional, Huang, Yu-Chun, additional, Wei, Kuo-Yen, additional, Huang, Jyh-Jaan, additional, Chen, Song-Chuen, additional, and Song, Sheng-Rong, additional

Published
2017
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30. Delivery of Antigen to CD8+ Dendritic Cells by Fusing Antigen With Formyl Peptide Receptor-Like 1 Inhibitor Protein Induces Antitumor Immunity.

Author

Chiang, Chen-Yi, Wu, Chiao-Chieh, Chen, Yi-Jyun, Liu, Shih-Jen, Leng, Chih-Hsiang, and Chen, Hsin-Wei

Subjects
DENDRITIC cells, BACTERIAL vaccines, IMMUNITY, PROTEIN binding, ANTIGEN presentation, ANTIGENS, T cells
Abstract

A major challenge for vaccine development is targeting antigens to dendritic cells (DCs) in vivo , enabling cross-presentation, and inducing the memory responses. Fcγ receptors (FcγRs) are expressed on many cell types including DCs. Therefore, targeting of antigen to DCs via FcγRs is an attractive strategy for vaccine development. This study employ formyl peptide receptor-like 1 inhibitory protein (FLIPr), an FcγR binding protein secreted by Staphylococcus aureus , to deliver antigen to DCs. Our results show that FLIPr is a competent vehicle in delivering antigen to CD8+ DCs for induction of potent immunities without extra adjuvant formulation. Fusion antigen with FLIPr enables effective antigen presentation on both MHC class II and class I to induce memory T cell responses. Altogether, using FLIPr as an antigen delivery vector has great potential to apply antigens for cancer immunotherapy as well as other infectious disease vaccines. [ABSTRACT FROM AUTHOR]

Published
2019
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31. dBRWD3 Regulates Tissue Overgrowth and Ectopic Gene Expression Caused by Polycomb Group Mutations

Author

Shih, Hsueh-Tzu, primary, Chen, Wei-Yu, additional, Liu, Kwei-Yan, additional, Shih, Zong-Siou, additional, Chen, Yi-Jyun, additional, Hsieh, Paul-Chen, additional, Kuo, Kuan-Lin, additional, Huang, Kuo-How, additional, Hsu, Pang-Hung, additional, Liu, Ya-Wen, additional, Chan, Shih-Peng, additional, Lee, Hsiu-Hsiang, additional, Tsai, Yu-Chen, additional, and Wu, June-Tai, additional

Published
2016
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32. Integrating RNA-seq and ChIP-seq data to characterize long non-coding RNAs in Drosophila melanogaster

Author

Chen, Mei-Ju May, primary, Chen, Li-Kai, additional, Lai, Yu-Shing, additional, Lin, Yu-Yu, additional, Wu, Dung-Chi, additional, Tung, Yi-An, additional, Liu, Kwei-Yan, additional, Shih, Hsueh-Tzu, additional, Chen, Yi-Jyun, additional, Lin, Yan-Liang, additional, Ma, Li-Ting, additional, Huang, Jian-Long, additional, Wu, Po-Chun, additional, Hong, Ming-Yi, additional, Chu, Fang-Hua, additional, Wu, June-Tai, additional, Li, Wen-Hsiung, additional, and Chen, Chien-Yu, additional

Published
2016
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40. p38α MAPK mediates 17β‐estradiol inhibition of MMP‐2 and ‐9 expression and cell migration in human lovo colon cancer cells

Author

Hsu, Hsi‐Hsien, primary, Liu, Chung‐Jung, additional, Shen, Chia‐Yao, additional, Chen, Yi‐Jyun, additional, Chen, Li‐Mien, additional, Kuo, Wu‐Hsien, additional, Lin, Yueh‐Min, additional, Chen, Ray‐Jade, additional, Tsai, Chang‐Hai, additional, Tsai, Fuu‐Jen, additional, and Huang, Chih‐Yang, additional

Published
2012
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43. Delivery of Antigen to CD8 + Dendritic Cells by Fusing Antigen With Formyl Peptide Receptor-Like 1 Inhibitor Protein Induces Antitumor Immunity.

Author

Chiang CY, Wu CC, Chen YJ, Liu SJ, Leng CH, and Chen HW

Subjects
Animals, Antigen Presentation immunology, Cross-Priming immunology, Female, Immunologic Memory immunology, Immunotherapy methods, Mice, Mice, Inbred C57BL, Mice, Transgenic, Receptors, IgG immunology, Staphylococcus aureus immunology, Antigens, Neoplasm immunology, CD8-Positive T-Lymphocytes immunology, Dendritic Cells immunology, Neoplasms immunology, Receptors, Formyl Peptide immunology
Abstract

A major challenge for vaccine development is targeting antigens to dendritic cells (DCs) in vivo , enabling cross-presentation, and inducing the memory responses. Fcγ receptors (FcγRs) are expressed on many cell types including DCs. Therefore, targeting of antigen to DCs via FcγRs is an attractive strategy for vaccine development. This study employ formyl peptide receptor-like 1 inhibitory protein (FLIPr), an FcγR binding protein secreted by Staphylococcus aureus , to deliver antigen to DCs. Our results show that FLIPr is a competent vehicle in delivering antigen to CD8 + DCs for induction of potent immunities without extra adjuvant formulation. Fusion antigen with FLIPr enables effective antigen presentation on both MHC class II and class I to induce memory T cell responses. Altogether, using FLIPr as an antigen delivery vector has great potential to apply antigens for cancer immunotherapy as well as other infectious disease vaccines.

Published
2019
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