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권호기사 목록 테이블로 기사명, 저자명, 페이지, 원문, 기사목차 순으로 되어있습니다.
기사명 저자명 페이지 원문 목차
Virus-like particles as antiviral vaccine : mechanism, design, and application Lei Zhang, Wen Xu, Xi Ma, XiaoJing Sun, JinBo Fan, Yang Wang p. 1-16
(An) overview on wound dressings and sutures fabricated by electrospinning Rezvan Mohamadinooripoor, Soheila Kashanian, Elham Arkan p. 17-35
Strategies to enhance the biosynthesis of monounsaturated fatty acids in escherichia coli Paul Matthay, Thomas Schalck, Natalie Verstraeten, Jan Michiels p. 36-50
Improvement of oxidative stress-induced cytotoxicity of Angelica keiskei (Miq.) koidz. leaves extract through activation of heme oxygenase-1 in C2C12 murine myoblasts Cheol Park, Da Hye Kim, Tae Hee Kim, Seong Un Jeong, Jae Hyun Yoon, Sung-Kwon Moon, Chan-Young Kwon, Shin-Hyung Park, Su Hyun Hong, Jung-Hyun Shim, Gi-Young Kim, Yung Huim Choi p. 51-62
Agarwood pill enhances immune function in cyclophosphamide-induced immunosuppressed mice Seon Yeong Ji, Hyesook Lee, Hyun Hwangbo, Min Young Kim, Da Hye Kim, Beom Su Park, Young Tae Koo, Jin Soo Kim, Ki Won Lee, Jong Cheul Ko, Gi-Young Kim, EunJin Bang, Yung Hyun Choi p. 63-73
Modulation of gut microbiota and intestinal barrier integrity and inflammation profile in high fat-fed rats Sungjin Eun, Hyunji Seo, Hee-jae Suh, Sehoon Jeong, Sunhye Lee p. 74-82
Self-assembled nanocomplex using cellulose nanocrystal based on zinc/DNA nanocluster for gene delivery Hongbin Kim, Seungmin Han, Kyoungcheol Choi, Jihyeon Lee, Seung-Hwan Lee, Young-Wook Won, Kwang Suk Lim p. 83-90
MiR-466d targeting MMP13 promotes the differentiation of osteoblasts exposed to a static magnetic field Fei Tong, Hongmeng Cheng, Jun Guo, Jianyong Wu, Hongshan Ge, Zhihua Li p. 91-100
Circ_0005280 protects human lens epithelial cells against H2O2-induced apoptosis and oxidative stress though miR-326/PLCD3 axis Yanxia Zhu, Yan Cheng, Linli Ma p. 101-111
CircBRMS1L participates in lipopolysaccharide-induced chondrocyte injury via the TLR4/NF-κB pathway through serving as a miR-142-5p decoy Ronghua Wang, Lianju Li, Jingxu Wang, Xiangzhuo Zhao, Jingfang Shen p. 112-124
Hsa_circ_0001165 regulates the malignant phenotype and angiogenesis of prostate cancer cells through miR-654-3p/DDAH1 Shiben Ji, Ci Zhang, Yang Xiang, Guohong Yin p. 125-136
(A) cell-free protein synthesis method for the detection of heavy metal ions using a personal glucose meter Ju-Hui Lee, Dong-Yeon Song, Hye Jin Lim, Dong-Myung Kim p. 137-142
Investigating the performance of machine learning methods in predicting functional properties of the hydrogenase variants Gyucheol Choi, Wonjun Kim, Jamin Koo p. 143-151
Detection of escherichia coli in food samples by magnetosome-based biosensor Sumana Sannigrahi, Shiva Kumar A, J Mathiyarasu, K Suthindhiran p. 152-161
In-vitro studies on copper nanoparticles and nano-hydroxyapatite infused biopolymeric composite scaffolds for bone bioengineering applications Shikha Kumari, Abha Mishra, Divakar Singh, Chenzhong Li, Pradeep Srivastava p. 162-180
Metallic vessel with mesh culture surface fabricated using three-dimensional printing engineers tissue culture environment Chikahiro Imashiro, Takashi Morikura, Motoaki Hayama, Atsushi Ezura, Jun Komotori, Shogo Miyata, Sakaguchi Katsuhisa, Shimizu Tatsuya p. 181-191
Cyclic AMP responsive element binding protein 3-like 4/AarF domain containing kinase 5 axis facilitates proliferation, migration and invasion of lung adenocarcinoma cells by modulating the TGFβ pathway Cheng Ai, Tenghao Rong, Zhengyu Chen, Wang Shen, Kaili Huang, Qiang Li, Jing Xiong, Wen Li p. 192-202
Hybrid model-based framework for soft sensing and forecasting key process variables in the production of hyaluronic acid by streptococcus zooepidemicus Sivakumar Rathinavelu, Satya Sai Pavan, Senthilkumar Sivaprakasam p. 203-214
(An) algicidal agent against harmful algae using novel N1-benzyl-N3, N3-diethylpropane-1,3-diamine derivatives Kang Seok Park, DuBok Choi, Hyeong Kyu Son, Young-Cheol Chang, Hoon Cho p. 215-225
Progress in top-down LC-MS analysis of antibodies : review Jiwon You, Hae-Min Park p. 226-233

참고문헌 (38건) : 자료제공( 네이버학술정보 )

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번호 참고문헌 국회도서관 소장유무
1 Qin, J., R. Li, J. Raes, M. Arumugam, K. S. Burgdorf, C. Manichanh, T. Nielsen, N. Pons, F. Levenez, T. Yamada, D. R. Mende, J. Li, J. Xu, S. Li, D. Li, J. Cao, B. Wang, H. Liang, H. Zheng, Y. Xie, J. Tap, P. Lepage, M. Bertalan, J. M. Batto, T. Hansen, D. Le Paslier, A. Linneberg, H. B. Nielsen, E. Pelletier, P. Renault, T. Sicheritz-Ponten, K. Turner, H. Zhu, C. Yu, S. Li, M. Jian, Y. Zhou, Y. Li, X. Zhang, S. Li, N. Qin, H. Yang, J. Wang, S. Brunak, J. Doré, F. Guarner, K. Kristiansen, O. Pedersen, J. Parkhill, J. Weissenbach, MetaHIT Consortium, P. Bork, S. D. Ehrlich, and J. Wang (2010) A human gut microbial gene catalogue established... 미소장
2 Lee, S. H. and C. B. de La Serre (2015) Gut microbiome-brain communications regulate host physiology and behavior. J. Nutrit. Health Food Sci. 3: 1-12. 미소장
3 Romaní-Pérez, M., A. Agusti, and Y. Sanz (2017) Innovation in microbiome-based strategies for promoting metabolic health. Curr. Opin. Clin. Nutr. Metab. Care 20: 484-491. 미소장
4 Carding, S., K. Verbeke, D. T. Vipond, B. M. Corfe, and L. J. Owen (2015) Dysbiosis of the gut microbiota in disease. Microb. Ecol. Health Dis. 26: 26191. 미소장
5 de La Serre, C. B., C. L. Ellis, J. Lee, A. L. Hartman, J. C. Rutledge, and H. E. Raybould (2010) Propensity to high-fat dietinduced obesity in rats is associated with changes in the gut microbiota and gut inflammation. Am. J. Physiol. Gastrointest. Liver Physiol. 299: G440-G448. 미소장
6 Cani, P. D., J. Amar, M. A. Iglesias, M. Poggi, C. Knauf, D. Bastelica, A. M. Neyrinck, F. Fava, K. M. Tuohy, C. Chabo, A. Waget, E. Delmée, B. Cousin, T. Sulpice, B. Chamontin, J. Ferrières, J. F. Tanti, G. R. Gibson, L. Casteilla, N. M. Delzenne, M. C. Alessi, and R. Burcelin (2007) Metabolic endotoxemia initiates obesity and insulin resistance. Diabetes 56: 1761-1772. 미소장
7 de La Serre, C. B., G. de Lartigue, and H. E. Raybould (2015)Chronic exposure to low dose bacterial lipopolysaccharide inhibits leptin signaling in vagal afferent neurons. Physiol. Behav. 139: 188-194. 미소장
8 Lee, S., K. I. Keirsey, R. Kirkland, Z. I. Grunewald, J. G. Fischer, and C. B. de La Serre (2018) Blueberry supplementation influences the gut microbiota, inflammation, and insulin resistance in highfat-diet-fed rats. J. Nutr. 148: 209-219. 미소장
9 Lee, S., M. Goodson, W. Vang, K. Kalanetra, D. Barile, and H. Raybould (2020) 2'-fucosyllactose supplementation improves gut-brain signaling and diet-induced obese phenotype and changes the gut microbiota in high fat-fed mice. Nutrients 12: 1003. 미소장
10 Jeong, S., M. Park, M. Kang, Y.-J. Park, M. Lee, C. You, U. Hwang, Y. Song, H. Park, S. Lee, and H. Suh (2021) Supplementation of non-fermented and fermented red ginseng improves obese phenotypes, lipid and inflammatory profiles, and antioxidant defense system in high fat-fed rats. J. Food Nutr. Res. (Newark)9: 154-162. 미소장
11 Lee, S., R. Kirkland, Z. I. Grunewald, Q. Sun, L. Wicker, and C. B. de La Serre (2019) Beneficial effects of non-encapsulated or encapsulated probiotic supplementation on microbiota composition, intestinal barrier functions, inflammatory profiles, and glucose tolerance in high fat fed rats. Nutrients 11: 1975. 미소장
12 Coon, J. T. and E. Ernst (2002) Panax ginseng: a systematic review of adverse effects and drug interactions. Drug Saf. 25:323-344. 미소장
13 Kim, J.-H. (2012) Cardiovascular diseases and Panax ginseng: a review on molecular mechanisms and medical applications. J. Ginseng Res. 36: 16-26. 미소장
14 Hasegawa, H. (2004) Proof of the mysterious efficacy of ginseng:basic and clinical trials: metabolic activation of ginsenoside:deglycosylation by intestinal bacteria and esterification with fatty acid. J. Pharmacol. Sci. 95: 153-157. 미소장
15 Guo, M., S. Ding, C. Zhao, X. Gu, X. He, K. Huang, Y. Luo, Z. Liang, H. Tian, and W. Xu (2015) Red Ginseng and Semen Coicis can improve the structure of gut microbiota and relieve the symptoms of ulcerative colitis. J. Ethnopharmacol. 162: 7-13. 미소장
16 Jeon, H., H.-Y. Kim, C.-H. Bae, Y. Lee, and S. Kim (2020)Korean red ginseng regulates intestinal tight junction and inflammation in the colon of a Parkinson's disease mouse model. J. Med. Food 23: 1231-1237. 미소장
17 Ahn, H., B.-C. Han, J. Kim, S. G. Kang, P.-H. Kim, K. H. Jang, S. H. So, S.-H. Lee, and G.-S. Lee (2019) Nonsaponin fraction of Korean Red Ginseng attenuates cytokine production via inhibition of TLR4 expression. J. Ginseng Res. 43: 291-299. 미소장
18 Truong, V.-L., M. J. Bak, and W.-S. Jeong (2019) Chemopreventive activity of red ginseng oil in a mouse model of azoxymethane/dextran sulfate sodium-induced inflammation-associated colon carcinogenesis. J. Med. Food 22: 578-586. 미소장
19 Jang, S.-H., J. Park, S.-H. Kim, K.-M. Choi, E.-S. Ko, J.-D. Cha, Y.-R. Lee, H. Jang, and Y.-S. Jang (2017) Oral administration of red ginseng powder fermented with probiotic alleviates the severity of dextran-sulfate sodium-induced colitis in a mouse model. Chin. J. Nat. Med. 15: 192-201. 미소장
20 Fan, J., S. Liu, Z. Ai, Y. Chen, Y. Wang, Y. Li, X. Li, S. Xiao, and Y. Wang (2021) Fermented ginseng attenuates lipopolysaccharideinduced inflammatory responses by activating the TLR4/MAPK signaling pathway and remediating gut barrier. Food Funct. 12: 852-861. 미소장
21 Bae, E.-A., Y.-I. Yoo, I.-A. Lee, M. J. Han, and D.-H. Kim (2008)The anti-inflammmatory effect of fermented red ginseng in experimental colitic mice. Food Agric. Immunol. 19: 313-323. 미소장
22 Livak, K. J. and T. D. Schmittgen (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 25: 402-408. 미소장
23 Caporaso, J. G., C. L. Lauber, W. A. Walters, D. Berg-Lyons, J. Huntley, N. Fierer, S. M. Owens, J. Betley, L. Fraser, M. Bauer, N. Gormley, J. A. Gilbert, G. Smith, and R. Knight (2012) Ultrahigh-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms. ISME J. 6: 1621-1624. 미소장
24 Arndt, D., J. Xia, Y. Liu, Y. Zhou, A. C. Guo, J. A. Cruz, I. Sinelnikov, K. Budwill, C. L. Nesbø, and D. S. Wishart (2012)METAGENassist: a comprehensive web server for comparative metagenomics. Nucleic Acids Res. 40(Web Server issue): W88-W95. 미소장
25 Segata, N., J. Izard, L. Waldron, D. Gevers, L. Miropolsky, W. S. Garrett, and C. Huttenhower (2011) Metagenomic biomarker discovery and explanation. Genome Biol. 12: R60. 미소장
26 Udayappan, S., L. Manneras-Holm, A. Chaplin-Scott, C. Belzer, H. Herrema, G. M. Dallinga-Thie, S. H. Duncan, E. S. G. Stroes, A. K. Groen, H. J. Flint, F. Backhed, W. M. de Vos, and M. Nieuwdorp (2016) Oral treatment with Eubacterium hallii improves insulin sensitivity in db/db mice. NPJ Biofilms Microbiomes 2: 16009. 미소장
27 Liu, S., P. Qin, and J. Wang (2019) High-fat diet alters the intestinal microbiota in streptozotocin-induced type 2 diabetic mice. Microorganisms 7: 176. 미소장
28 Lee, S., M. L. Goodson, W. Vang, J. Rutkowsky, K. Kalanetra, M. Bhattacharya, D. Barile, and H. E. Raybould (2021) Human milk oligosaccharide 2'-fucosyllactose supplementation improves gut barrier function and signaling in the vagal afferent pathway in mice. Food Funct. 12: 8507-8521. 미소장
29 Kanauchi, O., M. Fukuda, Y. Matsumoto, S. Ishii, T. Ozawa, M. Shimizu, K. Mitsuyama, and A. Andoh (2006) Eubacterium limosum ameliorates experimental colitis and metabolite of microbe attenuates colonic inflammatory action with increase of mucosal integrity. World J. Gastroenterol. 12: 1071-1077. 미소장
30 Xu, Y., N. Wang, H.-Y. Tan, S. Li, C. Zhang, and Y. Feng (2020)Function of Akkermansia muciniphila in obesity: interactions with lipid metabolism, immune response and gut systems. Front. Microbiol. 11: 219. 미소장
31 Chelakkot, C., J. Ghim, and S. H. Ryu (2018) Mechanisms regulating intestinal barrier integrity and its pathological implications. Exp. Mol. Med. 50: 1-9. 미소장
32 Dun, Y., M. Liu, J. Chen, D. Peng, H. Zhao, Z. Zhou, T. Wang, C. Liu, Y. Guo, C. Zhang, and D. Yuan (2018) Regulatory effects of saponins from Panax japonicus on colonic epithelial tight junctions in aging rats. J. Ginseng Res. 42: 50-56. 미소장
33 Zenewicz, L. A., G. D. Yancopoulos, D. M. Valenzuela, A. J. Murphy, S. Stevens, and R. A. Flavell (2008) Innate and adaptive interleukin-22 protects mice from inflammatory bowel disease. Immunity 29: 947-957. 미소장
34 Sabihi, M., M. Böttcher, P. Pelczar, and S. Huber (2020)Microbiota-dependent effects of IL-22. Cells 9: 2205. 미소장
35 Zenewicz, L. A. and R. A. Flavell (2011) Recent advances in IL-22 biology. Int. Immunol. 23: 159-163. 미소장
36 Ceccarelli, S., N. Panera, M. Mina, D. Gnani, C. De Stefanis, A. Crudele, C. Rychlicki, S. Petrini, G. Bruscalupi, L. Agostinelli, L. Stronati, S. Cucchiara, G. Musso, C. Furlanello, G. Svegliati-Baroni, V. Nobili, and A. Alisi (2015) LPS-induced TNF-α factor mediates pro-inflammatory and pro-fibrogenic pattern in nonalcoholic fatty liver disease. Oncotarget 6: 41434-41452. 미소장
37 Larrosa, M., M. Azorín-Ortuño, M. J. Yañez-Gascón, M. T. García-Conesa, F. Tomás-Barberán, and J. C. Espín (2011) Lack of effect of oral administration of resveratrol in LPS-induced systemic inflammation. Eur. J. Nutr. 50: 673-680. 미소장
38 Khan, H. U., K. Aamir, P. R. Jusuf, G. Sethi, S. P. Sisinthy, R. Ghildyal, and A. Arya (2021) Lauric acid ameliorates lipopolysaccharide (LPS)-induced liver inflammation by mediating TLR4/MyD88 pathway in Sprague Dawley (SD) rats. Life Sci. 265: 118750. 미소장