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For: Xia CM, Zhao Y, Jiang L, Jiang J, Zhang SC. Schistosoma japonicum ova maintains epithelial barrier function during experimental colitis. World J Gastroenterol 2011; 17(43): 4810-4816 [PMID: 22147983 DOI: 10.3748/wjg.v17.i43.4810]
URL: https://www.wjgnet.com/1007-9327/full/v17/i43/4810.htm
Number Citing Articles
1
Nitin Tandra, Peipei Wu, Xinyuan Hu, Fei Mao, Wenrong Xu, Hui Qian. Extracellular Vesicles: A New Nano Tool for the Treatment of Inflammatory Bowel DiseasesCurrent Nanoscience 2019; 15(6): 589 doi: 10.2174/1573413715666190411141126
2
Ya Liu, Qing Ye, Yu-Lan Liu, Jian Kang, Yan Chen, Wei-Guo Dong. <i>Schistosoma japonicum</i> attenuates dextran sodium sulfate-induced colitis in mice <i>via</i> reduction of endoplasmic reticulum stressWorld Journal of Gastroenterology 2017; 23(31): 5700-5712 doi: 10.3748/wjg.v23.i31.5700
3
Justyna Rzepecka, William Harnett. Helminth Infections and their Impact on Global Public Health2014; : 479 doi: 10.1007/978-3-7091-1782-8_16
4
Vishal Khatri, Nikhil Chauhan, Ramaswamy Kalyanasundaram. Parasite Cystatin: Immunomodulatory Molecule with Therapeutic Activity against Immune Mediated DisordersPathogens 2020; 9(6): 431 doi: 10.3390/pathogens9060431
5
Amir Abdoli, Alireza Badirzadeh, Nazanin Mojtabavi, Ahmadreza Meamar, Reza Falak. Translational Autoimmunity2022; : 395 doi: 10.1016/B978-0-12-824390-9.00005-0
6
Zhenyu Wu, Lifu Wang, Yanlai Tang, Xi Sun. Parasite-Derived Proteins for the Treatment of Allergies and Autoimmune DiseasesFrontiers in Microbiology 2017; 8 doi: 10.3389/fmicb.2017.02164
7
Joel V. Weinstock, David E. Elliott. Translatability of helminth therapy in inflammatory bowel diseasesInternational Journal for Parasitology 2013; 43(3-4): 245 doi: 10.1016/j.ijpara.2012.10.016
8
Deborah Boyett, Michael H. Hsieh, Laura J. Knoll. Wormholes in Host Defense: How Helminths Manipulate Host Tissues to Survive and ReproducePLoS Pathogens 2014; 10(4): e1004014 doi: 10.1371/journal.ppat.1004014
9
Amir Abdoli, Hoda Mirzaian Ardakani. Potential application of helminth therapy for resolution of neuroinflammation in neuropsychiatric disordersMetabolic Brain Disease 2020; 35(1): 95 doi: 10.1007/s11011-019-00466-5
10
Marthe Heylen, Nathalie E. Ruyssers, Els M. Gielis, Els Vanhomwegen, Paul A. Pelckmans, Tom G. Moreels, Joris G. De Man, Benedicte Y. De Winter. Of worms, mice and man: An overview of experimental and clinical helminth-based therapy for inflammatory bowel diseasePharmacology & Therapeutics 2014; 143(2): 153 doi: 10.1016/j.pharmthera.2014.02.011
11
Geom Seog Seo, Wen-Yi Jiang, Pil-Hoon Park, Dong Hwan Sohn, Jae Hee Cheon, Sung Hee Lee. Hirsutenone reduces deterioration of tight junction proteins through EGFR/Akt and ERK1/2 pathway both converging to HO-1 inductionBiochemical Pharmacology 2014; 90(2): 115 doi: 10.1016/j.bcp.2014.05.006
12
Wenqi Shan, Wenzhe Zhang, Fei Xue, Yongbin Ma, Liyang Dong, Ting Wang, Yu Zheng, Dingqi Feng, Ming Chang, Guoyue Yuan, Xuefeng Wang. Schistosoma japonicum peptide SJMHE1 inhibits acute and chronic colitis induced by dextran sulfate sodium in miceParasites & Vectors 2021; 14(1) doi: 10.1186/s13071-021-04977-y
13
Klara A. Stark, Gabriel Rinaldi, Alba Cortés, Alice Costain, Andrew S. MacDonald, Cinzia Cantacessi. The role of the host gut microbiome in the pathophysiology of schistosomiasisParasite Immunology 2023; 45(4) doi: 10.1111/pim.12970
14
Derek M. McKay, Adam Shute, Fernando Lopes. Helminths and intestinal barrier functionTissue Barriers 2017; 5(1): e1283385 doi: 10.1080/21688370.2017.1283385
15
Taylor B. Smallwood, Paul R. Giacomin, Alex Loukas, Jason P. Mulvenna, Richard J. Clark, John J. Miles. Helminth Immunomodulation in Autoimmune DiseaseFrontiers in Immunology 2017; 8 doi: 10.3389/fimmu.2017.00453
16
Toshio Arai, Fernando Lopes. Potential of human helminth therapy for resolution of inflammatory bowel disease: The future aheadExperimental Parasitology 2022; 232: 108189 doi: 10.1016/j.exppara.2021.108189
17
Irina Leonardi, Isabelle Frey, Gerhard Rogler. Helminth therapy for organic diseases?Translational Research 2015; 166(6): 586 doi: 10.1016/j.trsl.2015.06.016
18
Ibtissem Ghouzali, Caroline Lemaitre, Wafa Bahlouli, Saïda Azhar, Christine Bôle-Feysot, Mathieu Meleine, Philippe Ducrotté, Pierre Déchelotte, Moïse Coëffier. Targeting immunoproteasome and glutamine supplementation prevent intestinal hyperpermeabilityBiochimica et Biophysica Acta (BBA) - General Subjects 2017; 1861(1): 3278 doi: 10.1016/j.bbagen.2016.08.010
19
Alice H. Costain, Andrew S. MacDonald, Hermelijn H. Smits. Schistosome Egg Migration: Mechanisms, Pathogenesis and Host Immune ResponsesFrontiers in Immunology 2018; 9 doi: 10.3389/fimmu.2018.03042
20
Hilda Vargas-Robles, Karla Fabiola Castro-Ochoa, Alí Francisco Citalán-Madrid, Michael Schnoor. Beneficial effects of nutritional supplements on intestinal epithelial barrier functions in experimental colitis models <i>in vivo</i>World Journal of Gastroenterology 2019; 25(30): 4181-4198 doi: 10.3748/wjg.v25.i30.4181
21
Justyna Rzepecka, William Harnett. Helminth Infections and their Impact on Global Public Health2022; : 607 doi: 10.1007/978-3-031-00303-5_17
22
Junhua Wang, Christine Goepfert, Norbert Mueller, Alessandra Piersigilli, Renyong Lin, Hao Wen, Dominique A. Vuitton, Lucine Vuitton, Christoph Mueller, Bruno Gottstein. Larval Echinococcus multilocularis infection reduces dextran sulphate sodium‐induced colitis in mice by attenuating T helper type 1/type 17‐mediated immune reactionsImmunology 2018; 154(1): 76 doi: 10.1111/imm.12860
23
Lifu Wang, Zilong Yu, Shuo Wan, Feng Wu, Wei Chen, Beibei Zhang, Datao Lin, Jiahua Liu, Hui Xie, Xi Sun, Zhongdao Wu. Exosomes Derived from Dendritic Cells Treated with Schistosoma japonicum Soluble Egg Antigen Attenuate DSS-Induced ColitisFrontiers in Pharmacology 2017; 8 doi: 10.3389/fphar.2017.00651
24
Priya Prahalad, Justin I. Odegaard, Ajay Chawla. The Th2 Type Immune Response in Health and Disease2016; : 155 doi: 10.1007/978-1-4939-2911-5_9