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• N-terminomics profiling of host proteins targeted by excretory-secretory proteases of the nematode Angiostrongylus vasorum identifies points of interaction with canine coagulation and complement cascade
  Nina Germitsch, Tobias Kockmann, Manuela Schnyder, Lucienne Tritten, Elham Kazemirad
  PLOS ONE.2025; 20(1): e0316217.     CrossRef
• Administration of Trichinella spiralis Antigens Alleviated Diabetic Nephropathy in Diabetic Mice
  Asmaa M. El-kady, Sarah A. Altwaim, Haleema H. Albohiri, Majed H. Wakid, Khalil Mohamed, Eman Abdullah Alshehri, Hayam Elshazly, Hatem A. Elshabrawy, Dina hamed
  Acta Parasitologica.2025;[Epub]     CrossRef
• Characterization of a novel invasive virulence of chymotrypsin-like elastase family member 2A from Trichinella spiralis
  Xin Guo, Xin Zhuo Zhang, Yao Zhang, Ru Zhang, Shao Rong Long, Ruo Dan Liu, Jing Cui, Zhong Quan Wang
  Acta Tropica.2025; 270: 107803.     CrossRef
• Paying attention to attention: High attention sites as indicators of protein family and function in language models
  Gowri Nayar, Alp Tartici, Russ B. Altman, Serdar Bozdag
  PLOS Computational Biology.2025; 21(9): e1013424.     CrossRef
• Regulatory and coding changes underlying development and host detection in vertebrate-parasitizing blowflies
  Pedro Mariano-Martins, Diniz Lima Ferreira, Vanessa Araujo Soares da Cunha, Carolina Kurotusch Canettieri, Letícia Chiara Baldassio de Paula, Tatiana Teixeira Torres
  International Journal for Parasitology.2025;[Epub]     CrossRef
• Trichinella spiralis serine protease mediates larval invasion of gut epithelium via binding to CK8 and activating RhoA/ROCK1 pathway
  Wen Wen Zheng, Xin Zhuo Zhang, Pei Kun Cong, Ru Zhang, Shao Rong Long, Xi Zhang, Ruo Dan Liu, Zhong Quan Wang, Jing Cui, Feng Xue
  PLOS Neglected Tropical Diseases.2025; 19(11): e0013725.     CrossRef
• Host-parasite interactions: a study on the pathogenicity of different Mesanophrys sp. densities and hemocytes-mediated parasitic resistance of swimming crabs (Portunus trituberculatus)
  Lujia Yang, Ruiling Zhou, Chunlin Wang, Xiao Xie, Suming Zhou, Fei Yin
  Parasitology Research.2024;[Epub]     CrossRef
• Serine protease mediates Ovomermis sinensis‐inhibited host immune responses by inducing apoptosis: implications for successful parasitism and host mortality
  Zhenlong Jiao, Mingming Chen, Wenjing Zhao, Yuanming Wu, Guo Guo
  Pest Management Science.2024; 80(4): 1968.     CrossRef
• Application of a recombinant novel trypsin from Trichinella spiralis for serodiagnosis of trichinellosis
  Lu Lu Han, Qi Qi Lu, Yang Li Li, Wen Wen Zheng, Pian Ren, Ruo Dan Liu, Jing Cui, Zhong Quan Wang
  Parasites & Vectors.2024;[Epub]     CrossRef
• A novel Trichinella spiralis serine proteinase disrupted gut epithelial barrier and mediated larval invasion through binding to RACK1 and activating MAPK/ERK1/2 pathway
  Yan Yan Song, Xin Zhuo Zhang, Bo Ning Wang, Yong Kang Cheng, Xin Guo, Xi Zhang, Shao Rong Long, Ruo Dan Liu, Zhong Quan Wang, Jing Cui, Krystyna Cwiklinski
  PLOS Neglected Tropical Diseases.2024; 18(1): e0011872.     CrossRef
• Salmon louse labial gland enzymes: implications for host settlement and immune modulation
  Helena Marie Doherty Midtbø, Christiane Eichner, Lars Are Hamre, Michael Dondrup, Linn Flesland, Kristoffer Helland Tysseland, Heidi Kongshaug, Andreas Borchel, Renate Hvidsten Skoge, Frank Nilsen, Aina-Cathrine Øvergård
  Frontiers in Genetics.2024;[Epub]     CrossRef
• Moonlighting on the Fasciola hepatica tegument: Enolase, a glycolytic enzyme, interacts with the extracellular matrix and fibrinolytic system of the host
  Eve O’Kelly, Krystyna Cwiklinski, Carolina De Marco Verissimo, Nichola Eliza Davies Calvani, Jesús López Corrales, Heather Jewhurst, Andrew Flaus, Richard Lalor, Judit Serrat, John P. Dalton, Javier González-Miguel, Gabriel Rinaldi
  PLOS Neglected Tropical Diseases.2024; 18(8): e0012069.     CrossRef
• Excreted/Secreted 15-kDa Proteins and Serine Protease Peptides from Haemonchus contortus Act as Immune-Response Enhancers in Lambs
  René Camas-Pereyra, Génesis Andrea Bautista-García, Gustavo Pérez-Anzúrez, Zaira Carolina Duran-Cortes, David Emanuel Reyes-Guerrero, Jocelyn Maza-Lopez, Agustín Olmedo-Juárez, María Eugenia López-Arellano
  Pathogens.2024; 13(7): 604.     CrossRef
• Early diagnosis of Trichinella spiralis and Trichinella nativa: Expression of the serine protease gene at the invasive intestinal and muscular larva stages
  Orken S. Akibekov, Aissarat M. Gajimuradova, Alfiya S. Syzdykova, Aibek Kh. Zhumalin, Fariza S. Zhagipar, Fabio Tosini, Zhannara Zh. Akanova, Nurtai N. Gubaidullin, Nasipkhan A. Askarova
  Veterinary World.2024; : 2124.     CrossRef
• Trypsin, chymotrypsin and elastase in health and disease
  Oladoyin Grace Famutimi, Victor Gbolahan Adebiyi, Bukola Grace Akinmolu, Omoniyi Vincent Dada, Isaac Olusanjo Adewale
  Future Journal of Pharmaceutical Sciences.2024;[Epub]     CrossRef
• Protein profile of extracellular vesicles derived from adult Parascaris spp.
  Vishnu Manikantan, Nichol E. Ripley, Martin K. Nielsen, Sriveny Dangoudoubiyam
  Parasites & Vectors.2024;[Epub]     CrossRef
• In silico analysis of two Haemonchus spp. serine protease peptides (S28) and their immunomodulatory activity in vitro
  René Camas-Pereyra, Génesis A. Bautista-García, Guillermina Avila, Yazmin Alcala-Canto, Jocelyn Maza-Lopez, David E. Reyes-Guerrero, Rosa Isabel Higuera-Piedrahita, María Eugenia López-Arellano
  Molecular and Biochemical Parasitology.2023; 253: 111545.     CrossRef
• Proteases and their inhibitors involved in Schistosoma mansoni egg-host interaction revealed by comparative transcriptomics with Fasciola hepatica eggs
  Kristyna Peterkova, Jiri Vorel, Jana Ilgova, Pavel Ostasov, Pavla Fajtova, Lukas Konecny, Marta Chanova, Martin Kasny, Martin Horn, Jan Dvorak
  International Journal for Parasitology.2023; 53(5-6): 253.     CrossRef
• Secreted peptidases contribute to virulence of fish pathogen Flavobacterium columnare
  Nicole C. Thunes, Haitham H. Mohammed, Jason P. Evenhuis, Ryan S. Lipscomb, David Pérez-Pascual, Rebecca J. Stevick, Clayton Birkett, Rachel A. Conrad, Jean-Marc Ghigo, Mark J. McBride
  Frontiers in Cellular and Infection Microbiology.2023;[Epub]     CrossRef
• Biological control 2.0: Use of nematophagous fungi enzymes for nematode control
  Filippe Elias de Freitas Soares, Juliana Marques Ferreira, Hugo Leonardo André Genier, Laith Khalil Tawfeeq Al-Ani, Liliana Aguilar-Marcelino
  Journal of Natural Pesticide Research.2023; 4: 100025.     CrossRef
• In vitro knockdown of TsDNase II-7 suppresses Trichinella spiralis invasion into the host’s intestinal epithelial cells
  Jing Wang, Xuemin Jin, Chengyao Li, Xinhui Chen, Yanfeng Li, Mingyuan Liu, Xiaolei Liu, Jing Ding, Pamela Marie Pennington
  PLOS Neglected Tropical Diseases.2023; 17(6): e0011323.     CrossRef
• An insight into the functional genomics and species classification of Eudiplozoon nipponicum (Monogenea, Diplozoidae), a haematophagous parasite of the common carp Cyprinus carpio
  Jiří Vorel, Nikol Kmentová, Christoph Hahn, Petr Bureš, Martin Kašný
  BMC Genomics.2023;[Epub]     CrossRef
• The gut microbiota contributes to changes in the host immune response induced by Trichinella spiralis
  Chengyao Li, Yi Liu, Xiaolei Liu, Xue Bai, Xuemin Jin, Fengyan Xu, Hong Chen, Yuanyuan Zhang, Isabelle Vallee, Mingyuan Liu, Yong Yang, Krystyna Cwiklinski
  PLOS Neglected Tropical Diseases.2023; 17(8): e0011479.     CrossRef
• Molecular characterization of a novel serine proteinase from Trichinella spiralis and its participation in larval invasion of gut epithelium
  Yan Yan Song, Xin Zhuo Zhang, Bo Ning Wang, Min Min Weng, Zhao Yu Zhang, Xin Guo, Xi Zhang, Zhong Quan Wang, Jing Cui, jong-Yil Chai
  PLOS Neglected Tropical Diseases.2023; 17(9): e0011629.     CrossRef
• Oral immunization with attenuated Salmonella encoding an elastase elicits protective immunity against Trichinella spiralis infection
  Xin Zhuo Zhang, Wen Wen Yue, Sheng Jie Bai, Hui Nan Hao, Yan Yan Song, Shao Rong Long, Ruo Dan Liu, Jing Cui, Zhong Quan Wang
  Acta Tropica.2022; 226: 106263.     CrossRef
• Comparative transcriptome profiles of Schistosoma japonicum larval stages: Implications for parasite biology and host invasion
  Shaoyun Cheng, Bingkuan Zhu, Fang Luo, Xiying Lin, Chengsong Sun, Yanmin You, Cun Yi, Bin Xu, Jipeng Wang, Yan Lu, Wei Hu, James Cotton
  PLOS Neglected Tropical Diseases.2022; 16(1): e0009889.     CrossRef
• Characterization of the genome and serine protease of a novel Bacillus subtilis isolate
  Zahoor Khan, Maryam Shafique, Faizan Saleem, M. Kamran Azim, Nusrat Jabeen, Sehar Afshan Naz
  Antonie van Leeuwenhoek.2022; 115(2): 281.     CrossRef
• Functional Diversity of the Excretory/Secretory Proteins of Nematode Parasites
  Paritosh Joshi, Prasanta Kumar K. Mishra
  Acta Parasitologica.2022; 67(2): 619.     CrossRef
• Proteomic Profiling and In Silico Characterization of the Secretome of Anisakis simplex Sensu Stricto L3 Larvae
  Maciej Kochanowski, Joanna Dąbrowska, Mirosław Różycki, Jacek Sroka, Jacek Karamon, Aneta Bełcik, Weronika Korpysa-Dzirba, Tomasz Cencek
  Pathogens.2022; 11(2): 246.     CrossRef
• Transcriptomic Analysis of Steinernema Nematodes Highlights Metabolic Costs Associated to Xenorhabdus Endosymbiont Association and Rearing Conditions
  Emilie Lefoulon, John G. McMullen, S. Patricia Stock
  Frontiers in Physiology.2022;[Epub]     CrossRef
• Proteases secreted by Trichinella spiralis intestinal infective larvae damage the junctions of the intestinal epithelial cell monolayer and mediate larval invasion
  Yan Yan Song, Qi Qi Lu, Lu Lu Han, Shu Wei Yan, Xin Zhuo Zhang, Ruo Dan Liu, Shao Rong Long, Jing Cui, Zhong Quan Wang
  Veterinary Research.2022;[Epub]     CrossRef
• Proteomic Analysis of Plasma-Derived Extracellular Vesicles From Mice With Echinococcus granulosus at Different Infection Stages and Their Immunomodulatory Functions
  Chunli Shi, Xiaojing Zhou, Wenjuan Yang, Jianwen Wu, Min Bai, Ying Zhang, Wei Zhao, Hui Yang, Atsushi Nagai, Mei Yin, Xiaoping Gao, Shuqin Ding, Jiaqing Zhao
  Frontiers in Cellular and Infection Microbiology.2022;[Epub]     CrossRef
• Tandem Mass Tagging (TMT) Reveals Tissue-Specific Proteome of L4 Larvae of Anisakis simplex s. s.: Enzymes of Energy and/or Carbohydrate Metabolism as Potential Drug Targets in Anisakiasis
  Robert Stryiński, Jesús Mateos, Mónica Carrera, Jan Paweł Jastrzębski, Iwona Bogacka, Elżbieta Łopieńska-Biernat
  International Journal of Molecular Sciences.2022; 23(8): 4336.     CrossRef
• Novel Inhibitors and Activity-Based Probes Targeting Trypsin-Like Serine Proteases
  Timothy E. G. Ferguson, James A. Reihill, S. Lorraine Martin, Brian Walker
  Frontiers in Chemistry.2022;[Epub]     CrossRef
• Transcriptomic and proteomic profiling of peptidase expression in Fasciola hepatica eggs developing at host’s body temperature
  Jana Ilgová, Jiří Vorel, Pavel Roudnický, Lucie Škorpíková, Martin Horn, Martin Kašný
  Scientific Reports.2022;[Epub]     CrossRef
• Trichinella britovi recombinant proteins produced in Pichia pastoris expression system for specific IgG antibody detection in the sera of mice and pigs infected with Trichinella spp.
  Sylwia Grzelak, Justyna Bień-Kalinowska, Anna Stachyra
  Experimental Parasitology.2022; 242: 108386.     CrossRef
• A ShK-like Domain from Steinernema carpocapsae with Bioinsecticidal Potential
  Jorge Frias, Duarte Toubarro, Gro Elin Kjæreng Bjerga, Pål Puntervoll, João B. Vicente, Rui L. Reis, Nelson Simões
  Toxins.2022; 14(11): 754.     CrossRef
• Bioguided isolation of N-malonyl-(+)-tryptophan from the fruit of Pithecellobium dulce (Roxb.) Benth. that showed high activity against Hymenolepis nana
  Gabriela López-Angulo, Sara Elizabeth Verdugo-Gaxiola, Julio Montes-Avila, Sylvia Páz Díaz-Camacho, Valentín Miranda-Soto, Nancy Yareli Salazar-Salas, Francisco Delgado-Vargas
  Natural Product Research.2021; 35(4): 593.     CrossRef
• A putative lysozyme and serine carboxypeptidase from Heterorhabditis bacteriophora show differential virulence capacities in Drosophila melanogaster
  Eric Kenney, Amulya Yaparla, John M. Hawdon, Damien M. O’ Halloran, Leon Grayfer, Ioannis Eleftherianos
  Developmental & Comparative Immunology.2021; 114: 103820.     CrossRef
• A critical review on marine serine protease and its inhibitors: A new wave of drugs?
  Noora Barzkar, Zahoor Khan, Saeid Tamadoni Jahromi, Sajjad Pourmozaffar, Mohsen Gozari, Reza Nahavandi
  International Journal of Biological Macromolecules.2021; 170: 674.     CrossRef
• Proteomic analysis of hydrolytic proteases in excretory/secretory proteins from Trichinella spiralis intestinal infective larvae using zymography combined with shotgun LC-MS/MS approach
  Hua Nan Ren, Tong Xu Zhuo, Sheng Jie Bai, Ying Bai, Xiang Yuan Sun, Ruo Dan Liu, Shao Rong Long, Jing Cui, Zhong Quan Wang
  Acta Tropica.2021; 216: 105825.     CrossRef
• Disruption of Epithelial Barrier of Caco-2 Cell Monolayers by Excretory Secretory Products of Trichinella spiralis Might Be Related to Serine Protease
  Chengyao Li, Xue Bai, Xiaolei Liu, Yuanyuan Zhang, Lei Liu, Lixiao Zhang, Fengyan Xu, Yong Yang, Mingyuan Liu
  Frontiers in Microbiology.2021;[Epub]     CrossRef
• Immune Protection of a Helminth Protein in the DSS-Induced Colitis Model in Mice
  Shao Rong Long, Ruo Dan Liu, Deepak Vijaya Kumar, Zhong Quan Wang, Chien-Wen Su
  Frontiers in Immunology.2021;[Epub]     CrossRef
• The immune protection induced by a serine protease from the Trichinella spiralis adult against Trichinella spiralis infection in pigs
  Daoxiu Xu, Xue Bai, Jing Xu, Xuelin Wang, Zijian Dong, Wenjie Shi, Fengyan Xu, Yanfeng Li, Mingyuan Liu, Xiaolei Liu, Hernando A. del Portillo
  PLOS Neglected Tropical Diseases.2021; 15(5): e0009408.     CrossRef
• Spatial expression pattern of serine proteases in the blood fluke Schistosoma mansoni determined by fluorescence RNA in situ hybridization
  Lenka Ulrychová, Pavel Ostašov, Marta Chanová, Michael Mareš, Martin Horn, Jan Dvořák
  Parasites & Vectors.2021;[Epub]     CrossRef
• Characterization of a chymotrypsin-like enzyme from Trichinella spiralis and its facilitation of larva penetration into the host's enteral epithelial cells
  Jia Xu, Ruo Dan Liu, Shao Rong Long, Yan Yan Song, Peng Jiang, Xi Zhang, Jing Cui, Zhong Quan Wang
  Research in Veterinary Science.2020; 128: 1.     CrossRef
• In silico design of a T-cell epitope vaccine candidate for parasitic helminth infection
  Ayat Zawawi, Ruth Forman, Hannah Smith, Iris Mair, Murtala Jibril, Munirah H. Albaqshi, Andrew Brass, Jeremy P. Derrick, Kathryn J. Else, Maria Elena Bottazzi
  PLOS Pathogens.2020; 16(3): e1008243.     CrossRef
• Effect of recombinant serine protease from adult stage of Trichinella spiralis on TNBS-induced experimental colitis in mice
  Jianda Pang, Jing Ding, Lixiao Zhang, Yuanyuan Zhang, Yaming Yang, Xue Bai, Xiaolei Liu, Xuemin Jin, Heng Guo, Yong Yang, Mingyuan Liu
  International Immunopharmacology.2020; 86: 106699.     CrossRef
• Binding of elastase-1 and enterocytes facilitates Trichinella spiralis larval intrusion of the host's intestinal epithelium
  Chen Xi Hu, Jie Zeng, Da Qi Yang, Xin Yue, Ruo Dan Liu, Shao Rong Long, Xi Zhang, Peng Jiang, Jing Cui, Zhong Quan Wang
  Acta Tropica.2020; 211: 105592.     CrossRef
• Effect of recombinant serine protease from newborn larval stage of Trichinella spiralis on 2,4,6-trinitrobenzene sulfonic acid-induced experimental colitis in mice
  Zheng Qu, Xuemin Jin, Yang Wang, Yaming Yang, Yang Li, Xue Bai, Yong Yang, Ning Xu, Xuelin Wang, Mingyuan Liu
  Acta Tropica.2020; 211: 105553.     CrossRef
• Anisakis simplex products impair intestinal epithelial barrier function and occludin and zonula occludens-1 localisation in differentiated Caco-2 cells
  Noelia Carballeda-Sangiao, Isabel Sánchez-Alonso, Alfonso Navas, Susana C. Arcos, Pilar Fernández de Palencia, Mercedes Careche, Miguel González-Muñoz, Luisa Magalhães
  PLOS Neglected Tropical Diseases.2020; 14(7): e0008462.     CrossRef
• Comparative genomics and transcriptomics of 4 Paragonimus species provide insights into lung fluke parasitism and pathogenesis
  Bruce A Rosa, Young-Jun Choi, Samantha N McNulty, Hyeim Jung, John Martin, Takeshi Agatsuma, Hiromu Sugiyama, Thanh Hoa Le, Pham Ngoc Doanh, Wanchai Maleewong, David Blair, Paul J Brindley, Peter U Fischer, Makedonka Mitreva
  GigaScience.2020;[Epub]     CrossRef
• Vaccination of Mice with a Novel Trypsin from Trichinella spiralis Elicits the Immune Protection against Larval Challenge
  Yao Zhang, Jie Zeng, Yan Yan Song, Shao Rong Long, Ruo Dan Liu, Peng Jiang, Xi Zhang, Jing Cui, Zhong Quan Wang
  Vaccines.2020; 8(3): 437.     CrossRef
• Molecular cloning and characterization of a novel peptidase from Trichinella spiralis and protective immunity elicited by the peptidase in BALB/c mice
  Jun Jun Lei, Yuan Yuan Hu, Fang Liu, Shu Wei Yan, Ruo Dan Liu, Shao Rong Long, Peng Jiang, Jing Cui, Zhong Quan Wang
  Veterinary Research.2020;[Epub]     CrossRef
• Immunomodulation and Immune Escape Strategies of Gastrointestinal Helminths and Schistosomes
  Marie Wiedemann, David Voehringer
  Frontiers in Immunology.2020;[Epub]     CrossRef
• Proteases and pseudoproteases in parasitic arthropods of clinical importance
  Deepani Darshika Fernando, Katja Fischer
  The FEBS Journal.2020; 287(19): 4284.     CrossRef
• Molecular characterization of a Trichinella spiralis serine proteinase
  Xin Yue, Xiang Yuan Sun, Fang Liu, Chen Xi Hu, Ying Bai, Qi Da Yang, Ruo Dan Liu, Xi Zhang, Jing Cui, Zhong Quan Wang
  Veterinary Research.2020;[Epub]     CrossRef
• Activity of serine proteases from Fasciola hepatica eggs in relation to pH and temperature
  L. Kianifard, M. Yakhchali, M. Imani
  BULGARIAN JOURNAL OF VETERINARY MEDICINE.2020; 23(3): 350.     CrossRef
• Host Immunity and Inflammation to Pulmonary Helminth Infections
  Jill E. Weatherhead, Pedro Gazzinelli-Guimaraes, John M. Knight, Ricardo Fujiwara, Peter J. Hotez, Maria Elena Bottazzi, David B. Corry
  Frontiers in Immunology.2020;[Epub]     CrossRef
• Intranasal immunization with recombinant Trichinella spiralis serine protease elicits protective immunity in BALB/c mice
  Ge Ge Sun, Jun Jun Lei, Hua Nan Ren, Yao Zhang, Kai Xia Guo, Shao Rong Long, Ruo Dan Liu, Peng Jiang, Zhong Quan Wang, Jing Cui
  Experimental Parasitology.2019; 201: 1.     CrossRef
• Cloning, expression and characterization of a novel alkaline serine protease gene from native Iranian Bacillus sp.; a producer of protease for use in livestock
  Ahmadreza Ariyaei, Ayoub Farhadi, Fatemeh Moradian, Ghodrat Rahimi Mianji
  Gene.2019; 693: 10.     CrossRef
• Exploration of extracellular vesicles from Ascaris suum provides evidence of parasite–host cross talk
  Eline P. Hansen, Bastian Fromm, Sidsel D. Andersen, Antonio Marcilla, Kasper L. Andersen, Anne Borup, Andrew R. Williams, Aaron R. Jex, Robin B. Gasser, Neil D. Young, Ross S. Hall, Allan Stensballe, Vladimir Ovchinnikov, Yan Yan, Merete Fredholm, Stig M.
  Journal of Extracellular Vesicles.2019;[Epub]     CrossRef
• Hybrid Assembly of the Genome of the Entomopathogenic Nematode Steinernema carpocapsae Identifies the X-Chromosome
  Lorrayne Serra, Marissa Macchietto, Aide Macias-Muñoz, Cassandra Joan McGill, Isaryhia Maya Rodriguez, Bryan Rodriguez, Rabi Murad, Ali Mortazavi
  G3 Genes|Genomes|Genetics.2019; 9(8): 2687.     CrossRef
• Complex insight on microanatomy of larval “human broad tapeworm” Dibothriocephalus latus (Cestoda: Diphyllobothriidea)
  Daniel Barčák, Aneta Yoneva, Hana Sehadová, Mikuláš Oros, Andrea Gustinelli, Roman Kuchta
  Parasites & Vectors.2019;[Epub]     CrossRef
• Screening and verification for proteins that interact with leucine aminopeptidase of Taenia pisiformis using a yeast two-hybrid system
  Shaohua Zhang
  Parasitology Research.2019; 118(12): 3387.     CrossRef
• Proteases and protease inhibitors in infectious diseases
  Ayodeji A. Agbowuro, Wilhelmina M. Huston, Allan B. Gamble, Joel D. A. Tyndall
  Medicinal Research Reviews.2018; 38(4): 1295.     CrossRef
• Molecular cloning and characterization of leucine aminopeptidase gene from Taenia pisiformis
  Shaohua Zhang, Xuepeng Cai, Xuenong Luo, Shuai Wang, Aijiang Guo, Junling Hou, Run Wu
  Experimental Parasitology.2018; 186: 1.     CrossRef
• SmSP2: A serine protease secreted by the blood fluke pathogen Schistosoma mansoni with anti-hemostatic properties
  Adrian Leontovyč, Lenka Ulrychová, Anthony J. O’Donoghue, Jiří Vondrášek, Lucie Marešová, Martin Hubálek, Pavla Fajtová, Marta Chanová, Zhenze Jiang, Charles S. Craik, Conor R. Caffrey, Michael Mareš, Jan Dvořák, Martin Horn, Robert M. Greenberg
  PLOS Neglected Tropical Diseases.2018; 12(4): e0006446.     CrossRef
• Characterization of a Trichinella spiralis putative serine protease. Study of its potential as sero-diagnostic tool
  Ge Ge Sun, Yan Yan Song, Peng Jiang, Hua Na Ren, Shu Wei Yan, Yue Han, Ruo Dan Liu, Xi Zhang, Zhong Quan Wang, Jing Cui, Edoardo Pozio
  PLOS Neglected Tropical Diseases.2018; 12(5): e0006485.     CrossRef
• Trichuris muris whey acidic protein induces type 2 protective immunity against whipworm
  Neima Briggs, Junfei Wei, Leroy Versteeg, Bin Zhan, Brian Keegan, Ashish Damania, Jeroen Pollet, Kelly S. Hayes, Coreen Beaumier, Christopher A. Seid, Jamie Leong, Richard K. Grencis, Maria Elena Bottazzi, K. Jagannadha Sastry, Peter J. Hotez, Edward Mitr
  PLOS Pathogens.2018; 14(8): e1007273.     CrossRef
• The coagulation system helps control infection caused by the ciliate parasite Philasterides dicentrarchi in the turbot Scophthalmus maximus (L.)
  V. Blanco-Abad, M. Noia, A. Valle, F. Fontenla, I. Folgueira, A.P. De Felipe, P. Pereiro, J. Leiro, J. Lamas
  Developmental & Comparative Immunology.2018; 87: 147.     CrossRef
• Molecular characterization of a putative serine protease from Trichinella spiralis and its elicited immune protection
  Ge Ge Sun, Hua Nan Ren, Ruo Dan Liu, Yan Yan Song, Xin Qi, Chen Xi Hu, Fan Yang, Peng Jiang, Xi Zhang, Zhong Quan Wang, Jing Cui
  Veterinary Research.2018;[Epub]     CrossRef
• Silent Witness: Dual-Species Transcriptomics Reveals Epithelial Immunological Quiescence to Helminth Larval Encounter and Fostered Larval Development
  Friederike Ebner, Mathias Kuhring, Aleksandar Radonić, Ankur Midha, Bernhard Y. Renard, Susanne Hartmann
  Frontiers in Immunology.2018;[Epub]     CrossRef
• Protective immunity against Trichinella spiralis in mice elicited by oral vaccination with attenuated Salmonella-delivered TsSP1.2 DNA
  Jie Feng Li, Kai Xia Guo, Xin Qi, Jun Jun Lei, Yue Han, Shu Wei Yan, Peng Jiang, Chuan Yu, Xiang Chao Cheng, Zhong Quan Wang, Jing Cui
  Veterinary Research.2018;[Epub]     CrossRef
• Plasminogen-binding proteins as an evasion mechanism of the host’s innate immunity in infectious diseases
  Dolores A. Ayón-Núñez, Gladis Fragoso, Raúl J. Bobes, Juan P. Laclette
  Bioscience Reports.2018;[Epub]     CrossRef
• Editing the genome of Aphanomyces invadans using CRISPR/Cas9
  Muhammad Majeed, Hatem Soliman, Gokhlesh Kumar, Mansour El-Matbouli, Mona Saleh
  Parasites & Vectors.2018;[Epub]     CrossRef
• Activity profiling of peptidases in Angiostrongylus costaricensis first-stage larvae and adult worms
  Karina M. Rebello, James H. McKerrow, Ester M. Mota, Anthony J. O´Donoghue, Ana Gisele C. Neves-Ferreira, John Pius Dalton
  PLOS Neglected Tropical Diseases.2018; 12(10): e0006923.     CrossRef
• ВЛИЯНИЕ ЗАРАЖЕНИЯ ЦЕСТОДОЙ PROTEOCEPHALUS TORULOSUS BATSCH, 1786 НА АКТИВНОСТЬ ФЕРМЕНТОВ В КИШЕЧНИКЕ СИНЦА (BALLERUS BALLERUS L.), "Паразитология"
  Т.В. Фролова, Г.И. Извекова
  Паразитология.2018; (4): 292.     CrossRef
• Molecular characterization of a 31 kDa protein from Trichinella spiralis and its induced immune protection in BALB/c mice
  Hua Nan Ren, Kai Xia Guo, Yao Zhang, Ge Ge Sun, Ruo Dan Liu, Peng Jiang, Xi Zhang, Li Wang, Jing Cui, Zhong Quan Wang
  Parasites & Vectors.2018;[Epub]     CrossRef
• Recent advances in proteomic applications for schistosomiasis research: potential clinical impact
  Javier Sotillo, Denise Doolan, Alex Loukas
  Expert Review of Proteomics.2017; 14(2): 171.     CrossRef
• A critical review on serine protease: Key immune manipulator and pathology mediator
  S. Patel
  Allergologia et Immunopathologia.2017; 45(6): 579.     CrossRef
• Proteolytic enzymes and their inhibitors in cestodes
  G. I. Izvekova, T. V. Frolova
  Biology Bulletin Reviews.2017; 7(2): 150.     CrossRef
• Comparative proteomics of hydatid fluids from two Echinococcus multilocularis isolates
  Karina M. Monteiro, Karina R. Lorenzatto, Jeferson C. de Lima, Guilherme B. dos Santos, Sabine Förster, Gabriela P. Paludo, Paulo C. Carvalho, Klaus Brehm, Henrique B. Ferreira
  Journal of Proteomics.2017; 162: 40.     CrossRef
• Proteomic Analysis of Trichinella spiralis Adult Worm Excretory-Secretory Proteins Recognized by Sera of Patients with Early Trichinellosis
  Zhong Q. Wang, Ruo D. Liu, Ge G. Sun, Yan Y. Song, Peng Jiang, Xi Zhang, Jing Cui
  Frontiers in Microbiology.2017;[Epub]     CrossRef
• Immunoproteomic analysis of the excretory-secretory products of Trichinella pseudospiralis adult worms and newborn larvae
  Yang Wang, Xue Bai, Haichao Zhu, Xuelin Wang, Haining Shi, Bin Tang, Pascal Boireau, Xuepeng Cai, Xuenong Luo, Mingyuan Liu, Xiaolei Liu
  Parasites & Vectors.2017;[Epub]     CrossRef
• Effects of ionic liquids on the hydrolysis of casein by lumbrokinase
  Yunchang Fan, Xing Dong, Yingying Zhong, Jing Li, Juan Miao, Shaofeng Hua, Yan Li, Boyu Cheng, Wenqiong Chen
  Biochemical Engineering Journal.2016; 109: 35.     CrossRef
• Carbonic anhydrase enzyme as a potential therapeutic target for experimental trichinellosis
  Abeer E. Saad, Dalia S. Ashour, Dina M. Abou Rayia, Asmaa E. Bedeer
  Parasitology Research.2016; 115(6): 2331.     CrossRef
• Integrated Activity and Genetic Profiling of Secreted Peptidases in Cryptococcus neoformans Reveals an Aspartyl Peptidase Required for Low pH Survival and Virulence
  Starlynn C. Clarke, Phillip A. Dumesic, Christina M. Homer, Anthony J. O’Donoghue, Florencia La Greca, Lenka Pallova, Pavel Majer, Hiten D. Madhani, Charles S. Craik, Robin Charles May
  PLOS Pathogens.2016; 12(12): e1006051.     CrossRef

Citations

Citations to this article as recorded by  

• Assessing Zoonotic Risks of Blastocystis Infection in Singapore
  Thet Tun Aung, Charlotte Kai Qi How, Jean-Marc Chavatte, Nazmi Bin Nazir, Edgar Macabe Pena, Bryan Ogden, Grace Rou’en Lim, Yasmina Arditi Paramastri, Lois Anne Zitzow, Hanrong Chen, Niranjan Nagarajan, Kevin Shyong Wei Tan, Benoit Malleret
  Pathogens.2025; 14(8): 773.     CrossRef
• Prevalence and subtype distribution of Blastocystis infections among community participants in Thailand: a systematic review and meta-analysis
  Manas Kotepui, Supaluk Popruk, Kwuntida Uthaisar Kotepui, Frederick Ramirez Masangkay, Kinley Wangdi, Aongart Mahittikorn, Christen Rune Stensvold
  Parasite.2025; 32: 53.     CrossRef
• Subtype–host patterns and genetic differentiation of Blastocystis sp. in the Philippines
  Davin Edric V. Adao, Windell L. Rivera
  Heliyon.2024; 10(7): e29019.     CrossRef
• Blastocystis colonization and associations with population parameters in Thai adults
  Vasana Jinatham, Amara Yowang, Christen Rune Stensvold, Eleni Michalopoulou, Thanakrit Vichasilp, Picha Suwannahitatorn, Siam Popluechai, Anastasios D. Tsaousis, Eleni Gentekaki, Funda Dogruman-Al
  PLOS Neglected Tropical Diseases.2024; 18(7): e0012292.     CrossRef
• Occurrence and Genotypic Identification of Blastocystis spp. and Enterocytozoon bieneusi in Bamaxiang Pigs in Bama Yao Autonomous County of Guangxi Province, China
  Xingang Yu, Xuanru Mu, Kaijian Yuan, Sifan Wang, Yilong Li, Hui Xu, Qiaoyu Li, Wenjing Zeng, Zhili Li, Jianchao Guo, Yang Hong
  Animals.2024; 14(22): 3344.     CrossRef
• Phylogenetic relationship of nonmammalian and avian Blastocystis isolates and conventional subtypes
  Vanessa Yvonne B. Meclat, Keith Sigfred B. Ancheta, Davin Edric V. Adao, Windell L. Rivera
  Journal of Parasitic Diseases.2023; 47(1): 192.     CrossRef
• Prevalence and Subtype Distribution of Blastocystis Isolated from School-Aged Children in the Thai-Myanmar Border, Ratchaburi Province, Thailand
  Amanee Abu, Chantira Sutthikornchai, Aongart Mahittikorn, Khuanchai Koompapong, Rachatawan Chiabchalard, Dumrongkiet Arthan, Ngamphol Soonthornworasiri, Supaluk Popruk
  International Journal of Environmental Research and Public Health.2022; 20(1): 204.     CrossRef
• Prevalence and genotypes/subtypes of Enterocytozoon bieneusi and Blastocystis sp. in different breeds of cattle in Jiangxi Province, southeastern China
  Sen Li, Ping Wang, Xing-Quan Zhu, Yang Zou, Xiao-Qing Chen
  Infection, Genetics and Evolution.2022; 98: 105216.     CrossRef
• Molecular detection of Cryptosporidium spp., Giardia duodenalis, and Enterocytozoon bieneusi in school children at the Thai-Myanmar border
  Chantira Sutthikornchai, Supaluk Popruk, Aongart Mahittikorn, Dumrongkiet Arthan, Ngamphol Soonthornworasiri, Chirawat Paratthakonkun, Yaoyu Feng, Lihua Xiao
  Parasitology Research.2021; 120(8): 2887.     CrossRef
• Molecular prevalence and subtype distribution ofBlastocystissp. in Asia and in Australia
  Sara Nemati, Mohammad Reza Zali, Paul Johnson, Hamed Mirjalali, Panagiotis Karanis
  Journal of Water and Health.2021; 19(5): 687.     CrossRef
• Epidemiology and subtype distribution of Blastocystis in humans: A review
  Supaluk Popruk, Davin Edric V. Adao, Windell L. Rivera
  Infection, Genetics and Evolution.2021; 95: 105085.     CrossRef
• The Coexistence of Blastocystis spp. in Humans, Animals and Environmental Sources from 2010–2021 in Asia
  Adedolapo Aminat Rauff-Adedotun, Farah Haziqah Meor Termizi, Nurshafarina Shaari, Ii Li Lee
  Biology.2021; 10(10): 990.     CrossRef
• Prevalence, subtypes and risk factors of Blastocystis spp. infection among pre- and perimenopausal women
  Danuta Kosik-Bogacka, Małgorzata Lepczyńska, Karolina Kot, Małgorzata Szkup, Natalia Łanocha-Arendarczyk, Ewa Dzika, Elżbieta Grochans
  BMC Infectious Diseases.2021;[Epub]     CrossRef
• Molecular prevalence and subtypes of Blastocystis sp. in primates in northern China
  Lei Ma, Haixiav Qiao, Heqin Wang, Shuai Li, Pupu Zhai, Jing Huang, Yinghui Guo
  Transboundary and Emerging Diseases.2020; 67(6): 2789.     CrossRef
• Prevalence and Subtype Distribution of Blastocystis Infection in Patients with Diabetes Mellitus in Thailand
  Noppon Popruk, Satakamol Prasongwattana, Aongart Mahittikorn, Attakorn Palasuwan, Supaluk Popruk, Duangdao Palasuwan
  International Journal of Environmental Research and Public Health.2020; 17(23): 8877.     CrossRef
• Identifikasi Molekuler Blastocystis sp. pada Monyet Ekor Panjang (Macaca fascicularis) di Taman Nasional Baluran, Situbondo, Jawa Timur
  Dyah Ayu Kurniawati, Lucia Tri Suwanti, Nunuk Dyah Retno Lastuti, Setiawan Koesdarto, Endang Suprihati, Mufasirin Mufasirin, Arif Pratiwi
  Jurnal Medik Veteriner.2020; 3(2): 138.     CrossRef
• A Simple Genotyping Method for Rapid Differentiation of Blastocystis Subtypes and Subtype Distribution of Blastocystis spp. in Thailand
  Nittaya Srichaipon, Surang Nuchprayoon, Sarit Charuchaibovorn, Pattadon Sukkapan, Vivornpun Sanprasert
  Pathogens.2019; 8(1): 38.     CrossRef
• Evaluation of Blastocystis sp. Frequency in Referred Samples to Urban Laboratories: Is it a Potential Risk for Deployed Troops?
  Taher Elmi, Fariba Amni, Bahman Rahimi Esboei, Shirzad Gholami, Mostafa Akbariqomi, Mohsen Mortazavi, Mohammad Barati, Fatemeh Tabatabaie
  Journal of Archives in Military Medicine.2019;[Epub]     CrossRef
• Prevalence and subtype distribution of Blastocystis in ethnic minority groups on both sides of the China–Myanmar border, and assessment of risk factors
  Baiyan Gong, Xiaohua Liu, Yanchen Wu, Ning Xu, Meng Xu, Fengkun Yang, Lei Tong, Kexin Zhou, Jianping Cao, Aiqin Liu, Yujuan Shen
  Parasite.2019; 26: 46.     CrossRef
• Blastocystis subtypes detected in long-tailed macaques in Thailand—Further evidence of cryptic host specificity
  Kotchaphon Vaisusuk, Weerachai Saijuntha, Sutthira Sedlak, Thongchit Thanchomnang, Warayutt Pilap, Warong Suksavate, Christen Rune Stensvold, Chairat Tantrawatpan
  Acta Tropica.2018; 184: 78.     CrossRef
• Diagnosis and Identification of Blastocystis Subtypes in Primary School Children in Jakarta
  Ika P Sari, Martwinny R Benung, Sri Wahdini, Agnes Kurniawan
  Journal of Tropical Pediatrics.2018; 64(3): 208.     CrossRef
• Blastocystis subtype 5: Predominant subtype on pig farms, Thailand
  Ai-rada Pintong, Suparat Sunyanusin, Rapeepan Prasertbun, Aongart Mahittikorn, Hirotake Mori, Tanasak Changbunjong, Chalit Komalamisra, Yaowalark Sukthana, Supaluk Popruk
  Parasitology International.2018; 67(6): 824.     CrossRef
• Intestinal parasite infections in a rural community of Rio de Janeiro (Brazil): Prevalence and genetic diversity of Blastocystis subtypes
  Carolina Valença Barbosa, Magali Muniz Barreto, Rosemary de Jesus Andrade, Fernando Sodré, Claudia Masini d’Avila-Levy, José Mauro Peralta, Ricardo Pereira Igreja, Heloisa Werneck de Macedo, Helena Lucia Carneiro Santos, Maria Victoria Periago
  PLOS ONE.2018; 13(3): e0193860.     CrossRef
• Genetic diversity analysis of Blastocystis subtypes from both symptomatic and asymptomatic subjects using a barcoding region from the 18S rRNA gene
  Tahereh Rezaei Riabi, Hamed Mirjalali, Ali Haghighi, Mohammad Rostami Nejad, Mohammad Amin Pourhoseingholi, Philippe Poirier, Frederic Delbac, Ivan Wawrzyniak, Mohammad Reza Zali
  Infection, Genetics and Evolution.2018; 61: 119.     CrossRef
• Blastocystis subtypes and their association with Irritable Bowel Syndrome
  Susana Cifre, Mónica Gozalbo, Vicente Ortiz, José M. Soriano, J. Francisco Merino, María Trelis
  Medical Hypotheses.2018; 116: 4.     CrossRef
• Blastocystis infection and subtype distribution in humans, cattle, goats, and pigs in central and western Thailand
  Ruenruetai Udonsom, Rapeepan Prasertbun, Aongart Mahittikorn, Hirotake Mori, Tanasak Changbunjong, Chalit Komalamisra, Ai-rada Pintong, Yaowalark Sukthana, Supaluk Popruk
  Infection, Genetics and Evolution.2018;[Epub]     CrossRef
• High diversity of Blastocystis subtypes isolated from asymptomatic adults living in Chiang Rai, Thailand
  Amara Yowang, Anastasios D. Tsaousis, Tawatchai Chumphonsuk, Nontaphat Thongsin, Niwed Kullawong, Siam Popluechai, Eleni Gentekaki
  Infection, Genetics and Evolution.2018; 65: 270.     CrossRef
• Subtype identification of human Blastocystis spp. isolated from Lao People’s Democratic Republic
  Oranuch Sanpool, Sakhone Laymanivong, Tongjit Thanchomnang, Rutchanee Rodpai, Lakkhana Sadaow, Issarapong Phosuk, Wanchai Maleewong, Pewpan M. Intapan
  Acta Tropica.2017; 168: 37.     CrossRef
• Association of Blastocystis subtypes with diarrhea in children
  F Zulfa, I P Sari, A Kurniawan
  Journal of Physics: Conference Series.2017; 884: 012031.     CrossRef
• The relation between Blastocystis and the intestinal microbiota in Swedish travellers
  Joakim Forsell, Johan Bengtsson-Palme, Martin Angelin, Anders Johansson, Birgitta Evengård, Margareta Granlund
  BMC Microbiology.2017;[Epub]     CrossRef
• Are soil and waterborne parasitic infections health risk for worker populations in southeast Turkey?
  Sibel Ak, Fadime Eroğlu, Ali İhsan Nergiz, Furkan Hıyamlı
  Dicle Tıp Dergisi.2017; 44(2): 205.     CrossRef
• Subtype Distribution of Blastocystis in Communities along the Chao Phraya River, Thailand
  Attakorn Palasuwan, Duangdao Palasuwan, Aongart Mahittikorn, Rachatawan Chiabchalard, Valery Combes, Supaluk Popruk
  The Korean Journal of Parasitology.2016; 54(4): 455.     CrossRef
• The distribution of Blastocystis subtypes in isolates from Qatar
  Marawan Abu-Madi, Mahmoud Aly, Jerzy M. Behnke, C. Graham Clark, Hanan Balkhy
  Parasites & Vectors.2015;[Epub]     CrossRef

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• Thymus syriacus Essential Oil Extract: Potential Antileishmanial Activity Induced by an Apoptotic-like Death
  Basem Battah, Teresa Chianese, Luigi Rosati, Giacomo Petretto, Chadi Soukkarieh, Marco Ferrari, Vittorio Mazzarello, Aleksandra Barac, Aleksandar Peric, Matthew Gavino Donadu
  Antibiotics.2025; 14(3): 293.     CrossRef
• Antibacterial activity of Myrtus communis leaf extract against three pathogenic Xylella fastidiosa subspecies
  Giuseppe Incampo, Marwa Mourou, Davide Cornacchia, Vito Montilon, Graziana Difonzo, Paola Montoro, Francesco Caponio, Francesco Faretra, Franco Nigro, Stefania Pollastro
  Frontiers in Plant Science.2025;[Epub]     CrossRef
• Enantioselectivity of pinene against Leishmania amazonensis
  Ingrid S. Adão, Andreza R. Garcia, Kamila M. Sette, Camila M. Adade, Jefferson R. de Andrade Silva, Ana Claudia F. Amaral, Anderson S. Pinheiro, Igor A. Rodrigues
  Medicinal Chemistry Research.2024; 33(1): 127.     CrossRef
• The therapeutic value of Myrtus communis L.: an updated review
  Ali Esmail Al-Snafi, John Oluwafemi Teibo, Hazem M. Shaheen, Opeyemi Abigail Akinfe, Titilade Kehinde Ayandeyi Teibo, Numonde Emieseimokumo, Mohamed M. Elfiky, Hayder M. Al-kuraishy, Ali I. Al-Garbeeb, Athanasios Alexiou, Marios Papadakis, Hitham Alaa Moh
  Naunyn-Schmiedeberg's Archives of Pharmacology.2024; 397(7): 4579.     CrossRef
• Antileishmanial, Immune Modulation and Apoptosis Induction by Astragalus ecbatanus Extract Against Leishmania tropica
  Hossein Mahmoudvand, Amal Khudair Khalaf, Leila Masoori, Javad Ghasemian Yadegari
  Jundishapur Journal of Natural Pharmaceutical Products.2024;[Epub]     CrossRef
• A Review on Anti-leishmanial Activity of Terpenes and Chitosan as a Carrier for Nano-formulations
  Tanvi Goel, Deepali Bansode
  Current Traditional Medicine.2024;[Epub]     CrossRef
• Biological evaluation of CH3OH and C2H5OH of Berberis vulgaris for in vivo antileishmanial potential against Leishmania tropica in murine models
  Qasim Ali, Sumbal Haleem, Salman Ahmad, Qaisar Jamal, Tariq Ahmad, Afshan Khan, Shehzad Ali, Amal Alotaibi, Jyoti Singh, Adil Khan
  Open Chemistry.2024;[Epub]     CrossRef
• How to Naturally Support the Immune System in Inflammation—Essential Oils as Immune Boosters
  Magdalena Grazul, Paweł Kwiatkowski, Kacper Hartman, Anna Kilanowicz, Monika Sienkiewicz
  Biomedicines.2023; 11(9): 2381.     CrossRef
• Leishmanicidal and immunomodulatory activities of the formononetin (a natural isoflavone) against Leishmania tropica
  Hossein Mahmoudvand, Amal Khudair Khalaf, Pouya Zareh Rajabi, Nooshin Karbasian, Javad Ghasemian Yadegari
  BMC Research Notes.2023;[Epub]     CrossRef
• Synergistic antileishmanial activity of erythrodiol, uvaol, and oleanolic acid isolated from olive leaves of cv. Chemlali
  Oumayma Lafi, Rym Essid, Laurence Lachaud, Carlos Jimenez, Jaime Rodríguez, Lucía Ageitos, Ridha Mhamdi, Leila Abaza
  3 Biotech.2023;[Epub]     CrossRef
• Botanic Garden as a Factory of Molecules: Myrtus communis L. subsp. communis as a Case Study
  Claudia Giuliani, Martina Bottoni, Fabrizia Milani, Sefora Todero, Patrizia Berera, Filippo Maggi, Laura Santagostini, Gelsomina Fico
  Plants.2022; 11(6): 754.     CrossRef
• New developments in the treatment of cutaneous leishmaniasis
  Rasit Dinc
  Asian Pacific Journal of Tropical Medicine.2022; 15(5): 196.     CrossRef
• Assessment of anthelmintic potentials of Myrtus communis against Haemonchus contortus and Heligmosomoides polygyrus
  Essia Sebai, Amel Abidi, Raja Serairi, Bochra Ghawari, Mokhtar Dhibi, Hayet Benyedem, Hafidh Akkari
  Experimental Parasitology.2022; 240: 108320.     CrossRef
• Moroccan medicinal plants traditionally used for the treatment of skin diseases: From ethnobotany to clinical trials
  Mohammed Ajjoun, Loubna Kharchoufa, Ilyass Alami Merrouni, Mostafa Elachouri
  Journal of Ethnopharmacology.2022; 297: 115532.     CrossRef
• Chemical Composition and Potential of Eucalyptus camaldulensis Dehnh. Essential Oil and Its Major Components as Anti-inflammatory and Anti-leishmanial Agent
  Kamaljit Grewal, Jyoti Joshi, Sonia Rathee, Sukhbir Kaur, Harminder Pal Singh, Daizy R. Batish
  Journal of Essential Oil Bearing Plants.2022; 25(3): 419.     CrossRef
• Chemical composition, antileishmanial, and cytotoxic effects Ferula macrecolea essential oil against Leishmania tropica
  Hossein Mahmoudvand, Javad Ghasemian Yadegari, Amal Khudair Khalaf, Mohammad Javad Hashemi, Setareh Dastyarhaghighi, Iraj Salimikia
  Parasite Epidemiology and Control.2022; 19: e00270.     CrossRef
• HAS 1: A natural product from soil-isolated Streptomyces species with potent activity against cutaneous leishmaniasis caused by Leishmania tropica
  Bassel Awada, Maguy Hamie, Rana El Hajj, Ghada Derbaj, Rania Najm, Perla Makhoul, Dima Hajj Ali, Antoine G. Abou Fayad, Hiba El Hajj
  Frontiers in Pharmacology.2022;[Epub]     CrossRef
• Essential Oils in the Treatment of Various Types of Acne—A Review
  Renata Nurzyńska-Wierdak, Dominika Pietrasik, Magdalena Walasek-Janusz
  Plants.2022; 12(1): 90.     CrossRef
• A nanoemulsion-based nanogel of Citrus limon essential oil with leishmanicidal activity against Leishmania tropica and Leishmania major
  Elham Zarenezhad, Mahmoud Agholi, Ali Ghanbariasad, Ali Ranjbar, Mahmoud Osanloo
  Journal of Parasitic Diseases.2021; 45(2): 441.     CrossRef
• The potential role and apoptotic profile of three medicinal plant extracts on Leishmania tropica by MTT assay, macrophage model and flow cytometry analysis
  Mozhde Ilaghi, Iraj Sharifi, Fariba Sharififar, Fatemeh Sharifi, Razieh Tavakoli Oliaee, Zahra Babaei, Manzume Shamsi Meimamandi, Alireza Keyhani, Mehdi Bamorovat
  Parasite Epidemiology and Control.2021; 12: e00201.     CrossRef
• Myrtus communis Essential Oil; Anti-Parasitic Effects and Induction of the Innate Immune System in Mice with Toxoplasma gondii Infection
  Raafat M. Shaapan, Hiba Riyadh Al-Abodi, Abdullah D. Alanazi, Sobhy Abdel-Shafy, Marzieh Rashidipour, Abdullah F. Shater, Hossein Mahmoudvand
  Molecules.2021; 26(4): 819.     CrossRef
• Nanoformulating Cinnamomum zeylanicum essential oil with an extreme effect on Leishmania tropica and Leishmania major
  Ali Ghanbariasad, Alireza Valizadeh, Shamsi Noorpisheh Ghadimi, Zhila Fereidouni, Mahmoud Osanloo
  Journal of Drug Delivery Science and Technology.2021; 63: 102436.     CrossRef
• A Systematic Review of Curcumin and its Derivatives as Valuable Sources of Antileishmanial Agents
  Aishah E. Albalawi, Abdullah D. Alanazi, Iraj Sharifi, Fatemeh Ezzatkhah
  Acta Parasitologica.2021; 66(3): 797.     CrossRef
• Anti-Leishmania Effects of Volatile Oils and Their Isolates
  Patrícia Fampa, Melissa Florencio, Raissa Couto Santana, Dayana Rosa, Deivid Costa Soares, Herbert Leonel de Matos Guedes, Anabela Cordeiro da Silva, Douglas Siqueira A. Chaves, Lucia H. Pinto-da-Silva
  Revista Brasileira de Farmacognosia.2021; 31(5): 561.     CrossRef
• Myrtle (Myrtus communis L.) berries, seeds, leaves, and essential oils: New undiscovered sources of natural compounds with promising health benefits
  Francesca Giampieri, Danila Cianciosi, Tamara Y. Forbes‐Hernández
  Food Frontiers.2020; 1(3): 276.     CrossRef
• Chemical Composition of Myrtus communis L. and Proapoptotic Effects on the A549 Cell Line
  Nilufer Bilgic, Gulay Gulbol Duran
  Journal of Essential Oil Bearing Plants.2020; 23(6): 1283.     CrossRef
• Active Essential Oils and Their Components in Use against Neglected Diseases and Arboviruses
  Emanuela Coutinho Luna, Isadora Silva Luna, Luciana Scotti, Alex France M. Monteiro, Marcus Tullius Scotti, Ricardo Olímpio de Moura, Rodrigo Santos Aquino de Araújo, Kadja Luana Chagas Monteiro, Thiago Mendonça de Aquino, Frederico Fávaro Ribeiro, Franci
  Oxidative Medicine and Cellular Longevity.2019; 2019: 1.     CrossRef
• Myrtus communisessential oils: insecticidal, antioxidant and antimicrobial activities: a review
  Aicha Hennia, Said Nemmiche, Susana Dandlen, Maria Graça Miguel
  Journal of Essential Oil Research.2019; 31(6): 487.     CrossRef
• Essential Oil from Myrtle Leaves Growing in the Eastern Part of Saudi Arabia: Components, Anti-inflammatory and Cytotoxic Activities
  Maged E. Mohamed, Omar M. Mohafez, Hany E. Khalil, Ibrahim A. Alhaider
  Journal of Essential Oil Bearing Plants.2019; 22(4): 877.     CrossRef
• Linalool loaded on glutathione-modified gold nanoparticles: a drug delivery system for a successful antimicrobial therapy
  Majid S. Jabir, Ali A. Taha, Usama I. Sahib
  Artificial Cells, Nanomedicine, and Biotechnology.2018; 46(sup2): 345.     CrossRef
• Protective effect of standardized extract of Myrtus communis L. (myrtle) on experimentally bleomycin-induced pulmonary fibrosis: biochemical and histopathological study
  Mitra Samareh Fekri, Ali Mandegary, Fariba Sharififar, Hamid Reza Poursalehi, Mohammad Hadi Nematollahi, Atefe Izadi, Mohammad Mehdipour, Amir Asadi, Masoomeh Samareh Fekri
  Drug and Chemical Toxicology.2018; 41(4): 408.     CrossRef
• Antioxidant Activity of Myrtus communis L. and Myrtus nivellei Batt. & Trab. Extracts: A Brief Review
  Aicha Hennia, Maria Graça Miguel, Said Nemmiche
  Medicines.2018; 5(3): 89.     CrossRef
• Myrtus communis Linn: A review on ethnobotanical, ethnopharmacological and phytochemical studies
  Sisay Mekonnen, Gashaw Tigist
  Journal of Pharmacognosy and Phytotherapy.2017; 9(6): 77.     CrossRef
• Medicinal plants with promising antileishmanial activity in Iran: a systematic review and meta-analysis
  Masoud Soosaraei, Mahdi Fakhar, Saeed Hosseini Teshnizi, Hajar Ziaei Hezarjaribi, Elham Sadat Banimostafavi
  Annals of Medicine and Surgery.2017; 21: 63.     CrossRef
• Ethnobotanical, Ethnopharmacological, and Phytochemical Studies of Myrtus communis Linn: A Popular Herb in Unani System of Medicine
  Mekonnen Sisay, Tigist Gashaw
  Journal of Evidence-Based Complementary & Alternative Medicine.2017; 22(4): 1035.     CrossRef
• Leishmanicidal Activity of Biogenic Fe3O4 Nanoparticles
  Mehrdad Khatami, Hajar Alijani, Iraj Sharifi, Fatemeh Sharifi, Shahram Pourseyedi, Sam Kharazi, Marcos Augusto Lima Nobre, Manouchehr Khatami
  Scientia Pharmaceutica.2017; 85(4): 36.     CrossRef
• Chemical composition along with anti-leishmanial and cytotoxic activity of Zataria multiflora
  Ebrahim Saedi Dezaki, Hossein Mahmoudvand, Fariba Sharififar, Shirzad Fallahi, Lianet Monzote, Fatemeh Ezatkhah
  Pharmaceutical Biology.2016; 54(5): 752.     CrossRef
• In vitro anti-leishmanial activity of Satureja hortensis and Artemisia dracunculus extracts on Leishmania major promastigotes
  Farzaneh Mirzaei, Ali Fattahi Bafghi, Mohammad Ali Mohaghegh, Hossein Zarei Jaliani, Roghiyeh Faridnia, Hamed Kalani
  Journal of Parasitic Diseases.2016; 40(4): 1571.     CrossRef
• Antileishmanial, antioxidant, and cytotoxic activities of Quercus infectoria Olivier extract
  Farnaz Kheirandish, Bahram Delfan, Hossein Mahmoudvand, Nasim Moradi, Behrouz Ezatpour, Farzad Ebrahimzadeh, Marzieh Rashidipour
  Biomedicine & Pharmacotherapy.2016; 82: 208.     CrossRef
• Efficacy and Safety ofBunium Persicum(Boiss) to Inactivate Protoscoleces during Hydatid Cyst Operations
  Hossein Mahmoudvand, Razieh Tavakoli Oliaei, Seyed Reza Mirbadie, Farnaz Kheirandish, Amir Tavakoli Kareshk, Behrouz Ezatpour, Hormoz Mahmoudvand
  Surgical Infections.2016; 17(6): 713.     CrossRef
• In VitroandIn VivoAntileishmanial Effects ofPistacia khinjuk against Leishmania tropicaandLeishmania major
  Behrouz Ezatpour, Ebrahim Saedi Dezaki, Hossein Mahmoudvand, Mojgan Azadpour, Fatemeh Ezzatkhah
  Evidence-Based Complementary and Alternative Medicine.2015; 2015: 1.     CrossRef
• In vitro Studies on the Antileishmanial Activity of Herbicides and Plant Extracts Against Leishmania major Parasites
  Judith A. Makwali, Frederick M.E. Wanja, Johnstone Ingonga, Christopher O. Anjili
  Research Journal of Medicinal Plant.2015; 9(3): 90.     CrossRef

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• Reconsidering Toxoplasmosis Prevention and Treatment Due to Its Relation to Neuropsychiatric Disturbances
  Fabrizio Bruschi, Silvia Fabiani
  Zoonotic Diseases.2025; 5(2): 8.     CrossRef
• Seroprevalence and Associated Risk Factors of Toxoplasma gondii in Patients Diagnosed with Schizophrenia: A Case–Control Cross Sectional Study
  Sebastian Grada, Alin Gabriel Mihu, Daniela Adriana Oatis, Constantin Catalin Marc, Liana Maria Chicea, Cristina Petrescu, Alina Maria Lupu, Tudor Rares Olariu
  Biomedicines.2024; 12(5): 998.     CrossRef
• Seroprevalence and sociodemographic characteristics of Toxoplasma gondii infection in patients with psychiatric disorders in Malaysia
  Alia Maisarah, Suharni Mohamad, Maruzairi Husain, Sarimah Abdullah, Rahmah Noordin
  Acta Tropica.2024; 255: 107241.     CrossRef
• The Spread of Toxoplasmosis in Women within Al-Rifai District
  Rehab Issa Hashem Suhail, Shimaa Ahmed Mutab Nayef, Teeba Sabah Daham Mohammed, Yaqeen Mohammed Mahmud, Abdalrhman Falah Omar Ali
  European Journal of Medical and Health Research.2024; 2(4): 257.     CrossRef
• Infección por Toxoplasma gondii como factor de riesgo para desarrollar esquizofrenia: revisión de la literatura
  Felipe Botero Rodríguez, Ana María Zárate, Damaris Cote Martínez, Carlos Gómez Restrepo, Andrés Duarte Osorio
  Universitas Médica.2023;[Epub]     CrossRef
• Metabolomic Profiling Reveals Common Metabolic Alterations in Plasma of Patients with Toxoplasma Infection and Schizophrenia
  Emelia Osman, Anis Safirah Mohammad Zahariluddin, Shalisah Sharip, Zulkarnain Md Idris, Jen Kit Tan
  Genes.2022; 13(8): 1482.     CrossRef
• Association between exposure to toxoplasmosis and major psychiatric disorders: a systematic review
  Santiago M. Fernandes, Alan R. Dias, Ângela Miranda-Scippa
  Brazilian Journal of Psychiatry.2021; 43(4): 438.     CrossRef
• Seroprevalence of ToRCH Pathogens in Southeast Asia
  Franziska E. Fuchs, Maude Pauly, Antony P. Black, Judith M. Hübschen
  Microorganisms.2021; 9(3): 574.     CrossRef
• A Review on the Prevalence of Toxoplasma gondii in Humans and Animals Reported in Malaysia from 2008–2018
  Mohammed Nasiru Wana, Mohamad Aris Mohd Moklas, Malaika Watanabe, Norshariza Nordin, Ngah Zasmy Unyah, Sharif Alhassan Abdullahi, Ashraf Ahmad Issa Alapid, Tijjani Mustapha, Rusliza Basir, Roslaini Abd. Majid
  International Journal of Environmental Research and Public Health.2020; 17(13): 4809.     CrossRef
• Molecular Detection and Genetic Diversity of Toxoplasma gondii Oocysts in Cat Faeces from Klang Valley, Malaysia, Using B1 and REP Genes in 2018
  Mohammed Nasiru Wana, Mohamad Aris Mohd Moklas, Malaika Watanabe, Ngah Zasmy Unyah, Sharif Alhassan Abdullahi, Ashraf Ahmad Issa Alapid, Norshariza Nordin, Rusliza Basir, Roslaini Abd Majid
  Pathogens.2020; 9(7): 576.     CrossRef
• Depression and Toxoplasma gondii infection: assess the possible relationship through a seromolecular case–control study
  Saber Nasirpour, Farnaz Kheirandish, Shirzad Fallahi
  Archives of Microbiology.2020; 202(10): 2689.     CrossRef
• Toxoplasmosis in a Cohort of Italian Patients With Bipolar and Psychotic Disorders
  Claudia Del Grande, Elisa Schiavi, Isabella Masci, Margherita Barbuti, Giuseppe Maccariello, Gabriele Massimetti, Fabrizio Bruschi, Liliana Dell'Osso
  Journal of Nervous & Mental Disease.2020; 208(2): 118.     CrossRef
• Cerebral Malaria and Toxoplasmosis: Could their Concomitant Presentation Worsen Psychotic Condition?
  Mohammed A. Ibrahim, Olayinka Atilola, Aminu Mohammed, Emmanuel J. Awosanya, Ismail A. Odetokun, Aliyu Muhammad, Chinwe U. Chukwudi, Kingsley N. Ukwaja, Oyetunde T. Oyeyemi
  Annals of Science and Technology.2020; 5(2): 24.     CrossRef
• Serological and molecular detection of Toxoplasma gondii in terrestrial and marine wildlife harvested for food in Nunavik, Canada
  Nicholas Bachand, André Ravel, Patrick Leighton, Craig Stephen, Momar Ndao, Ellen Avard, Emily Jenkins
  Parasites & Vectors.2019;[Epub]     CrossRef
• Lack of circulating toxoplasma gondii DNA in seropositive patients with bipolar or schizophrenia spectrum disorders
  L. Galli, C. Del Grande, L. Rindi, C. Mangia, V. Mangano, E. Schiavi, I. Masci, B. Pinto, L. Kramer, L. Dell'Osso, F. Bruschi
  Psychiatry Research.2019; 273: 706.     CrossRef
• A Case–Control Seroprevalence Study on the Association Between Toxoplasma gondii Infection and Bipolar Disorder
  Cosme Alvarado-Esquivel, Sergio Estrada-Martínez, Alma Rosa Pérez-Alamos
  Frontiers in Psychiatry.2019;[Epub]     CrossRef
• Associations of mental disorders and neurotropic parasitic diseases: a meta-analysis in developing and emerging countries
  Labanté Outcha Daré, Pierre-Emile Bruand, Daniel Gérard, Benoît Marin, Valerie Lameyre, Farid Boumédiène, Pierre-Marie Preux
  BMC Public Health.2019;[Epub]     CrossRef
• Foxes (Vulpes vulpes) as sentinels for parasitic zoonoses, Toxoplasma gondii and Trichinella nativa, in the northeastern Canadian Arctic
  Bachand Nicholas, A. Ravel, P. Leighton, C. Stephen, A. Iqbal, M. Ndao, K. Konecsni, C. Fernando, E. Jenkins
  International Journal for Parasitology: Parasites and Wildlife.2018; 7(3): 391.     CrossRef
• Possible Link Between Toxoplasma gondii Infection and Mood Disorders in Lorestan Province, Western Iran
  Farnaz Kheirandish, Hedayat Nazari, Hossein Mahmoudvand, Yaser Yaseri, Mohammad Javad Tarahi, Shirzad Fallahi, Behrouz Ezatpour
  Archives of Clinical Infectious Diseases.2016;[Epub]     CrossRef
• Mental Health Disorders Associated with Foodborne Pathogens
  Declan J. Bolton, Lucy J. Robertson
  Journal of Food Protection.2016; 79(11): 2005.     CrossRef

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Citations to this article as recorded by  

• Evaluation Algorithm of Volleyball Players’ Competitive Ability Based on the Random Matrix Model
  Tailin Wang, Hua Zheng, Fangshu Li, Nian Jia, Zengliang Cai, Ning Cao
  Mathematical Problems in Engineering.2022; 2022: 1.     CrossRef

Citations

Citations to this article as recorded by  

• Indigenous Plasmodium vivax upsurge in the Eastern Mediterranean, Western Pacific, and South East Asia regions – beyond the constant culpability of climate change, COVID-19, and armed conflicts
  Loick P. Kojom Foko, Amit Sharma
  International Journal for Parasitology.2025;[Epub]     CrossRef
• Low Genetic Diversity of Plasmodium vivax Circumsporozoite Surface Protein in Clinical Isolates from Southern Thailand
  Tachin Khulmanee, Thanyapit Thita, Kanyanan Kritsiriwutinan, Usa Boonyuen, Aminoh Saai, Kanjana Inkabjan, Rimi Chakrabarti, Pradipsinh K. Rathod, Srivicha Krudsood, Mathirut Mungthin, Rapatbhorn Patrapuvich
  Tropical Medicine and Infectious Disease.2024; 9(5): 94.     CrossRef
• Drug resistance markers in Plasmodium vivax isolates from a Kanchanaburi province, Thailand between January to May 2023
  Thanawat Sridapan, Paweesuda Rattanakoch, Kaewkanha Kijprasong, Suttipat Srisutham, Kristan Alexander Schneider
  PLOS ONE.2024; 19(7): e0304337.     CrossRef
• Investigation of Mutations in the crt-o and mdr1 Genes of Plasmodium vivax for the Molecular Surveillance of Chloroquine Resistance in Parasites from Gold Mining Areas in Roraima, Brazil
  Jacqueline de Aguiar Barros, Fabiana Granja, Rebecca de Abreu-Fernandes, Lucas Tavares de Queiroz, Daniel da Silva e Silva, Arthur Camurça Citó, Natália Ketrin Almeida-de-Oliveira Mocelin, Cláudio Tadeu Daniel-Ribeiro, Maria de Fátima Ferreira-da-Cruz
  Microorganisms.2024; 12(8): 1680.     CrossRef
• Molecular epidemiology of potential candidate markers for chloroquine resistance in imported Plasmodium vivax malaria cases in Iran
  Sakineh Pirahmadi, Shima Afzali, Akram Abouie Mehrizi, Abbasali Raz, Ahmad Raeisi
  Malaria Journal.2023;[Epub]     CrossRef
• Toxins from Animal Venoms as a Potential Source of Antimalarials: A Comprehensive Review
  Zeca M. Salimo, André L. Barros, Asenate A. X. Adrião, Aline M. Rodrigues, Marco A. Sartim, Isadora S. de Oliveira, Manuela B. Pucca, Djane C. Baia-da-Silva, Wuelton M. Monteiro, Gisely C. de Melo, Hector H. F. Koolen
  Toxins.2023; 15(6): 375.     CrossRef
• Characteristics of molecular markers associated with chloroquine resistance in Plasmodium vivax strains from vivax malaria cases in Yunnan Province, China
  Hongyun Ding, Ying Dong, Yan Deng, Yanchun Xu, Yan Liu, Jing Wu, Mengni Chen, Canglin Zhang, Weibin Zheng
  Malaria Journal.2023;[Epub]     CrossRef
• Distinct Allelic Diversity of Plasmodium vivax Merozoite Surface Protein 3-Alpha (PvMSP-3α) Gene in Thailand Using PCR-RFLP
  Kanyanan Kritsiriwuthinan, Warunee Ngrenngarmlert, Rapatbhorn Patrapuvich, Supaksajee Phuagthong, Kantima Choosang, Jianbing Mu
  Journal of Tropical Medicine.2023; 2023: 1.     CrossRef
• Nationwide spatiotemporal drug resistance genetic profiling from over three decades in Indian Plasmodium falciparum and Plasmodium vivax isolates
  Loick P. Kojom Foko, Geetika Narang, Jahnvi Jakhan, Suman Tamang, Amit Moun, Vineeta Singh
  Malaria Journal.2023;[Epub]     CrossRef
• Surveillance of drug resistance molecular markers in Plasmodium vivax before and after introduction of dihydroartemisinin and piperaquine in Thailand: 2009–2019
  Nutnicha Suphakhonchuwong, Kanchana Rungsihirunrat, Jiraporn Kuesap
  Parasitology Research.2023; 122(12): 2871.     CrossRef
• Genomic analysis of Plasmodium vivax describes patterns of connectivity and putative drivers of adaptation in Ethiopia
  Alebachew Messele Kebede, Edwin Sutanto, Hidayat Trimarsanto, Ernest Diez Benavente, Mariana Barnes, Richard D. Pearson, Sasha V. Siegel, Berhanu Erko, Ashenafi Assefa, Sisay Getachew, Abraham Aseffa, Beyene Petros, Eugenia Lo, Rezika Mohammed, Daniel Yil
  Scientific Reports.2023;[Epub]     CrossRef
• Genetic Diversity of Plasmodium vivax Merozoite Surface Protein-3 Alpha and Beta from Diverse Geographic Areas of Thailand
  Jiraporn Kuesap, Kanchana Rungsihirunrat, Wanna Chaijaroenkul, Mathirut Mungthin
  Japanese Journal of Infectious Diseases.2022; 75(3): 241.     CrossRef
• Polymorphisms of potential drug resistant molecular markers in Plasmodium vivax from China–Myanmar border during 2008‒2017
  Zhensheng Wang, Chunyan Wei, Yunchun Pan, Zhihua Wang, Xin Ji, Qianqian Chen, Lianhui Zhang, Zenglei Wang, Heng Wang
  Infectious Diseases of Poverty.2022;[Epub]     CrossRef
• Global scenario of Plasmodium vivax occurrence and resistance pattern
  Davinder Kaur, Shweta Sinha, Rakesh Sehgal
  Journal of Basic Microbiology.2022; 62(12): 1417.     CrossRef
• Assessing the in vitro sensitivity with associated drug resistance polymorphisms in Plasmodium vivax clinical isolates from Delhi, India
  Monika Matlani, Amit Kumar, Vineeta Singh
  Experimental Parasitology.2021; 220: 108047.     CrossRef
• Monitoring Plasmodium vivax resistance to antimalarials: Persisting challenges and future directions
  Marcelo U. Ferreira, Tais Nobrega de Sousa, Gabriel W. Rangel, Igor C. Johansen, Rodrigo M. Corder, Simone Ladeia-Andrade, José Pedro Gil
  International Journal for Parasitology: Drugs and Drug Resistance.2021; 15: 9.     CrossRef
• Ten-Year Molecular Surveillance of Drug-Resistant Plasmodium spp. Isolated From the China–Myanmar Border
  Tongke Tang, Yanchun Xu, Long Cao, Penghai Tian, Jiang Shao, Yan Deng, Hongning Zhou, Bo Xiao
  Frontiers in Cellular and Infection Microbiology.2021;[Epub]     CrossRef
• Global assessment of genetic paradigms of Pvmdr1 mutations in chloroquine-resistant Plasmodium vivax isolates
  Adel Spotin, Mahmoud Mahami-Oskouei, Ehsan Ahmadpour, Mahdi Parsaei, Ali Rostami, Shima Emami, Saba Gholipour, Mostafa Farmani
  Transactions of The Royal Society of Tropical Medicine and Hygiene.2020; 114(5): 339.     CrossRef
• Molecular Detection of Antimalarial Drug Resistance in Plasmodium vivax from Returned Travellers to NSW, Australia during 2008–2018
  Chaturong Noisang, Wieland Meyer, Nongyao Sawangjaroen, John Ellis, Rogan Lee
  Pathogens.2020; 9(2): 101.     CrossRef
• Plasmodium vivax drug resistance markers: Genetic polymorphisms and mutation patterns in isolates from Malaysia
  Fei-Wen Cheong, Shairah Dzul, Mun-Yik Fong, Yee-Ling Lau, Sasheela Ponnampalavanar
  Acta Tropica.2020; 206: 105454.     CrossRef
• Case report: recurrence of Plasmodium vivax malaria due to defective cytochrome P450 2D6 function in Pos Lenjang, Pahang, Malaysia
  Noor Hafizan Mat Salleh, Mohd Faizal Abdul Rahman, Samsiah Samsusah, Jeremy Ryan De Silva, David Chun-Ern Ng, Azilawati Hanim Ghozali, Jia Hui Tan, Meng Yee Lai, Amirah Amir, Jonathan Wee Kent Liew, Yee Ling Lau
  Transactions of The Royal Society of Tropical Medicine and Hygiene.2020; 114(9): 700.     CrossRef
• Ex vivo susceptibilities of Plasmodium vivax isolates from the China-Myanmar border to antimalarial drugs and association with polymorphisms in Pvmdr1 and Pvcrt-o genes
  Jiangyan Li, Jie Zhang, Qian Li, Yue Hu, Yonghua Ruan, Zhiyong Tao, Hui Xia, Jichen Qiao, Lingwen Meng, Weilin Zeng, Cuiying Li, Xi He, Luyi Zhao, Faiza A. Siddiqui, Jun Miao, Zhaoqing Yang, Qiang Fang, Liwang Cui, Kamala Thriemer
  PLOS Neglected Tropical Diseases.2020; 14(6): e0008255.     CrossRef
• An unlabelled probe-based real time PCR and modified semi-nested PCR as molecular tools for analysis of chloroquine resistant Plasmodium vivax isolates from Afghanistan
  Sayed Hussain Mosawi, Abdolhossein Dalimi, Najibullah Safi, Reza Fotouhi-Ardakani, Fatemeh Ghaffarifar, Javid Sadraei
  Malaria Journal.2020;[Epub]     CrossRef
• Molecular surveillance for drug resistance markers in Plasmodium vivax isolates from symptomatic and asymptomatic infections at the China–Myanmar border
  Yan Zhao, Lin Wang, Myat Thu Soe, Pyae Linn Aung, Haichao Wei, Ziling Liu, Tongyu Ma, Yuanyuan Huang, Lynette J. Menezes, Qinghui Wang, Myat Phone Kyaw, Myat Htut Nyunt, Liwang Cui, Yaming Cao
  Malaria Journal.2020;[Epub]     CrossRef
• Molecular surveillance of the Plasmodium vivax multidrug resistance 1 gene in Peru between 2006 and 2015
  Fredy E. Villena, Jorge L. Maguiña, Meddly L. Santolalla, Edwar Pozo, Carola J. Salas, Julia S. Ampuero, Andres G. Lescano, Danett K. Bishop, Hugo O. Valdivia
  Malaria Journal.2020;[Epub]     CrossRef
• Molecular detection of drug resistant malaria in Southern Thailand
  Chaturong Noisang, Christiane Prosser, Wieland Meyer, Waenurama Chemoh, John Ellis, Nongyao Sawangjaroen, Rogan Lee
  Malaria Journal.2019;[Epub]     CrossRef
• Promising approach to reducing Malaria transmission by ivermectin: Sporontocidal effect against Plasmodium vivax in the South American vectors Anopheles aquasalis and Anopheles darlingi
  Yudi T. Pinilla, Stefanie C. P. Lopes, Vanderson S. Sampaio, Francys S. Andrade, Gisely C. Melo, Alessandra S. Orfanó, Nágila F. C. Secundino, Maria G. V. B. Guerra, Marcus V. G. Lacerda, Kevin C. Kobylinski, Karin S. Escobedo-Vargas, Victor M. López-Sifu
  PLOS Neglected Tropical Diseases.2018; 12(2): e0006221.     CrossRef
• The prevalence of molecular markers of drug resistance in Plasmodium vivax from the border regions of Thailand in 2008 and 2014
  Kritpaphat Tantiamornkul, Tepanata Pumpaibool, Jittima Piriyapongsa, Richard Culleton, Usa Lek-Uthai
  International Journal for Parasitology: Drugs and Drug Resistance.2018; 8(2): 229.     CrossRef
• Genetic diversity of the Plasmodium vivax multidrug resistance 1 gene in Thai parasite populations
  Veerayuth Kittichai, Wang Nguitragool, Huguette Gaelle Ngassa Mbenda, Jetsumon Sattabongkot, Liwang Cui
  Infection, Genetics and Evolution.2018; 64: 168.     CrossRef
• Molecular Evidence of Drug Resistance in Asymptomatic Malaria Infections, Myanmar, 2015
  Myat Htut Nyunt, Thinzar Shein, Ni Ni Zaw, Soe Soe Han, Fauzi Muh, Seong-Kyun Lee, Jin-Hee Han, Kyaw Zin Thant, Eun-Taek Han, Myat Phone Kyaw
  Emerging Infectious Diseases.2017; 23(3): 517.     CrossRef
• Genetic diversity of Plasmodium vivax metacaspase 1 and Plasmodium vivax multi-drug resistance 1 genes of field isolates from Mauritania, Sudan and Oman
  Fatimata Sow, Guillaume Bonnot, Bilal Rabah Ahmed, Sidi Mohamed Diagana, Hachim Kebe, Mohamedou Koita, Ba Malado Samba, Said K. Al-Mukhaini, Majed Al-Zadjali, Seif S. Al-Abri, Osama A. M. Ali, Abdallah M. Samy, Muzamil Mahdi Abdel Hamid, Musab M. Ali Albs
  Malaria Journal.2017;[Epub]     CrossRef
• Clinical and molecular surveillance of drug resistant vivax malaria in Myanmar (2009–2016)
  Myat Htut Nyunt, Jin-Hee Han, Bo Wang, Khin Myo Aye, Kyin Hla Aye, Seong-Kyun Lee, Ye Htut, Myat Phone Kyaw, Kay Thwe Han, Eun-Taek Han
  Malaria Journal.2017;[Epub]     CrossRef
• Measuring ex vivo drug susceptibility in Plasmodium vivax isolates from Cambodia
  Suwanna Chaorattanakawee, Chanthap Lon, Soklyda Chann, Kheang Heng Thay, Nareth Kong, Yom You, Siratchana Sundrakes, Chatchadaporn Thamnurak, Sorayut Chattrakarn, Chantida Praditpol, Kritsanai Yingyuen, Mariusz Wojnarski, Rekol Huy, Michele D. Spring, Dou
  Malaria Journal.2017;[Epub]     CrossRef
• Plasmodium vivax mdr1 genotypes in isolates from successfully cured patients living in endemic and non-endemic Brazilian areas
  Larissa Rodrigues Gomes, Natália Ketrin Almeida-de-Oliveira, Aline Rosa de Lavigne, Suelen Rezende Félix de Lima, Anielle de Pina-Costa, Patrícia Brasil, Cláudio Tadeu Daniel-Ribeiro, Didier Ménard, Maria de Fatima Ferreira-da-Cruz
  Malaria Journal.2016;[Epub]     CrossRef
• Plasmodium vivax multidrug resistance-1 gene polymorphism in French Guiana
  Emilie Faway, Lise Musset, Stéphane Pelleau, Béatrice Volney, Jessica Casteras, Valérie Caro, Didier Menard, Sébastien Briolant, Eric Legrand
  Malaria Journal.2016;[Epub]     CrossRef
• Evaluation of single nucleotide polymorphisms of pvmdr1 and microsatellite genotype in Plasmodium vivax isolates from Republic of Korea military personnel
  Dong-Il Chung, Sookwan Jeong, Sylvatrie-Danne Dinzouna-Boutamba, Hye-Won Yang, Sang-Geon Yeo, Yeonchul Hong, Youn-Kyoung Goo
  Malaria Journal.2015;[Epub]     CrossRef

Citations

Citations to this article as recorded by  

• Toxocara canis infections in mice: from subtle to severe consequences in 100 weeks
  Nicol Bernardová, Jan Novák, Chia-Kwung Fan, Libuše Kolářová, Marta Chanová
  Journal of Helminthology.2025;[Epub]     CrossRef
• Using Biocontrol Fungi to Control Helminthosis in Wild Animals: An Innovative Proposal for the Health and Conservation of Species
  Júlia dos Santos Fonseca, Beatriz Bacelar Barbosa, Adolfo Paz Silva, María Sol Arias Vázquez, Cristiana Filipa Cazapal Monteiro, Huarrisson Azevedo Santos, Jackson Victor de Araújo
  Pathogens.2025; 14(8): 775.     CrossRef
• The potential relationship between Toxocara canis infection and epilepsy in a rat model
  Amina M. Salama, Dina I. Elgendy, Rasha A. Elmahy, Asmaa F. Eltantawy, Monira A. Seleem, Ahmed M. Elgohary, Omaima K. Docmac, Marwa E. F. Al Mwafy, Ahmed A. Almeldin, Mahmoud S. Sharaf
  Parasitology Research.2025;[Epub]     CrossRef
• Efficacy of artemether against toxocariasis in mice: parasitological and immunopathological changes in brain, liver, and lung
  Dina I. Elgendy, Rasha A. Elmahy, Alaa Ibrahim Mohamed Amer, Hoda A. Ibrahim, Asmaa Fawzy Eltantawy, Fotouh Rashed Mansour, Amina M. Salama
  Pathogens and Global Health.2024; 118(1): 47.     CrossRef
• Neurobehavioral Disorders and Pathological Changes in the Brain of Mice Are Caused by Chronic Toxocara canis Larval Invasion with Low to Moderate Inoculum
  Nicol Bernardová, Jan Novák, Petr Horák, Chia-Kwung Fan, Libuše Kolářová
  Acta Parasitologica.2024; 69(4): 1736.     CrossRef
• Effects of metformin on parasitological, pathological changes in the brain and liver and immunological aspects during visceral toxocariasis in mice
  Amina M. Salama, Rasha A. Elmahy, Hoda A. Ibrahim, Alaa Ibrahim Mohamed Amer, Asmaa Fawzy Eltantawy, Dina I. Elgendy
  Parasitology Research.2023; 122(12): 3213.     CrossRef
• Cyclosporine A increases the intensity of Toxocara canis infection in swiss mice
  W. D. S. Terto, M. Q. de Moura, J. L. Borchardt, F. D. S. Santos, L. F. da Costa Avila, N. B. Pinheiro, F. P. Leivas Leite, M. M. Villela, M. E. A. Berne
  Brazilian Journal of Biology.2022;[Epub]     CrossRef
• Glial Fibrillary Acidic Protein and Ionized Calcium-Binding Adapter Molecule 1 Immunostaining Score for the Central Nervous System of Horses With Non-suppurative Encephalitis and Encephalopathies
  Gisele Silva Boos, Klaus Failing, Edson Moleta Colodel, David Driemeier, Márcio Botelho de Castro, Daniele Mariath Bassuino, José Diomedes Barbosa, Christiane Herden
  Frontiers in Veterinary Science.2021;[Epub]     CrossRef
• Diallyl sulfide alleviates cyclophosphamide-induced nephropathic encephalopathy in rats
  Shereen M. Galal, Heba H. Mansour, Abeer A. Elkhoely
  Toxicology Mechanisms and Methods.2020; 30(3): 208.     CrossRef
• Mesenchymal stem cells combined with albendazole as a novel therapeutic approach for experimental neurotoxocariasis
  E. V. N. Beshay, S. A. El-Refai, G. S. Sadek, A. A. Elbadry, F. H. Shalan, A. F. Afifi
  Parasitology.2020; 147(7): 799.     CrossRef
• Histopathological characterization of Toxocara canis- and T. cati-induced neurotoxocarosis in the mouse model
  Andrea Springer, Lea Heuer, Elisabeth Janecek-Erfurth, Andreas Beineke, Christina Strube
  Parasitology Research.2019; 118(9): 2591.     CrossRef
• Developmental stages and viability of Toxocara canis eggs outside the host
  Iman Fathy Abou-El-Naga
  Biomédica.2018; 38(2): 189.     CrossRef
• Seroprevalence and Risk Factors for Toxocara canis Infection in Serbia During 2015
  Simona Gabrielli, Suzana Tasić-Otašević, Aleksandra Ignjatović, Maurizio Fraulo, Marija Trenkić-Božinović, Stefan Momčilović, Gabriella Cancrini
  Foodborne Pathogens and Disease.2017; 14(1): 43.     CrossRef

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• Knowledge and Awareness of Bovine Fasciolosis Among Dairy Farm Personnel in the Eastern Cape Province, South Africa
  Zuko Mpisana, Mandla Yawa, Mhlangabezi Slayi, Nkululeko Nyangiwe, James Oguttu, Ishmael Festus Jaja
  Parasitologia.2025; 5(3): 33.     CrossRef
• Prevalence and risk factors of fasciolosis in a bovine population from farms in Taiping, Malaysia
  Naim Che-Kamaruddin, Nur Fazila Saulol Hamid, Lokman Hakim Idris, Ferdaus Mohamat Yusuff, Zulfa Hanan Ashaari, Hasmawati Yahaya, Norhidayu Sahimin, Nur Mahiza Md Isa
  Veterinary Parasitology: Regional Studies and Reports.2024; 49: 100998.     CrossRef
• Coproprevalence, seroprevalence, and geographic distribution of Fasciola spp. infection in beef and dairy cattle in Pak Chong highland, Nakhon-Ratchasima Province, Northeast Thailand
  Pongsakorn Martviset, Amornrat Geadkaew-Krenc, Pantip Piyatadsananon, Ruttiroj Jirojwong, Pathanin Chantree, Wansika Phadungsil, Chompunoot Wangboon, Mantana Jamklang, Sirilak Chumkiew, Rawipreeya Poomkhokrak, Aree Taylor, Nanthawat Kosa, Rudi Grams
  Parasitology International.2024; 98: 102809.     CrossRef
• Investigation of Fasciola gigantica in freshwater snail Radix ( Lymnaea ) spp. In the highly parasite-prevalent area of Nakhon Ratchasima Province, Thailand
  Pongsakorn Martviset, Pathanin Chantree, Amornrat Geadkaew-Krenc, Pantip Piyatadsananon, Ruttiroj Jirojwong, Chompunoot Wangboon, Mantana Jamklang, Sirilak Chumkiew, Rawipreeya Poomkhokrak, Nanthawat Kosa, Salisa Chaimon, Bumpenporn Sanannam, Rudi Grams,
  International Journal of Veterinary Science and Medicine.2024; 12(1): 125.     CrossRef
• Towards the comprehension of fasciolosis (re-)emergence: an integrative overview
  Annia Alba, Antonio A. Vazquez, Sylvie Hurtrez-Boussès
  Parasitology.2021; 148(4): 385.     CrossRef
• Differential expression of microRNAs and tRNA fragments mediate the adaptation of the liver fluke Fasciola gigantica to its intermediate snail and definitive mammalian hosts
  Rui-Si Hu, Xiao-Xuan Zhang, Qiao-Ni Ma, Hany M. Elsheikha, Muhammad Ehsan, Quan Zhao, Bastian Fromm, Xing-Quan Zhu
  International Journal for Parasitology.2021; 51(5): 405.     CrossRef
• Identification of Fasciola spp. based on ITS-2 reveals the Fasciola gigantica infection in buffaloes in Nanning city, South China
  Zhengjiao Wu, Jinhui Wang, Zhen Meng, Weikun Jin, Kangxin He, Weiyu Zhang, Wenda Di
  Veterinary Parasitology.2021; 300: 109585.     CrossRef
• An annotated checklist of the eukaryotic parasites of humans, exclusive of fungi and algae
  Blaine A. Mathison, Sarah G. H. Sapp
  ZooKeys.2021; 1069: 1.     CrossRef
• Molecular detection of natural infection ofLymnaea(Pseudosuccinea)columella(Gastropoda: Lymnaeidae) withFasciola gigantica(Digenea: Fasciolidae) from two provinces of South Africa
  M.P. Malatji, S. Mukaratirwa
  Journal of Helminthology.2020;[Epub]     CrossRef
• Adaptive Radiation of the Flukes of the Family Fasciolidae Inferred from Genome-Wide Comparisons of Key Species
  Young-Jun Choi, Santiago Fontenla, Peter U Fischer, Thanh Hoa Le, Alicia Costábile, David Blair, Paul J Brindley, Jose F Tort, Miguel M Cabada, Makedonka Mitreva, Keith Crandall
  Molecular Biology and Evolution.2020; 37(1): 84.     CrossRef
• Lymnaeidae from Santander and bordering departments of Colombia: Morphological characterization, molecular identification and natural infection with Fasciola hepatica
  Andrés Esteban Pereira, Nelson Uribe, Jean-Pierre Pointier
  Veterinary Parasitology: Regional Studies and Reports.2020; 20: 100408.     CrossRef
• Prevalence, risk factors, and spatial distribution of Fasciola in carabao and intermediate host in Baybay, Leyte, Philippines
  Harvie P. Portugaliza, Ivy Mae C. Balaso, June Clyde B. Descallar, Eugene B. Lañada
  Veterinary Parasitology: Regional Studies and Reports.2019; 15: 100261.     CrossRef
• Les helminthoses à tropisme hépatique
  Brice Autier, Hélène Guegan, Kévin Ory, Sorya Belaz, Sarah Dion, Brigitte Degeilh, Florence Robert-Gangneux, Jean-Pierre Gangneux
  Revue Francophone des Laboratoires.2019; 2019(512): 73.     CrossRef
• Complex and dynamic transcriptional changes allow the helminth Fasciola gigantica to adjust to its intermediate snail and definitive mammalian hosts
  Xiao-Xuan Zhang, Krystyna Cwiklinski, Rui-Si Hu, Wen-Bin Zheng, Zhao-An Sheng, Fu-Kai Zhang, Hany M. Elsheikha, John P. Dalton, Xing-Quan Zhu
  BMC Genomics.2019;[Epub]     CrossRef
• Expression profiles of genes involved in TLRs and NLRs signaling pathways of water buffaloes infected with Fasciola gigantica
  Fu-Kai Zhang, Jun-Ling Hou, Ai-Jiang Guo, Ai-Ling Tian, Zhao-An Sheng, Wen-Bin Zheng, Wei-Yi Huang, Hany M. Elsheikha, Xing-Quan Zhu
  Molecular Immunology.2018; 94: 18.     CrossRef
• Transcriptomic responses of water buffalo liver to infection with the digenetic fluke Fasciola gigantica
  Fu-Kai Zhang, Xiao-Xuan Zhang, Hany M. Elsheikha, Jun-Jun He, Zhao-An Sheng, Wen-Bin Zheng, Jian-Gang Ma, Wei-Yi Huang, Ai-Jiang Guo, Xing-Quan Zhu
  Parasites & Vectors.2017;[Epub]     CrossRef
• High prevalence of cattle fascioliasis in coastal areas of Thua Thien Hue province, Vietnam
  Nga Thi NGUYEN, Thinh Cong LE, Minh Duc Co VO, Hoang VAN CAO, Ly Thi NGUYEN, Khanh Thi HO, Quyet Ngoc NGUYEN, Vui Quang TRAN, Yasunobu MATSUMOTO
  Journal of Veterinary Medical Science.2017; 79(6): 1035.     CrossRef
• Serum levels of cytokines in water buffaloes experimentally infected with Fasciola gigantica
  Fu-Kai Zhang, Ai-Jiang Guo, Jun-Ling Hou, Miao-Miao Sun, Zhao-An Sheng, Xiao-Xuan Zhang, Wei-Yi Huang, Hany M. Elsheikha, Xing-Quan Zhu
  Veterinary Parasitology.2017; 244: 97.     CrossRef

Citations

Citations to this article as recorded by  

• Characterization of a novel organic solute transporter homologue from Clonorchis sinensis
  Yanyan Lu, Won Gi Yoo, Fuhong Dai, Ji-Yun Lee, Jhang Ho Pak, Woon-Mok Sohn, Sung-Jong Hong, John Pius Dalton
  PLOS Neglected Tropical Diseases.2018; 12(4): e0006459.     CrossRef
• Molecular and structural characteristics of multidrug resistance-associated protein 7 in Chinese liver fluke Clonorchis sinensis
  Fuhong Dai, Won Gi Yoo, Ji-Yun Lee, Yanyan Lu, Jhang Ho Pak, Woon-Mok Sohn, Sung-Jong Hong
  Parasitology Research.2017; 116(3): 953.     CrossRef

Citations

Citations to this article as recorded by  

• Current Gaps in Survey Design and Analysis for Molecular Xenomonitoring of Vector‐Borne Neglected Tropical Diseases: A Systematic Review
  Angus McLure, Tilahun Alamnia, Zhiwei Xu, Colleen L. Lau, Helen J. Mayfield
  Tropical Medicine & International Health.2025; 30(9): 893.     CrossRef
• Synthesis, larvicidal efficiency and molecular docking studies of novel annulated pyrano[2,3-c]pyrazoles against Culex pipiens L. and Musca domestica L. larvae
  Mahmoud K.F. El-Sayed, Manal M. El-Shahawi, Yasmeen M. Ali, Doaa R. Abdel-Haleem, Fatma S.M. Abu El-Azm
  Bioorganic Chemistry.2023; 130: 106258.     CrossRef
• Mosquito Vectors (Diptera: Culicidae) and Mosquito-Borne Diseases in North Africa
  Amira Nebbak, Lionel Almeras, Philippe Parola, Idir Bitam
  Insects.2022; 13(10): 962.     CrossRef
• The use of molecular xenomonitoring for surveillance of mosquito-borne diseases
  Mary M. Cameron, Anita Ramesh
  Philosophical Transactions of the Royal Society B: Biological Sciences.2021; 376(1818): 20190816.     CrossRef
• Bancroftian Filariasis Still Endemic in Some Foci in Sohag Governorate, Upper Egypt
  Refaat MA Khalifa, Amal M Ahmed, Mohamed AA Taha, Nasr Eldeen MM Ali, Haitham KA Abd El Samea, Dabbu Jaijyan
  Journal of Parasite Research.2019; 1(1): 1.     CrossRef
• Comparative evaluation of dry and liquid RIME LAMP in detecting trypanosomes in dead tsetse flies
  Peter Nambala, Janelisa Musaya, Kyoko Hayashida, Emmanuel Maganga, Edward Senga, Kelita Kamoto, John Chisi, Chihiro Sugimoto
  Onderstepoort Journal of Veterinary Research.2018;[Epub]     CrossRef
• Implementing a community vector collection strategy using xenomonitoring for the endgame of lymphatic filariasis elimination
  Sellase Pi-Bansa, Joseph Harold Nyarko Osei, Joannitta Joannides, Maame Esi Woode, David Agyemang, Elizabeth Elhassan, Samuel Kweku Dadzie, Maxwell Alexander Appawu, Michael David Wilson, Benjamin Guibehi Koudou, Dziedzom Komi de Souza, Jürg Utzinger, Dan
  Parasites & Vectors.2018;[Epub]     CrossRef
• Finding Wolbachia in Filarial larvae and Culicidae Mosquitoes in Upper Egypt Governorate
  Ahmed K. Dyab, Lamia A. Galal, Abeer E. Mahmoud, Yasser Mokhtar
  The Korean Journal of Parasitology.2016; 54(3): 265.     CrossRef
• Trypanosome infection rates in tsetse flies in the “silent” sleeping sickness focus of Bafia in the Centre Region in Cameroon
  Gustave Simo, Pierre Fongho, Oumarou Farikou, Prosper Innocent Ndjeuto Ndjeuto-Tchouli, Judith Tchouomene-Labou, Flobert Njiokou, Tazoacha Asonganyi
  Parasites & Vectors.2015;[Epub]     CrossRef

Citations

Citations to this article as recorded by  

• Developmental Proteomics Reveals the Dynamic Expression Profile of Global Proteins of Haemaphysalis longicornis (Parthenogenesis)
  Min-Xuan Liu, Xiao-Pei Xu, Fan-Ming Meng, Bing Zhang, Wei-Gang Li, Yuan-Yuan Zhang, Qiao-Ying Zen, Wen-Ge Liu
  Life.2025; 15(1): 59.     CrossRef
• Haemaphysalis longicornis calreticulin is not an effective molecular tool for tick bite diagnosis and disruption of tick infestations
  Weiqing Zheng, Haijun Hu, Jiafu Jiang, Xiangrong Sun, Renlong Fu, Huiying Tao, Yangqing Liu, Haiying Chen, Hongmei Ma, Shengen Chen
  Veterinary Parasitology.2022; 309: 109775.     CrossRef
• Trypanosoma cruzi Calreticulin: Immune Evasion, Infectivity, and Tumorigenesis
  Galia Ramírez-Toloza, Eduardo Sosoniuk-Roche, Carolina Valck, Lorena Aguilar-Guzmán, Viviana P. Ferreira, Arturo Ferreira
  Trends in Parasitology.2020; 36(4): 368.     CrossRef
• Catalogue of stage-specific transcripts in Ixodes ricinus and their potential functions during the tick life-cycle
  Pavlina Vechtova, Zoltan Fussy, Radim Cegan, Jan Sterba, Jan Erhart, Vladimir Benes, Libor Grubhoffer
  Parasites & Vectors.2020;[Epub]     CrossRef
• Comparative Tandem Mass Tag-Based Quantitative Proteomic Analysis of Tachaea chinensis Isopod During Parasitism
  Yingdong Li, Xin Li, Zhibin Han, Weibin Xu, Xiaodong Li, Qijun Chen
  Frontiers in Cellular and Infection Microbiology.2019;[Epub]     CrossRef
• Applying proteomics to tick vaccine development: where are we?
  Margarita Villar, Anabel Marina, José de la Fuente
  Expert Review of Proteomics.2017; 14(3): 211.     CrossRef
• Screening and Identification of Antigenic Proteins from the Hard Tick <i>Dermacentor silvarum</i> (Acari: Ixodidae)
  Tiantian Zhang, Xuejiao Cui, Jincheng Zhang, Hui Wang, Meng Wu, Hua Zeng, Yuanyuan Cao, Jingze Liu, Yonghong Hu
  The Korean Journal of Parasitology.2015; 53(6): 789.     CrossRef

Citations

Citations to this article as recorded by  

• Helminth-induced immune modulation in colorectal cancer: exploring therapeutic applications
  Hongyu Li, Chaojun Shan, Yunhuan Zhu, Xiaodong Yao, Lijun Lin, Xiaofen Zhang, Yuncheng Qian, Yuqing Wang, Jialu Xu, Yijie Zhang, Hairun Li, Ling Zhao, Keda Chen
  Frontiers in Immunology.2025;[Epub]     CrossRef
• Relationship between parasites and lung cancer: Unveiling the link
  Mariam T. El Khadrawe, Nahla El Skhawy, Maha M. Eissa
  Tropical Medicine & International Health.2025; 30(7): 613.     CrossRef
• NEOPLASIA AND PROLIFERATIVE LESIONS IN FREE-RANGING MOUNTAIN AND GRAUER'S GORILLAS (GORILLA BERINGEI)
  Maya L. Iyer, Kirsten V. Gilardi, Michael R. Cranfield, Sarah M. Corner, Eddy Kambale Syaluha, Jean Bosco Noheri, Benard Ssebide, Jean Felix Kinani, Fred Nizeyimana, Ricky Okwir Okello, Julius Nziza, Martin Kabuyaya, Methode Bahizi, Richard Muvunyi, Elisa
  Journal of Zoo and Wildlife Medicine.2025;[Epub]     CrossRef
• Gastroduodenal Strongyloidiasis Diagnosed during Iron Deficiency Anemia Workup
  Malek Kreidieh, Neville Mobarakai, Sherif Andrawes, Robert Colef, Lara Kreidieh, Hassan Al Moussawi, Jean M. Chalhoub
  Case Reports in Gastroenterology.2025; 19(1): 467.     CrossRef
• The Parasitism and Tumors Carcinogenesis: A Review Subject
  Ahmed Salih Alshewered
  Acta Parasitologica.2024; 69(1): 183.     CrossRef
• A case of disseminated strongyloidiasis diagnosed by worms in the urinary sediment
  Young-Ha Lee
  Parasites, Hosts and Diseases.2024; 62(2): 238.     CrossRef
• Mining parasites for their potential as novel therapeutic agents against cancer
  Neha Sylvia Walter, Shalmoli Bhattacharyya
  Medical Oncology.2024;[Epub]     CrossRef
• Association between Some Helminths and Tumorigenesis through Immunological and Biochemical Factors
  Maryam Fasihi-Karami, Reza Afrisham, Saina Karami, Ehsan Beigzadeh, Forough Kazemi
  Current Cancer Therapy Reviews.2023; 19(2): 96.     CrossRef
• STRONGYLOIDES STERCORALIS: A RARE CASE DIAGNOSED WITH ESOPHAGEAL SWAB SAMPLE
  Arzu Hazal AYDIN, Buse BAYAZIT GÖZÜKÜÇÜK, Nesrin TURHAN
  Kırıkkale Üniversitesi Tıp Fakültesi Dergisi.2023; 25(1): 166.     CrossRef
• Is Gastric Involvement by Strongyloides stercoralis in an Immunocompetent Patient a Common Finding? A Case Report and Review of the Literature
  Irene Pecorella, Tom Richard Okello, Gaia Ciardi, David Martin Ogwang
  Acta Parasitologica.2022; 67(1): 94.     CrossRef
• Seropositivity Rates of Strongyloides stercoralis Antibody in the Southeastern Region of Republic of Korea: A Single-Center Retrospective Study
  Taehwa Kim, Seungjin Lim
  The Korean Journal of Parasitology.2022; 60(3): 181.     CrossRef
• Strongyloides Hyperinfection Causing Gastrointestinal Bleeding and Bacteremia in an Immunocompromised Patient
  Juan Carlos De la Cruz Mayhua, Bisharah Rizvi
  Cureus.2021;[Epub]     CrossRef
• Bacterial and Parasitic Pathogens as Risk Factors for Cancers in the Gastrointestinal Tract: A Review of Current Epidemiological Knowledge
  Janneke W. Duijster, Eelco Franz, Jacques Neefjes, Lapo Mughini-Gras
  Frontiers in Microbiology.2021;[Epub]     CrossRef
• Colorectal Cancer Related to Chronic Strongyloides stercoralis Infection
  M. Sava, T. Huynh, A. Frugoli, L. Kong, M. Salehpour, B. Barrows
  Case Reports in Gastrointestinal Medicine.2020; 2020: 1.     CrossRef
• Phylogenetic Positioning of a Strongyloides stercoralis Isolate Recovered from a Korean Patient and Comparison with Other Asian Isolates
  Jaeho Bae, Mi Jin Jeong, Dong hoon Shin, Hyun Woo Kim, Sung Ho Ahn, Jun Ho Choi, Hak Sun Yu
  The Korean Journal of Parasitology.2020; 58(6): 689.     CrossRef
• Microbiome signatures in prostate cancer
  Sagarika Banerjee, James C Alwine, Zhi Wei, Tian Tian, Natalie Shih, Colin Sperling, Thomas Guzzo, Michael D Feldman, Erle S Robertson
  Carcinogenesis.2019; 40(6): 749.     CrossRef
• Pathologic Features of Infectious Gastritis
  Eric U. Yee, Enoch Kuo, Jeffrey D. Goldsmith
  Advances in Anatomic Pathology.2018; 25(4): 238.     CrossRef
• The Clean India Mission: Public and animal health benefits
  Rashmi Thakur, Balbir Bagicha Singh, Prateek Jindal, Rabinder Singh Aulakh, Jatinder Paul Singh Gill
  Acta Tropica.2018; 186: 5.     CrossRef
• Compensatory gastric stretching following subtotal gastric resection due to gastric adenocarcinoma in a diamond python (Morelia spilota spilota)
  HR Baron, J Šlapeta, SL Donahoe, RTJ Doneley, DN Phalen
  Australian Veterinary Journal.2018; 96(12): 481.     CrossRef
• Parasite Infection, Carcinogenesis and Human Malignancy
  Hoang van Tong, Paul J. Brindley, Christian G. Meyer, Thirumalaisamy P. Velavan
  EBioMedicine.2017; 15: 12.     CrossRef
• Gastric Strongyloidiasis: Report of 2 Cases and Brief Review of the Literature
  Rawia Mohamed, Mowafak M. Hamodat, Mousa A. Al-Abbadi
  Laboratory Medicine.2017; 48(1): 93.     CrossRef
• Strongyloidiasis Current Status with Emphasis in Diagnosis and Drug Research
  Tiago Mendes, Karen Minori, Marlene Ueta, Danilo Ciccone Miguel, Silmara Marques Allegretti
  Journal of Parasitology Research.2017; 2017: 1.     CrossRef
• A case of adenocarcinoma developed in the small intestine with chronic strongyloidiasis
  Satoshi Ishikawa, Tamaki Maeda, Kimiaki Hattori, Takahiro Watanabe, Takanori Kuramoto, Saori Ueno, Goro Ueno, Tadahiro Yamada, Akifumi Kanazawa, Masahiro Sakaguchi, Yoshitane Tsukamoto
  Clinical Journal of Gastroenterology.2017; 10(6): 519.     CrossRef
• Colorectal Cancer Associated with Strongyloides stercoralis Colitis
  Carmine Catalano, Joshua Aron, Raghav Bansal, Anatoly Leytin
  ACG Case Reports Journal.2017; 4(1): e104.     CrossRef
• Carcinogenesis associated with parasites other than Schistosoma, Opisthorchis and Clonorchis: A systematic review
  Claudia Machicado, Luis A. Marcos
  International Journal of Cancer.2016; 138(12): 2915.     CrossRef

Citations

Citations to this article as recorded by  

• Morphological and molecular data on acuariid nematodes in European great cormorants (Phalacrocorax carbo sinensis) and pygmy cormorants (Microcarbo pygmaeus)
  Perla Tedesco, Monica Caffara, Nadav Davidovich, Valentina Luci, Alessia Cantori, Maria Letizia Fioravanti, Andrea Gustinelli
  Scientific Reports.2024;[Epub]     CrossRef
• Helminths of the black-headed gull (Chroicocephalus ridibundus) from breeding colonies in north-central Poland
  Agata N. Stapf, Izabella Rząd, Katarzyna Królaczyk, Piotr Indykiewicz, Wojciech Gruszka
  Scientific Reports.2024;[Epub]     CrossRef
• Bir Martıda (Larus cachinnans) Türkiye Faunası için İki Yeni Nematod Türü; Cosmocephalus obvelatus (Creplin, 1825) ve Paracuaria adunca (Creplin, 1846)
  Şinasi UMUR, Gökmen Zafer PEKMEZCİ, Cenk Soner BÖLÜKBAŞ, Celil ATEŞ
  Erciyes Üniversitesi Veteriner Fakültesi Dergisi.2019; 16(3): 238.     CrossRef

Citations

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• Dietary footprints of a global parasite: diagnosing Dibothriocephalus nihonkaiensis in non-endemic regions
  Wilson G.W. Goh, Jean-Marc Chavatte, Gabriel Z.R. Yan, Yuan Yi Constance Chen, Mark Dhinesh Muthiah, Lionel H.W. Lum
  Gut Pathogens.2025;[Epub]     CrossRef
• Human diphyllobothriosis in Taiwan: A review of cases and molecular evidence of Dibothriocephalus nihonkaiensis
  Chia-Kwung Fan, Daniel Barčák, Tomáš Scholz, Pasaikou Sonko, Martina Orosová, Kua-Eyre Su, Chun-Chao Chang, Yuarn-Jang Lee, Roman Kuchta, Mikuláš Oros
  Food and Waterborne Parasitology.2023; 33: e00213.     CrossRef
• Population genetic structure of diphyllobothriid tapeworms (Cestoda: Diphyllobothriidea) parasitising fish in the Baikal Rift Zone
  IA Kutyrev, VA Mordvinov
  Diseases of Aquatic Organisms.2022; 148: 113.     CrossRef
• Molecular Identification of Diphyllobothrium latum from a Pediatric Case in Taiwan
  Yu-Chin An, Chia-Cheng Sung, Chih-Chien Wang, Hsin-Chung Lin, Kuang-Yao Chen, Fu-Man Ku, Ruei-Min Chen, Mei-Li Chen, Kuo-Yang Huang
  The Korean Journal of Parasitology.2017; 55(4): 425.     CrossRef
• Four Human Cases of Diphyllobothrium nihonkaiense (Eucestoda: Diphyllobothriidae) in China with a Brief Review of Chinese Cases
  Yu-Chun Cai, Shao-Hong Chen, Hiroshi Yamasaki, Jia-Xu Chen, Yan Lu, Yong-Nian Zhang, Hao Li, Lin Ai, Hai-Ning Chen
  The Korean Journal of Parasitology.2017; 55(3): 319.     CrossRef
• Molecular Identification of <i>Diphyllobothrium nihonkaiense</i> from 3 Human Cases in Heilongjiang Province with a Brief Literature Review in China
  Weizhe Zhang, Fei Che, Song Tian, Jing Shu, Xiaoli Zhang
  The Korean Journal of Parasitology.2015; 53(6): 683.     CrossRef

Citations

Citations to this article as recorded by  

• Dietary footprints of a global parasite: diagnosing Dibothriocephalus nihonkaiensis in non-endemic regions
  Wilson G.W. Goh, Jean-Marc Chavatte, Gabriel Z.R. Yan, Yuan Yi Constance Chen, Mark Dhinesh Muthiah, Lionel H.W. Lum
  Gut Pathogens.2025;[Epub]     CrossRef
• Tapeworm Infection Diagnosed after Campylobacter jejuni-induced Enteritis
  Sotaro Ozaka, Ryusuke Soma, Haruhiko Takahashi, Yuta Shimomori, Masahide Fukuda, Koshiro Tsutsumi, Yuka Hirashita, Kensuke Fukuda, Ryo Ogawa, Kazuhiro Mizukami, Yomei Kagoshima, Nozomi Sachi, Naganori Kamiyama, Hideo Hasegawa, Takashi Kobayashi, Masaaki K
  Internal Medicine.2024; 63(21): 2939.     CrossRef
• Epidemiology ofDiphyllobothrium nihonkaienseDiphyllobothriasis, Japan, 2001–2016
  Hiroshi Ikuno, Shinkichi Akao, Hiroshi Yamasaki
  Emerging Infectious Diseases.2018;[Epub]     CrossRef
• RETROSPECTIVE ANALYSIS OF THE EPIDEMIOLOGIC LITERATURE, 1990–2015, ON WILDLIFE-ASSOCIATED DISEASES FROM THE REPUBLIC OF KOREA
  Jusun Hwang, Kyunglee Lee, Young-Jun Kim, Jonathan M. Sleeman, Hang Lee
  Journal of Wildlife Diseases.2017; 53(1): 5.     CrossRef

Citations

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• Molecular identification and diversity of gastrointestinal apicomplexan protozoa in pigs in the Republic of Korea
  Subin Lee, Sang-Hyup Lee, Badriah Alkathiri, Kyung-Duk Min, Dong Hyeon Kwon, Mi-Hye Hwang, Gyu-Tae Jeon, Bok Kyung Ku, Jae-Won Byun, Seung-Hun Lee
  Scientific Reports.2025;[Epub]     CrossRef
• Occurrence and Molecular Characterization of Cryptosporidium spp. in Swine Farms in Northeastern Spain
  Laura Garza-Moreno, Celia León, Joaquín Quílez
  Pathogens.2025; 14(7): 665.     CrossRef
• Infections and genetic diversity of Cryptosporidium spp. and Giardia spp. in small wild mammals on the Eastern Tibetan plateau: public health implications
  Qingqiu Zuo, Zhuoma Bianba, Chuizhao Xue, Hua Liu, Xiaoxue Peng, Hao Zhou, Xiaocheng Zhang, Quan Chen, Mengqing Li, Yang Yang, Yan Zhou, Jianping Cao, Jianhai Yin, Xu Wang, Yujuan Shen
  BMC Microbiology.2025;[Epub]     CrossRef
• Global prevalence of Cryptosporidium spp. in pigs: a systematic review and meta-analysis
  Yuancai Chen, Huikai Qin, Yayun Wu, Huiyan Xu, Jianying Huang, Junqiang Li, Longxian Zhang
  Parasitology.2023; 150(6): 531.     CrossRef
• Outbreak of severe diarrhea due to zoonotic Cryptosporidium parvum and C. xiaoi in goat kids in Chungcheongbuk-do, Korea
  Ah-Young Kim, Badriah Alkathiri, Subin Lee, Kyung-Duk Min, Soochong Kim, Sang-Myeong Lee, Wan-Kyu Lee, Dongmi Kwak, Seung-Hun Lee
  Parasitology Research.2023; 122(9): 2045.     CrossRef
• The infection and molecular characterization of Cryptosporidium spp. in diarrheic pigs in southern China
  Pei Wang, Sen Li, Yang Zou, Zi-Cheng Du, De-Ping Song, Ping Wang, Xiao-Qing Chen
  Microbial Pathogenesis.2022; 165: 105459.     CrossRef
• First Characterization and Zoonotic Potential of Cryptosporidium spp. and Giardia duodenalis in Pigs in Hubei Province of China
  Dongfang Li, Han Deng, Yaxin Zheng, Hongyan Zhang, Sen Wang, Lan He, Junlong Zhao
  Frontiers in Cellular and Infection Microbiology.2022;[Epub]     CrossRef
• Prevalence ofCryptosporidiumin pigs in China: A systematic review and meta‐analysis
  Wei Wang, Qing‐Long Gong, Ao Zeng, Ming‐Han Li, Quan Zhao, Hong‐Bo Ni
  Transboundary and Emerging Diseases.2021; 68(3): 1400.     CrossRef
• Genotyping and zoonotic potential of Cryptosporidium and Enterocytozoon bieneusi in pigs transported across regions in China
  Hua Liu, Hongxia Ni, Jie Xu, Rong Wang, Yongdong Li, Yujuan Shen, Jianping Cao, Jianhai Yin
  Microbial Pathogenesis.2021; 154: 104823.     CrossRef
• Prevalence and Characterization of Cryptosporidium Species in Tibetan Antelope (Pantholops hodgsonii)
  Si-Yuan Qin, He-Ting Sun, Chuang Lyu, Jun-Hui Zhu, Zhen-Jun Wang, Tao Ma, Quan Zhao, Yun-Gang Lan, Wen-Qi He
  Frontiers in Cellular and Infection Microbiology.2021;[Epub]     CrossRef
• A retrospective epidemiological analysis of human Cryptosporidium infection in China during the past three decades (1987-2018)
  Aiqin Liu, Baiyan Gong, Xiaohua Liu, Yujuan Shen, Yanchen Wu, Weizhe Zhang, Jianping Cao, Luther A. Bartelt
  PLOS Neglected Tropical Diseases.2020; 14(3): e0008146.     CrossRef
• High prevalence of Cryptosporidium infection caused by C. scrofarum and C. suis among pigs in Thailand
  Umaporn Thathaisong, Suradej Siripattanapipong, Tawin Inpankaew, Saovanee Leelayoova, Mathirut Mungthin
  Parasitology International.2020; 77: 102122.     CrossRef
• Prevalence and molecular characterization of Cryptosporidium spp. in pigs in Xinjiang, China
  Meng Qi, Qiyuan Zhang, Chunyan Xu, Ying Zhang, Jinming Xing, Dayong Tao, Junqiang Li, Longxian Zhang
  Acta Tropica.2020; 209: 105551.     CrossRef
• Molecular identification and epidemiological comparison of Cryptosporidium spp. among different pig breeds in Tibet and Henan, China
  Shuangjian Zheng, Dongfang Li, Chunxiang Zhou, Sumei Zhang, Yayun Wu, Yankai Chang, Yuancai Chen, Jianying Huang, Changshen Ning, Gaiping Zhang, Longxian Zhang
  BMC Veterinary Research.2019;[Epub]     CrossRef
• Occurrence, Molecular Characterization, and Assessment of Zoonotic Risk of Cryptosporidium spp., Giardia duodenalis, and Enterocytozoon bieneusi in Pigs in Henan, Central China
  Haiyan Wang, Yiqi Zhang, Yayun Wu, Junqiang Li, Meng Qi, Tingwen Li, Jianling Wang, Rongjun Wang, Sumei Zhang, Fuchun Jian, Changshen Ning, Longxian Zhang
  Journal of Eukaryotic Microbiology.2018; 65(6): 893.     CrossRef
• Presence of zoonotic Cryptosporidium scrofarum, Giardia duodenalis assemblage A and Enterocytozoon bieneusi genotypes in captive Eurasian wild boars (Sus scrofa) in China: potential for zoonotic transmission
  Wei Li, Lei Deng, Kongju Wu, Xiangming Huang, Yuan Song, Huaiyi Su, Yanchun Hu, Hualin Fu, Zhijun Zhong, Guangneng Peng
  Parasites & Vectors.2017;[Epub]     CrossRef
• Prevalence and risk factors of Cryptosporidium infection in farmed pigs in Zhejiang, Guangdong, and Yunnan provinces, China
  Yang Zou, Jian-Gang Ma, Dong-Mei Yue, Wen-Bin Zheng, Xiao-Xuan Zhang, Quan Zhao, Xing-Quan Zhu
  Tropical Animal Health and Production.2017; 49(3): 653.     CrossRef
• Molecular Epidemiology of Cryptosporidiosis in China
  Yaoyu Feng, Lihua Xiao
  Frontiers in Microbiology.2017;[Epub]     CrossRef
• Identification of pig-specific Cryptosporidium species in mixed infections using Illumina sequencing technology
  A. Kaupke, J. Gawor, A. Rzeżutka, R. Gromadka
  Experimental Parasitology.2017; 182: 22.     CrossRef

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• Global prevalence of Giardia infection in nonhuman mammalian hosts: A systematic review and meta-analysis of five million animals
  Kareem Hatam-Nahavandi, Ehsan Ahmadpour, Milad Badri, Aida Vafae Eslahi, Davood Anvari, David Carmena, Lihua Xiao, Aysegul Taylan Ozkan
  PLOS Neglected Tropical Diseases.2025; 19(4): e0013021.     CrossRef
• Molecular characterization of Cryptosporidium spp. and Giardia duodenalis in pet cats in Henan Province, central China
  Liangliang Li, Yuzhen Sui, Xinmiao Li, Pengtao Song, Guizhen Chen, Hu Liu, Shoujun Zuo, Jinjie Guo, Qiong Wang, Qiyuan Sun, Hongyu Dai, Junqiang Li, Tao Zhang, Fang Liu, Longxian Zhang, Haiju Dong
  Acta Tropica.2024; 254: 107188.     CrossRef
• Cryptosporidium and Giardia in cats and dogs: What is the real zoonotic risk?
  Amanda D. Barbosa, Siobhon Egan, Yaoyu Feng, Lihua Xiao, Una Ryan
  Current Research in Parasitology & Vector-Borne Diseases.2023; 4: 100158.     CrossRef
• Genetic characterization of Cryptosporidium spp. and Giardia duodenalis in dogs and cats in Guangdong, China
  Jiayu Li, Xiaoyu Dan, Kexin Zhu, Na Li, Yaqiong Guo, Zezhong Zheng, Yaoyu Feng, Lihua Xiao
  Parasites & Vectors.2019;[Epub]     CrossRef
• Giardia in a selected population of dogs and cats in Germany – diagnostics, coinfections and assemblages
  M.F. Sommer, P. Rupp, M. Pietsch, A. Kaspar, P. Beelitz
  Veterinary Parasitology.2018; 249: 49.     CrossRef
• Prevalence and risk factors of Giardia duodenalis in domestic rabbbits (Oryctolagus cuniculus) in Jilin and Liaoning province, northeastern China
  Jing Jiang, Jian-Gang Ma, Nian-Zhang Zhang, Peng Xu, Guangyu Hou, Quan Zhao, Xiao-Xuan Zhang
  Journal of Infection and Public Health.2018; 11(5): 723.     CrossRef
• Development of T m -shift genotyping method for detection of cat-derived Giardia lamblia
  Weida Pan, Yeqi Fu, Auwalu Yusuf Abdullahi, Mingwei Wang, Xianli Shi, Fang Yang, Xingang Yu, Xinxin Yan, Pan Zhang, Jianxiong Hang, Guoqing Li
  Parasitology Research.2017; 116(4): 1151.     CrossRef
• Giardia duodenalis Infections in Humans and Other Animals in China
  Junqiang Li, Haiyan Wang, Rongjun Wang, Longxian Zhang
  Frontiers in Microbiology.2017;[Epub]     CrossRef
• Genotypes of Cryptosporidium spp., Enterocytozoon bieneusi and Giardia duodenalis in dogs and cats in Shanghai, China
  Hailing Xu, Yue Jin, Wenxian Wu, Pei Li, Lin Wang, Na Li, Yaoyu Feng, Lihua Xiao
  Parasites & Vectors.2016;[Epub]     CrossRef
• A Multiplex PCR for Simultaneous Detection of Three Zoonotic ParasitesAncylostoma ceylanicum,A. caninum,andGiardia lambliaAssemblage A
  Wei Hu, Sheng Wu, Xingang Yu, Auwalu Yusuf Abullahi, Meiran Song, Liping Tan, Zhen Wang, Biao Jiang, Guoqing Li
  BioMed Research International.2015; 2015: 1.     CrossRef

Citations

Citations to this article as recorded by  

• Global geographical distribution of Toxoplasma gondii genotypes from dogs: A systematic review
  Maryam Hataminejad, Mahbobeh Montazeri, Asal Tanzifi, Tahereh Mikaeili Galeh
  Parasite Epidemiology and Control.2025; 30: e00433.     CrossRef
• Can cloning and sequencing help to genotype positive Toxoplasma gondii clinical samples? Results and validation using SAG3 as a model
  Claudia Patricia Rico-Torres, Luis Fernando Valenzuela-Moreno, Sara Teresa Méndez-Cruz, Carlos Cedillo-Peláez, Heriberto Caballero-Ortega
  Infection, Genetics and Evolution.2022; 101: 105283.     CrossRef
• Low Prevalence of Toxoplasma gondii in Dogs From Central China
  Niuping Zhu, Liulu Yang, Shilin Xin, Wei Huang, Yibao Jiang, Yurong Yang
  Frontiers in Cellular and Infection Microbiology.2022;[Epub]     CrossRef
• Molecular Detection and Genotyping ofToxoplasma gondiiandNeospora caninumin Slaughtered Goats in Central China
  Weifeng Qian, Wenchao Yan, Chaochao Lv, Rongzhen Bai, Tianqi Wang, Zhiguo Wei, Min Zhang
  Foodborne Pathogens and Disease.2020; 17(5): 348.     CrossRef
• A Review on the Prevalence of Toxoplasma gondii in Humans and Animals Reported in Malaysia from 2008–2018
  Mohammed Nasiru Wana, Mohamad Aris Mohd Moklas, Malaika Watanabe, Norshariza Nordin, Ngah Zasmy Unyah, Sharif Alhassan Abdullahi, Ashraf Ahmad Issa Alapid, Tijjani Mustapha, Rusliza Basir, Roslaini Abd. Majid
  International Journal of Environmental Research and Public Health.2020; 17(13): 4809.     CrossRef
• Toxoplasma gondii infections in dogs: 2009-2020
  Jitender P. Dubey, Fernando H.A. Murata, Camila K. Cerqueira-Cézar, Oliver C.H. Kwok, Yurong Yang, Chunlei Su
  Veterinary Parasitology.2020; 287: 109223.     CrossRef
• Molecular Detection and Genetic Characterization of Toxoplasma gondii from Horses in Three Provinces of China
  Wei-Xin Ren, Xiao-Xuan Zhang, Cui-Yu Long, Quan Zhao, Tian Cheng, Jian-Gang Ma, Peng Xu, Guangyu Hou, Hong-Bo Ni
  Vector-Borne and Zoonotic Diseases.2019; 19(9): 703.     CrossRef
• Occurrence and genetic characterization of Toxoplasma gondii and Neospora caninum in slaughtered domestic rabbits in central China
  Weifeng Qian, Wenchao Yan, Chaochao Lv, Rongzhen Bai, Tianqi Wang
  Parasite.2019; 26: 36.     CrossRef
• Prevalence, risk factors and genetic characterization of Toxoplasma gondii in sick pigs and stray cats in Jiangsu Province, eastern China
  Zhao-feng Hou, Shi-jie Su, Dan-dan Liu, Le-le Wang, Chuan-li Jia, Zhen-xing Zhao, Yi-fei Ma, Qiao-qiao Li, Jin-jun Xu, Jian-ping Tao
  Infection, Genetics and Evolution.2018; 60: 17.     CrossRef
• Geographical distribution of Toxoplasma gondii genotypes in Asia: A link with neighboring continents
  P. Chaichan, A. Mercier, L. Galal, A. Mahittikorn, F. Ariey, S. Morand, F. Boumédiène, R. Udonsom, A. Hamidovic, J.B. Murat, Y. Sukthana, M.L. Dardé
  Infection, Genetics and Evolution.2017; 53: 227.     CrossRef
• Prevalence and genetic characterization of Toxoplasma gondii in donkeys in northeastern China
  Xiao-Xuan Zhang, Wei Shi, Nian-Zhang Zhang, Kun Shi, Jian-Ming Li, Peng Xu, Quan Zhao, Rui Du
  Infection, Genetics and Evolution.2017; 54: 455.     CrossRef
• Seroprevalence and genotypes of Toxoplasma gondii isolated from pigs intended for human consumption in Liaoning province, northeastern China
  Dawei Wang, Yan Liu, Tiantian Jiang, Guoxin Zhang, Gaoming Yuan, Jianbin He, Chunlei Su, Na Yang
  Parasites & Vectors.2016;[Epub]     CrossRef
• Seroprevalence ofToxoplasma gondiiin goats in Hunan province, China
  Fen Li, Shi-Ping Wang, Chang-Jian Wang, Shi-Cheng He, Xiang Wu, Guo-Hua Liu
  Parasite.2016; 23: 44.     CrossRef
• Prevalence of <i>Toxoplasma gondii</i> in Dogs in Zhanjiang, Southern China
  Hai-Hai Jiang, Ming-Wei Li, Min-Jun Xu, Wei Cong, Xing-Quan Zhu
  The Korean Journal of Parasitology.2015; 53(4): 493.     CrossRef
• Seroprevalence and risk factors of Toxoplasma gondii infection in stray dogs in northern China
  Xiao-Xuan Zhang, Ya-Nan Cai, Chun-Feng Wang, Jing Jiang, Ying-Tian Xu, Gui-Lian Yang, Quan Zhao
  Parasitology Research.2015; 114(12): 4725.     CrossRef

Citations

Citations to this article as recorded by  

• Evidence of high genetic diversity among parasite populations in a schistosomiasis hotspot
  Yvonne Aryeetey Ashong, Emmanuel Odartei Armah, Jewelna Akorli, Frank Twum Aboagye, Isaac Owusu-Frimpong, Linda Batsa Debrah, Rhoda Lims Diyie, Samuel Armoo, Alexander Yaw Debrah, Mike Yaw Osei-Atweneboana, Clinton J. Jones, Marcello Otake Sato
  Microbiology Spectrum.2025;[Epub]     CrossRef
• Geographical Influence on Morphometric Variability of Genetically “Pure” Schistosoma haematobium Eggs from Sub-Saharan Migrants in Spain
  Marta Reguera-Gómez, Maria Adela Valero, Patricio Artigas, Alejandra De Elías-Escribano, Maria Cecilia Fantozzi, Maria Pilar Luzón-García, Joaquín Salas-Coronas, Jérôme Boissier, Santiago Mas-Coma, Maria Dolores Bargues
  Tropical Medicine and Infectious Disease.2023; 8(3): 144.     CrossRef
• Genetic Diversity of Schistosoma haematobium in Sub-Saharan Africa: A Systematic Review
  Rabecca Tembo, Panji Nkhoma, Mildred Zulu, Florence Mwaba, John Yabe, Hikabasa Halwiindi, Moses Kamwela, King S Nalubamba, Chummy S Sikasunge, Andrew M Phri
  University of Zambia Journal of Agricultural and Biomedical Sciences.2022;[Epub]     CrossRef
• Membrane Technology for Rapid Point-of-Care Diagnostics for Parasitic Neglected Tropical Diseases
  Madeleine J. Rogers, Donald P. McManus, Stephen Muhi, Catherine A. Gordon
  Clinical Microbiology Reviews.2021;[Epub]     CrossRef
• Detection of Schistosoma DNA in genital specimens and urine: A comparison between five female African study populations originating from S. haematobium and/or S. mansoni endemic areas
  P. Pillay, J.A. Downs, J.M. Changalucha, E.A.T. Brienen, C.E. Ramarokoto, P.D.C. Leutscher, B.J. Vennervald, M. Taylor, E.F. Kjetland, L. Van Lieshout
  Acta Tropica.2020; 204: 105363.     CrossRef
• RETRACTED: Diversity and Compatibility of Human Schistosomes and Their Intermediate Snail Hosts
  Benjamin Sanogo, Dongjuan Yuan, Xin Zeng, Yanhua Zhang, Zhongdao Wu
  Trends in Parasitology.2018; 34(6): 493.     CrossRef
• Geographic strain differentiation of Schistosoma japonicum in the Philippines using microsatellite markers
  Kharleezelle J. Moendeg, Jose Ma M. Angeles, Ryo Nakao, Lydia R. Leonardo, Ian Kendrich C. Fontanilla, Yasuyuki Goto, Masashi Kirinoki, Elena A. Villacorte, Pilarita T. Rivera, Noboru Inoue, Yuichi Chigusa, Shin-ichiro Kawazu, Aaron R. Jex
  PLOS Neglected Tropical Diseases.2017; 11(7): e0005749.     CrossRef
• Genetic Diversity of <i>Schistosoma haematobium</i> Eggs Isolated from Human Urine in Sudan
  Juan-Hua Quan, In-Wook Choi, Hassan Ahmed Hassan Ahmed Ismail, Abdoelohab Saed Mohamed, Hoo-Gn Jeong, Jin-Su Lee, Sung-Tae Hong, Tai-Soon Yong, Guang-Ho Cha, Young-Ha Lee
  The Korean Journal of Parasitology.2015; 53(3): 271.     CrossRef

Citations

Citations to this article as recorded by  

• Intestinal parasites in rodents from five different Himas in Lebanon
  M. Abi Said, T. Maroun, H. Shaib
  Helminthologia.2025; 62(2): 120.     CrossRef
• Helminthofauna Diversity in Synanthropic Rodents of the Emilia-Romagna Region (Italy): Implications for Public Health and Rodent Control
  Filippo Maria Dini, Carlotta Mazzoni Tondi, Roberta Galuppi
  Veterinary Sciences.2024; 11(11): 585.     CrossRef
• The Parasites that can be Found in the Mus musculus House Mice
  Dilara KARAMAN, Ahmet Onur GİRİŞGİN
  Commagene Journal of Biology.2022;[Epub]     CrossRef
• A newly identified secreted larval antigen elicits basophil-dependent protective immunity against N. brasiliensis infection
  Natalie Thuma, Daniela Döhler, Dirk Mielenz, Heinrich Sticht, Daniel Radtke, Lena Reimann, Bettina Warscheid, David Voehringer
  Frontiers in Immunology.2022;[Epub]     CrossRef
• IL‐4/IL‐13‐producing ILC2s are required for timely control of intestinal helminth infection in mice
  Filipa Varela, Cornelia Symowski, Jonathan Pollock, Stefan Wirtz, David Voehringer
  European Journal of Immunology.2022; 52(12): 1925.     CrossRef
• Rictularia jiyeoni n. sp. (Nematoda: Rictulariidae) from the Striped Field Mouse, Apodemus agrarius, in Korea
  Bae Keun Park, Hyeon Cheol Kim, Eui Ju Hong, Si Yun Ryu, Joon Seok Chae
  Journal of Parasitology.2021;[Epub]     CrossRef
• A helminth-derived suppressor of ST2 blocks allergic responses
  Francesco Vacca, Caroline Chauché, Abhishek Jamwal, Elizabeth C Hinchy, Graham Heieis, Holly Webster, Adefunke Ogunkanbi, Zala Sekne, William F Gregory, Martin Wear, Georgia Perona-Wright, Matthew K Higgins, Josquin A Nys, E Suzanne Cohen, Henry J McSorle
  eLife.2020;[Epub]     CrossRef
• Immunomodulation and Immune Escape Strategies of Gastrointestinal Helminths and Schistosomes
  Marie Wiedemann, David Voehringer
  Frontiers in Immunology.2020;[Epub]     CrossRef
• Selective expression of constitutively activated STAT6 in intestinal epithelial cells promotes differentiation of secretory cells and protection against helminths
  Christoph Schubart, Branislav Krljanac, Manuel Otte, Cornelia Symowski, Eva Martini, Claudia Günther, Christoph Becker, Christoph Daniel, David Voehringer
  Mucosal Immunology.2019; 12(2): 413.     CrossRef
• A novel controlled release microsponges containing Albendazole against Haemonchus contortus in experimentally infected goats
  Ahmed A.H. Abdellatif, Gamal M. Zayed, H.H. Kamel, Ahmed G. Mohamed, Waleed M. Arafa, Abdelrhman M. Khatib, Ossama M. Sayed
  Journal of Drug Delivery Science and Technology.2018; 43: 469.     CrossRef
• Infections of Intestinal Helminth at Two Species of Field Mice, Apodemus agrarius and A. Peninsulae, in Gangwondo and Chungcheongnam-do, Korea
  Jae-Hyung Lee, Shuang Gong, Yung Chul Park, Hyun-Ju Kim, In-Wook Choi, Young-Ha Lee
  The Korean Journal of Parasitology.2018; 56(3): 301.     CrossRef
• The Distribution and Habitat Characteristic of Tscherskia triton (Rodentia; Cricetidae) in Jeju Island, Korea
  Jun-Ho Park, Kang Il Kim, Man-Ho Kim, Hong-Shik Oh
  Environmental Biology Research.2018; 36(3): 412.     CrossRef
• Seroprevalence of Toxoplasmosis with ELISA and Rapid Diagnostic Test among Residents in Gyodong-do, Inchon city, Korea: A Four-Year Follow-up
  Yeong Hoon Kim, Ji hoo Lee, Seong kyu Ahn, Tong-Soo Kim, Sung-Jong Hong, Chom-Kyu Chong, Hye-Jin Ahn, Ho-Woo Nam
  The Korean Journal of Parasitology.2017; 55(3): 247.     CrossRef
• Seroprevalence of Toxoplasmosis Detected by RDT in Residents near the DMZ (demilitarized zone) of Cheorwon-gun, Gangwon-do, Korea
  Yeong Hoon Kim, Jihoo Lee, Young-Eun Kim, Seongkyu Ahn, Tong-Soo Kim, Sung-Jong Hong, Chom-Kyu Chong, Hye-Jin Ahn, Ho-Woo Nam
  The Korean Journal of Parasitology.2017; 55(4): 385.     CrossRef