Articles citing this article

The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).

Cited article:

The first commercially approved efficacious cryptosporidium vaccine protecting New-Born calves from severe diarrhea

Marina Timmermans, Willem Hubers, Dianne Schroer, Koen Gevers, Ruud PAM Segers, Ron Niessen and Mark H van Roosmalen
Veterinary Vaccine 3 (1) 100054 (2024)
https://doi.org/10.1016/j.vetvac.2024.100054

miR-181d targets BCL2 to regulate HCT-8 cell apoptosis and parasite burden in response to Cryptosporidium parvum infection via the intrinsic apoptosis pathway

Juanfeng Li, Ruiying Feng, Xiaotian Zhang, Wenyan Hou, Yingying Zhang, Junqiang Li, Xiaoying Li, Fuchun Jian, Longxian Zhang, Sumei Zhang and Rongjun Wang
Veterinary Parasitology 330 110237 (2024)
https://doi.org/10.1016/j.vetpar.2024.110237

Pharmacokinetics and tissue distribution of LN002, a new compound alternative oxidase inhibitor against Cryptosporidium in rats

Minglang Ma, Yongxiang Zhang, Yanjun Fang, Yixing Lu, Huiguo Huang, Zhenling Zeng and Dongping Zeng
Frontiers in Pharmacology 15 (2024)
https://doi.org/10.3389/fphar.2024.1413872

Herbal-based compounds: A review on treatments of cryptosporidiosis

Fatemeh Namazi and Seyed Mostafa Razavi
International Journal for Parasitology: Drugs and Drug Resistance 24 100521 (2024)
https://doi.org/10.1016/j.ijpddr.2024.100521

Efficacy of Lactobacillus taiwanensis S29 and Lactiplantibacillus plantarum S27 against tapeworm infection in Swiss Albino rats

Sudeshna Mandal, Chandrani Mondal, Sinchan Ghosh, Samiparna Saha, Mou Singha Ray and Larisha M. Lyndem
Experimental Parasitology 259 108715 (2024)
https://doi.org/10.1016/j.exppara.2024.108715

Therapeutic Potency of Ginger, Garlic, and Pomegranate Extracts Against Cryptosporidium parvum-Mediated Gastro-Splenic Damage in Mice

Dina M. M. EL-Shewehy, Gehad E. Elshopakey, Amira Ismail, Shimaa S. Hassan and Amany M. Ramez
Acta Parasitologica 68 (1) 32 (2023)
https://doi.org/10.1007/s11686-022-00635-0

Therapeutic efficacy of proton pump inhibitor (omeprazole) on cryptosporidiosis parvum in immunosuppressed experimental mice

Engy V. N. Beshay, Nashaat E. Nassef, Omaima K. El Shafei, Mona M. Saleh, Mona A. Kora and Fatma H. Shalaan
Journal of Parasitic Diseases 47 (3) 535 (2023)
https://doi.org/10.1007/s12639-023-01592-9

Cost-effective In Vivo and In Vitro Mouse Models for Evaluating Anticryptosporidial Drug Efficacy: Assessing Vorinostat, Docetaxel, and Baicalein

Mingxiao Liu, Di Zhang, Dongqiang Wang, Xiaodong Wu, Ying Zhang, Jigang Yin and Guan Zhu
The Journal of Infectious Diseases 228 (10) 1430 (2023)
https://doi.org/10.1093/infdis/jiad243

Investigation of the prophylactic and therapeutic effectiveness of oral thyme extract in rats experimentally infected with cryptosporidium parvum

Erdal Kara, Sibel Yasa Duru, Sami Gökpinar, Özkan Duru, Sedat Sevin, Yasin Şenel and Ufuk Kaya
Veterinary Research Communications 47 (2) 663 (2023)
https://doi.org/10.1007/s11259-022-10025-6

Evaluation of the therapeutic efficacy of some essential oils in experimentally immunosuppressed mice infected with Cryptosporidium parvum

Noha Madbouly Taha, Rabab Sayed Zalat, Eman Khaled and Basma M. Elmansory
Journal of Parasitic Diseases 47 (4) 733 (2023)
https://doi.org/10.1007/s12639-023-01621-7

A multi-epitope vaccine candidate developed from unique immunogenic epitopes against Cryptosporidium hominis by utilizing an immunoinformatics-driven approach

Nirali Pandya and Amit Kumar
Journal of Biomolecular Structure and Dynamics 41 (10) 4614 (2023)
https://doi.org/10.1080/07391102.2022.2070284

Pathobiology of Parasitic Protozoa: Dynamics and Dimensions

Amresh Kumar Singh, Suraiya Khanam Ansari, Alok Raghav and Vivek Gaur
Pathobiology of Parasitic Protozoa: Dynamics and Dimensions 45 (2023)
https://doi.org/10.1007/978-981-19-8225-5_3

The potential therapeutic effect of Nigella sativa and Zingiber officinale extracts versus Nitazoxanide drug against experimentally induced cryptosporidiosis in laboratory mice

Samah Hassan Yahia, Reda Lamei El gamal, Ghada Mahmoud Fathy, et al.
Journal of Parasitic Diseases 47 (2) 329 (2023)
https://doi.org/10.1007/s12639-023-01572-z

QSAR and deep learning model for virtual screening of potential inhibitors against Inosine 5’ Monophosphate dehydrogenase (IMPDH) of Cryptosporidium parvum

Misgana Mengistu Asmare, Nitin Nitin, Soon-IL Yun and Rajani Kanta Mahapatra
Journal of Molecular Graphics and Modelling 111 108108 (2022)
https://doi.org/10.1016/j.jmgm.2021.108108

Parasitic Helminths and Zoonoses - From Basic to Applied Research

Osama M. Darwesh and Hoda Samir El-Sayed
Parasitic Helminths and Zoonoses - From Basic to Applied Research (2022)
https://doi.org/10.5772/intechopen.103744

Anti-cryptosporidial activity of Camellia sinensis (green tea extract) in experimentally infected immunocompromised mice

Eman S. El-Wakil, Eman Ali Mohamed, Eman Ahmed El-Wakil, Tarek S. AbouShousha and Neimat Mousa Amer
Acta Protozoologica 61 23 (2022)
https://doi.org/10.4467/16890027AP.22.002.16205

In vivo evaluation of anticryptosporidial effects of wheat germ extracts in immunocompromised mice

Hagar F. Abdelmaksoud, Ezzat E. A. Osman, Sayed S. Abdel-Hameed, Tarek Aboushousha and Heba M. El Naggar
Journal of Parasitic Diseases 46 (3) 833 (2022)
https://doi.org/10.1007/s12639-022-01502-5

Garlic (Allium sativum Linnaeus) improved inflammation and reduced cryptosporidiosis burden in immunocompromised mice

Alyaa Farid, Mona Yousry and Gehan Safwat
Journal of Ethnopharmacology 292 115174 (2022)
https://doi.org/10.1016/j.jep.2022.115174

Chemical profiling of Verbena officinalis and assessment of its anti-cryptosporidial activity in experimentally infected immunocompromised mice

Eman S. El-Wakil, Maha A.M. El-Shazly, Ayman M. El-Ashkar, Tarek Aboushousha and Mosad A. Ghareeb
Arabian Journal of Chemistry 15 (7) 103945 (2022)
https://doi.org/10.1016/j.arabjc.2022.103945

Efficacy of clofazimine and nitazoxanide combination in treating intestinal cryptosporidiosis and enhancing intestinal cellular regeneration in immunocompromised mice

Marwa Esmat, Amany A. Abdel-Aal, Maisa A. Shalaby, et al.
Food and Waterborne Parasitology 27 e00161 (2022)
https://doi.org/10.1016/j.fawpar.2022.e00161

Bioactive Peptides against Human Apicomplexan Parasites

Norma Rivera-Fernández, Jhony Anacleto-Santos, Brenda Casarrubias-Tabarez, Teresa de Jesús López-Pérez, Marcela Rojas-Lemus, Nelly López-Valdez and Teresa I. Fortoul
Antibiotics 11 (11) 1658 (2022)
https://doi.org/10.3390/antibiotics11111658

The Efficacy of Citrus maxima Peels Aqueous Extract Against Cryptosporidiosis in Immunecompromised Mice

Eman Naser Hafez and Wafaa Fayez Abd El Hamed
Acta Parasitologica 66 (2) 638 (2021)
https://doi.org/10.1007/s11686-020-00315-x

The immunomodulatory activity of secnidazole–nitazoxanide in a murine cryptosporidiosis model

Neveen Madbouly, Azza El Amir, Asmaa Abdel Kader, Ibraheem Rabee and Alyaa Farid
Journal of Medical Microbiology 70 (3) (2021)
https://doi.org/10.1099/jmm.0.001327

Persistent Cryptosporidium parvum Infection Leads to the Development of the Tumor Microenvironment in an Experimental Mouse Model: Results of a Microarray Approach

Manasi Sawant, Sadia Benamrouz-Vanneste, Anthony Mouray, Peggy Bouquet, Nausicaa Gantois, Colette Creusy, Erika Duval, Adriana Mihalache, Pierre Gosset, Magali Chabé, David Hot, Eric Viscogliosi and Gabriela Certad
Microorganisms 9 (12) 2569 (2021)
https://doi.org/10.3390/microorganisms9122569

Giardia and Cryptosporidium in Neo-Tropical Rodents and Marsupials: Is There Any Zoonotic Potential?

Kegan Romelle Jones and Laura Tardieu
Life 11 (3) 256 (2021)
https://doi.org/10.3390/life11030256

Evaluation of possible prophylactic and therapeutic effect of mefloquine on experimental cryptosporidiosis in immunocompromised mice

Eman S. El-Wakil, Amal E. Salem and Asmaa M. F. Al-Ghandour
Journal of Parasitic Diseases 45 (2) 380 (2021)
https://doi.org/10.1007/s12639-020-01315-4

Etiological Treatment of Protozoer Diarrhea in Neonatal Ruminants

İlker Yusuf AKINCI and Metin Koray ALBAY
Veterinary Journal of Mehmet Akif Ersoy University 5 (1) 28 (2020)
https://doi.org/10.24880/maeuvfd.681052

Potential therapeutic and prophylactic effects of Asafoetida in murine cryptosporidiosis

Hagar F. Abdelmaksoud, Ayman M. El-Ashkar, Sh. A. Elgohary and Eman S. El-Wakil
Journal of Parasitic Diseases 44 (3) 646 (2020)
https://doi.org/10.1007/s12639-020-01241-5

S-Methylcysteine (SMC) Ameliorates Intestinal, Hepatic, and Splenic Damage Induced by Cryptosporidium parvum Infection Via Targeting Inflammatory Modulators and Oxidative Stress in Swiss Albino Mice

Ehab Kotb Elmahallawy, Gehad E. Elshopakey, Amira A. Saleh, Ahmad Agil, Ahmed El-Morsey, Dina M. M. EL-shewehy, Ahmed S. Sad, Tokuma Yanai and Walied Abdo
Biomedicines 8 (10) 423 (2020)
https://doi.org/10.3390/biomedicines8100423

Parasitology and Microbiology Research

Helena Lúcia Carneiro Santos, Karina Mastropasqua Rebello and Teresa Cristina Bergamo Bomfim
Parasitology and Microbiology Research (2020)
https://doi.org/10.5772/intechopen.88387

Oocysticidal Effect of Essential Oils (EOs) and their Major Components on Cryptosporidium baileyi and Cryptosporidium galli

M. Tanghort, H. Chefchaou, A. Mzabi, et al.
International Journal of Poultry Science 18 (10) 475 (2019)
https://doi.org/10.3923/ijps.2019.475.482

Effect of oregano essential oil and carvacrol on Cryptosporidium parvum infectivity in HCT-8 cells

Shashank Gaur, Theresa B. Kuhlenschmidt, Mark S. Kuhlenschmidt and Juan E. Andrade
Parasitology International 67 (2) 170 (2018)
https://doi.org/10.1016/j.parint.2017.11.001

Limitations in the screening of potentially anti-cryptosporidial agents using laboratory rodents with gastric cryptosporidiosis

Andrea Valigurova, Radka Peckova, Karel Dolezal, et al.
Folia Parasitologica 65 (2018)
https://doi.org/10.14411/fp.2018.010

The anti-parasitic effect of probiotic bacteria via limiting the fecundity of Trichinella spiralis female adults

B. Bucková, Z. Hurníková, A. Lauková, V. Revajová and E. Dvorožňáková
Helminthologia 55 (2) 102 (2018)
https://doi.org/10.2478/helm-2018-0010

Public health significance of zoonotic Cryptosporidium species in wildlife: Critical insights into better drinking water management

Alireza Zahedi, Andrea Paparini, Fuchun Jian, Ian Robertson and Una Ryan
International Journal for Parasitology: Parasites and Wildlife 5 (1) 88 (2016)
https://doi.org/10.1016/j.ijppaw.2015.12.001

Cryptosporidium canis in Two Mexican Toddlers

Mariana González-Díaz, Alejandro Urrea-Quezada, Isaac Villegas-Gómez, et al.
Pediatric Infectious Disease Journal 35 (11) 1265 (2016)
https://doi.org/10.1097/INF.0000000000001287

Target validation of the inosine monophosphate dehydrogenase (IMPDH) gene in Cryptosporidium using Phylomer® peptides

R. Jefferies, R. Yang, C.K. Woh, et al.
Experimental Parasitology 148 40 (2015)
https://doi.org/10.1016/j.exppara.2014.11.003

Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases

David A. Bobak and Richard L. Guerrant
Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases 1253 (2015)
https://doi.org/10.1016/B978-1-4557-4801-3.00100-4

Validation of cell-free culture using scanning electron microscopy (SEM) and gene expression studies

R. Yang, Y. Elankumaran, N. Hijjawi and U. Ryan
Experimental Parasitology 153 55 (2015)
https://doi.org/10.1016/j.exppara.2015.03.002

An evaluation of the potential use ofCryptosporidiumspecies as agents for deliberate release

Ralf Matthias Hagen, U Loderstaedt and H Frickmann
Journal of the Royal Army Medical Corps 160 (4) 289 (2014)
https://doi.org/10.1136/jramc-2013-000186

CDPKs of Cryptosporidium parvum—stage-specific expression in vitro

Manja Etzold, Matthias Lendner, Arwid Daugschies and Viktor Dyachenko
Parasitology Research 113 (7) 2525 (2014)
https://doi.org/10.1007/s00436-014-3902-0

Role of COX-2 in Pathogenesis of Intestinal Cryptosporidiosis and Effect of some Drugs on Treatment of Infection

Gehan S. Sadek and Bahaa El Deen W. El Aswa
Research Journal of Parasitology 9 (2) 21 (2014)
https://doi.org/10.3923/jp.2014.21.40

Manual of Security Sensitive Microbes and Toxins

Lihua Xiao and Yaoyu Feng
Manual of Security Sensitive Microbes and Toxins 427 (2014)
https://doi.org/10.1201/b16752-42

Infectivity of Cryptosporidium andersoni and Cryptosporidium muris to Normal and Immunosuppressive Cynomolgus Monkeys

Koichi MASUNO, Yasuhiro FUKUDA, Masahito KUBO, et al.
Journal of Veterinary Medical Science 76 (2) 169 (2014)
https://doi.org/10.1292/jvms.13-0350

Assessment of Cryptosporidium parvum infection in immunocompetent and immunocompromised mice and its role in triggering intestinal dysplasia

Asmaa Gaber Abdou, Nancy Mahmoud Harba, Amira Fathy Afifi and Nada Farag Elnaidany
International Journal of Infectious Diseases 17 (8) e593 (2013)
https://doi.org/10.1016/j.ijid.2012.11.023

Effect of Nitaxozanide and Pyrimethamine on Astrocytes Infected by Toxoplasma gondii In Vitro

Ma. de la Luz Galván-Ramírez, Judith Marcela Dueñas Jiménez, Laura Rocío Rodríguez Pérez, et al.
Archives of Medical Research 44 (6) 415 (2013)
https://doi.org/10.1016/j.arcmed.2013.07.002

Nitazoxanide suppresses IL-6 production in LPS-stimulated mouse macrophages and TG-injected mice

Seong Keun Hong, Hee Joo Kim, Chang Seon Song, et al.
International Immunopharmacology 13 (1) 23 (2012)
https://doi.org/10.1016/j.intimp.2012.03.002

A Rapid, High-Throughput Viability Assay for Blastocystis spp. Reveals Metronidazole Resistance and Extensive Subtype-Dependent Variations in Drug Susceptibilities

Haris Mirza, Joshua D. W. Teo, Jacqui Upcroft and Kevin S. W. Tan
Antimicrobial Agents and Chemotherapy 55 (2) 637 (2011)
https://doi.org/10.1128/AAC.00900-10

Antibody responses following administration of a Cryptosporidium parvum rCP15/60 vaccine to pregnant cattle

A.J. Burton, D.V. Nydam, G. Jones, et al.
Veterinary Parasitology 175 (1-2) 178 (2011)
https://doi.org/10.1016/j.vetpar.2010.09.013

Structure of triosephosphate isomerase fromCryptosporidium parvum

Trang N. Nguyen, Jan Abendroth, David J. Leibly, et al.
Acta Crystallographica Section F Structural Biology and Crystallization Communications 67 (9) 1095 (2011)
https://doi.org/10.1107/S1744309111019178

Current and Evolving Clinical Options for HIV-Infected Patients with Chronic Diarrhoea

Tom Wingfield, Ashley Pennell and Tom J. Blanchard
Clinical Medicine Insights: Therapeutics 3 (2011)
https://doi.org/10.4137/CMT.S6386

The loading of labelled antibody-engineered nanoparticles with Indinavir increases itsin vitroefficacy againstCryptosporidium parvum

L. BONDIOLI, A. LUDOVISI, G. TOSI, et al.
Parasitology 138 (11) 1384 (2011)
https://doi.org/10.1017/S0031182011001119

Probiotics for the Control of Parasites: An Overview

Marie-Agnès Travers, Isabelle Florent, Linda Kohl and Philippe Grellier
Journal of Parasitology Research 2011 1 (2011)
https://doi.org/10.1155/2011/610769

Cryptosporidium-Malnutrition Interactions: Mucosal Disruption, Cytokines, and TLR Signaling In A Weaned Murine Model

Lourrany B Costa, Eric A JohnBull, Jordan T Reeves, et al.
Journal of Parasitology 97 (6) 1113 (2011)
https://doi.org/10.1645/GE-2848.1

Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases

DAVID A. BOBAK and RICHARD L. GUERRANT
Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases 1359 (2010)
https://doi.org/10.1016/B978-0-443-06839-3.00095-3

Complete development and multiplication of Cryptosporidium hominis in cell-free culture

Nawal Hijjawi, Annika Estcourt, Rongchang Yang, Paul Monis and Una Ryan
Veterinary Parasitology 169 (1-2) 29 (2010)
https://doi.org/10.1016/j.vetpar.2009.12.021

Update on the Diagnosis and Management of Cryptosporidium spp Infections in Dogs and Cats

Valeria Scorza and Sahatchai Tangtrongsup
Topics in Companion Animal Medicine 25 (3) 163 (2010)
https://doi.org/10.1053/j.tcam.2010.07.007

Triazole Inhibitors of Cryptosporidium parvum Inosine 5′-Monophosphate Dehydrogenase

Sushil K. Maurya, Deviprasad R. Gollapalli, Shivapriya Kirubakaran, et al.
Journal of Medicinal Chemistry 52 (15) 4623 (2009)
https://doi.org/10.1021/jm900410u

Functional Expression of a DNA‐Topoisomerase IB from Cryptosporidium parvum

César Ordóñez, Javier Alfonso, Rafael Balaña-Fouce, David Ordóñez and Ali Ouaissi
BioMed Research International 2009 (1) (2009)
https://doi.org/10.1155/2009/837608