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Blastocystis: past pitfalls and future perspectives
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1 of the 87 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1007/s11739-010-0451-0 (notice 2014-12-10).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ibd.20084openalex-snapshot
Patchy distribution of mucosal lesions in ileal Crohnʼs disease is not linked to differences in the dominant mucosa-associated bacteria
inferredcites →https://doi.org/10.1002/ibd.20783openalex-snapshot
Twin studies reveal specific imbalances in the mucosa-associated microbiota of patients with ileal Crohn's disease.
inferredcites →https://doi.org/10.1002/ibd.21339openalex-snapshot
Disease phenotype and genotype are associated with shifts in intestinal-associated microbiota in inflammatory bowel diseases
inferredcites →https://doi.org/10.1002/ibd.21436openalex-snapshot
Highlighting new phylogenetic specificities of Crohnʼs disease microbiota
inferredcites →https://doi.org/10.1007/s00436-005-0033-7openalex-snapshot
Predominance of amoeboid forms of Blastocystis hominis in isolates from symptomatic patients
inferredcites →https://doi.org/10.1007/s00436-006-0439-xopenalex-snapshot
Morphology and reproductive mode of Blastocystis hominis in diarrhea and in vitro
inferredcites →https://doi.org/10.1007/s00436-007-0808-0openalex-snapshot
Predominance of subtype 3 among Blastocystis isolates from a major hospital in Singapore
inferredcites →https://doi.org/10.1007/s00436-007-0833-zopenalex-snapshot
Pathophysiological variability of different genotypes of human Blastocystis hominis Egyptian isolates in experimentally infected rats
inferredcites →https://doi.org/10.1007/s00436-008-1006-4openalex-snapshot
Detection of Blastocystis from stool samples using real-time PCR
inferredcites →https://doi.org/10.1007/s00436-008-1203-1openalex-snapshot
Blastocystis exhibits inter- and intra-subtype variation in cysteine protease activity
inferredcites →https://doi.org/10.1007/s00436-009-1398-9openalex-snapshot
Molecular epidemiology of human Blastocystis isolates in France
inferredcites →https://doi.org/10.1007/s00436-009-1485-yopenalex-snapshot
High prevalence of subtype 4 among isolates of Blastocystis hominis from symptomatic patients of a health district of Valencia (Spain)
inferredcites →https://doi.org/10.1007/s00436-009-1693-5openalex-snapshot
Subtype analysis of Blastocystis isolates from symptomatic patients in Egypt
inferredcites →https://doi.org/10.1007/s00436-010-1761-xopenalex-snapshot
Irritable bowel syndrome: is it associated with genotypes of Blastocystis hominis
inferredcites →https://doi.org/10.1007/s00436-010-2244-9openalex-snapshot
Development of a new PCR protocol to detect and subtype Blastocystis spp. from humans and animals
inferredcites →https://doi.org/10.1007/s00436-011-2626-7openalex-snapshot
Blastocystis infection is associated with irritable bowel syndrome in a Mexican patient population
inferredcites →https://doi.org/10.1007/s004360050329openalex-snapshot
Observations on the surface coat of Blastocystishominis
inferredcites →https://doi.org/10.1007/s11739-010-0451-0openalex-snapshot
RETRACTED ARTICLE: Gut microbiota and related diseases: clinical features
inferredcites →https://doi.org/10.1007/s11908-009-0073-8openalex-snapshot
Current Views on the Clinical Relevance of Blastocystis spp.
inferredcites →https://doi.org/10.1016/0020-7519(91)90069-jopenalex-snapshot
A cyst-like stage of Blastocystis hominis
inferredcites →https://doi.org/10.1016/0020-7519(91)90149-2openalex-snapshot
Ultrastructure of Blastocystis hominis in human stool samples
inferredcites →https://doi.org/10.1016/j.diagmicrobio.2007.06.003openalex-snapshot
Detecting Blastocystis using parasitologic and DNA-based methods: a comparative study
inferredcites →https://doi.org/10.1016/j.ijpara.2006.09.009openalex-snapshot
Irritable bowel syndrome: A review on the role of intestinal protozoa and the importance of their detection and diagnosis
inferredcites →https://doi.org/10.1016/j.ijpara.2008.07.006openalex-snapshot
Subtype distribution of Blastocystis isolates from synanthropic and zoo animals and identification of a new subtype
inferredcites →https://doi.org/10.1016/j.mcp.2007.06.007openalex-snapshot
Direct detection of Blastocystis sp. in human faecal samples and subtype assignment using single strand conformational polymorphism and sequencing
inferredcites →https://doi.org/10.1016/j.meegid.2011.11.002openalex-snapshot
Levels of genetic diversity vary dramatically between Blastocystis subtypes
inferredcites →https://doi.org/10.1016/j.mehy.2007.01.027openalex-snapshot
Is this recently characterized gastrointestinal pathogen responsible for rising rates of inflammatory bowel disease (IBD) and IBD associated autism in Europe and the United States in the 1990s?
inferredcites →https://doi.org/10.1016/j.parint.2006.12.004openalex-snapshot
Infectivity of different genotypes of human Blastocystis hominis isolates in chickens and rats
inferredcites →https://doi.org/10.1016/j.parint.2012.02.007openalex-snapshot
Characterization of two cysteine proteases secreted by Blastocystis ST7, a human intestinal parasite
inferredcites →https://doi.org/10.1016/j.pt.2007.01.004openalex-snapshot
Terminology for Blastocystis subtypes – a consensus
inferredcites →https://doi.org/10.1016/j.tim.2005.05.009openalex-snapshot
Off the hook – how bacteria survive protozoan grazing
inferredcites →https://doi.org/10.1016/j.vetpar.2004.09.017openalex-snapshot
Blastocystis in humans and animals: new insights using modern methodologies
inferredcites →https://doi.org/10.1016/j.vetpar.2009.12.032openalex-snapshot
Molecular characterization of Blastocystis isolates from zoo animals and their animal-keepers
inferredcites →https://doi.org/10.1016/s0020-7519(99)00045-4openalex-snapshot
The functional importance of parasites in animal communities: many roles at many levels?
inferredcites →https://doi.org/10.1016/s0166-6851(97)00046-7openalex-snapshot
Extensive genetic diversity in Blastocystis hominis
inferredcites →https://doi.org/10.1016/s0966-842x(02)02428-9openalex-snapshot
Population biology of emerging and re-emerging pathogens
inferredcites →https://doi.org/10.1016/s0966-842x(98)01425-5openalex-snapshot
Unexplored reservoirs of pathogenic bacteria: protozoa and biofilms
inferredcites →https://doi.org/10.1023/a:1020505204959openalex-snapshot
Predation as a shaping force for the phenotypic and genotypic composition of planktonic bacteria
inferredcites →https://doi.org/10.1038/cmi.2010.67openalex-snapshot
The role of gut microbiota (commensal bacteria) and the mucosal barrier in the pathogenesis of inflammatory and autoimmune diseases and cancer: contribution of germ-free and gnotobiotic animal models of human diseases
inferredcites →https://doi.org/10.1038/ismej.2008.76openalex-snapshot
Micro-eukaryotic diversity of the human distal gut microbiota: qualitative assessment using culture-dependent and -independent analysis of faeces
inferredcites →https://doi.org/10.1053/j.gastro.2004.01.063openalex-snapshot
Clinical epidemiology of inflammatory bowel disease: incidence, prevalence, and environmental influences
inferredcites →https://doi.org/10.1053/j.gastro.2004.03.054openalex-snapshot
Enhanced Escherichia coli adherence and invasion in Crohn’s disease and colon cancer 1 1The authors thank Professor T. K. Korhonen (Division of General Microbiology, University of Helsinki, Finland), who kindly donated Escherichia coli IH11165; Professor J.-F. Colombel (Laboratoire de Recherche…
inferredcites →https://doi.org/10.1053/j.gastro.2004.04.061openalex-snapshot
High prevalence of adherent-invasive Escherichia coli associated with ileal mucosa in Crohn’s disease
inferredcites →https://doi.org/10.1053/j.gastro.2005.11.033openalex-snapshot
Hypothalamic-Pituitary-Gut Axis Dysregulation in Irritable Bowel Syndrome: Plasma Cytokines as a Potential Biomarker?
inferredcites →https://doi.org/10.1073/pnas.0404028101openalex-snapshot
Protozoan predation, diversifying selection, and the evolution of antigenic diversity in Salmonella
inferredcites →https://doi.org/10.1097/mog.0b013e32832b12efopenalex-snapshot
The evolving epidemiology of inflammatory bowel disease
inferredcites →https://doi.org/10.1098/rspb.2007.0245openalex-snapshot
Grazing protozoa and the evolution of the Escherichia coli O157:H7 Shiga toxin-encoding prophage
inferredcites →https://doi.org/10.1098/rstb.2008.0249openalex-snapshot
Introduction. Ecological immunology
inferredcites →https://doi.org/10.1099/00221287-140-6-1253openalex-snapshot
Trojan Horses of the microbial world: protozoa and the survival of bacterial pathogens in the environment
inferredcites →https://doi.org/10.1111/j.1445-5994.2011.02626.xopenalex-snapshot
Blastocystis subtypes in symptomatic and asymptomatic family members and pets and response to therapy
inferredcites →https://doi.org/10.1111/j.1462-2920.2007.01369.xopenalex-snapshot
Diversity of the human gastrointestinal tract microbiota revisited
inferredcites →https://doi.org/10.1111/j.1462-2920.2010.02283.xopenalex-snapshot
Closely related protist strains have different grazing impacts on natural bacterial communities
inferredcites →https://doi.org/10.1111/j.1462-5822.2005.00639.xopenalex-snapshot
The Crohn's disease-associated adherent-invasive Escherichia coli strain LF82 replicates in mature phagolysosomes within J774 macrophages
inferredcites →https://doi.org/10.1111/j.1550-7408.2002.tb00339.xopenalex-snapshot
Phylogenetic Position of Blastocystis hominis and of Stramenopiles Inferred from Multiple Molecular Sequence Data
inferredcites →https://doi.org/10.1111/j.1574-6941.2008.00511.xopenalex-snapshot
Selective grazing of methanotrophs by protozoa in a rice field soil
inferredcites →https://doi.org/10.1126/science.1155725openalex-snapshot
Evolution of Mammals and Their Gut Microbes
inferredcites →https://doi.org/10.1128/cmr.00022-08openalex-snapshot
New Insights on Classification, Identification, and Clinical Relevance ofBlastocystisspp
inferredcites →https://doi.org/10.1128/cmr.13.2.196openalex-snapshot
Cysteine Proteinases and the Pathogenesis of Amebiasis
inferredcites →https://doi.org/10.1128/cmr.14.1.114-128.2001openalex-snapshot
Treatment of Giardiasis
inferredcites →https://doi.org/10.1128/cmr.4.1.61openalex-snapshot
Blastocystis hominis--past and future
inferredcites →https://doi.org/10.1128/ec.00371-07openalex-snapshot
Blastocystis rattiContains Cysteine Proteases That Mediate Interleukin-8 Response from Human Intestinal Epithelial Cells in an NF-κB-Dependent Manner
inferredcites →https://doi.org/10.1128/iai.00328-06openalex-snapshot
Blastocystis rattiInduces Contact-Independent Apoptosis, F-Actin Rearrangement, and Barrier Function Disruption in IEC-6 Cells
inferredcites →https://doi.org/10.1128/iai.05632-11openalex-snapshot
A Metronidazole-Resistant Isolate of Blastocystis spp. Is Susceptible to Nitric Oxide and Downregulates Intestinal Epithelial Inducible Nitric Oxide Synthase by a Novel Parasite Survival Mechanism
inferredcites →https://doi.org/10.1128/iai.67.9.4499-4509.1999openalex-snapshot
Invasive Ability of an Escherichia coli Strain Isolated from the Ileal Mucosa of a Patient with Crohn’s Disease
inferredcites →https://doi.org/10.1128/iai.69.9.5529-5537.2001openalex-snapshot
Adherent Invasive Escherichia coli Strains from Patients with Crohn's Disease Survive and Replicate within Macrophages without Inducing Host Cell Death
inferredcites →https://doi.org/10.1128/jcm.00312-06openalex-snapshot
Culture-Independent Analyses of Temporal Variation of the Dominant Fecal Microbiota and Targeted Bacterial Subgroups in Crohn's Disease
inferredcites →https://doi.org/10.1128/jcm.01392-10openalex-snapshot
Development and Evaluation of a Real-Time PCR Assay for Detection and Quantification of Blastocystis Parasites in Human Stool Samples: Prospective Study of Patients with Hematological Malignancies
inferredcites →https://doi.org/10.1128/jcm.29.3.662-663.1991openalex-snapshot
Pathogenicity of Blastocystis hominis
inferredcites →https://doi.org/10.1136/gut.2007.134668openalex-snapshot
Dysbiosis in inflammatory bowel disease: a role for bacteriophages?
inferredcites →https://doi.org/10.1136/gut.38.2.216openalex-snapshot
Increased interleukin 8 expression in the colon mucosa of patients with inflammatory bowel disease.
inferredcites →https://doi.org/10.1152/physrev.00045.2009openalex-snapshot
Gut Microbiota in Health and Disease
inferredcites →https://doi.org/10.1186/1756-3305-1-40openalex-snapshot
Oh my aching gut: irritable bowel syndrome, Blastocystis, and asymptomatic infection
inferredcites →https://doi.org/10.1186/gb-2011-12-3-r29openalex-snapshot
Genome sequence of the stramenopile Blastocystis, a human anaerobic parasite
inferredcites →https://doi.org/10.1371/journal.pone.0006761openalex-snapshot
Predation on Multiple Trophic Levels Shapes the Evolution of Pathogen Virulence
inferredcites →https://doi.org/10.1371/journal.pone.0015484openalex-snapshot
Comparison of Methods for Detection of Blastocystis Infection in Routinely Submitted Stool Samples, and also in IBS/IBD Patients in Ankara, Turkey
inferredcites →https://doi.org/10.1371/journal.ppat.1002545openalex-snapshot
New Insights into Blastocystis spp.: A Potential Link with Irritable Bowel Syndrome
inferredcites →https://doi.org/10.1590/s0074-02762009000500011openalex-snapshot
Blastocystis subtypes in irritable bowel syndrome and inflammatory bowel disease in Ankara, Turkey
inferredcites →https://doi.org/10.2307/3281615openalex-snapshot
Host Genetics: A Key Factor in Regulating the Distribution of Parasites in Natural Host Populations
inferredcites →https://doi.org/10.3109/08916931003674709openalex-snapshot
Inflammatory bowel disease—From mechanisms to treatment strategies
inferredcites →https://doi.org/10.4269/ajtmh.2001.65.393openalex-snapshot
Ribodemes of Blastocystis hominis isolated in Japan.
inferredcites →https://doi.org/10.4269/ajtmh.2011.10-0447openalex-snapshot
Comparison of Microscopy, Culture, and Conventional Polymerase Chain Reaction for Detection of Blastocystis sp. in Clinical Stool Samples
inferredcites →https://doi.org/10.4269/ajtmh.2011.11-0005openalex-snapshot
Blastocystis sp. Subtype 4 is Common in Danish Blastocystis-Positive Patients Presenting with Acute Diarrhea
inferredcites →https://doi.org/10.4314/eajph.v7i1.64706openalex-snapshot
A case-control study of blastocystis hominis among Iranian population
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.12688/openreseurope.18046.1zenodo-depositor-declared
Advancing research on Blastocystis through a One Health approach
inferred← citeshttps://doi.org/10.1002/vms3.70609openalex-snapshot
Subtype Identification of Blastocystis sp . Among Humans and Domestic Animals in the West of Iran
inferred← citeshttps://doi.org/10.1007/978-3-030-84224-6_8openalex-snapshot
Diagnosis and Treatment of Neglected Tropical Diseases in Europe: Laboratory Infrastructure, Diagnostic Techniques, Disease Notification, and Surveillance Systems
inferred← citeshttps://doi.org/10.1007/s00436-013-3536-7openalex-snapshot
A rat model to study Blastocytis subtype 1 infections
inferred← citeshttps://doi.org/10.1007/s00436-014-3805-0openalex-snapshot
Do not forget the stool examination!—cutaneous and gastrointestinal manifestations of Blastocystis sp. infection
inferred← citeshttps://doi.org/10.1007/s00436-015-4540-xopenalex-snapshot
Features of Blastocystis spp. in xenic culture revealed by deconvolutional microscopy
inferred← citeshttps://doi.org/10.1007/s00436-017-5506-yopenalex-snapshot
Molecular characterization of Blastocystis sp. in captive wild animals in Qinling Mountains
inferred← citeshttps://doi.org/10.1007/s00436-018-6103-4openalex-snapshot
Is the genetic variability of Cathepsin B important in the pathogenesis of Blastocystis spp.?
inferred← citeshttps://doi.org/10.1007/s00436-019-06574-6openalex-snapshot
Assessment of the subtypes and the zoonotic risk of Blastocystis sp. of experimental macaques in Yunnan province, southwestern China
inferred← citeshttps://doi.org/10.1007/s00436-023-07973-6openalex-snapshot
Genetic characteristics of Blastocystis sp. ST3 at the genome level in the Chinese population
inferred← citeshttps://doi.org/10.1007/s10096-017-3065-xopenalex-snapshot
Distribution and phylogenetic analysis of Blastocystis sp. subtypes isolated from IBD patients and healthy individuals in Iran
inferred← citeshttps://doi.org/10.1007/s11686-021-00360-0openalex-snapshot
Comparative molecular prevalence and subtypes distribution of Blastocystis sp. a potentially zoonotic infection isolated from symptomatic and asymptomatic patients in Iran: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1007/s11686-021-00419-yopenalex-snapshot
Blastocystis Subtypes and Culture Characteristics of Isolates from Human Stools Related with the Presence of Gastrointestinal Symptoms: A Case–Control Study
inferred← citeshttps://doi.org/10.1007/s11686-021-00435-yopenalex-snapshot
Diagnostic Features of Blastocystis Life Cycle Forms in the Small Intestine in an HIV-Infected Patient
inferred← citeshttps://doi.org/10.1007/s12639-019-01092-9openalex-snapshot
Surface ultrastructure, protein profile and zymography of Blastocystis species isolated from patients with colorectal carcinoma
inferred← citeshttps://doi.org/10.1007/s12639-019-01177-5openalex-snapshot
Molecular epidemiology of Blastocystis spp. in children referred to Qods hospital in northwest of Iran
inferred← citeshttps://doi.org/10.1007/s12639-021-01442-6openalex-snapshot
Influence of Blastocystis hominis on the small intestine and lactase enzyme activity
inferred← citeshttps://doi.org/10.1016/b978-0-323-55512-8.00153-8openalex-snapshot
Persistent Abdominal Symptoms in the Returned Traveler
inferred← citeshttps://doi.org/10.1016/j.actatropica.2013.05.005openalex-snapshot
Abdominal pain and asthenia as common clinical features in hospitalized children for giardiasis
inferred← citeshttps://doi.org/10.1016/j.actatropica.2017.06.014openalex-snapshot
Molecular characterization of Blastocystis from pigs in Shaanxi province of China
inferred← citeshttps://doi.org/10.1016/j.arcmed.2017.11.015openalex-snapshot
Human Intestinal Microbiota: Interaction Between Parasites and the Host Immune Response
inferred← citeshttps://doi.org/10.1016/j.cimid.2018.11.013openalex-snapshot
First molecular identification and subtype distribution of Blastocystis sp. isolated from hooded crows (Corvus cornix) and pigeons (Columba livia) in Tehran Province, Iran
inferred← citeshttps://doi.org/10.1016/j.exppara.2022.108341openalex-snapshot
Blastocystis hominis undergoing programmed cell death via cytotoxic gamma irradiation
inferred← citeshttps://doi.org/10.1016/j.heliyon.2020.e05729openalex-snapshot
Blastocystis infection frequency and subtype distribution in university students
inferred← citeshttps://doi.org/10.1016/j.jiph.2017.03.009openalex-snapshot
PCR-based molecular characterization of Blastocystis hominis subtypes in southwest of Iran
inferred← citeshttps://doi.org/10.1016/j.meegid.2015.02.012openalex-snapshot
Prevalence and subtype analysis of Blastocystis in healthy Indian individuals
inferred← citeshttps://doi.org/10.1016/j.meegid.2016.07.036openalex-snapshot
Comparison of the genetic variability of Blastocystis subtypes between human carriers from two contrasting climatic regions of México
inferred← citeshttps://doi.org/10.1016/j.meegid.2016.08.018openalex-snapshot
Prevalence and genetic diversity of Blastocystis in family units living in the United States
inferred← citeshttps://doi.org/10.1016/j.meegid.2017.02.016openalex-snapshot
Inter- and intra-subtype variation of Blastocystis subtypes isolated from diarrheic and non-diarrheic patients in Iran
inferred← citeshttps://doi.org/10.1016/j.molbiopara.2016.02.002openalex-snapshot
Evolution of the microtubular cytoskeleton (flagellar apparatus) in parasitic protists
inferred← citeshttps://doi.org/10.1016/j.onehlt.2021.100347openalex-snapshot
Prevalence of Blastocystis infection in free-range Tibetan sheep and Tibetan goats in the Qinghai-Tibetan Plateau in China
inferred← citeshttps://doi.org/10.1016/j.parepi.2019.e00124openalex-snapshot
Characterization of subtypes of Blastocystis sp. isolated from patients with urticaria, São Paulo, Brazil
inferred← citeshttps://doi.org/10.1016/j.parint.2016.05.007openalex-snapshot
Pathogenic mechanisms in Blastocystis spp. — Interpreting results from in vitro and in vivo studies
inferred← citeshttps://doi.org/10.1016/j.parint.2025.103075openalex-snapshot
Blastocystis colonization among inland and forest periphery Negritos in Malaysia: The crucial role of sanitation and hygiene practices
inferred← citeshttps://doi.org/10.1016/j.poamed.2015.04.001openalex-snapshot
The role of Blastocystis sp. as an etiology of irritable bowel syndrome
inferred← citeshttps://doi.org/10.1016/j.pt.2013.08.006openalex-snapshot
Blastocystis: getting to grips with our guileful guest
inferred← citeshttps://doi.org/10.1016/j.rgmx.2021.02.003openalex-snapshot
Prevalencia e impacto de resistencias a antimicrobianos en infecciones gastrointestinales: una revisión
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Prevalence and impact of antimicrobial resistance in gastrointestinal infections: A review
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10.1016/s1155-1968(14)62908-4
inferred← citeshttps://doi.org/10.1016/s1155-1968(21)42355-2openalex-snapshot
10.1016/s1155-1968(21)42355-2
inferred← citeshttps://doi.org/10.1016/s2222-1808(14)60626-5openalex-snapshot
Prevalence and diagnostic approach for a neglected protozoon Blastocystis hominis
inferred← citeshttps://doi.org/10.1017/pao.2017.3openalex-snapshot
Identification of Blastocystis subtypes in clinical stool samples from Sao Paulo City, Brazil
inferred← citeshttps://doi.org/10.1017/s0950268823000596openalex-snapshot
Circulation and colonisation ofBlastocystissubtypes in schoolchildren of various ethnicities in rural northern Thailand
inferred← citeshttps://doi.org/10.1038/s41598-020-72286-yopenalex-snapshot
Contrasting microbiota profiles observed in children carrying either Blastocystis spp. or the commensal amoebas Entamoeba coli or Endolimax nana
inferred← citeshttps://doi.org/10.1038/srep25255openalex-snapshot
Colonization with the enteric protozoa Blastocystis is associated with increased diversity of human gut bacterial microbiota
inferred← citeshttps://doi.org/10.1097/mib.0000000000000405openalex-snapshot
Donor Recruitment for Fecal Microbiota Transplantation
inferred← citeshttps://doi.org/10.1097/pat.0000000000000243openalex-snapshot
Advances in molecular diagnosis of parasitic enteropathogens
inferred← citeshttps://doi.org/10.1111/1574-6941.12396openalex-snapshot
The microbial eukaryote Blastocystis is a prevalent and diverse member of the healthy human gut microbiota
inferred← citeshttps://doi.org/10.1111/1749-4877.12634openalex-snapshot
Simultaneous analysis of the intestinal parasites and diet through eDNA metabarcoding
inferred← citeshttps://doi.org/10.1111/ijd.13064openalex-snapshot
Mysterious chronic urticaria caused by Blastocystis spp.?
inferred← citeshttps://doi.org/10.1111/jeu.12766openalex-snapshot
Contrasting Strategies: Human Eukaryotic Versus Bacterial Microbiome Research
inferred← citeshttps://doi.org/10.1128/aem.00520-15openalex-snapshot
Development and Application of a Blastocystis Subtype-Specific PCR Assay Reveals that Mixed-Subtype Infections Are Common in a Healthy Human Population
inferred← citeshttps://doi.org/10.1128/cmr.00025-17openalex-snapshot
Practical Guidance for Clinical Microbiology Laboratories: Laboratory Diagnosis of Parasites from the Gastrointestinal Tract
inferred← citeshttps://doi.org/10.1128/iai.02279-14openalex-snapshot
Differential Regulation of Proinflammatory Cytokine Expression by Mitogen-Activated Protein Kinases in Macrophages in Response to Intestinal Parasite Infection
inferred← citeshttps://doi.org/10.11606/d.99.2017.tde-08022017-071309openalex-snapshot
Identificação de subtipos de Blastocystis sp. isolados de indivíduos acompanhados no Hospital das Clínicas de São Paulo (HC/FMUSP), São Paulo, Brasil
inferred← citeshttps://doi.org/10.11606/d.99.2019.tde-30082019-143424openalex-snapshot
Detecção de DNA de Blastocystis sp. em pacientes candidatos a transplantes atendidos no Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP)
inferred← citeshttps://doi.org/10.11606/t.5.2022.tde-16022023-131406openalex-snapshot
Blastocystis sp.: epidemiologia molecular e relação com doenças em cenários brasileiros
inferred← citeshttps://doi.org/10.1177/2049936113504754openalex-snapshot
Blastocystis , an unrecognized parasite: an overview of pathogenesis and diagnosis
inferred← citeshttps://doi.org/10.1186/1471-2334-13-37openalex-snapshot
Persistent digestive disorders in the tropics: causative infectious pathogens and reference diagnostic tests
inferred← citeshttps://doi.org/10.1186/1756-3305-6-295openalex-snapshot
Amoebic forms of Blastocystis spp. - evidence for a pathogenic role
inferred← citeshttps://doi.org/10.1186/1756-3305-7-207openalex-snapshot
Blastocystis sp. in splenic cysts: causative agent or accidental association? A unique case report
inferred← citeshttps://doi.org/10.1186/s12866-021-02341-9openalex-snapshot
Association of Blastocystis ST6 with higher protease activity among symptomatic subjects
inferred← citeshttps://doi.org/10.1186/s13027-022-00447-xopenalex-snapshot
Are Blastocystis hominis and Cryptosporidium spp. playing a positive role in colorectal cancer risk? A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1186/s13071-018-3141-9openalex-snapshot
Can the pyruvate: ferredoxin oxidoreductase (PFOR) gene be used as an additional marker to discriminate among Blastocystis strains or subtypes?
inferred← citeshttps://doi.org/10.12688/f1000research.19481.1openalex-snapshot
Metabolic phenotyping of the human microbiome
inferred← citeshttps://doi.org/10.13105/wjma.v12.i3.95631openalex-snapshot
Blastocystis hominis as a cause of chronic diarrhea in low-resource settings: A systematic review
inferred← citeshttps://doi.org/10.1371/journal.pntd.0002885openalex-snapshot
Intra-Subtype Variation in Enteroadhesion Accounts for Differences in Epithelial Barrier Disruption and Is Associated with Metronidazole Resistance in Blastocystis Subtype-7
inferred← citeshttps://doi.org/10.1371/journal.pone.0084372openalex-snapshot
Subtype Distribution of Blastocystis Isolates in Sebha, Libya
inferred← citeshttps://doi.org/10.1371/journal.pone.0089036openalex-snapshot
Pleiotropic Effects of Blastocystis spp. Subtypes 4 and 7 on Ligand-Specific Toll-Like Receptor Signaling and NF-κB Activation in a Human Monocyte Cell Line
inferred← citeshttps://doi.org/10.1371/journal.pone.0091452openalex-snapshot
Intestinal Parasitic Infections in HIV-Infected Patients, Lao People’s Democratic Republic
inferred← citeshttps://doi.org/10.1371/journal.pone.0212542openalex-snapshot
Resistance towards metronidazole in Blastocystis sp.: A pathogenic consequence
inferred← citeshttps://doi.org/10.14260/jemds/2016/380openalex-snapshot
INTESTINAL PARASITES IN PATIENTS HAVING HAEMATOLOGICAL MALIGNANCIES
inferred← citeshttps://doi.org/10.14393/ufu.te.2019.2480openalex-snapshot
Caracterização molecular de Blastocystis spp. e Enterocytozoon bieneusi em animais de produção de propriedades rurais da microrregião de Uberlândia, Minas Gerais, Brasil
inferred← citeshttps://doi.org/10.17151/biosa.2016.15.2.8openalex-snapshot
Blastocystis sp: evidencias de su rol patógeno
inferred← citeshttps://doi.org/10.18502/ijpa.v17i2.9534openalex-snapshot
Molecular Identification, Subtypes Distribution, and Alleles Discrimination of Blastocystis sp., Isolated from Immunocompromised Subjects in Iran
inferred← citeshttps://doi.org/10.18502/ijpa.v17i3.10619openalex-snapshot
Detection of Blastocystis Subtypes in Children with Functional Abdominal Pain and Celiac Disease in Çorum, Turkey
inferred← citeshttps://doi.org/10.18502/ijpa.v17i3.10629openalex-snapshot
Prevalence and Associated Risk Factors of Intestinal Parasitic Infections among Patients Visiting a Referral Hospital in Tehran Province, Iran
inferred← citeshttps://doi.org/10.20431/2454-9428.0303001openalex-snapshot
Blastocystis Hominis Infection Pathogenic or Commensal: Short Review
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2134372/v1openalex-snapshot
Global Trends on Blastocystis sp. Research: A Scientometric Study
inferred← citeshttps://doi.org/10.21608/eajbse.2022.259102openalex-snapshot
Assessment of Protease Enzymatic Activity Among Symptomatic Blastocystosis Patients
inferred← citeshttps://doi.org/10.21608/jesp.2020.131115openalex-snapshot
BLASTOCYSTIS HOMINIS IN DIABETIC AND NON-DIABETIC PATIENTS WITH IRRITABLE BOWEL SYNDROME IN BENI-SUEF CITY, EGYPT
inferred← citeshttps://doi.org/10.21608/jesp.2021.193314openalex-snapshot
SILVER NANOPARTICLES AS APROMISING TREATMENT FOR BLASTOCYSTIS HOMINIS IN EXPERIMENTALLY INFECTED MICE
inferred← citeshttps://doi.org/10.21608/puj.2018.6111.1024openalex-snapshot
Expression of cysteine proteinases and cystatins in parasites and use of cysteine proteinase inhibitors in parasitic diseases. Part II: Arthropods
inferred← citeshttps://doi.org/10.22190/fumb161027001topenalex-snapshot
BLASTOCYSTIS HOMINIS: A MYSTERIOUS AND COMMONLY DISREGARDED PARASITE
inferred← citeshttps://doi.org/10.2478/s11686-018-00002-yopenalex-snapshot
Determination the Subtypes of Blastocystis sp. and Evaluate the Effect of These Subtypes on Pathogenicity
inferred← citeshttps://doi.org/10.2478/s11686-020-00186-2openalex-snapshot
Molecular identification and subtypes distribution of Blastocystis sp. isolated from children and adolescent with cancer in Iran: evaluation of possible risk factors and clinical features
inferred← citeshttps://doi.org/10.2478/s11686-020-00229-8openalex-snapshot
Prevalence, Molecular Characterization and Risk Factors of Blastocystis sp. from Farmed Pigs in Yunnan Province, Southwestern China
inferred← citeshttps://doi.org/10.26444/aaem/81315openalex-snapshot
Genetic diversity and pathogenicity of Blastocystis
inferred← citeshttps://doi.org/10.31038/ijvb.2017122openalex-snapshot
Identification by Light Microscopy of Blastocystis Sp. in Oysters Crassotrea Virginica
inferred← citeshttps://doi.org/10.31254/jmr.2015.1110openalex-snapshot
Recent insights into the genetic diversity, epidemiology and clinical relevance of Blastocystis species.
inferred← citeshttps://doi.org/10.32734/sumej.v2i2.724openalex-snapshot
Blastocytosis hominis: Unboxing Its Clinical Significance
inferred← citeshttps://doi.org/10.3347/kjp.2020.58.5.571openalex-snapshot
An Unusual Case of Extra-Enteric Blastocystosis in the Uterine Cervix
inferred← citeshttps://doi.org/10.3389/fcimb.2022.822475openalex-snapshot
Collateral Damage in the Human Gut Microbiome - Blastocystis Is Significantly Less Prevalent in an Antibiotic-Treated Adult Population Compared to Non-Antibiotic Treated Controls
inferred← citeshttps://doi.org/10.3389/fmicb.2017.01835openalex-snapshot
Genotyping of Enterocytozoon bieneusi and Subtyping of Blastocystis in Cancer Patients: Relationship to Diarrhea and Assessment of Zoonotic Transmission
inferred← citeshttps://doi.org/10.3390/jcm14113928openalex-snapshot
Molecular Identification of Blastocystis Subtypes in the Cervix: A Study on Polish Patients
inferred← citeshttps://doi.org/10.34172/ijep.2022.5561openalex-snapshot
Investigating the Effect of Silver, Chitosan, and Curcumin Nanoparticles on Blastocystis spp. and Comparing it With Metronidazole In Vitro
inferred← citeshttps://doi.org/10.4103/1995-7645.269905openalex-snapshot
Molecular characterization and subtyping of Blastocystis in urticarial patients in Turkey
inferred← citeshttps://doi.org/10.4103/2229-5070.113894openalex-snapshot
Blastocystis: Taxonomy, biology and virulence
inferred← citeshttps://doi.org/10.4103/tp.tp_4_18openalex-snapshot
Detection of Blastocystis in clinical stool specimens using three different methods and morphological examination in Jones' medium
inferred← citeshttps://doi.org/10.4269/ajtmh.12-0777openalex-snapshot
Molecular Epidemiology of Blastocystis in Lebanon and Correlation between Subtype 1 and Gastrointestinal Symptoms
inferred← citeshttps://doi.org/10.4269/ajtmh.13-0006openalex-snapshot
Intestinal Parasitic Infections among Long-Term-Residents and Settled Immigrants in Qatar in the Period 2005 to 2011
inferred← citeshttps://doi.org/10.4274/imj.galenos.2021.01058openalex-snapshot
First Case-Control Study of Intestinal Parasites in Follow-up Schizophrenia Patients: Are We Overlooking the Role of These Agents?
inferred← citeshttps://doi.org/10.4314/ahs.v20i3.21openalex-snapshot
Distribution and molecular analysis of Blastocystis subtypes from gastrointestinal symptomatic and asymptomatic patients in Iran
inferred← citeshttps://doi.org/10.47278/book.zoon/2023.69openalex-snapshot
Epizootiology of Blastocystis spp.: A Parasite with Zoonotic Concern
inferred← citeshttps://doi.org/10.5505/turkhijyen.2014.29053openalex-snapshot
TBHEB 2014-4 Vol 71 Full Printed Journal
inferred← citeshttps://doi.org/10.5505/turkhijyen.2014.38980openalex-snapshot
Blastocystis sp. infection in patients with gastrointestinal complaints: a Cuban study
inferred← citeshttps://doi.org/10.55374/jseamed.v1i2.32openalex-snapshot
PREVALENCE AND RISK FACTORS OF BLASTOCYSTIS SP. INFECTION AMONG PRIMARY SCHOOL CHILDREN IN A RURAL COMMUNITY, CENTRAL THAILAND
inferred← citeshttps://doi.org/10.55905/oelv22n1-201openalex-snapshot
Blastocystis spp. em diferentes hospedeiros dos biomas da região Centro-Oeste do Brasil
inferred← citeshttps://doi.org/10.5812/archcid.36648openalex-snapshot
Prevalence and Genotype Analysis of Blastocystis hominis in Iran: A Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.58837/chula.the.2020.1044openalex-snapshot
การหาความชกและการกระจายสายพนธของเชอบลาสโตซสตสในผปวยโรคเบาหวานและผทไมเปนโรคเบาหวาน ณ อำเภอบางปะอน จงหวดพระนครศรอยธยา ประเทศไทย
inferred← citeshttps://doi.org/10.5897/ajpp2015.4375openalex-snapshot
Susceptibility of Blastocystis hominis to monolaurine (Lauric acid), lactoferine (Lactobacillus acidophillus) and metronidazole: An in vitro and in vivo studies
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