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Association of Blastocystis and Gut Microbiota in Type 2 Diabetic Mellitus Patients and non-Diabetic Individuals

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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.it.2018.06.002openalex-snapshot
Helminth–Bacterial Interactions: Cause and Consequence
inferredcites →https://doi.org/10.1016/j.micpath.2017.08.038openalex-snapshot
Comparison of gut microbiota in adult patients with type 2 diabetes and healthy individuals
inferredcites →https://doi.org/10.1016/j.parepi.2020.e00134openalex-snapshot
Occurrence of Blastocystis-subtypes in patients from Italy revealed association of ST3 with a healthy gut microbiota
inferredcites →https://doi.org/10.1016/j.parint.2016.05.007openalex-snapshot
Pathogenic mechanisms in Blastocystis spp. — Interpreting results from in vitro and in vivo studies
inferredcites →https://doi.org/10.1016/j.protis.2005.12.001openalex-snapshot
DNA Barcoding of Blastocystis
inferredcites →https://doi.org/10.1016/j.pt.2017.08.005openalex-snapshot
Gut Protozoa: Friends or Foes of the Human Gut Microbiota?
inferredcites →https://doi.org/10.1016/j.pt.2018.02.004openalex-snapshot
Associations between Gut Microbiota and Common Luminal Intestinal Parasites
inferredcites →https://doi.org/10.1038/ismej.2017.139openalex-snapshot
Large-scale comparative metagenomics of Blastocystis, a common member of the human gut microbiome
inferredcites →https://doi.org/10.1038/nature12506openalex-snapshot
Richness of human gut microbiome correlates with metabolic markers
inferredcites →https://doi.org/10.1038/nri.2017.7openalex-snapshot
Dysbiosis and the immune system
inferredcites →https://doi.org/10.1038/s41591-020-01183-8openalex-snapshot
Microbiome connections with host metabolism and habitual diet from 1,098 deeply phenotyped individuals
inferredcites →https://doi.org/10.1038/s41598-020-59121-0openalex-snapshot
SLIM: Simultaneous Logic-in-Memory Computing Exploiting Bilayer Analog OxRAM Devices
inferredcites →https://doi.org/10.1111/j.1574-6968.2009.01514.xopenalex-snapshot
Diversity, metabolism and microbial ecology of butyrate-producing bacteria from the human large intestine
inferredcites →https://doi.org/10.1136/gutjnl-2018-316106openalex-snapshot
Population-level analysis of Blastocystis subtype prevalence and variation in the human gut microbiota
inferredcites →https://doi.org/10.1136/gutjnl-2020-323071openalex-snapshot
Gut microbiota-derived metabolites as central regulators in metabolic disorders
inferredcites →https://doi.org/10.1155/2020/7253978openalex-snapshot
Alterations of Gut Microbiota in Type 2 Diabetes Individuals and the Confounding Effect of Antidiabetic Agents
inferredcites →https://doi.org/10.1186/s12866-021-02146-wopenalex-snapshot
Changes in the gut microbiome community of nonhuman primates following radiation injury
inferredcites →https://doi.org/10.1186/s13071-017-2294-2openalex-snapshot
Molecular epidemiology of blastocystosis in Malaysia: does seasonal variation play an important role in determining the distribution and risk factors of Blastocystis subtype infections in the Aboriginal community?
inferredcites →https://doi.org/10.1186/s13071-020-04392-9openalex-snapshot
Microbiota characterization in Blastocystis-colonized and Blastocystis-free school-age children from Colombia
inferredcites →https://doi.org/10.1186/s40168-019-0644-3openalex-snapshot
Interactions between a pathogenic Blastocystis subtype and gut microbiota: in vitro and in vivo studies
inferredcites →https://doi.org/10.1371/journal.pone.0111868openalex-snapshot
Blastocystis Is Associated with Decrease of Fecal Microbiota Protective Bacteria: Comparative Analysis between Patients with Irritable Bowel Syndrome and Control Subjects
inferredcites →https://doi.org/10.1371/journal.pone.0232391openalex-snapshot
Machine learning using intrinsic genomic signatures for rapid classification of novel pathogens: COVID-19 case study
inferredcites →https://doi.org/10.1371/journal.ppat.1009501openalex-snapshot
Mutations derived from horseshoe bat ACE2 orthologs enhance ACE2-Fc neutralization of SARS-CoV-2
inferredcites →https://doi.org/10.1515/tjb-2022-0110openalex-snapshot
Biochemical analysis of microbiotas obtained from healthy, prediabetic, type 2 diabetes, and obese individuals
inferredcites →https://doi.org/10.1590/s1678-9946202163032openalex-snapshot
Blastocystis subtypes in patients with diabetes mellitus from the Midwest region of Brazil
inferredcites →https://doi.org/10.17140/droj-2-123openalex-snapshot
Intestinal Parasites in Diabetes Mellitus Patients in the Limbe and Buea Municipalities, Cameroon
inferredcites →https://doi.org/10.2166/wh.2021.011openalex-snapshot
Molecular prevalence and subtype distribution ofBlastocystissp. in Asia and in Australia
inferredcites →https://doi.org/10.2337/db11-0227openalex-snapshot
Responses of Gut Microbiota and Glucose and Lipid Metabolism to Prebiotics in Genetic Obese and Diet-Induced Leptin-Resistant Mice
inferredcites →https://doi.org/10.33140/ijdmd.05.01.02openalex-snapshot
Intestinal Parasites in the Diabetic Patient
inferredcites →https://doi.org/10.3389/fmicb.2018.00803openalex-snapshot
Comparing Microbiome Sampling Methods in a Wild Mammal: Fecal and Intestinal Samples Record Different Signals of Host Ecology, Evolution
inferredcites →https://doi.org/10.3389/fmicb.2021.713347openalex-snapshot
Prokaryotic and Eukaryotic Fecal Microbiota in Irritable Bowel Syndrome Patients and Healthy Individuals Colonized With Blastocystis
inferredcites →https://doi.org/10.3390/ijerph17186591openalex-snapshot
Physical Activity Changes and Its Risk Factors among Community-Dwelling Japanese Older Adults during the COVID-19 Epidemic: Associations with Subjective Well-Being and Health-Related Quality of Life
inferredcites →https://doi.org/10.3390/microorganisms10020326openalex-snapshot
Stool Microbiota Diversity Analysis of Blastocystis-Positive and Blastocystis-Negative Individuals
inferredcites →https://doi.org/10.3390/microorganisms9061343openalex-snapshot
Wide Genetic Diversity of Blastocystis in White-Tailed Deer (Odocoileus virginianus) from Maryland, USA
inferredcites →https://doi.org/10.3390/nu10050591openalex-snapshot
Dietary Neurotransmitters: A Narrative Review on Current Knowledge
inferredcites →https://doi.org/10.3390/pathogens9040283openalex-snapshot
Occurrence of Blastocystis in Patients with Clostridioides difficile Infection
inferredcites →https://doi.org/10.3390/tropicalmed7090226openalex-snapshot
Prevalence and Associated Factors of Blastocystis sp. Infection in Patients with Gastrointestinal Symptoms in Spain: A Case-Control Study
inferredcites →https://doi.org/10.5152/tjg.2021.19644openalex-snapshot
Blastocystis and Clostridioides difficile: Evidence for a Synergistic Role in Colonization Among IBD Patients with Emphasis on Ulcerative Colitis
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