John Penders
www.penderslab.com
0000-0001-9146-5919
Maastricht University
109 papers found
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Global phylogenetic analysis of Escherichia coli and plasmids carrying the mcr-1 gene indicates bacterial diversity but plasmid restriction
Influence of vitamin D on key bacterial taxa in infant microbiota in the KOALA Birth Cohort Study
Towards standards for human fecal sample processing in metagenomic studies
Travel-related acquisition of diarrhoeagenic bacteria, enteral viruses and parasites in a prospective cohort of 98 Dutch travellers
Gut microbiota composition strongly correlates to peripheral insulin sensitivity in obese men but not in women
Gut microbiota composition in relation to the metabolic response to 12-week combined polyphenol supplementation in overweight men and women
Study protocol on the role of intestinal microbiota in colorectal cancer treatment: a pathway to personalized medicine 2.0
Gut Colonization by Methanogenic Archaea Is Associated with Organic Dairy Consumption in Children
Does a prenatal bacterial microbiota exist?
Import and spread of extended-spectrum β-lactamase-producing Enterobacteriaceae by international travellers (COMBAT study) : a prospective, multicentre cohort study
The fecal microbiota as a biomarker for disease activity in Crohn’s disease
Can the composition of the intestinal microbiota predict the development of urinary tract infections?
Early Life Antibiotic Exposure and Weight Development in Children
Detection of the plasmid-mediated colistin-resistance genemcr-1in faecal metagenomes of Dutch travellers
Prolonged carriage and potential onward transmission of carbapenemase-producing Enterobacteriaceae in Dutch travelers
Long-Term Green Tea Supplementation Does Not Change the Human Gut Microbiota
The gut resistome is highly dynamic during the first months of life
1098 Mucosal and Fecal Microbiota in Patients With Compensated and Decompensated Liver Cirrhosis
Dissemination of Antimicrobial Resistance in Microbial Ecosystems through Horizontal Gene Transfer
Advantages and Limitations of Direct PCR Amplification of Bacterial 16S-rDNA from Resected Heart Tissue or Swabs Followed by Direct Sequencing for Diagnosing Infective Endocarditis: A Retrospective Analysis in the Routine Clinical Setting
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