Fecal Human β-Defensin 2 in Children with Cystic Fibrosis: Is There a Diminished Intestinal Innate Immune Response?
Published 2015 View Full Article
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Title
Fecal Human β-Defensin 2 in Children with Cystic Fibrosis: Is There a Diminished Intestinal Innate Immune Response?
Authors
Keywords
Cystic fibrosis, Innate immunity, Inflammation, Biological markers
Journal
DIGESTIVE DISEASES AND SCIENCES
Volume 60, Issue 10, Pages 2946-2952
Publisher
Springer Nature
Online
2015-08-13
DOI
10.1007/s10620-015-3842-2
References
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Related references
Note: Only part of the references are listed.- Elevated fecal M2-pyruvate kinase in children with cystic fibrosis: A clue to the increased risk of intestinal malignancy in adulthood?
- (2015) Tamara Pang et al. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
- Intestinal Inflammation and Impact on Growth in Children With Cystic Fibrosis
- (2015) Jasbir Dhaliwal et al. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
- Associations between Gut Microbial Colonization in Early Life and Respiratory Outcomes in Cystic Fibrosis
- (2015) Anne G. Hoen et al. JOURNAL OF PEDIATRICS
- Improvement of digestive health and reduction in proteobacterial populations in the gut microbiota of cystic fibrosis patients using a Lactobacillus reuteri probiotic preparation: A double blind prospective study
- (2014) Rosa del Campo et al. Journal of Cystic Fibrosis
- Disrupted Intestinal Microbiota and Intestinal Inflammation in Children with Cystic Fibrosis and Its Restoration with Lactobacillus GG: A Randomised Clinical Trial
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- Fecal Biomarkers of Intestinal Health and Disease in Children
- (2014) Tamara Pang et al. Frontiers in Pediatrics
- Fecal calprotectin, MMP-9, and human beta-defensin-2 levels in pediatric inflammatory bowel disease
- (2013) Kaija-Leena Kolho et al. INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
- Adult intestinal stem cells: critical drivers of epithelial homeostasis and regeneration
- (2013) Nick Barker NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Allelic Variants Relate to Shifts in Faecal Microbiota of Cystic Fibrosis Patients
- (2013) Serena Schippa et al. PLoS One
- S100A12 and hBD2 Correlate with the Composition of the Fecal Microflora in ELBW Infants and Expansion ofE. coliIs Associated with NEC
- (2013) A. C. Jenke et al. Biomed Research International
- Intestinal pH and Gastrointestinal Transit Profiles in Cystic Fibrosis Patients Measured by Wireless Motility Capsule
- (2012) Daniel Gelfond et al. DIGESTIVE DISEASES AND SCIENCES
- Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in pancreatitis
- (2012) Chee Y. Ooi et al. Journal of Cystic Fibrosis
- Human β-defensin 2 expression in ELBW infants with severe necrotizing enterocolitis
- (2012) Andreas C.W. Jenke et al. PEDIATRIC RESEARCH
- Type of CFTR Mutation Determines Risk of Pancreatitis in Patients With Cystic Fibrosis
- (2010) Chee Y. Ooi et al. GASTROENTEROLOGY
- Cystic Fibrosis Pigs Develop Lung Disease and Exhibit Defective Bacterial Eradication at Birth
- (2010) D. A. Stoltz et al. Science Translational Medicine
- Elevated Human β-Defensin-2 Levels Indicate an Activation of the Innate Immune System in Patients With Irritable Bowel Syndrome
- (2009) Jost Langhorst et al. AMERICAN JOURNAL OF GASTROENTEROLOGY
- Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator–dependent bicarbonate secretion
- (2009) Mary Abigail S. Garcia et al. JOURNAL OF CLINICAL INVESTIGATION
- Fecal β-Defensin-2 in Children With Inflammatory Bowel Diseases
- (2009) Nathalie Kapel et al. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION
- Innate immune activation and cystic fibrosis
- (2008) Siobhain Brennan Paediatric Respiratory Reviews
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