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Publications by Daniel Lawton
Antibody to Pseudomonas Aeruginosa Mucoid Exopolysaccharide and to Sodium Alginate in Cystic Fibrosis Serum
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
ClpXP Proteases Positively Regulate Alginate Overexpression and Mucoid Conversion in Pseudomonas Aeruginosa
Microbiology
Microbiology
Eradication of Pseudomonas Aeruginosa in Cystic Fibrosis
European Respiratory Journal
Medicine
Pulmonary
Respiratory Medicine
Cystic Fibrosis: Inflammatory Response to Infection With Burkholderia Cepacia and Pseudomonas Aeruginosa
European Respiratory Journal
Medicine
Pulmonary
Respiratory Medicine
Pseudomonas Aeruginosa in Cystic Fibrosis: A Chronic Cheater
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Treatment of Pseudomonas Aeruginosa Colonisation in Cystic Fibrosis.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
The AlgT-Dependent Transcriptional Regulator AmrZ (AlgZ) Inhibits Flagellum Biosynthesis in Mucoid, Nonmotile Pseudomonas Aeruginosa Cystic Fibrosis Isolates
Journal of Bacteriology
Microbiology
Molecular Biology
Reduction in the Adherence of Pseudomonas Aeruginosa to Native Cystic Fibrosis Epithelium With Anti-asialoGM1 Antibody and Neuraminidase Inhibition
European Respiratory Journal
Medicine
Pulmonary
Respiratory Medicine
The Susceptibility of Pseudomonas Aeruginosa Strains From Cystic Fibrosis Patients to Bacteriophages
PLoS ONE
Multidisciplinary
Pulmonary Outcome in Cystic Fibrosis Is Influenced Primarily by Mucoid Pseudomonas Aeruginosa Infection and Immune Status and Only Modestly by Genotype
Infection and Immunity
Parasitology
Infectious Diseases
Immunology
Microbiology