Compounds > arabinose

arabinose and Cystic Fibrosis

arabinose has been researched along with Cystic Fibrosis in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's1 (16.67)18.2507
2000's1 (16.67)29.6817
2010's1 (16.67)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Bar-Yoseph, R; Bentur, L; Gur, M; Hakim, F; Hanna, M; Laghi, L; Levanon, S; Marazzato, M; Masarweh, K; Wilschanski, M; Zuckerman-Levin, N1
Brannon, MK; Gutu, AD; Haugen, E; Høiby, N; Jacobs, MA; Johansen, HK; Kaul, RK; Moskowitz, SM; Sgambati, N; Strasbourger, P1
Adams, KN; Burns, JL; Emerson, JC; Ernst, RK; Harvey, MD; Kraig, GM; Miller, SI; Moskowitz, SM; Ramsey, B; Speert, DP1
Burns, JL; Ernst, RK; Guo, L; Hackett, M; Lim, KB; Miller, SI; Yi, EC1
Bain, AD; Butterworth, J; McCrae, WM; Scott, F1
Beyreiss, K; Hoepffner, W1

Other Studies

6 other study(ies) available for arabinose and Cystic Fibrosis

ArticleYear
The effect of probiotic administration on metabolomics and glucose metabolism in CF patients.
    Pediatric pulmonology, 2022, Volume: 57, Issue:10

    Topics: Adolescent; Adult; Arabinose; Blood Glucose; Blood Glucose Self-Monitoring; Child; Cysteine; Cystic Fibrosis; Cytokines; Diabetes Mellitus; Dysbiosis; Glucose Intolerance; Glutamine; Humans; Indoles; Insulin Resistance; Lactates; Lactulose; Mannitol; Pilot Projects; Probiotics; Prospective Studies; Quality of Life; Young Adult

2022
Polymyxin resistance of Pseudomonas aeruginosa phoQ mutants is dependent on additional two-component regulatory systems.
    Antimicrobial agents and chemotherapy, 2013, Volume: 57, Issue:5

    Topics: Anti-Bacterial Agents; Arabinose; Bacterial Proteins; Cystic Fibrosis; DNA Transposable Elements; Drug Resistance, Bacterial; Gene Deletion; Gene Expression Regulation, Bacterial; Genes, Regulator; Genetic Complementation Test; Genetic Loci; Humans; Lipid A; Mutation; Plasmids; Polymyxins; Pseudomonas aeruginosa; Pseudomonas Infections

2013
Unique lipid a modifications in Pseudomonas aeruginosa isolated from the airways of patients with cystic fibrosis.
    The Journal of infectious diseases, 2007, Oct-01, Volume: 196, Issue:7

    Topics: Arabinose; Child; Child, Preschool; Chronic Disease; Cystic Fibrosis; Decanoic Acids; Humans; Infant; Lipid A; Lung Diseases; Palmitates; Prevalence; Pseudomonas aeruginosa; Pseudomonas Infections

2007
Specific lipopolysaccharide found in cystic fibrosis airway Pseudomonas aeruginosa.
    Science (New York, N.Y.), 1999, Nov-19, Volume: 286, Issue:5444

    Topics: Acylation; Antimicrobial Cationic Peptides; Arabinose; Bacterial Proteins; Cells, Cultured; Cystic Fibrosis; Drug Resistance, Microbial; Humans; Infant; Interleukin-8; Lipid A; Lipopolysaccharides; Magnesium; Mutation; Palmitates; Peptides; Polymyxins; Pseudomonas aeruginosa; Pseudomonas Infections; Respiratory System; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Virulence

1999
Lysosomal enzymes of cultured fibroblasts of cystic fibrosis patients.
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 40, Issue:1

    Topics: Acetates; Acid Phosphatase; Arabinose; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Child; Chondroitin; Cystic Fibrosis; Fibroblasts; Fucose; Galactosidases; Glucosidases; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Lysosomes; Mannose; Mucopolysaccharidoses

1972
[Resorption of 3-0-methylglucose, D-xylose and L-arabinose. II. Comparative studies in infants with malabsorption syndromes].
    Padiatrie und Grenzgebiete, 1971, Volume: 10, Issue:4

    Topics: Arabinose; Celiac Disease; Child, Preschool; Cystic Fibrosis; Diet Therapy; Glucose; Humans; Infant; Infant, Newborn; Intestinal Absorption; Malabsorption Syndromes; Xylose

1971