Page last updated: 2024-09-04

3-o-sulfogalactose and Cystic Fibrosis

3-o-sulfogalactose has been researched along with Cystic Fibrosis in 1 studies

*Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. [MeSH]

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cummings, RD; Damera, G; Royall, JA; Sachdev, GP; Xia, B1

Other Studies

1 other study(ies) available for 3-o-sulfogalactose and Cystic Fibrosis

ArticleYear
Altered O-glycosylation and sulfation of airway mucins associated with cystic fibrosis.
    Glycobiology, 2005, Volume: 15, Issue:8

    Topics: Acetylgalactosamine; Acetylglucosamine; Carbohydrate Sequence; Case-Control Studies; Chromatography, High Pressure Liquid; Cystic Fibrosis; Fucose; Galactose; Gas Chromatography-Mass Spectrometry; Glycosylation; Humans; Molecular Sequence Data; Mucins; N-Acetylneuraminic Acid; Oligosaccharides; Respiratory Mucosa; Spectrometry, Mass, Fast Atom Bombardment; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Sulfates; Sulfuric Acid Esters

2005