Page last updated: 2024-10-21

5,5-dimethyl-1-pyrroline-1-oxide and Cystic Fibrosis

5,5-dimethyl-1-pyrroline-1-oxide has been researched along with Cystic Fibrosis in 1 studies

5,5-dimethyl-1-pyrroline-1-oxide: do not confuse with DMPO (4',5'-dihydroxy-7-methoxy-4-phenyl-5,2'-oxidocoumarin)
5,5-dimethyl-1-pyrroline N-oxide : A member of the class of 1-pyrroline nitrones (1-pyrroline N-oxides) resulting from the formal N-oxidation of 5,5-dimethyl-1-pyrroline. Used as a spin trap for the study of radicals formed by enzymatic acetaldehyde oxidation.

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.

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
Rosias, PP1
Den Hartog, GJ1
Robroeks, CM1
Bast, A1
Donckerwolcke, RA1
Heynens, JW1
Suykerbuyk, J1
Hendriks, HJ1
Jöbsis, Q1
Dompeling, E1

Other Studies

1 other study available for 5,5-dimethyl-1-pyrroline-1-oxide and Cystic Fibrosis

ArticleYear
Free radicals in exhaled breath condensate in cystic fibrosis and healthy subjects.
    Free radical research, 2006, Volume: 40, Issue:9

    Topics: Adolescent; Adult; Breath Tests; Catalase; Child; Cyclic N-Oxides; Cystic Fibrosis; Electron Spin Re

2006