Page last updated: 2024-10-25

dapi and Cystic Fibrosis

dapi has been researched along with Cystic Fibrosis in 2 studies

DAPI: RN given refers to parent cpd.

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 (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Yang, L1
Reece, J1
Gabriel, SE1
Shears, SB1
Heng, HH1
Tsui, LC1

Other Studies

2 other studies available for dapi and Cystic Fibrosis

ArticleYear
Apical localization of ITPK1 enhances its ability to be a modifier gene product in a murine tracheal cell model of cystic fibrosis.
    Journal of cell science, 2006, Apr-01, Volume: 119, Issue:Pt 7

    Topics: Animals; Cell Line; Cell Membrane; Cell Polarity; Cystic Fibrosis; Disease Models, Animal; Fluoresce

2006
Modes of DAPI banding and simultaneous in situ hybridization.
    Chromosoma, 1993, Volume: 102, Issue:5

    Topics: Cells, Cultured; Chromosome Banding; Cystic Fibrosis; Fluorescent Dyes; Formamides; Hot Temperature;

1993