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.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Yang, L | 1 |
Reece, J | 1 |
Gabriel, SE | 1 |
Shears, SB | 1 |
Heng, HH | 1 |
Tsui, LC | 1 |
2 other studies available for dapi and Cystic Fibrosis
Article | Year |
---|---|
Apical localization of ITPK1 enhances its ability to be a modifier gene product in a murine tracheal cell model of cystic fibrosis.
Topics: Animals; Cell Line; Cell Membrane; Cell Polarity; Cystic Fibrosis; Disease Models, Animal; Fluoresce | 2006 |
Modes of DAPI banding and simultaneous in situ hybridization.
Topics: Cells, Cultured; Chromosome Banding; Cystic Fibrosis; Fluorescent Dyes; Formamides; Hot Temperature; | 1993 |