gamma-aminobutyric acid has been researched along with Cystic Fibrosis in 3 studies
gamma-Aminobutyric Acid: The most common inhibitory neurotransmitter in the central nervous system.
gamma-aminobutyric acid : A gamma-amino acid that is butanoic acid with the amino substituent located at C-4.
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 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Chung, WJ | 1 |
| Goeckeler-Fried, JL | 1 |
| Havasi, V | 1 |
| Chiang, A | 1 |
| Rowe, SM | 1 |
| Plyler, ZE | 1 |
| Hong, JS | 1 |
| Mazur, M | 1 |
| Piazza, GA | 1 |
| Keeton, AB | 1 |
| White, EL | 1 |
| Rasmussen, L | 1 |
| Weissman, AM | 1 |
| Denny, RA | 1 |
| Brodsky, JL | 1 |
| Sorscher, EJ | 1 |
| Saha, K | 1 |
| Chevalier, B | 1 |
| Doly, S | 1 |
| Baatallah, N | 1 |
| Guilbert, T | 1 |
| Pranke, I | 1 |
| Scott, MGH | 1 |
| Enslen, H | 1 |
| Guerrera, C | 1 |
| Chuon, C | 1 |
| Edelman, A | 1 |
| Sermet-Gaudelus, I | 1 |
| Hinzpeter, A | 1 |
| Marullo, S | 1 |
| Franciolini, F | 1 |
| Petris, A | 1 |
1 review available for gamma-aminobutyric acid and Cystic Fibrosis
| Article | Year |
|---|---|
Chloride channels of biological membranes.
Topics: Animals; Biological Transport; Calcium; Cell Membrane; Chloride Channels; Chlorides; Cystic Fibrosis | 1990 |
2 other studies available for gamma-aminobutyric acid and Cystic Fibrosis
| Article | Year |
|---|---|
Increasing the Endoplasmic Reticulum Pool of the F508del Allele of the Cystic Fibrosis Transmembrane Conductance Regulator Leads to Greater Folding Correction by Small Molecule Therapeutics.
Topics: Alleles; Benzoates; Cells, Cultured; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regu | 2016 |
Pharmacological chaperone-rescued cystic fibrosis CFTR-F508del mutant overcomes PRAF2-gated access to endoplasmic reticulum exit sites.
Topics: Carrier Proteins; Cell Membrane; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulato | 2022 |