Page last updated: 2024-10-16

gamma-aminobutyric acid and Cystic Fibrosis

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.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (33.33)18.2507
2000's0 (0.00)29.6817
2010's1 (33.33)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Chung, WJ1
Goeckeler-Fried, JL1
Havasi, V1
Chiang, A1
Rowe, SM1
Plyler, ZE1
Hong, JS1
Mazur, M1
Piazza, GA1
Keeton, AB1
White, EL1
Rasmussen, L1
Weissman, AM1
Denny, RA1
Brodsky, JL1
Sorscher, EJ1
Saha, K1
Chevalier, B1
Doly, S1
Baatallah, N1
Guilbert, T1
Pranke, I1
Scott, MGH1
Enslen, H1
Guerrera, C1
Chuon, C1
Edelman, A1
Sermet-Gaudelus, I1
Hinzpeter, A1
Marullo, S1
Franciolini, F1
Petris, A1

Reviews

1 review available for gamma-aminobutyric acid and Cystic Fibrosis

ArticleYear
Chloride channels of biological membranes.
    Biochimica et biophysica acta, 1990, May-07, Volume: 1031, Issue:2

    Topics: Animals; Biological Transport; Calcium; Cell Membrane; Chloride Channels; Chlorides; Cystic Fibrosis

1990

Other Studies

2 other studies available for gamma-aminobutyric acid and Cystic Fibrosis

ArticleYear
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.
    PloS one, 2016, Volume: 11, Issue:10

    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.
    Cellular and molecular life sciences : CMLS, 2022, Sep-27, Volume: 79, Issue:10

    Topics: Carrier Proteins; Cell Membrane; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulato

2022