glycerol has been researched along with Cystic Fibrosis in 17 studies
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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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Pseudomonas aeruginosa NM48, a non-mucoid derivative of an alginate-producing strain isolated from a cystic fibrosis patient, was grown in batch culture with glycerol, glucose or succinate as carbon source, and in continuous culture (D 0." | 3.69 | The effect of nutrient limitation on glycerol uptake and metabolism in continuous cultures of Pseudomonas aeruginosa. ( Greenwood, JA; Jones, CW; Williams, SG, 1994) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (17.65) | 18.7374 |
| 1990's | 4 (23.53) | 18.2507 |
| 2000's | 3 (17.65) | 29.6817 |
| 2010's | 5 (29.41) | 24.3611 |
| 2020's | 2 (11.76) | 2.80 |
| Authors | Studies |
|---|---|
| Ross, BS | 1 |
| Lofgren, LA | 1 |
| Ashare, A | 1 |
| Stajich, JE | 1 |
| Cramer, RA | 1 |
| Liu, Y | 1 |
| Sun, W | 1 |
| Ma, L | 1 |
| Xu, R | 1 |
| Yang, C | 1 |
| Xu, P | 1 |
| Ma, C | 1 |
| Gao, C | 1 |
| Matamouros, S | 1 |
| Hayden, HS | 1 |
| Hager, KR | 1 |
| Brittnacher, MJ | 1 |
| Lachance, K | 1 |
| Weiss, EJ | 1 |
| Pope, CE | 1 |
| Imhaus, AF | 1 |
| McNally, CP | 1 |
| Borenstein, E | 1 |
| Hoffman, LR | 1 |
| Miller, SI | 1 |
| Servidoni, MF | 1 |
| Sousa, M | 1 |
| Vinagre, AM | 1 |
| Cardoso, SR | 1 |
| Ribeiro, MA | 1 |
| Meirelles, LR | 1 |
| de Carvalho, RB | 1 |
| Kunzelmann, K | 1 |
| Ribeiro, AF | 1 |
| Ribeiro, JD | 1 |
| Amaral, MD | 1 |
| Sun, Z | 1 |
| Kang, Y | 1 |
| Norris, MH | 1 |
| Troyer, RM | 1 |
| Son, MS | 1 |
| Schweizer, HP | 1 |
| Dow, SW | 1 |
| Hoang, TT | 1 |
| Daniels, JB | 1 |
| Scoffield, J | 2 |
| Woolnough, JL | 1 |
| Silo-Suh, L | 2 |
| Ross, SA | 1 |
| Shaffer, EA | 1 |
| Williams, SG | 1 |
| Greenwood, JA | 1 |
| Jones, CW | 1 |
| Brown, CR | 1 |
| Hong-Brown, LQ | 1 |
| Biwersi, J | 1 |
| Verkman, AS | 1 |
| Welch, WJ | 1 |
| Serrano, J | 1 |
| Sanchis, J | 1 |
| Kollen, WJ | 1 |
| Schembri, FM | 1 |
| Gerwig, GJ | 1 |
| Vliegenthart, JF | 1 |
| Glick, MC | 1 |
| Scanlin, TF | 1 |
| Rubenstein, RC | 1 |
| Zeitlin, PL | 1 |
| Morello, JP | 1 |
| Petäjä-Repo, UE | 1 |
| Bichet, DG | 1 |
| Bouvier, M | 1 |
| Cérantola, S | 1 |
| Montrozier, H | 1 |
| Berger, HM | 1 |
| Reynolds, SJ | 1 |
| Lee, KH | 1 |
| Allué, X | 1 |
| Sanjurjo, P | 1 |
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Phenylbutyrate for Monogenetic Developmental and Epileptic Encephalopathy[NCT04937062] | Early Phase 1 | 50 participants (Anticipated) | Interventional | 2021-03-01 | Enrolling by invitation | ||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
2 reviews available for glycerol and Cystic Fibrosis
| Article | Year |
|---|---|
[Usefulness of mucoactive drugs in respiratory diseases].
Topics: Acetylcysteine; Ambroxol; Bromhexine; Bronchiectasis; Bronchitis; Cystic Fibrosis; Deoxyribonuclease | 1998 |
Pharmacological chaperones: a new twist on receptor folding.
Topics: Animals; Cryoprotective Agents; Cystic Fibrosis; Diabetes Insipidus, Nephrogenic; Dimethyl Sulfoxide | 2000 |
15 other studies available for glycerol and Cystic Fibrosis
| Article | Year |
|---|---|
Aspergillus fumigatus In-Host HOG Pathway Mutation for Cystic Fibrosis Lung Microenvironment Persistence.
Topics: Aspergillosis, Allergic Bronchopulmonary; Aspergillus fumigatus; Cystic Fibrosis; Genomics; Genotype | 2021 |
Metabolic Mechanism and Physiological Role of Glycerol 3-Phosphate in Pseudomonas aeruginosa PAO1.
Topics: Anti-Bacterial Agents; Cystic Fibrosis; Glycerol; Humans; Kanamycin; Oxidoreductases; Pseudomonas ae | 2022 |
Adaptation of commensal proliferating
Topics: Case-Control Studies; Child, Preschool; Cystic Fibrosis; Dietary Fats; Escherichia coli; Escherichia | 2018 |
Rectal forceps biopsy procedure in cystic fibrosis: technical aspects and patients perspective for clinical trials feasibility.
Topics: Adult; Anesthetics, Intravenous; Biopsy; Blotting, Western; Cathartics; Child; Cystic Fibrosis; Cyst | 2013 |
Blocking phosphatidylcholine utilization in Pseudomonas aeruginosa, via mutagenesis of fatty acid, glycerol and choline degradation pathways, confirms the importance of this nutrient source in vivo.
Topics: 3-Hydroxyacyl-CoA Dehydrogenase; Amino Acid Sequence; Animals; Bacterial Proteins; Choline; Cystic F | 2014 |
Impact of glycerol-3-phosphate dehydrogenase on virulence factor production by Pseudomonas aeruginosa.
Topics: Adaptation, Physiological; Culture Media; Cystic Fibrosis; Genes, Bacterial; Glycerol; Glycerolphosp | 2014 |
Glycerol metabolism promotes biofilm formation by Pseudomonas aeruginosa.
Topics: Biofilms; Choline; Cystic Fibrosis; Glycerol; Humans; Pseudomonas aeruginosa; Pseudomonas Infections | 2016 |
The importance of triglyceride hydrolysis for the release of gastric inhibitory polypeptide.
Topics: Adolescent; Adult; Antibodies; Child; Cystic Fibrosis; Female; Gastric Inhibitory Polypeptide; Gastr | 1981 |
The effect of nutrient limitation on glycerol uptake and metabolism in continuous cultures of Pseudomonas aeruginosa.
Topics: Adaptation, Biological; Alginates; Amino Acid Sequence; Bacterial Proteins; Cell Membrane; Culture M | 1994 |
Chemical chaperones correct the mutant phenotype of the delta F508 cystic fibrosis transmembrane conductance regulator protein.
Topics: 3T3 Cells; Animals; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; | 1996 |
Enhanced efficiency of lactosylated poly-L-lysine-mediated gene transfer into cystic fibrosis airway epithelial cells.
Topics: Amino Acid Sequence; Cell Line, Transformed; Chloroquine; Cystic Fibrosis; Gene Expression Regulatio | 1999 |
Sodium 4-phenylbutyrate downregulates Hsc70: implications for intracellular trafficking of DeltaF508-CFTR.
Topics: Animals; Antineoplastic Agents; Biological Transport; Butyrates; Calcium-Binding Proteins; Calnexin; | 2000 |
Production in vitro, on different solid culture media, of two distinct exopolysaccharides by a mucoid clinical strain of Burkholderia cepacia.
Topics: Burkholderia cepacia; Carbohydrate Conformation; Carbohydrate Sequence; Culture Media; Cystic Fibros | 2001 |
False-positive meconium screen.
Topics: Cystic Fibrosis; False Positive Reactions; Glycerol; Humans; Infant, Newborn; Infant, Newborn, Disea | 1977 |
Triglyceride levels after Intralipid infusion in children with cystic fibrosis.
Topics: Child, Preschool; Cystic Fibrosis; Dietary Fats; Drug Combinations; Fatty Acids, Essential; Fatty Ac | 1978 |