copper gluconate has been researched along with Cystic Fibrosis of Pancreas in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (11.11) | 18.7374 |
| 1990's | 3 (33.33) | 18.2507 |
| 2000's | 3 (33.33) | 29.6817 |
| 2010's | 2 (22.22) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ashraf, SN; Behrends, V; Bell, TJ; Bundy, JG; Cordes-Blauert, A; Liebeke, M; Nair, C; Williams, HD; Zlosnik, JE | 1 |
| Broutin, I; Fournier, D; Llanes, C; Monlezun, L; Plésiat, P; Richardot, C | 1 |
| Hebestreit, A; Hebestreit, H; Kersting, U | 1 |
| Erbacher, P; Glick, MC; Kollen, WJ; Midoux, P; Monsigny, M; Roche, AC; Scanlin, TF; Yip, A | 1 |
| Boisseau, P; Chailleux, E; Danner, I; Escande, D | 1 |
| Boucher, RC; Gabriel, SE; Lethem, MI; Makhlina, M; Martsen, E; Thomas, EJ | 1 |
| Eben-Brunnen, J; Götz, H; Hellmann, KP; Hellmann, T; Hilschmann, N; Kiafard, Z; Merker, R; Schwarzer, C; Thinnes, FP; Walter, G | 1 |
| Mastrocola, T; Rugolo, M | 1 |
| Bijman, J; Frömter, E | 1 |
1 trial(s) available for copper gluconate and Cystic Fibrosis of Pancreas
| Article | Year |
|---|---|
Hypertonic saline inhibits luminal sodium channels in respiratory epithelium.
Topics: Adolescent; Adrenergic beta-Agonists; Adult; Amiloride; Case-Control Studies; Cystic Fibrosis; Dose-Response Relationship, Drug; Gluconates; Humans; Isoproterenol; Nasal Mucosa; Saline Solution, Hypertonic; Sodium Channel Blockers; Sodium Channels | 2007 |
8 other study(ies) available for copper gluconate and Cystic Fibrosis of Pancreas
| Article | Year |
|---|---|
Metabolite profiling to characterize disease-related bacteria: gluconate excretion by Pseudomonas aeruginosa mutants and clinical isolates from cystic fibrosis patients.
Topics: Bacterial Proteins; Cystic Fibrosis; Drug Resistance, Bacterial; Female; Gluconates; Humans; Male; Metabolome; Pseudomonas aeruginosa; Pseudomonas Infections; Random Amplified Polymorphic DNA Technique | 2013 |
Carbapenem resistance in cystic fibrosis strains of Pseudomonas aeruginosa as a result of amino acid substitutions in porin OprD.
Topics: Amino Acid Substitution; Anti-Bacterial Agents; beta-Lactam Resistance; Carbapenems; Culture Media; Cystic Fibrosis; Gene Deletion; Genetic Complementation Test; Gluconates; Humans; Mutant Proteins; Porins; Pseudomonas aeruginosa; Pseudomonas Infections | 2015 |
Gluconoylated and glycosylated polylysines as vectors for gene transfer into cystic fibrosis airway epithelial cells.
Topics: Cell Count; Cells, Cultured; Chloroquine; Cystic Fibrosis; Epithelium; Gene Expression; Gene Transfer Techniques; Genes, Reporter; Genetic Therapy; Genetic Vectors; Gluconates; Glycosylation; Humans; Lactones; Lactose; Luciferases; Plasmids; Polylysine; Trachea; Transfection | 1996 |
Respiratory epithelial ion transport in patients with disseminated bronchiectasis.
Topics: Adolescent; Adult; Amiloride; Bronchiectasis; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Diagnosis, Differential; Epithelium; Female; Genotype; Gluconates; Humans; Ion Transport; Isoproterenol; Male; Membrane Potentials; Middle Aged; Nasal Mucosa; Uridine Triphosphate | 1999 |
Permeabilization via the P2X7 purinoreceptor reveals the presence of a Ca2+-activated Cl- conductance in the apical membrane of murine tracheal epithelial cells.
Topics: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Animals; Bromine; Calcium; Calcium Channel Blockers; Calixarenes; Cell Line; Cell Membrane; Chelating Agents; Chlorides; Cystic Fibrosis; DNA, Complementary; Electrophysiology; Epithelium; Gluconates; Glyburide; Hypoglycemic Agents; Iodine; Ions; Mice; Niflumic Acid; Nitrobenzoates; ortho-Aminobenzoates; Phenols; Receptors, Purinergic P2; Receptors, Purinergic P2X7; Tamoxifen; Time Factors; Trachea; Uridine Triphosphate | 2000 |
Gadolinium as an opener of the outwardly rectifying Cl(-) channel (ORCC). Is there relevance for cystic fibrosis therapy?
Topics: Anti-Inflammatory Agents; Antibodies; Chloride Channels; Cystic Fibrosis; Gadolinium; Gluconates; HeLa Cells; Humans; Hypotonic Solutions; Ion Channel Gating; Isotonic Solutions; Porins; Ringer's Solution; Voltage-Dependent Anion Channels; Water-Electrolyte Balance | 2001 |
The response of chloride transport to cyclic AMP, calcium and hypotonic shock in normal and cystic fibrosis fibroblasts.
Topics: 8-Bromo Cyclic Adenosine Monophosphate; Bucladesine; Calcimycin; Calcium; Cell Line; Cells, Cultured; Chlorides; Cyclic AMP; Cystic Fibrosis; Fibroblasts; Furosemide; Gluconates; Humans; Hypotonic Solutions; Isoproterenol | 1990 |
Direct demonstration of high transepithelial chloride-conductance in normal human sweat duct which is absent in cystic fibrosis.
Topics: Adult; Amiloride; Cell Membrane Permeability; Chlorides; Cystic Fibrosis; Epithelium; Gluconates; Humans; In Vitro Techniques; Male; Sweat Glands | 1986 |