fenamic acid has been researched along with Cystic Fibrosis of Pancreas in 17 studies
fenamic acid: has chloride and potassium channel-blocking activity; RN given refers to parent cpd
fenamic acid : An aminobenzoic acid that is the N-phenyl derivative of anthranilic acid. It acts as a parent skeleton for the synthesis of several non-steroidal anti-inflammatory drugs.
Excerpt | Relevance | Reference |
---|---|---|
"Cystic fibrosis is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel, which mediates transepithelial Cl- transport in a variety of epithelia, including airway, intestine, pancreas, and sweat duct." | 1.30 | Exocytosis is not involved in activation of Cl- secretion via CFTR in Calu-3 airway epithelial cells. ( Loffing, J; McCoy, D; Moyer, BD; Stanton, BA, 1998) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (5.88) | 18.7374 |
1990's | 10 (58.82) | 18.2507 |
2000's | 4 (23.53) | 29.6817 |
2010's | 2 (11.76) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Michoud, MC | 1 |
Robert, R | 1 |
Hassan, M | 1 |
Moynihan, B | 1 |
Haston, C | 1 |
Govindaraju, V | 1 |
Ferraro, P | 1 |
Hanrahan, JW | 1 |
Martin, JG | 1 |
Finkbeiner, WE | 1 |
Zlock, LT | 1 |
Morikawa, M | 1 |
Lao, AY | 1 |
Dasari, V | 1 |
Widdicombe, JH | 1 |
Shen, B | 1 |
Li, X | 1 |
Wang, F | 1 |
Yao, X | 1 |
Yang, D | 1 |
Paradiso, AM | 1 |
Coakley, RD | 1 |
Boucher, RC | 2 |
Reisin, IL | 1 |
Prat, AG | 1 |
Abraham, EH | 1 |
Amara, JF | 1 |
Gregory, RJ | 1 |
Ausiello, DA | 1 |
Cantiello, HF | 1 |
McDonough, S | 2 |
Davidson, N | 2 |
Lester, HA | 2 |
McCarty, NA | 2 |
Faller, DP | 1 |
Egan, DA | 1 |
Ryan, MP | 1 |
Cohen, BN | 1 |
Riordan, JR | 1 |
Rückes, C | 1 |
Blank, U | 1 |
Möller, K | 1 |
Rieboldt, J | 1 |
Lindemann, H | 2 |
Münker, G | 2 |
Clauss, W | 2 |
Weber, WM | 2 |
Kelley, TJ | 1 |
Cotton, CU | 1 |
Drumm, ML | 1 |
Mailleau, C | 1 |
Capeau, J | 1 |
Brahimi-Horn, MC | 1 |
Loffing, J | 1 |
Moyer, BD | 1 |
McCoy, D | 1 |
Stanton, BA | 1 |
Pedersen, PS | 1 |
Frederiksen, O | 1 |
Holstein-Rathlou, NH | 1 |
Larsen, PL | 1 |
Qvortrup, K | 1 |
Rückes-Nilges, C | 1 |
Weber, U | 1 |
Gabriel, SE | 1 |
Makhlina, M | 1 |
Martsen, E | 1 |
Thomas, EJ | 1 |
Lethem, MI | 1 |
Walsh, DE | 1 |
Harvey, BJ | 1 |
Urbach, V | 1 |
Bijman, J | 1 |
Englert, HC | 1 |
Lang, HJ | 1 |
Greger, R | 1 |
Frömter, E | 1 |
17 other studies available for fenamic acid and Cystic Fibrosis of Pancreas
Article | Year |
---|---|
Role of the cystic fibrosis transmembrane conductance channel in human airway smooth muscle.
Topics: Asthma; Bronchi; Calcium; Calcium Channel Blockers; Cells, Cultured; Cystic Fibrosis; Cystic Fibrosi | 2009 |
Cystic fibrosis and the relationship between mucin and chloride secretion by cultures of human airway gland mucous cells.
Topics: Adenosine Triphosphate; Adrenergic alpha-1 Receptor Agonists; Adrenergic beta-Agonists; Adult; Bronc | 2011 |
A synthetic chloride channel restores chloride conductance in human cystic fibrosis epithelial cells.
Topics: 4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic Acid; 4,4'-Diisothiocyanostilbene-2,2'-Disulfo | 2012 |
Polarized distribution of HCO3- transport in human normal and cystic fibrosis nasal epithelia.
Topics: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Adult; Amiloride; Barium; Bicarbonates; Biological | 2003 |
The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel.
Topics: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Adenosine Triphosphate; Animals; Chloride Channels | 1994 |
Novel pore-lining residues in CFTR that govern permeation and open-channel block.
Topics: Amino Acid Sequence; Animals; Calcium Channel Blockers; Cystic Fibrosis; Cystic Fibrosis Transmembra | 1994 |
Evidence for location of the CFTR in human placental apical membrane vesicles.
Topics: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Adenosine Triphosphate; Anions; Bumetanide; Cell M | 1995 |
Voltage-dependent block of the cystic fibrosis transmembrane conductance regulator Cl- channel by two closely related arylaminobenzoates.
Topics: Animals; Cell Membrane; Chloride Channels; Chlorides; Cyclic AMP; Cystic Fibrosis; Electrophysiology | 1993 |
Amiloride-sensitive Na+ channels in human nasal epithelium are different from classical epithelial Na+ channels.
Topics: 1-Methyl-3-isobutylxanthine; 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Amiloride; Anti-Infla | 1997 |
In vivo activation of CFTR-dependent chloride transport in murine airway epithelium by CNP.
Topics: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Amiloride; Animals; Anti-Inflammatory Agents, Non- | 1997 |
Interrelationship between the Na+/glucose cotransporter and CFTR in Caco-2 cells: relevance to cystic fibrosis.
Topics: Biological Transport; Caco-2 Cells; Calcium Channel Blockers; Cell Differentiation; Chlorides; Colfo | 1998 |
Exocytosis is not involved in activation of Cl- secretion via CFTR in Calu-3 airway epithelial cells.
Topics: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Acetazolamide; Amiloride; Cell Membrane; Chloride | 1998 |
Ion transport in epithelial spheroids derived from human airway cells.
Topics: Absorption; Adenosine Triphosphate; Amiloride; Biological Transport; Chlorides; Cyclic AMP; Cystic F | 1999 |
Minor role of Cl- secretion in non-cystic fibrosis and cystic fibrosis human nasal epithelium.
Topics: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Adenosine Triphosphate; Amiloride; Calcium Channel | 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 Blocker | 2000 |
CFTR regulation of intracellular calcium in normal and cystic fibrosis human airway epithelia.
Topics: Adenosine Triphosphate; Calcium; Cell Line; Cells, Cultured; Colforsin; Cystic Fibrosis; Cystic Fibr | 2000 |
Characterization of human sweat duct chloride conductance by chloride channel blockers.
Topics: Chlorides; Cystic Fibrosis; Electric Conductivity; Humans; Ion Channels; ortho-Aminobenzoates; Sweat | 1987 |