carbachol has been researched along with Cystic Fibrosis of Pancreas in 51 studies
Carbachol: A slowly hydrolyzed CHOLINERGIC AGONIST that acts at both MUSCARINIC RECEPTORS and NICOTINIC RECEPTORS.
Excerpt | Relevance | Reference |
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"The chronically pilocarpine-treated rat has been proposed as an animal model for the disease cystic fibrosis, a generalized exocrinopathy." | 7.67 | The chronically pilocarpine-treated rat in the study of cystic fibrosis: investigations on submandibular gland and pancreas. ( Bardon, A; Ceder, O; Kuijpers, GA; Müller, RM; Roomans, GM, 1985) |
"We used mass-spectrometry based proteomic analysis of unstimulated and carbachol stimulated newborn wild-type (WT) and cystic fibrosis transmembrane conductance regulator (CFTR) null (CF) piglet airways to study proteins in the airway surface liquid and mucus, to investigate if levels of MUC5AC and MUC5B were affected by carbachol stimulation and whether the proteins clustered according to function." | 4.31 | Proteome of airway surface liquid and mucus in newborn wildtype and cystic fibrosis piglets. ( Bähr, A; Ermund, A; Hansson, GC; Jaudas, F; Klymiuk, N; Rodriguez-Piñeiro, AM, 2023) |
"Rectal biopsies from cystic fibrosis (CF) patients show defective cAMP-activated Cl(-) secretion and an inverse response of the short-circuit current (I(sc)) toward stimulation with carbachol (CCh)." | 3.70 | Defective cholinergic Cl(-) secretion and detection of K(+) secretion in rectal biopsies from cystic fibrosis patients. ( Brandis, M; Greger, R; Kuehr, J; Kunzelmann, K; Mall, M; Seydewitz, HH; Wissner, A, 2000) |
"Chronic reserpine treatment of animals, an experimental model for cystic fibrosis (CF), results in generalized exocrinopathy, impaired secretion, and decreased pancreatic content of amylase." | 3.68 | Alterations of amylase secretion in the chronically reserpinized rat: an acetylcholine-mediated phenomenon. ( Benrezzak, O; Bérubé, FL; Morisset, J, 1991) |
"Airway reactivity to cold air and methacholine, alpha-adrenergic and cholinergic reactivity measured as pupillary responses to phenylephrine and carbachol, respectively, and beta-adrenergic reactivity assessed by lymphocyte adenosine 3',5'-cyclic monophosphate (cAMP) response to isoproterenol were compared in 108 parents of patients with cystic fibrosis (CF) and 133 healthy adult controls." | 3.67 | Heterozygotes for cystic fibrosis: models for study of airway and autonomic reactivity. ( Byard, PJ; Davis, PB, 1989) |
"The chronically pilocarpine-treated rat has been proposed as an animal model for the disease cystic fibrosis, a generalized exocrinopathy." | 3.67 | The chronically pilocarpine-treated rat in the study of cystic fibrosis: investigations on submandibular gland and pancreas. ( Bardon, A; Ceder, O; Kuijpers, GA; Müller, RM; Roomans, GM, 1985) |
"1 µM carbachol was ∼4 times greater in adult than in neonatal nasal glands." | 1.37 | Defective fluid secretion from submucosal glands of nasal turbinates from CFTR-/- and CFTR (ΔF508/ΔF508) pigs. ( Cho, HJ; Joo, NS; Wine, JJ, 2011) |
"Lubiprostone is shown to increase submucosal gland secretion in pigs, sheep, and humans and to increase short-circuit current (SCC) in the surface epithelium of pigs and sheep." | 1.35 | Lubiprostone stimulates secretion from tracheal submucosal glands of sheep, pigs, and humans. ( Cuthbert, AW; Joo, NS; Wine, JJ, 2009) |
"Methoxsalen failed to increase I(sc)." | 1.30 | Psoralens: novel modulators of Cl- secretion. ( Bridges, RJ; Devor, DC; Frizzell, RA; Singh, AK, 1997) |
"Reserpine treatment resulted in altered enzyme secretion from rat pancreatic acini in response to carbamylcholine and secretin (1,2)." | 1.29 | Alterations of pancreatic amylase secretion in the reserpinized rat model of cystic fibrosis. Effects of cerulein and EGF. ( Benrezzak, O; Bérubé, FL; Morisset, J; Vanier, M, 1994) |
"Treatment with carbachol, calcium ionophores or phorbol ester did not acutely affect chloride efflux." | 1.29 | Effects of mutations in cAMP-dependent protein kinase on chloride efflux in Caco-2 human colonic carcinoma cells. ( Bear, CE; Krolczyk, AJ; Lai, PF; Schimmer, BP, 1995) |
" No effects specific to cystic fibrosis serum were demonstrated upon the following parameters of potassium transport: (1) maximal stimulation of K+ efflux by the cholinergic agonists carbamylcholine; (2) the dose-response curve of K+ efflux in response to carbamylcholine; (3) re-entry of K+ into cells after carbamylcholine stimulation; (4) the maintenance of K+ in the absence of added effectors." | 1.26 | Cystic fibrosis factors: effect of serum on the secretory response of dispersed rat submandibular cells. ( Barzen, KA; Flux, M; Lafferty, JL; Quissell, DO; Rennert, OM; Seale, TW, 1980) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 8 (15.69) | 18.7374 |
1990's | 19 (37.25) | 18.2507 |
2000's | 13 (25.49) | 29.6817 |
2010's | 8 (15.69) | 24.3611 |
2020's | 3 (5.88) | 2.80 |
Authors | Studies |
---|---|
Joo, NS | 8 |
Cho, HJ | 3 |
Shinbashi, M | 1 |
Choi, JY | 3 |
Milla, CE | 1 |
Engelhardt, JF | 1 |
Wine, JJ | 8 |
Rodriguez-Piñeiro, AM | 1 |
Jaudas, F | 1 |
Klymiuk, N | 1 |
Bähr, A | 1 |
Hansson, GC | 1 |
Ermund, A | 1 |
Luan, X | 1 |
Tam, JS | 1 |
Jagadeeshan, S | 1 |
Grishchenko, N | 1 |
Hassan, N | 1 |
Gioino, P | 1 |
Shipley, AM | 1 |
Machen, TE | 1 |
Ianowski, JP | 2 |
Abu-Arish, A | 1 |
Pandžić, E | 1 |
Kim, D | 1 |
Tseng, HW | 1 |
Wiseman, PW | 1 |
Hanrahan, JW | 2 |
Collaco, AM | 1 |
Jakab, RL | 1 |
Hoekstra, NE | 1 |
Mitchell, KA | 1 |
Brooks, A | 1 |
Ameen, NA | 1 |
Jeong, JH | 1 |
Hwang, PH | 1 |
Cuthbert, AW | 6 |
Khansaheb, M | 2 |
Krouse, ME | 2 |
Robbins, RC | 3 |
Weill, D | 1 |
Lee, RJ | 1 |
Foskett, JK | 1 |
Shenoy, A | 1 |
Kopic, S | 1 |
Murek, M | 1 |
Caputo, C | 1 |
Geibel, JP | 1 |
Egan, ME | 1 |
Sousa, M | 1 |
Servidoni, MF | 1 |
Vinagre, AM | 1 |
Ramalho, AS | 1 |
Bonadia, LC | 1 |
Felício, V | 1 |
Ribeiro, MA | 1 |
Uliyakina, I | 1 |
Marson, FA | 1 |
Kmit, A | 1 |
Cardoso, SR | 1 |
Ribeiro, JD | 1 |
Bertuzzo, CS | 1 |
Sousa, L | 1 |
Kunzelmann, K | 2 |
Ribeiro, AF | 1 |
Amaral, MD | 1 |
Irokawa, T | 1 |
Wu, JV | 2 |
Whyte, RI | 1 |
Del Castillo, IC | 1 |
Alvarez, JG | 1 |
Freedman, SD | 1 |
Ollero, M | 2 |
Claros, L | 1 |
Song, JC | 1 |
Yoo, J | 1 |
Matthews, JB | 1 |
Brouillard, F | 1 |
Bensalem, N | 1 |
Hinzpeter, A | 1 |
Tondelier, D | 1 |
Trudel, S | 1 |
Gruber, AD | 1 |
Edelman, A | 1 |
Tuo, B | 1 |
Riederer, B | 1 |
Wang, Z | 1 |
Colledge, WH | 5 |
Soleimani, M | 1 |
Seidler, U | 1 |
van Barneveld, A | 1 |
Stanke, F | 2 |
Ballmann, M | 1 |
Naim, HY | 1 |
Tümmler, B | 2 |
MacVinish, LJ | 3 |
Cope, G | 1 |
Ropenga, A | 1 |
Tóth, B | 1 |
Wilke, M | 1 |
Dorsch, M | 1 |
Jansen, S | 1 |
Wedekind, D | 1 |
Charizopoulou, N | 1 |
Bot, A | 1 |
Burmester, M | 1 |
Leonhard-Marek, S | 1 |
de Jonge, HR | 2 |
Hedrich, HJ | 1 |
Breves, G | 1 |
Davis, PB | 3 |
Shelhamer, JR | 1 |
Kaliner, M | 2 |
Seale, TW | 1 |
Flux, M | 1 |
Rennert, OM | 1 |
Quissell, DO | 1 |
Barzen, KA | 1 |
Lafferty, JL | 1 |
Mills, CL | 1 |
Dorin, JR | 1 |
Davidson, DJ | 1 |
Porteus, DJ | 1 |
Alton, EW | 1 |
Dormer, RL | 2 |
McPherson, MA | 2 |
Valverde, MA | 1 |
O'Brien, JA | 1 |
Sepúlveda, FV | 1 |
Ratcliff, R | 3 |
Evans, MJ | 4 |
Morisset, J | 2 |
Bérubé, FL | 2 |
Vanier, M | 1 |
Benrezzak, O | 2 |
Krolczyk, AJ | 1 |
Bear, CE | 1 |
Lai, PF | 1 |
Schimmer, BP | 1 |
Schröder, UH | 1 |
Frömter, E | 1 |
Yankaskas, JR | 1 |
Haizlip, JE | 1 |
Conrad, M | 1 |
Koval, D | 1 |
Lazarowski, E | 1 |
Paradiso, AM | 1 |
Rinehart, CA | 1 |
Sarkadi, B | 1 |
Schlegel, R | 1 |
Boucher, RC | 1 |
Halstead, J | 1 |
Hickman, ME | 1 |
Veeze, HJ | 1 |
Halley, DJ | 1 |
Bijman, J | 1 |
de Jongste, JC | 1 |
Sinaasappel, M | 1 |
Montserrat, C | 1 |
Merten, M | 1 |
Figarella, C | 2 |
Devor, DC | 1 |
Singh, AK | 1 |
Bridges, RJ | 1 |
Frizzell, RA | 1 |
Manson, AL | 1 |
Trezise, AE | 1 |
Kasschau, KD | 1 |
Birchall, N | 1 |
Episkopou, V | 1 |
Vassaux, G | 1 |
Huxley, C | 1 |
Kammouni, W | 1 |
Baeza, N | 1 |
Marchand, S | 1 |
Merten, MD | 1 |
Tang, S | 1 |
Beharry, S | 1 |
Kent, G | 1 |
Durie, PR | 1 |
Grubb, BR | 1 |
Mall, M | 1 |
Wissner, A | 1 |
Seydewitz, HH | 1 |
Kuehr, J | 1 |
Brandis, M | 1 |
Greger, R | 1 |
Pratha, VS | 1 |
Hogan, DL | 1 |
Martensson, BA | 1 |
Bernard, J | 1 |
Zhou, R | 1 |
Isenberg, JI | 1 |
Smitham, JE | 1 |
Barrett, KE | 1 |
Cozens, AL | 1 |
Yezzi, MJ | 1 |
Chin, L | 1 |
Simon, EM | 1 |
Finkbeiner, WE | 1 |
Wagner, JA | 1 |
Gruenert, DC | 1 |
Brayden, DJ | 1 |
Pickles, RJ | 1 |
McCool, DJ | 1 |
Marcon, MA | 1 |
Forstner, JF | 1 |
Forstner, GG | 1 |
Izutsu, KT | 1 |
Ensign, WY | 1 |
Ramsey, BW | 1 |
Schubert, MM | 1 |
Allan, BJ | 1 |
Truelove, EL | 1 |
Byard, PJ | 1 |
Doughney, C | 1 |
Pedersen, PS | 1 |
Müller, RM | 1 |
Kuijpers, GA | 1 |
Bardon, A | 1 |
Ceder, O | 1 |
Roomans, GM | 1 |
Wasserman, SI | 1 |
Austen, KF | 1 |
51 other studies available for carbachol and Cystic Fibrosis of Pancreas
Article | Year |
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Combined agonists act synergistically to increase mucociliary clearance in a cystic fibrosis airway model.
Topics: Animals; Carbachol; Colforsin; Cystic Fibrosis; Disease Models, Animal; Drug Synergism; Drug Therapy | 2021 |
Proteome of airway surface liquid and mucus in newborn wildtype and cystic fibrosis piglets.
Topics: Animals; Carbachol; Cystic Fibrosis; Goblet Cells; Mucins; Mucus; Proteome; Proteomics; Swine | 2023 |
Airway submucosal glands from cystic fibrosis swine suffer from abnormal ion transport across the serous acini, collecting duct, and ciliated duct.
Topics: Acinar Cells; Animals; Carbachol; Cations, Monovalent; Chlorides; Cilia; Colforsin; Cystic Fibrosis; | 2020 |
Agonists that stimulate secretion promote the recruitment of CFTR into membrane lipid microdomains.
Topics: Amitriptyline; Apoptosis; Carbachol; Cell Line; Cystic Fibrosis; Cystic Fibrosis Transmembrane Condu | 2019 |
Regulated traffic of anion transporters in mammalian Brunner's glands: a role for water and fluid transport.
Topics: Animals; Anion Transport Proteins; Aquaporin 5; Bicarbonates; Biological Transport; Brunner Glands; | 2013 |
Mucociliary clearance and submucosal gland secretion in the ex vivo ferret trachea.
Topics: Analgesics, Non-Narcotic; Angiogenesis Inhibitors; Animals; Bronchodilator Agents; Bumetanide; Calci | 2014 |
Lubiprostone stimulates secretion from tracheal submucosal glands of sheep, pigs, and humans.
Topics: Alprostadil; Animals; Anions; Carbachol; Chloride Channels; Cystic Fibrosis; Dose-Response Relations | 2009 |
Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process.
Topics: Age Factors; Animals; Calcium Signaling; Capsicum; Carbachol; Chelating Agents; Clotrimazole; Colfor | 2009 |
Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs.
Topics: Animals; Animals, Newborn; Body Fluids; Carbachol; Colforsin; Cystic Fibrosis; Cystic Fibrosis Trans | 2010 |
cAMP-activated Ca2+ signaling is required for CFTR-mediated serous cell fluid secretion in porcine and human airways.
Topics: Adult; Animals; Animals, Newborn; Body Fluids; Bronchioles; Calcium Signaling; Carbachol; Cyclic AMP | 2010 |
Calcium-modulated chloride pathways contribute to chloride flux in murine cystic fibrosis-affected macrophages.
Topics: Animals; Calcium; Carbachol; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance R | 2011 |
Defective fluid secretion from submucosal glands of nasal turbinates from CFTR-/- and CFTR (ΔF508/ΔF508) pigs.
Topics: Aging; Animals; Animals, Newborn; Body Fluids; Carbachol; Colforsin; Cystic Fibrosis; Cystic Fibrosi | 2011 |
Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis.
Topics: 1-Methyl-3-isobutylxanthine; Biomarkers; Biopsy; Carbachol; Chlorides; Colforsin; Cystic Fibrosis; C | 2012 |
Absent secretion to vasoactive intestinal peptide in cystic fibrosis airway glands.
Topics: Adult; Biopsy; Bronchi; Carbachol; Colforsin; Cystic Fibrosis; Female; Humans; Kinetics; Lung Transp | 2002 |
Docosahexaenoic acid selectively augments muscarinic stimulation of epithelial Cl- secretion.
Topics: Carbachol; Cell Line; Chlorides; Cystic Fibrosis; Docosahexaenoic Acids; Humans; Intestinal Mucosa; | 2003 |
Blue native/SDS-PAGE analysis reveals reduced expression of the mClCA3 protein in cystic fibrosis knock-out mice.
Topics: Amino Acid Sequence; Animals; Carbachol; Chloride Channels; Colon; Cystic Fibrosis; Cystic Fibrosis | 2005 |
Involvement of the anion exchanger SLC26A6 in prostaglandin E2- but not forskolin-stimulated duodenal HCO3- secretion.
Topics: Animals; Antiporters; Bicarbonates; Carbachol; Colforsin; Cystic Fibrosis; Cystic Fibrosis Transmemb | 2006 |
Ex vivo biochemical analysis of CFTR in human rectal biopsies.
Topics: Adolescent; Adult; Biopsy; Carbachol; Child; Child, Preschool; Colforsin; Cysteine; Cystic Fibrosis; | 2006 |
Chloride transporting capability of Calu-3 epithelia following persistent knockdown of the cystic fibrosis transmembrane conductance regulator, CFTR.
Topics: Adenylyl Cyclases; Alprostadil; Carbachol; Cell Line; Chloride Channels; Chlorides; CLC-2 Chloride C | 2007 |
Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.
Topics: Acetylcholine; Animals; Carbachol; Cholinergic Agonists; Cyclic AMP; Cystic Fibrosis; Cystic Fibrosi | 2007 |
Very mild disease phenotype of congenic CftrTgH(neoim)Hgu cystic fibrosis mice.
Topics: Analysis of Variance; Animals; Body Weight; Carbachol; Chlorides; Colforsin; Cystic Fibrosis; Cystic | 2008 |
Abnormal adrenergic and cholinergic sensitivity in cystic fibrosis.
Topics: Adolescent; Adult; Autonomic Nervous System; Carbachol; Cystic Fibrosis; Female; Humans; Isoproteren | 1980 |
Autonomic and airway reactivity in obligate heterozygotes for cystic fibrosis.
Topics: Adult; Autonomic Nervous System; Bronchi; Bronchial Provocation Tests; Carbachol; Cyclic AMP; Cystic | 1984 |
Cystic fibrosis factors: effect of serum on the secretory response of dispersed rat submandibular cells.
Topics: Adolescent; Adult; Animals; Biological Transport; Body Fluids; Carbachol; Cells, Cultured; Child; Cu | 1980 |
Decreased beta-adrenergic stimulation of glycoprotein secretion in CF mice submandibular glands: reversal by the methylxanthine, IBMX.
Topics: 1-Methyl-3-isobutylxanthine; Adrenergic beta-Agonists; Amylases; Animals; Carbachol; Cyclic AMP; Cys | 1995 |
Inactivation of the murine cftr gene abolishes cAMP-mediated but not Ca(2+)-mediated secretagogue-induced volume decrease in small-intestinal crypts.
Topics: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Animals; Calcium; Carbachol; Chloride Channels; Cy | 1993 |
Alterations of pancreatic amylase secretion in the reserpinized rat model of cystic fibrosis. Effects of cerulein and EGF.
Topics: Amylases; Animals; Carbachol; Ceruletide; Cystic Fibrosis; Disease Models, Animal; Epidermal Growth | 1994 |
Effects of mutations in cAMP-dependent protein kinase on chloride efflux in Caco-2 human colonic carcinoma cells.
Topics: Carbachol; Chloride Channels; Colforsin; Colonic Neoplasms; Cyclic AMP; Cyclic AMP-Dependent Protein | 1995 |
Characterization of two distinct Cl- conductances in fused human respiratory epithelial cells. I. Anion selectivities, stimulation and intermeshing signal transduction pathways.
Topics: Anions; Calcimycin; Carbachol; Cell Fusion; Cells, Cultured; Chloride Channels; Colforsin; Cyclic AM | 1995 |
Papilloma virus immortalized tracheal epithelial cells retain a well-differentiated phenotype.
Topics: Adult; Animals; Bradykinin; Calcium; Carbachol; Cell Differentiation; Cell Division; Cell Line, Tran | 1993 |
The genetic advantage hypothesis in cystic fibrosis heterozygotes: a murine study.
Topics: Animals; Bacterial Toxins; Calcium; Carbachol; Chloride Channels; Cholera Toxin; Colforsin; Colon; C | 1995 |
Ion-transporting activity in the murine colonic epithelium of normal animals and animals with cystic fibrosis.
Topics: Amiloride; Animals; Biological Transport; Carbachol; Colforsin; Colon; Cystic Fibrosis; Epithelium; | 1994 |
Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype.
Topics: Adolescent; Adult; Aged; Alleles; Biopsy; Carbachol; Child; Child, Preschool; Chlorides; Cystic Fibr | 1994 |
Defective ATP-dependent mucin secretion by cystic fibrosis pancreatic epithelial cells.
Topics: Adenocarcinoma; Adenosine; Adenosine Diphosphate; Adenosine Monophosphate; Adenosine Triphosphate; A | 1996 |
Psoralens: novel modulators of Cl- secretion.
Topics: Animals; Atropine; Benzimidazoles; Calcium; Carbachol; Cell Line; Chloride Channels; Chlorides; Chlo | 1997 |
Complementation of null CF mice with a human CFTR YAC transgene.
Topics: Animals; Carbachol; Chlorides; Chromosomes, Artificial, Yeast; Colforsin; Cystic Fibrosis; Cystic Fi | 1997 |
Pseudomonas aeruginosa lipopolysaccharide induces CF-like alteration of protein secretion by human tracheal gland cells.
Topics: Adenosine Triphosphate; Adrenergic beta-Agonists; Carbachol; Cells, Cultured; Cholinergic Agonists; | 1997 |
Synergistic effects of cAMP- and calcium-mediated amylase secretion in isolated pancreatic acini from cystic fibrosis mice.
Topics: 8-Bromo Cyclic Adenosine Monophosphate; Amylases; Animals; Body Weight; Calcium; Carbachol; Colforsi | 1999 |
Ion transport across the normal and CF neonatal murine intestine.
Topics: Amiloride; Amino Acid Transport Systems; Amino Acid Transport Systems, Neutral; Animals; Animals, Ne | 1999 |
Defective cholinergic Cl(-) secretion and detection of K(+) secretion in rectal biopsies from cystic fibrosis patients.
Topics: Adolescent; Adult; Biopsy; Carbachol; Child; Child, Preschool; Chlorides; Cholinergic Agonists; Chol | 2000 |
Identification of transport abnormalities in duodenal mucosa and duodenal enterocytes from patients with cystic fibrosis.
Topics: Acid-Base Equilibrium; Acids; Adult; Alkalies; Ammonium Chloride; Antiporters; Bacterial Toxins; Bic | 2000 |
Differential effects of apical and basolateral uridine triphosphate on intestinal epithelial chloride secretion.
Topics: Bucladesine; Calcium; Carbachol; Cell Line; Cell Polarity; Chlorides; Cholinergic Agonists; Colon; C | 2001 |
Characterization of immortal cystic fibrosis tracheobronchial gland epithelial cells.
Topics: Base Sequence; Bronchi; Calcium; Carbachol; Cell Transformation, Viral; Cells, Cultured; Chlorides; | 1992 |
Ion transport in cultured epithelia from human sweat glands: comparison of normal and cystic fibrosis tissues.
Topics: Adenylyl Cyclases; Amiloride; Barium; Calcium; Carbachol; Cells, Cultured; Colforsin; Cyclic AMP; Cy | 1991 |
Alterations of amylase secretion in the chronically reserpinized rat: an acetylcholine-mediated phenomenon.
Topics: Acetylcholine; Amylases; Animals; Body Weight; Carbachol; Ceruletide; Cystic Fibrosis; Disease Model | 1991 |
The T84 human colonic adenocarcinoma cell line produces mucin in culture and releases it in response to various secretagogues.
Topics: Adenocarcinoma; Calcimycin; Carbachol; Cell Line; Cholera Toxin; Colonic Neoplasms; Cystic Fibrosis; | 1990 |
Potassium release in labial glands from controls and patients with cystic fibrosis.
Topics: 1-Methyl-3-isobutylxanthine; Carbachol; Cystic Fibrosis; Humans; Potassium; Salivary Glands; Salivar | 1989 |
Heterozygotes for cystic fibrosis: models for study of airway and autonomic reactivity.
Topics: Adult; Aged; Autonomic Nervous System; Carbachol; Cold Temperature; Cyclic AMP; Cystic Fibrosis; Gen | 1989 |
Formation of inositol polyphosphates in cultured human sweat duct cells in response to cholinergic stimulation.
Topics: Calcium; Carbachol; Cells, Cultured; Chlorides; Cystic Fibrosis; Humans; Inositol Phosphates; Parasy | 1989 |
The chronically pilocarpine-treated rat in the study of cystic fibrosis: investigations on submandibular gland and pancreas.
Topics: Animals; Carbachol; Cystic Fibrosis; Disease Models, Animal; Electron Probe Microanalysis; Energy Me | 1985 |
Immunologic release of chemical mediators from human nasal polyps.
Topics: Allergens; Anaphylaxis; Butyrates; Carbachol; Chemotaxis; Cholera; Cyclic AMP; Cystic Fibrosis; Depr | 1973 |