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Liquid secretion properties of airway submucosal glands
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9780470720356.ch7openalex-snapshot
Regulation of Na+and Cl−Transport and Mucous Gland Secretion in Airway Epithelium
inferredcites →https://doi.org/10.1002/aja.1001170302openalex-snapshot
On the cytology and cytochemistry of the opossum's bronchial glands
inferredcites →https://doi.org/10.1002/ajmg.1320280420openalex-snapshot
Pathological confirmation of cystic fibrosis in the fetus following prenatal diagnosis
inferredcites →https://doi.org/10.1002/ar.1092100303openalex-snapshot
Intercellular junctions in upper airway submucosal glands of the rat: A tracer and freeze fracture study
inferredcites →https://doi.org/10.1007/bf01870568openalex-snapshot
Chloride secretion by canine tracheal epithelium: IV. Basolateral membrane K permeability parallels secretion rate
inferredcites →https://doi.org/10.1016/0014-2999(87)90075-6openalex-snapshot
Platelet activating factor (PAF) is a potent stimulator of porcine tracheal fluid secretion in vitro
inferredcites →https://doi.org/10.1016/0014-5793(93)80624-4openalex-snapshot
Characterization of cAMP dependent CFTR‐chloride channels in human trache gland cells
inferredcites →https://doi.org/10.1016/0034-5687(90)90097-iopenalex-snapshot
Reflex and chemical responses of tracheal submucosal glands in piglets
inferredcites →https://doi.org/10.1016/0034-5687(93)90008-xopenalex-snapshot
A stimulatory role of protein kinase C in feline tracheal submucosal gland secretion
inferredcites →https://doi.org/10.1016/0034-5687(94)90040-xopenalex-snapshot
Tachykinins induce a [Ca2+]i rise in the acinar cells of feline tracheal submucosal gland
inferredcites →https://doi.org/10.1016/s0014-2999(99)00694-9openalex-snapshot
Effect of non-peptide tachykinin NK1 receptor antagonists on non-adrenergic, non-cholinergic neurogenic mucus secretion in ferret trachea
inferredcites →https://doi.org/10.1016/s0034-5687(00)00209-7openalex-snapshot
Motor control of airway goblet cells and glands
inferredcites →https://doi.org/10.1016/s0169-2607(01)00170-5openalex-snapshot
Computer assisted measurement of airway gland secretions by the hillocks technique
inferredcites →https://doi.org/10.1038/279551a0openalex-snapshot
Composition and control of secretions from tracheal bronchial submucosal glands
inferredcites →https://doi.org/10.1038/301421a0openalex-snapshot
Chloride impermeability in cystic fibrosis
inferredcites →https://doi.org/10.1038/352628a0openalex-snapshot
Phosphorylation-regulated CI− channel in CHO cells stably expressing the cystic fibrosis gene
inferredcites →https://doi.org/10.1038/labinvest.3780283openalex-snapshot
Expression and Distribution of Vasoactive Intestinal Polypeptide Receptor VPAC2 mRNA in Human Airways
inferredcites →https://doi.org/10.1038/ng1192-240openalex-snapshot
Submucosal glands are the predominant site of CFTR expression in the human bronchus
inferredcites →https://doi.org/10.1038/sj.bjp.0705029openalex-snapshot
Tachykinin NK3 and NK1 receptor activation elicits secretion from porcine airway submucosal glands
inferredcites →https://doi.org/10.1046/j.1469-7580.2000.19730361.xopenalex-snapshot
A comparative study of mammalian tracheal mucous glands
inferredcites →https://doi.org/10.1046/j.1469-7580.2001.19820207.xopenalex-snapshot
Distribution of tracheal and laryngeal mucous glands in some rodents and the rabbit
inferredcites →https://doi.org/10.1073/pnas.131087598openalex-snapshot
Submucosal gland secretions in airways from cystic fibrosis patients have normal [Na + ] and pH but elevated viscosity
inferredcites →https://doi.org/10.1073/pnas.241318498openalex-snapshot
Compartmentalized autocrine signaling to cystic fibrosis transmembrane conductance regulator at the apical membrane of airway epithelial cells
inferredcites →https://doi.org/10.1073/pnas.91.12.5340openalex-snapshot
Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator.
inferredcites →https://doi.org/10.1074/jbc.m107257200openalex-snapshot
Aquaporin-5 Dependent Fluid Secretion in Airway Submucosal Glands
inferredcites →https://doi.org/10.1074/jbc.m202712200openalex-snapshot
Mucus Secretion from Single Submucosal Glands of Pig
inferredcites →https://doi.org/10.1074/jbc.m208826200openalex-snapshot
Absent Secretion to Vasoactive Intestinal Peptide in Cystic Fibrosis Airway Glands
inferredcites →https://doi.org/10.1083/jcb.33.3.c7openalex-snapshot
HEXAGONAL ARRAY OF SUBUNITS IN INTERCELLULAR JUNCTIONS OF THE MOUSE HEART AND LIVER
inferredcites →https://doi.org/10.1085/jgp.113.5.743openalex-snapshot
Bicarbonate and Chloride Secretion in Calu-3 Human Airway Epithelial Cells
inferredcites →https://doi.org/10.1111/j.1469-7793.2003.00079.xopenalex-snapshot
Bicarbonate-dependent chloride secretion in Calu-3 epithelia in response to 7,8-benzoquinoline
inferredcites →https://doi.org/10.1111/j.1476-5381.1989.tb12665.xopenalex-snapshot
Receptors mediating the effects of substance P and neurokinin A on mucus secretion and smooth muscle tone of the ferret trachea: potentiation by an enkephalinase inhibitor
inferredcites →https://doi.org/10.1111/j.1476-5381.1991.tb12135.xopenalex-snapshot
The effects of calcitonin gene‐related peptide on submucosal gland secretion and epithelial albumin transport in the ferret trachea in vitro
inferredcites →https://doi.org/10.1111/j.1749-6632.1963.tb16665.xopenalex-snapshot
COMPARISON OF MUCUS GLANDS IN THE TRACHEOBRONCHIAL TREE OF MAN AND ANIMALS*
inferredcites →https://doi.org/10.1111/j.1749-6632.1996.tb17547.xopenalex-snapshot
Correlation of Vasoactive Intestinal Peptide and Nitric Oxide Synthase with Choline Acetyltransferase in the Airway Innervation
inferredcites →https://doi.org/10.1113/jphysiol.2001.012806openalex-snapshot
Regulation of intracellular pH in Calu‐3 human airway cells
inferredcites →https://doi.org/10.1113/jphysiol.2001.013300openalex-snapshot
Characterization of basolateral K+ channels underlying anion secretion in the human airway cell line Calu‐3
inferredcites →https://doi.org/10.1113/jphysiol.2002.030148openalex-snapshot
ATP release from human airway epithelial cells studied using a capillary cell culture system
inferredcites →https://doi.org/10.1113/jphysiol.2002.035923openalex-snapshot
Disruptive effects of Anion Secretion Inhibitors on Airway Mucus Morphology in Isolated Perfused Pig Lung
inferredcites →https://doi.org/10.1113/jphysiol.2003.046482openalex-snapshot
Bicarbonate-dependent chloride secretion in Calu-3 epithelia in response to 7,8-benzoquinoline
inferredcites →https://doi.org/10.1126/science.1712984openalex-snapshot
Demonstration That CFTR Is a Chloride Channel by Alteration of Its Anion Selectivity
inferredcites →https://doi.org/10.1126/science.2475911openalex-snapshot
Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
inferredcites →https://doi.org/10.1136/adc.51.1.82-aopenalex-snapshot
Perspectives in Pediatric Pathology
inferredcites →https://doi.org/10.1136/thx.24.6.729openalex-snapshot
A reconstruction of the duct system and secretory tubules of the human bronchial submucosal gland
inferredcites →https://doi.org/10.1152/ajpcell.1981.241.1.c25openalex-snapshot
Possible mechanisms of stimulus-induced vacuolation in serous cells of tracheal secretory glands
inferredcites →https://doi.org/10.1152/ajpcell.1995.269.2.c511openalex-snapshot
Relative expression of the human epithelial Na+ channel subunits in normal and cystic fibrosis airways
inferredcites →https://doi.org/10.1152/ajpcell.2000.279.4.c1016openalex-snapshot
Functional and molecular characterization of an anion exchanger in airway serous epithelial cells
inferredcites →https://doi.org/10.1152/ajplung.00277.2001openalex-snapshot
Liquid secretion inhibitors reduce mucociliary transport in glandular airways
inferredcites →https://doi.org/10.1152/ajplung.00348.2002openalex-snapshot
Secretion of acid and base equivalents by intact distal airways
inferredcites →https://doi.org/10.1152/ajplung.1990.258.2.l112openalex-snapshot
Sodium efflux from isolated submucosal gland in feline trachea
inferredcites →https://doi.org/10.1152/ajplung.1992.262.1.l86openalex-snapshot
Neutrophil elastase stimulates tracheal submucosal gland secretion that is inhibited by ICI 200,355
inferredcites →https://doi.org/10.1152/ajplung.1992.262.2.l223openalex-snapshot
Muscarinic receptor subtypes in feline tracheal submucosal gland secretion
inferredcites →https://doi.org/10.1152/ajplung.1993.265.2.l170openalex-snapshot
Calcium-dependent chloride secretion across cultures of human tracheal surface epithelium and glands
inferredcites →https://doi.org/10.1152/ajplung.1994.266.5.l493openalex-snapshot
Calu-3: a human airway epithelial cell line that shows cAMP-dependent Cl- secretion
inferredcites →https://doi.org/10.1152/ajplung.1994.266.5.l502openalex-snapshot
CFTR in Calu-3 human airway cells: channel properties and role in cAMP-activated Cl- conductance
inferredcites →https://doi.org/10.1152/ajplung.1994.267.2.l152openalex-snapshot
Apically localized IP3 receptors control chloride current in airway gland acinar cells
inferredcites →https://doi.org/10.1152/ajplung.1995.268.3.l526openalex-snapshot
Chloride secretion across distal airway epithelium: relationship to submucosal gland distribution
inferredcites →https://doi.org/10.1152/ajplung.1996.270.6.l979openalex-snapshot
P2u-purinoceptor regulation of chloride secretion in cultured human tracheal submucosal glands
inferredcites →https://doi.org/10.1152/ajplung.1997.272.2.l203openalex-snapshot
In situ visualization of bronchial submucosal glands and their secretory response to acetylcholine
inferredcites →https://doi.org/10.1152/ajplung.1997.272.2.l372openalex-snapshot
Effect of anion transport inhibition on mucus secretion by airway submucosal glands
inferredcites →https://doi.org/10.1152/ajplung.1997.273.6.l1208openalex-snapshot
Calcium-stimulated Cl−secretion in Calu-3 human airway cells requires CFTR
inferredcites →https://doi.org/10.1152/ajplung.1998.274.2.l258openalex-snapshot
Inhibition of airway liquid secretion and its effect on the physical properties of airway mucus
inferredcites →https://doi.org/10.1152/ajplung.1998.275.6.l1095openalex-snapshot
Acetylcholine-induced liquid secretion by bronchial epithelium: role of Cl− and HCO 3 − transport
inferredcites →https://doi.org/10.1152/ajplung.1999.277.4.l694openalex-snapshot
CFTR involvement in chloride, bicarbonate, and liquid secretion by airway submucosal glands
inferredcites →https://doi.org/10.1152/ajplung.2001.281.2.l458openalex-snapshot
Optical method for quantifying rates of mucus secretion from single submucosal glands
inferredcites →https://doi.org/10.1152/ajplung.2001.281.3.l639openalex-snapshot
Mechanism of substance P-induced liquid secretion across bronchial epithelium
inferredcites →https://doi.org/10.1152/ajplung.2002.282.1.l12openalex-snapshot
A2adenosine receptors regulate CFTR through PKA and PLA2
inferredcites →https://doi.org/10.1152/jappl.1980.49.6.1027openalex-snapshot
Adrenergic and cholinergic nerves mediate fluid secretion from tracheal glands of ferrets
inferredcites →https://doi.org/10.1152/jappl.1982.52.4.893openalex-snapshot
Regional effects of autonomic agents on ion transport across excised canine airways
inferredcites →https://doi.org/10.1152/jappl.1982.53.4.985openalex-snapshot
Reflex tracheal gland secretion evoked by stimulation of bronchial C-fibers in dogs
inferredcites →https://doi.org/10.1152/jappl.1986.60.4.1237openalex-snapshot
Contractility of isolated single submucosal gland from trachea
inferredcites →https://doi.org/10.1152/jappl.1987.62.6.2404openalex-snapshot
Neural control of contraction in isolated submucosal gland from feline trachea
inferredcites →https://doi.org/10.1152/jappl.1988.65.4.1891openalex-snapshot
Acetylcholine-stimulated chloride flux in tracheal submucosal gland cells
inferredcites →https://doi.org/10.1152/jappl.1995.78.5.1651openalex-snapshot
Effect of hypoxia on reflex responses of tracheal submucosal glands
inferredcites →https://doi.org/10.1152/japplphysiol.00174.2002openalex-snapshot
Effects of ion transport inhibitors on MCh-mediated secretion from porcine airway submucosal glands
inferredcites →https://doi.org/10.1152/physrev.1999.79.1.s3openalex-snapshot
Physiological Basis of Cystic Fibrosis: A Historical Perspective
inferredcites →https://doi.org/10.1159/000350071openalex-snapshot
Therapy of CF-Patients with Amitriptyline and Placebo - a Randomised, Double-Blind, Placebo-Controlled Phase IIb Multicenter, Cohort-Study
inferredcites →https://doi.org/10.1164/arrd.1971.103.6.774openalex-snapshot
A comparative study of four methods of assessing the morphologic changes in chronic bronchitis.
inferredcites →https://doi.org/10.1164/arrd.1980.121.2.351openalex-snapshot
Micropipette measurement of airway submucosal gland secretion. Autonomic effects.
inferredcites →https://doi.org/10.1165/ajrcmb.20.6.3475openalex-snapshot
Murine Submucosal Glands Are Clonally Derived and Show a Cystic Fibrosis Gene–Dependent Distribution Pattern
inferredcites →https://doi.org/10.1165/ajrcmb.24.3.4367openalex-snapshot
Expression and Localization of Epithelial Aquaporins in the Adult Human Lung
inferredcites →https://doi.org/10.1165/ajrcmb/2.1.41openalex-snapshot
Human Tracheobronchial Submucosal Gland Cells in Culture
inferredcites →https://doi.org/10.1177/30.9.6813372openalex-snapshot
Immunocytochemical demonstration of carbonic anhydrase in human epithelial cells.
inferredcites →https://doi.org/10.1183/09031936.93.06020169openalex-snapshot
Localization of the cystic fibrosis transmembrane conductance regulator in airway secretory glands
inferredcites →https://doi.org/10.1542/peds.4.1.53openalex-snapshot
THE PATHOGENESIS OF FIBROCYSTIC DISEASE OF THE PANCREAS
inferredcites →https://doi.org/10.3109/00016487609120896openalex-snapshot
Mucous Elements in the Airways
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/0471142956.cy1228s60openalex-snapshot
Live Imaging of the Lung
inferred← citeshttps://doi.org/10.1002/ppul.20183openalex-snapshot
Cystic fibrosis and airway submucosal glands
inferred← citeshttps://doi.org/10.1007/978-1-4419-9745-6_1openalex-snapshot
Macro- and Microstructure of the Airways for Drug Delivery
inferred← citeshttps://doi.org/10.1007/978-94-024-1057-0_4openalex-snapshot
Aquaporins and Gland Secretion
inferred← citeshttps://doi.org/10.1007/978-981-19-7415-1_16openalex-snapshot
Aquaporins in Glandular Secretion
inferred← citeshttps://doi.org/10.1007/s00424-008-0527-0openalex-snapshot
Substance P stimulates CFTR-dependent fluid secretion by mouse tracheal submucosal glands
inferred← citeshttps://doi.org/10.1007/s12011-025-04630-0openalex-snapshot
Effect of NiCl2 Intake Through Respiratory Tract on Antioxidant Capacity, Lung, and Trace Element Content in Mice
inferred← citeshttps://doi.org/10.1007/s12551-012-0068-9openalex-snapshot
CFTR–SLC26 transporter interactions in epithelia
inferred← citeshttps://doi.org/10.1016/b978-0-323-48063-5.00001-0openalex-snapshot
Nanotechnologies for early diagnosis, in situ disease monitoring, and prevention
inferred← citeshttps://doi.org/10.1016/j.applthermaleng.2021.117265openalex-snapshot
Design of membrane humidifier using obstacles in the flow channels for ventilator
inferred← citeshttps://doi.org/10.1016/j.autneu.2007.01.008openalex-snapshot
Parasympathetic control of airway submucosal glands: Central reflexes and the airway intrinsic nervous system
inferred← citeshttps://doi.org/10.1016/j.bbrc.2004.05.101openalex-snapshot
Regulation of apical surface fluid and protein secretion in human airway epithelial cell line Calu-3
inferred← citeshttps://doi.org/10.1016/j.biomaterials.2024.122546openalex-snapshot
A functional 3D full-thickness model for comprehending the interaction between airway epithelium and connective tissue in cystic fibrosis
inferred← citeshttps://doi.org/10.1016/j.ceca.2014.02.001openalex-snapshot
Ca2+ signaling and fluid secretion by secretory cells of the airway epithelium
inferred← citeshttps://doi.org/10.1016/j.icheatmasstransfer.2022.105931openalex-snapshot
Numerical modeling of a membrane humidifier for mechanical ventilation
inferred← citeshttps://doi.org/10.1016/j.jconrel.2015.09.047openalex-snapshot
Respiratory nanoparticle-based vaccines and challenges associated with animal models and translation
inferred← citeshttps://doi.org/10.1016/j.morpho.2018.11.001openalex-snapshot
Update on the cellular and molecular aspects of cystic fibrosis transmembrane conductance regulator (CFTR) and male fertility
inferred← citeshttps://doi.org/10.1016/j.resp.2007.06.005openalex-snapshot
Liquid movement across the surface epithelium of large airways
inferred← citeshttps://doi.org/10.1016/j.resp.2007.06.017openalex-snapshot
Fluid secretion by submucosal glands of the tracheobronchial airways
inferred← citeshttps://doi.org/10.1016/j.suc.2011.06.001openalex-snapshot
Nutritional Considerations in Adult Cardiothoracic Surgical Patients
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2016.04.057openalex-snapshot
Lessons learned from the cystic fibrosis pig
inferred← citeshttps://doi.org/10.1016/s0070-2153(04)64003-8openalex-snapshot
Airway Glandular Development and Stem Cells
inferred← citeshttps://doi.org/10.1017/cbo9781139018760.004openalex-snapshot
The normal lung: histology, embryology, development, aging and function
inferred← citeshttps://doi.org/10.1038/s41467-017-00835-7openalex-snapshot
Cystic fibrosis swine fail to secrete airway surface liquid in response to inhalation of pathogens
inferred← citeshttps://doi.org/10.1073/pnas.2119759119openalex-snapshot
Cellular and molecular architecture of submucosal glands in wild-type and cystic fibrosis pigs
inferred← citeshttps://doi.org/10.1074/jbc.m111.266734openalex-snapshot
Novel Role for Pendrin in Orchestrating Bicarbonate Secretion in Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-expressing Airway Serous Cells
inferred← citeshttps://doi.org/10.1074/jbc.m112.412817openalex-snapshot
Why Mouse Airway Submucosal Gland Serous Cells Do Not Secrete Fluid in Response to cAMP Stimulation
inferred← citeshttps://doi.org/10.1074/jbc.m512766200openalex-snapshot
Hyposecretion, Not Hyperabsorption, Is the Basic Defect of Cystic Fibrosis Airway Glands
inferred← citeshttps://doi.org/10.1085/jgp.200810017openalex-snapshot
HCO3− Secretion by Murine Nasal Submucosal Gland Serous Acinar Cells during Ca2+-stimulated Fluid Secretion
inferred← citeshttps://doi.org/10.1088/1752-7163/ad7a9aopenalex-snapshot
Exhaled breath condensate (EBC) in respiratory diseases: recent advances and future perspectives in the age of omic sciences
inferred← citeshttps://doi.org/10.1091/mbc.e04-11-1010openalex-snapshot
Characterization of Wild-Type and ΔF508 Cystic Fibrosis Transmembrane Regulator in Human Respiratory Epithelia
inferred← citeshttps://doi.org/10.1101/cshperspect.a009589openalex-snapshot
CFTR, Mucins, and Mucus Obstruction in Cystic Fibrosis
inferred← citeshttps://doi.org/10.1111/bph.12085openalex-snapshot
Protein phosphatase 1 coordinates CFTR ‐dependent airway epithelial HCO3 − secretion by reciprocal regulation of apical and basolateral membrane Cl −‐ HCO3 − exchangers
inferred← citeshttps://doi.org/10.1111/j.1748-1716.2011.02253.xopenalex-snapshot
Anion secretion by a model epithelium: more lessons from Calu‐3
inferred← citeshttps://doi.org/10.1113/ep087221openalex-snapshot
TLR7 agonist attenuates acetylcholine‐induced, Ca2+‐dependent ionic currents in swine tracheal submucosal gland cells
inferred← citeshttps://doi.org/10.1113/jphysiol.2006.123653openalex-snapshot
Mucus secretion by single tracheal submucosal glands from normal and cystic fibrosis transmembrane conductance regulator knockout mice
inferred← citeshttps://doi.org/10.1113/jphysiol.2007.131995openalex-snapshot
Optical imaging of Ca2+‐evoked fluid secretion by murine nasal submucosal gland serous acinar cells
inferred← citeshttps://doi.org/10.1113/jphysiol.2007.135855openalex-snapshot
SLC26A9 is a Cl− channel regulated by the WNK kinases
inferred← citeshttps://doi.org/10.1113/jphysiol.2012.236919openalex-snapshot
Basolateral chloride loading by the anion exchanger type 2: role in fluid secretion by the human airway epithelial cell line Calu‐3
inferred← citeshttps://doi.org/10.1124/jpet.105.088542openalex-snapshot
Prostanoids Secreted by Alveolar Macrophages Enhance Ionic Currents in Swine Tracheal Submucosal Gland Cells
inferred← citeshttps://doi.org/10.1124/jpet.107.120154openalex-snapshot
Prostaglandin E2 Enhances Acetylcholine-Induced, Ca2+-Dependent Ionic Currents in Swine Tracheal Mucous Gland Cells
inferred← citeshttps://doi.org/10.1126/science.1255825openalex-snapshot
Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis
inferred← citeshttps://doi.org/10.1139/y05-112openalex-snapshot
Expression of the chloride channel CLC-K in human airway epithelial cells
inferred← citeshttps://doi.org/10.1139/y09-009openalex-snapshot
Volume regulation in the human airway epithelial cell line Calu-3
inferred← citeshttps://doi.org/10.1146/annurev-physiol-021113-170331openalex-snapshot
Live Imaging of the Lung
inferred← citeshttps://doi.org/10.1146/annurev.med.58.071905.105316openalex-snapshot
Airway Surface Dehydration in Cystic Fibrosis: Pathogenesis and Therapy
inferred← citeshttps://doi.org/10.1148/rg.230136openalex-snapshot
2021 WHO Classification of Lung Cancer: Molecular Biology Research and Radiologic-Pathologic Correlation
inferred← citeshttps://doi.org/10.1152/ajpcell.00341.2018openalex-snapshot
Oxidative stress, autophagy and airway ion transport
inferred← citeshttps://doi.org/10.1152/ajpcell.00379.2005openalex-snapshot
Hyperacidity of secreted fluid from submucosal glands in early cystic fibrosis
inferred← citeshttps://doi.org/10.1152/ajpcell.00525.2005openalex-snapshot
Acid in the airways. Focus on “Hyperacidity of secreted fluid from submucosal glands in early cystic fibrosis”
inferred← citeshttps://doi.org/10.1152/ajpcell.00605.2005openalex-snapshot
Innate immune response in CF airway epithelia: hyperinflammatory?
inferred← citeshttps://doi.org/10.1152/ajplung.00009.2014openalex-snapshot
Mucociliary clearance and submucosal gland secretion in the ex vivo ferret trachea
inferred← citeshttps://doi.org/10.1152/ajplung.00053.2013openalex-snapshot
Flagellin/TLR5 signaling potentiates airway serous secretion from swine tracheal submucosal glands
inferred← citeshttps://doi.org/10.1152/ajplung.00056.2013openalex-snapshot
Protein composition of bronchoalveolar lavage fluid and airway surface liquid from newborn pigs
inferred← citeshttps://doi.org/10.1152/ajplung.00085.2009openalex-snapshot
Airway surface liquid depth measured in ex vivo fragments of pig and human trachea: dependence on Na+ and Cl− channel function
inferred← citeshttps://doi.org/10.1152/ajplung.00143.2012openalex-snapshot
Mucociliary transport in porcine trachea: differential effects of inhibiting chloride and bicarbonate secretion
inferred← citeshttps://doi.org/10.1152/ajplung.00159.2005openalex-snapshot
Ionic mechanism of forskolin-induced liquid secretion by porcine bronchi
inferred← citeshttps://doi.org/10.1152/ajplung.00253.2009openalex-snapshot
Effects of secretagogues on net and unidirectional liquid fluxes across porcine bronchial airways
inferred← citeshttps://doi.org/10.1152/ajplung.00342.2009openalex-snapshot
Mechanisms of Ca2+-stimulated fluid secretion by porcine bronchial submucosal gland serous acinar cells
inferred← citeshttps://doi.org/10.1152/ajplung.00372.2010openalex-snapshot
Properties of substance P-stimulated mucus secretion from porcine tracheal submucosal glands
inferred← citeshttps://doi.org/10.1152/ajplung.00388.2010openalex-snapshot
Mucous solids and liquid secretion by airways: studies with normal pig, cystic fibrosis human, and non-cystic fibrosis human bronchi
inferred← citeshttps://doi.org/10.1152/ajplung.00411.2020openalex-snapshot
PAR-2-activated secretion by airway gland serous cells: role for CFTR and inhibition byPseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1152/ajplung.90203.2008openalex-snapshot
The porcine lung as a potential model for cystic fibrosis
inferred← citeshttps://doi.org/10.1152/ajplung.90292.2008openalex-snapshot
Flagellin-stimulated Cl− secretion and innate immune responses in airway epithelia: role for p38
inferred← citeshttps://doi.org/10.1155/2014/715434openalex-snapshot
Humidification during Mechanical Ventilation in the Adult Patient
inferred← citeshttps://doi.org/10.1159/000087235openalex-snapshot
Characterization of Novel Airway Submucosal Gland Cell Models for Cystic Fibrosis
inferred← citeshttps://doi.org/10.1164/rccm.200506-987ocopenalex-snapshot
Ion and Fluid Transport Properties of Small Airways in Cystic Fibrosis
inferred← citeshttps://doi.org/10.1165/rcmb.2005-0059ocopenalex-snapshot
Lysozyme Secretion by Submucosal Glands Protects the Airway from Bacterial Infection
inferred← citeshttps://doi.org/10.1165/rcmb.2006-0286ocopenalex-snapshot
Bioelectric Properties of Chloride Channels in Human, Pig, Ferret, and Mouse Airway Epithelia
inferred← citeshttps://doi.org/10.1165/rcmb.2006-0347ocopenalex-snapshot
Chloride-Dependent Secretion of Alveolar Wall Liquid Determined by Optical-Sectioning Microscopy
inferred← citeshttps://doi.org/10.1165/rcmb.2008-0240ocopenalex-snapshot
Differential Gene Expression in Human Conducting Airway Surface Epithelia and Submucosal Glands
inferred← citeshttps://doi.org/10.1165/rcmb.2013-0453tropenalex-snapshot
Anatomy and Bronchoscopy of the Porcine Lung. A Model for Translational Respiratory Medicine
inferred← citeshttps://doi.org/10.1165/rcmb.2015-0090ocopenalex-snapshot
Glandular Proteome Identifies Antiprotease Cystatin C as a Critical Modulator of Airway Hydration and Clearance
inferred← citeshttps://doi.org/10.1165/rcmb.2015-0238rcopenalex-snapshot
Site of Fluid Secretion in Small Airways
inferred← citeshttps://doi.org/10.1165/rcmb.2018-0158ocopenalex-snapshot
Pendrin Mediates Bicarbonate Secretion and Enhances Cystic Fibrosis Transmembrane Conductance Regulator Function in Airway Surface Epithelia
inferred← citeshttps://doi.org/10.1172/jci.insight.89752openalex-snapshot
Defective postsecretory maturation of MUC5B mucin in cystic fibrosis airways
inferred← citeshttps://doi.org/10.1172/jci37284openalex-snapshot
Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process
inferred← citeshttps://doi.org/10.1183/13993003.01386-2019openalex-snapshot
Neuropeptide regulation of secretion and inflammation in human airway gland serous cells
inferred← citeshttps://doi.org/10.1186/s12890-016-0339-5openalex-snapshot
Cystic fibrosis lung environment and Pseudomonas aeruginosa infection
inferred← citeshttps://doi.org/10.1371/journal.pone.0007591openalex-snapshot
Enhanced Edar Signalling Has Pleiotropic Effects on Craniofacial and Cutaneous Glands
inferred← citeshttps://doi.org/10.1371/journal.pone.0024424openalex-snapshot
Defective Fluid Secretion from Submucosal Glands of Nasal Turbinates from CFTR-/- and CFTRΔF508/ΔF508 Pigs
inferred← citeshttps://doi.org/10.1513/pats.200801-003awopenalex-snapshot
The Glandular Stem/Progenitor Cell Niche in Airway Development and Repair
inferred← citeshttps://doi.org/10.17077/etd.3ijtk1ftopenalex-snapshot
Innate immune responses in the lung and liver
inferred← citeshttps://doi.org/10.17077/etd.9hpirtqhopenalex-snapshot
Augmenting antiviral host defense in the respiratory epithelium
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1508610/v1openalex-snapshot
Effects of different anesthetic depths monitored by Narcotrend on glandular secretion in patients undergoing laparoscopic total hysterectomy
inferred← citeshttps://doi.org/10.2174/1874306401509010104openalex-snapshot
Humidification on Ventilated Patients: Heated Humidifications or Heat and Moisture Exchangers?
inferred← citeshttps://doi.org/10.3389/fanes.2023.1237970openalex-snapshot
Effects of different anesthetic depths monitored by processed EEG analysis on glandular secretion in patients undergoing laparoscopic total hysterectomy
inferred← citeshttps://doi.org/10.3389/fchem.2017.00040openalex-snapshot
D-BMAP18 Antimicrobial Peptide Is Active In vitro, Resists to Pulmonary Proteases but Loses Its Activity in a Murine Model of Pseudomonas aeruginosa Lung Infection
inferred← citeshttps://doi.org/10.35366/55381openalex-snapshot
Manejo integral del paciente con traqueostomía
inferred← citeshttps://doi.org/10.4161/tisb.24997openalex-snapshot
Barrier function of airway tract epithelium
inferred← citeshttps://doi.org/10.5772/52342openalex-snapshot
Cystic Fibrosis: Does CFTR Malfunction Alter pH Regulation?
inferred← citeshttps://doi.org/10.5772/55650openalex-snapshot
Placenta-Derived Stem Cells as a Source for Treatment of Lung and Liver Disease in Cystic Fibrosis
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