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Cystic fibrosis and airway submucosal glands

https://doi.org/10.1002/ppul.20183
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ajmg.1320280420openalex-snapshot
Pathological confirmation of cystic fibrosis in the fetus following prenatal diagnosis
inferredcites →https://doi.org/10.1006/taap.1996.0179openalex-snapshot
Cocaine Inhibits Chloride Secretion by Swine Tracheal Submucosal Gland Cells Grown in Culture
inferredcites →https://doi.org/10.1007/bf00234174openalex-snapshot
The distribution and structure of cells in the tracheal epithelium of the mouse
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/s0034-5687(00)00209-7openalex-snapshot
Motor control of airway goblet cells and glands
inferredcites →https://doi.org/10.1016/s0092-8674(00)81724-9openalex-snapshot
Evidence for Periciliary Liquid Layer Depletion, Not Abnormal Ion Composition, in the Pathogenesis of Cystic Fibrosis Airways Disease
inferredcites →https://doi.org/10.1016/s1569-9048(02)00118-0openalex-snapshot
Differential effect of epidermal growth factor on serous and mucous cells in porcine airway submucosal gland
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/ng1192-240openalex-snapshot
Submucosal glands are the predominant site of CFTR expression in the human bronchus
inferredcites →https://doi.org/10.1038/nm1028openalex-snapshot
Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice
inferredcites →https://doi.org/10.1063/1.339474openalex-snapshot
High-density magnetic recording: Theory and practical considerations
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/10.1074/jbc.m405367200openalex-snapshot
Nucleotide Release Provides a Mechanism for Airway Surface Liquid Homeostasis
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/10.1085/jgp.118.2.223openalex-snapshot
The Relative Roles of Passive Surface Forces and Active Ion Transport in the Modulation of Airway Surface Liquid Volume and Composition
inferredcites →https://doi.org/10.1093/hmg/6.13.2191openalex-snapshot
Towards an ovine model of cystic fibrosis
inferredcites →https://doi.org/10.1096/fj.03-1248fjeopenalex-snapshot
A small molecule CFTR inhibitor produces cystic fibrosis‐like submucosal gland fluid secretions in normal airways
inferredcites →https://doi.org/10.1111/j.1469-7793.1997.637bm.xopenalex-snapshot
Fluid transport across cultures of human tracheal glands is altered in cystic fibrosis
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.2003.052779openalex-snapshot
Liquid secretion properties of airway submucosal glands
inferredcites →https://doi.org/10.1126/science.2772657openalex-snapshot
Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
inferredcites →https://doi.org/10.1126/science.8211164openalex-snapshot
Altered Fluid Transport Across Airway Epithelium in Cystic Fibrosis
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.00417.2002openalex-snapshot
Role of airway surface liquid and submucosal glands in cystic fibrosis lung disease
inferredcites →https://doi.org/10.1152/ajpcell.1989.256.4.c893openalex-snapshot
Na+ and Cl- transport across rabbit nonciliated bronchiolar epithelial (Clara) cells
inferredcites →https://doi.org/10.1152/ajpcell.1997.272.1.c203openalex-snapshot
Reduced Mg2+ inhibition of Ca2+ release in muscle fibers of pigs susceptible to malignant hyperthermia
inferredcites →https://doi.org/10.1152/ajpcell.1997.273.5.c1562openalex-snapshot
Aqp1 expression in erythroleukemia cells: genetic regulation of glucocorticoid and chemical induction
inferredcites →https://doi.org/10.1152/ajpcell.1998.275.4.c1095openalex-snapshot
Minor role of a Ca2+-depleted sarcoplasmic reticulum in heterologous desensitization of smooth muscle to K+
inferredcites →https://doi.org/10.1152/ajpcell.2000.279.6.c1925openalex-snapshot
Properties of CFTR activated by the xanthine derivative X-33 in human airway Calu-3 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.00326.2003openalex-snapshot
Secretion of lactoferrin and lysozyme by cultures of human airway epithelium
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.1991.261.6.l485openalex-snapshot
Ion transport by cultures of human tracheobronchial submucosal glands
inferredcites →https://doi.org/10.1152/ajplung.1991.261.6.l491openalex-snapshot
Altered ion transport by tracheal glands in cystic fibrosis
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.1994.267.1.l79openalex-snapshot
Bioelectric properties of proximal bronchiolar epithelium
inferredcites →https://doi.org/10.1152/ajplung.1994.267.2.l206openalex-snapshot
Chloride secretion and function of serous and mucous cells of human airway glands
inferredcites →https://doi.org/10.1152/ajplung.1996.270.2.l289openalex-snapshot
Regulation of ion transport across porcine distal bronchi
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.1998.274.5.l762openalex-snapshot
Effect of anion secretion inhibitors on mucin content of airway submucosal gland ducts
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/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/10.1164/ajrccm.150.2.8049852openalex-snapshot
Human Airway Ion Transport. Part Two
inferredcites →https://doi.org/10.1164/ajrccm.153.6.8665037openalex-snapshot
Effect of Uridine 5'-Triphosphate Plus Amiloride on Mucociliary Clearance in Adult Cystic Fibrosis
inferredcites →https://doi.org/10.1164/ajrccm/141.5_pt_1.1280openalex-snapshot
Culture and Characterization of Human Tracheal Gland Cells
inferredcites →https://doi.org/10.1164/arrd.1968.98.3.449openalex-snapshot
A hypothesis for pulmonary clearance and its implications.
inferredcites →https://doi.org/10.1165/ajrcmb.24.2.3918openalex-snapshot
New Models of the Tracheal Airway Define the Glandular Contribution to Airway Surface Fluid and Electrolyte Composition
inferredcites →https://doi.org/10.1165/ajrcmb/2.1.41openalex-snapshot
Human Tracheobronchial Submucosal Gland Cells in Culture
inferredcites →https://doi.org/10.1165/rcmb.2003-0109ocopenalex-snapshot
The Role of the Basolateral Outwardly Rectifying Chloride Channel in Human Airway Epithelial Anion Secretion
inferredcites →https://doi.org/10.1172/jci111385openalex-snapshot
Defective beta adrenergic response of cystic fibrosis sweat glands in vivo and in vitro.
inferredcites →https://doi.org/10.1172/jci2687openalex-snapshot
Coordinated clearance of periciliary liquid and mucus from airway surfaces.
inferredcites →https://doi.org/10.1542/peds.4.1.53openalex-snapshot
THE PATHOGENESIS OF FIBROCYSTIC DISEASE OF THE PANCREAS
inferredcites →https://doi.org/10.3109/10520299109109965openalex-snapshot
Preservation of Tracheal Mucus by Nonaqueous Fixative
inferredcites →https://doi.org/10.3109/15513818409041187openalex-snapshot
Scanning Electron Microscopic Study of the Airways in Normal Children and in Patients with Cystic Fibrosis and Other Lung Diseases

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4656875openalex-extracted
inferred← citeshttps://doi.org/10.1002/ppul.20690openalex-snapshot
Evolution of CFTR protein distribution in lung tissue from normal and CF human fetuses
inferred← citeshttps://doi.org/10.1002/ppul.21154openalex-snapshot
Cystic fibrosis lung disease starts in the small airways: Can we treat it more effectively?
inferred← citeshttps://doi.org/10.1007/978-0-387-84841-9_4openalex-snapshot
Emerging Issues in Pulmonary Infections of Cystic Fibrosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-374001-4.00016-xopenalex-snapshot
Epithelial Cells
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.ecoenv.2024.117318openalex-snapshot
Alteration of growth performance and characterization of pathological lesions in long-term ammonia-exposed pigs
inferred← citeshttps://doi.org/10.1016/j.molmed.2007.05.001openalex-snapshot
Cystic fibrosis: a disease of vulnerability to airway surface dehydration
inferred← citeshttps://doi.org/10.1016/j.pccm.2026.05.001openalex-snapshot
Structural and cellular mechanisms of mucus plugging in the larger airways
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/10.1017/cbo9781139018760.006openalex-snapshot
Congenital abnormalities and pediatric lung diseases, including neoplasms
inferred← citeshttps://doi.org/10.1080/01926230601060025openalex-snapshot
Cystic Fibrosis and Other Respiratory Diseases of Impaired Mucus Clearance
inferred← citeshttps://doi.org/10.1111/j.1476-5381.2010.01137.xopenalex-snapshot
New horizons in the treatment of cystic fibrosis
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/10.1152/ajpcell.00379.2005openalex-snapshot
Hyperacidity of secreted fluid from submucosal glands in early cystic fibrosis
inferred← citeshttps://doi.org/10.1152/ajplung.00039.2007openalex-snapshot
A new tool to investigate differences between human SP-A1 and SP-A2
inferred← citeshttps://doi.org/10.1152/ajplung.00279.2024openalex-snapshot
CFTR-independent prostaglandin E 2 -stimulated chloride secretion in human airway
inferred← citeshttps://doi.org/10.1152/ajplung.90203.2008openalex-snapshot
The porcine lung as a potential model for cystic fibrosis
inferred← citeshttps://doi.org/10.1159/000295859openalex-snapshot
Cystic Fibrosis Transmembrane Conductance Regulator Can Export Hyaluronan
inferred← citeshttps://doi.org/10.1371/journal.pbio.3000675openalex-snapshot
SCRINSHOT enables spatial mapping of cell states in tissue sections with single-cell resolution
inferred← citeshttps://doi.org/10.1371/journal.pone.0005357openalex-snapshot
New Microbicidal Functions of Tracheal Glands: Defective Anti-Infectious Response to Pseudomonas aeruginosa in Cystic Fibrosis
inferred← citeshttps://doi.org/10.2353/ajpath.2010.090849openalex-snapshot
Pathology of Gastrointestinal Organs in a Porcine Model of Cystic Fibrosis
inferred← citeshttps://doi.org/10.3109/15376516.2013.879504openalex-snapshot
Tiotropium bromide suppresses smoke inhalation and burn injury-induced ERK 1/2 and SMAD 2/3 signaling in sheep bronchial submucosal glands
inferred← citeshttps://doi.org/10.3390/cells9061371openalex-snapshot
Intrinsic Abnormalities of Cystic Fibrosis Airway Connective Tissue Revealed by an In Vitro 3D Stromal Model
inferred← citeshttps://doi.org/10.3390/ijms25031933openalex-snapshot
Mucus Structure, Viscoelastic Properties, and Composition in Chronic Respiratory Diseases
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