UB Paderborn / Katalog / Suche / in CDI

Airway Gland Structure and Function

Physiological reviews, 2015-10, Vol.95 (4), p.1241-1319

2015

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Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809

Proceedings of the National Academy of Sciences - PNAS, 2011-11, Vol.108 (46), p.18843-18848

2011

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Variation in CFTR-dependent 'β-sweating' among healthy adults

PloS one, 2022-03, Vol.17 (3), p.e0265432-e0265432

2022

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Disease phenotype of a ferret CFTR-knockout model of cystic fibrosis

The Journal of clinical investigation, 2010-09, Vol.120 (9), p.3149-3160

2010

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Parasympathetic control of airway submucosal glands: Central reflexes and the airway intrinsic nervous system

Autonomic neuroscience, 2007-04, Vol.133 (1), p.35-54

Wine, Jeffrey J

2007

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Evaporimeter and Bubble-Imaging Measures of Sweat Gland Secretion Rates

PloS one, 2016-10, Vol.11 (10), p.e0165254-e0165254

2016

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Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs

The Journal of clinical investigation, 2010-09, Vol.120 (9), p.3161-3166

2010

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Proteomic analysis of pure human airway gland mucus reveals a large component of protective proteins

PloS one, 2015-02, Vol.10 (2), p.e0116756-e0116756

2015

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Combined agonists act synergistically to increase mucociliary clearance in a cystic fibrosis airway model

Scientific reports, 2021-09, Vol.11 (1), p.18828-18828, Article 18828

2021

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In vivo readout of CFTR function: ratiometric measurement of CFTR-dependent secretion by individual, identifiable human sweat glands

PloS one, 2013-10, Vol.8 (10), p.e77114

2013

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A little CFTR goes a long way: CFTR-dependent sweat secretion from G551D and R117H-5T cystic fibrosis subjects taking ivacaftor

PloS one, 2014-02, Vol.9 (2), p.e88564

2014

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The magnitude of ivacaftor effects on fluid secretion via R117H-CFTR channels: Human in vivo measurements

PloS one, 2017-04, Vol.12 (4), p.e0175486-e0175486

2017

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How the sweat gland reveals levels of CFTR activity

Journal of cystic fibrosis, 2022-05, Vol.21 (3), p.396-406

Wine, Jeffrey J.

2022

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The development of lung disease in cystic fibrosis pigs

Science translational medicine, 2010-04, Vol.2 (29), p.29ps20

Wine, Jeffrey J

2010

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Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease

PloS one, 2017, Vol.12 (12), p.e0189894-e0189894

2017

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Hyposecretion, Not Hyperabsorption, Is the Basic Defect of Cystic Fibrosis Airway Glands

The Journal of biological chemistry, 2006-03, Vol.281 (11), p.7392-7398

2006

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Mucus secretion from individual submucosal glands of the ferret trachea

American journal of physiology. Lung cellular and molecular physiology, 2010-07, Vol.299 (1), p.L124-L136

2010

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How to live a long and healthy life with cystic fibrosis: Lessons from the CF ferret

Journal of cystic fibrosis, 2019-01, Vol.18 (1), p.8-9

Wine, Jeffrey J.

2019

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Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis

The Journal of clinical investigation, 2007-10, Vol.117 (10), p.3118-3127

2007

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Mucus secretion by single tracheal submucosal glands from normal and cystic fibrosis transmembrane conductance regulator knockout mice

The Journal of physiology, 2007-04, Vol.580 (1), p.301-314

2007

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Submucosal Gland Secretions in Airways from Cystic Fibrosis Patients Have Normal [Na+]and pH but Elevated Viscosity

Proceedings of the National Academy of Sciences - PNAS, 2001-07, Vol.98 (14), p.8119-8123

2001

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The normal trachea is cleaned by MUC5B mucin bundles from the submucosal glands coated with the MUC5AC mucin

Biochemical and biophysical research communications, 2017-10, Vol.492 (3), p.331-337

2017

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Measuring mucociliary transport and mucus properties in multiple regions of airway epithelial surfaces helps clarify cystic fibrosis defects

American journal of respiratory and critical care medicine, 2014-08, Vol.190 (4), p.364-365

Wine, Jeffrey J

2014

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Medicine. Letting go of mucus

Science (American Association for the Advancement of Science), 2014-08, Vol.345 (6198), p.730-731

Wine, Jeffrey J

2014

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Airway Gland Structure and Function

Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809

High-Efficiency, Selection-free Gene Repair in Airway Stem Cells from Cystic Fibrosis Patients Rescues CFTR Function in Differentiated Epithelia

Variation in CFTR-dependent 'β-sweating' among healthy adults

Disease phenotype of a ferret CFTR-knockout model of cystic fibrosis

Parasympathetic control of airway submucosal glands: Central reflexes and the airway intrinsic nervous system

Evaporimeter and Bubble-Imaging Measures of Sweat Gland Secretion Rates

Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs

Proteomic analysis of pure human airway gland mucus reveals a large component of protective proteins

Combined agonists act synergistically to increase mucociliary clearance in a cystic fibrosis airway model

In vivo readout of CFTR function: ratiometric measurement of CFTR-dependent secretion by individual, identifiable human sweat glands

A little CFTR goes a long way: CFTR-dependent sweat secretion from G551D and R117H-5T cystic fibrosis subjects taking ivacaftor

The magnitude of ivacaftor effects on fluid secretion via R117H-CFTR channels: Human in vivo measurements

How the sweat gland reveals levels of CFTR activity

The development of lung disease in cystic fibrosis pigs

Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease

Hyposecretion, Not Hyperabsorption, Is the Basic Defect of Cystic Fibrosis Airway Glands

Mucus secretion from individual submucosal glands of the ferret trachea

How to live a long and healthy life with cystic fibrosis: Lessons from the CF ferret

Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis

Mucus secretion by single tracheal submucosal glands from normal and cystic fibrosis transmembrane conductance regulator knockout mice

Submucosal Gland Secretions in Airways from Cystic Fibrosis Patients Have Normal [Na+]and pH but Elevated Viscosity

The normal trachea is cleaned by MUC5B mucin bundles from the submucosal glands coated with the MUC5AC mucin

Measuring mucociliary transport and mucus properties in multiple regions of airway epithelial surfaces helps clarify cystic fibrosis defects

Medicine. Letting go of mucus

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