Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis. (Q42563377)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25124441%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

title

Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis (English)

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12 March 2020

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2

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12 March 2020

Lynda S Ostedgaard

4

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12 March 2020

Maged S Awadalla

6

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12 March 2020

Eric A Hoffman

9

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12 March 2020

Joseph Zabner

10

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12 March 2020

David Stoltz

11

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12 March 2020

author name string

Mark J Hoegger

1

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12 March 2020

James D McMenimen

3

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12 March 2020

Alex J Tucker

5

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12 March 2020

Thomas O Moninger

7

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12 March 2020

Andrew S Michalski

8

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12 March 2020

Michael J Welsh

12

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12 March 2020

language of work or name

English

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publication date

1 August 2014

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12 March 2020

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12 March 2020

volume

345

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12 March 2020

issue

6198

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12 March 2020

page(s)

818-822

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Assessing mucociliary transport of single particles in vivo shows variable speed and preference for the ventral trachea in newborn pigs

12 March 2020

cites work

1 reference

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Conditions associated with the cystic fibrosis defect promote chronic Pseudomonas aeruginosa infection

28 May 2018

1 reference

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The secret life of CFTR as a calcium-activated chloride channel

28 May 2018

1 reference

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Protein composition of bronchoalveolar lavage fluid and airway surface liquid from newborn pigs

28 May 2018

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Why mouse airway submucosal gland serous cells do not secrete fluid in response to cAMP stimulation.

28 May 2018

1 reference

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Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis lung

28 May 2018

1 reference

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Bicarbonate and functional CFTR channel are required for proper mucin secretion and link cystic fibrosis with its mucus phenotype.

28 May 2018

1 reference

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Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epithelia

28 May 2018

1 reference

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Airway mucus function and dysfunction

28 May 2018

1 reference

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Role of epithelial HCO3⁻ transport in mucin secretion: lessons from cystic fibrosis

28 May 2018

1 reference

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

28 May 2018

1 reference

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Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children

28 May 2018

1 reference

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Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth

28 May 2018

1 reference

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Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs

28 May 2018

1 reference

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Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis

28 May 2018

1 reference

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HCO3(-) secretion by murine nasal submucosal gland serous acinar cells during Ca2+-stimulated fluid secretion.

28 May 2018

1 reference

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Fluid secretion by submucosal glands of the tracheobronchial airways

28 May 2018

1 reference

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

28 May 2018

1 reference

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Evidence for airway surface dehydration as the initiating event in CF airway disease

28 May 2018

1 reference

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Submucosal glands and airway defense

28 May 2018

1 reference

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Liquid secretion properties of airway submucosal glands

28 May 2018

1 reference

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Mucociliary clearance in cystic fibrosis

28 May 2018

1 reference

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Evidence for periciliary liquid layer depletion, not abnormal ion composition, in the pathogenesis of cystic fibrosis airways disease

28 May 2018

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Calcium-stimulated Cl- secretion in Calu-3 human airway cells requires CFTR.

28 May 2018

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Heterogeneity of the composition and thickness of tracheal mucus in rats.

28 May 2018

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Mucociliary clearance in the airways

28 May 2018

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Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator

28 May 2018

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Quantification of periciliary fluid height in human airway biopsies is feasible, but not suitable as a biomarker

28 May 2018

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Normal nasal mucociliary clearance in CF children: evidence against a CFTR-related defect

16 August 2018

1 reference

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16 August 2018

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16 August 2018

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Submucosal glands are the predominant site of CFTR expression in the human bronchus

16 August 2018

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12 December 2020

Mucociliary clearance in patients with cystic fibrosis and in normal subjects

1 reference

12 December 2020

Acetylcholine-induced liquid secretion by bronchial epithelium: role of Cl- and HCO3- transport

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12 December 2020

Differences in disease expression between primary ciliary dyskinesia and cystic fibrosis with and without pancreatic insufficiency

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12 December 2020

Identifiers

DOI

10.1126/SCIENCE.1255825

1 reference

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12 March 2020

Fatcat ID

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mapped directly with Wikidata item

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12 March 2020

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