Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs. - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q34090231

about

Understanding protein kinase CK2 mis-regulation upon F508del CFTR expression Origins of cystic fibrosis lung disease Airway Gland Structure and Function Marked increases in mucociliary clearance produced by synergistic secretory agonists or inhibition of the epithelial sodium channel.A little CFTR goes a long way: CFTR-dependent sweat secretion from G551D and R117H-5T cystic fibrosis subjects taking ivacaftor Mechanism and synergism in epithelial fluid and electrolyte secretion.cAMP and Ca²⁺ signaling in secretory epithelia: crosstalk and synergism.Gel-forming mucins form distinct morphologic structures in airways Distribution and size of mucous glands in the ferret tracheobronchial tree.Defective fluid secretion from submucosal glands of nasal turbinates from CFTR-/- and CFTR (ΔF508/ΔF508) pigs.Pseudomonas aeruginosa triggers CFTR-mediated airway surface liquid secretion in swine trachea.Genetic therapies for cystic fibrosis lung disease CGRP induction in cystic fibrosis airways alters the submucosal gland progenitor cell niche in mice.Proteomic analysis of pure human airway gland mucus reveals a large component of protective proteins.The magnitude of ivacaftor effects on fluid secretion via R117H-CFTR channels: Human in vivo measurements Acidic pH increases airway surface liquid viscosity in cystic fibrosis New animal models of cystic fibrosis: what are they teaching us?Glandular Proteome Identifies Antiprotease Cystatin C as a Critical Modulator of Airway Hydration and Clearance.Lessons learned from the cystic fibrosis pig.Protein composition of bronchoalveolar lavage fluid and airway surface liquid from newborn pigs.Tachykinins and their receptors: contributions to physiological control and the mechanisms of disease.The secret life of CFTR as a calcium-activated chloride channel.Cystic Fibrosis and the Nervous System.Role of tyrosine phosphorylation in the muscarinic activation of the cystic fibrosis transmembrane conductance regulator (CFTR).Protein phosphatase 1 coordinates CFTR-dependent airway epithelial HCO3- secretion by reciprocal regulation of apical and basolateral membrane Cl(-)-HCO3- exchangers Novel role for pendrin in orchestrating bicarbonate secretion in cystic fibrosis transmembrane conductance regulator (CFTR)-expressing airway serous cells.Acute intratracheal Pseudomonas aeruginosa infection in cystic fibrosis mice is age-independent.Why mouse airway submucosal gland serous cells do not secrete fluid in response to cAMP stimulation.Transgenic animals may help resolve a sticky situation in cystic fibrosis.Roadmap for an early gene therapy for cystic fibrosis airway disease.Cystic fibrosis swine fail to secrete airway surface liquid in response to inhalation of pathogens.Mucociliary clearance and submucosal gland secretion in the ex vivo ferret trachea.Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.Flagellin/TLR5 signaling potentiates airway serous secretion from swine tracheal submucosal glands.Measuring mucociliary transport and mucus properties in multiple regions of airway epithelial surfaces helps clarify cystic fibrosis defects.The cytokines interleukin-1β and tumor necrosis factor-α stimulate CFTR-mediated fluid secretion by swine airway submucosal glands.Medicine. Letting go of mucus.Toll-like receptor 4 potentiates Ca2+-dependent secretion of electrolytes from swine tracheal glands.New insights into the mechanisms controlling the bronchial mucus balance.Sweat rate analysis of ivacaftor potentiation of CFTR in non-CF adults

P2860

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P2860

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

http://www.wikidata.org/entity/Q34090231

description

2010 nî lūn-bûn

@nan

2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

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

@ast

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

@en

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

@nl

type

label

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

@ast

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

@en

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

@nl

prefLabel

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

@ast

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

@en

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

@nl

P1433

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P2860

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P1433

Journal of Clinical Investigation

P1476

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

@en

P2093

Hyung-Ju Cho

http://www.w3.org/2001/XMLSchema#string

Jeffrey J Wine

http://www.w3.org/2001/XMLSchema#string

Monal Khansaheb

http://www.w3.org/2001/XMLSchema#string

Nam Soo Joo

http://www.w3.org/2001/XMLSchema#string

P2860

A novel host defense system of airways is defective in cystic fibrosis

The lactoperoxidase system links anion transport to host defense in cystic fibrosis

Cystic fibrosis

Production of CFTR-null and CFTR-DeltaF508 heterozygous pigs by adeno-associated virus-mediated gene targeting and somatic cell nuclear transfer

Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process.

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

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

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

Submucosal glands and airway defense.

Submucosal gland secretions in airways from cystic fibrosis patients have normal [Na(+)] and pH but elevated viscosity

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3161-3166

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10.1172/JCI43466

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9

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120

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2010-08-25T00:00:00Z

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20739758

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2929738

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