Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis ; volume:9 ; number:1 ; day:24 ; month:4 ; year:2019 ; pages:1-11 ; date:12.2019
Scientific reports ; 9, Heft 1 (24.4.2019), 1-11, 12.2019

Classification: Naturwissenschaften

Creator: Simonin, Juliette
Bille, Emmanuelle
Crambert, Gilles
Noel, Sabrina
Dreano, Elise
Edwards, Aurélie
Hatton, Aurélie
Pranke, Iwona
Villeret, Bérengère
Cottart, Charles-Henry
Vrel, Jean-Patrick
Urbach, Valérie
Baatallah, Nesrine
Hinzpeter, Alexandre
Golec, Anita
Touqui, Lhousseine
Nassif, Xavier
Galietta, Luis J. V.
Planelles, Gabrielle
Sallenave, Jean-Michel
Edelman, Aleksander
Sermet-Gaudelus, Isabelle

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-019-42751-4

URN: urn:nbn:de:101:1-2019051323353458700648

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:51 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Simonin, Juliette
Bille, Emmanuelle
Crambert, Gilles
Noel, Sabrina
Dreano, Elise
Edwards, Aurélie
Hatton, Aurélie
Pranke, Iwona
Villeret, Bérengère
Cottart, Charles-Henry
Vrel, Jean-Patrick
Urbach, Valérie
Baatallah, Nesrine
Hinzpeter, Alexandre
Golec, Anita
Touqui, Lhousseine
Nassif, Xavier
Galietta, Luis J. V.
Planelles, Gabrielle
Sallenave, Jean-Michel
Edelman, Aleksander
Sermet-Gaudelus, Isabelle
SpringerLink (Online service)

Other Objects (12)

Regional analysis of airway abnormalities in cystic fibrosis employing Electrical Impedance Tomography

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

A Practical Approach to Glucose Abnormalities in Cystic Fibrosis

Airway disease phenotypes in animal models of cystic fibrosis

Bronchiectasis, Bulla and Ciliary Dyskinesia (Pulmonary Structural/Functional Airway Abnormalities)

Increased susceptibility of cystic fibrosis airway epithelial cells to ferroptosis

Quantitative imaging analysis detects subtle airway abnormalities in symptomatic military deployers

Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification

Longitudinal development of the airway microbiota in infants with cystic fibrosis

A longitudinal characterization of the Non-Cystic Fibrosis Bronchiectasis airway microbiome

The metabolic footprint of the airway bacterial community in cystic fibrosis

CREB-dependent LPA-induced signaling initiates a pro-fibrotic feedback loop between small airway basal cells and fibroblasts

Regional analysis of airway abnormalities in cystic fibrosis employing Electrical Impedance Tomography

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

A Practical Approach to Glucose Abnormalities in Cystic Fibrosis

Airway disease phenotypes in animal models of cystic fibrosis

Bronchiectasis, Bulla and Ciliary Dyskinesia (Pulmonary Structural/Functional Airway Abnormalities)

Increased susceptibility of cystic fibrosis airway epithelial cells to ferroptosis

Quantitative imaging analysis detects subtle airway abnormalities in symptomatic military deployers

Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification

Longitudinal development of the airway microbiota in infants with cystic fibrosis

A longitudinal characterization of the Non-Cystic Fibrosis Bronchiectasis airway microbiome

The metabolic footprint of the airway bacterial community in cystic fibrosis

CREB-dependent LPA-induced signaling initiates a pro-fibrotic feedback loop between small airway basal cells and fibroblasts

Regional analysis of airway abnormalities in cystic fibrosis employing Electrical Impedance Tomography

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

A Practical Approach to Glucose Abnormalities in Cystic Fibrosis

Airway disease phenotypes in animal models of cystic fibrosis

Bronchiectasis, Bulla and Ciliary Dyskinesia (Pulmonary Structural/Functional Airway Abnormalities)

Increased susceptibility of cystic fibrosis airway epithelial cells to ferroptosis

Quantitative imaging analysis detects subtle airway abnormalities in symptomatic military deployers

Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification

Longitudinal development of the airway microbiota in infants with cystic fibrosis

A longitudinal characterization of the Non-Cystic Fibrosis Bronchiectasis airway microbiome

The metabolic footprint of the airway bacterial community in cystic fibrosis

CREB-dependent LPA-induced signaling initiates a pro-fibrotic feedback loop between small airway basal cells and fibroblasts

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis

Object Details

References and Relationships

Classification and Topics

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Regional analysis of airway abnormalities in cystic fibrosis employing Electrical Impedance Tomography

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

A Practical Approach to Glucose Abnormalities in Cystic Fibrosis

Airway disease phenotypes in animal models of cystic fibrosis

Bronchiectasis, Bulla and Ciliary Dyskinesia (Pulmonary Structural/Functional Airway Abnormalities)

Increased susceptibility of cystic fibrosis airway epithelial cells to ferroptosis

Quantitative imaging analysis detects subtle airway abnormalities in symptomatic military deployers

Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification

Longitudinal development of the airway microbiota in infants with cystic fibrosis

A longitudinal characterization of the Non-Cystic Fibrosis Bronchiectasis airway microbiome

The metabolic footprint of the airway bacterial community in cystic fibrosis

CREB-dependent LPA-induced signaling initiates a pro-fibrotic feedback loop between small airway basal cells and fibroblasts

Regional analysis of airway abnormalities in cystic fibrosis employing Electrical Impedance Tomography

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

A Practical Approach to Glucose Abnormalities in Cystic Fibrosis

Airway disease phenotypes in animal models of cystic fibrosis

Bronchiectasis, Bulla and Ciliary Dyskinesia (Pulmonary Structural/Functional Airway Abnormalities)

Increased susceptibility of cystic fibrosis airway epithelial cells to ferroptosis

Quantitative imaging analysis detects subtle airway abnormalities in symptomatic military deployers

Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification

Longitudinal development of the airway microbiota in infants with cystic fibrosis

A longitudinal characterization of the Non-Cystic Fibrosis Bronchiectasis airway microbiome

The metabolic footprint of the airway bacterial community in cystic fibrosis

CREB-dependent LPA-induced signaling initiates a pro-fibrotic feedback loop between small airway basal cells and fibroblasts

Regional analysis of airway abnormalities in cystic fibrosis employing Electrical Impedance Tomography

Alteration of cystic airway mesenchyme in congenital pulmonary airway malformation

A Practical Approach to Glucose Abnormalities in Cystic Fibrosis

Airway disease phenotypes in animal models of cystic fibrosis

Bronchiectasis, Bulla and Ciliary Dyskinesia (Pulmonary Structural/Functional Airway Abnormalities)

Increased susceptibility of cystic fibrosis airway epithelial cells to ferroptosis

Quantitative imaging analysis detects subtle airway abnormalities in symptomatic military deployers

Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification

Longitudinal development of the airway microbiota in infants with cystic fibrosis

A longitudinal characterization of the Non-Cystic Fibrosis Bronchiectasis airway microbiome

The metabolic footprint of the airway bacterial community in cystic fibrosis

CREB-dependent LPA-induced signaling initiates a pro-fibrotic feedback loop between small airway basal cells and fibroblasts

Related objects

Reset password