Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis-Reference-Cited by-同舟云学术

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Genetic variations in inflammatory mediators influence lung disease progression in cystic fibrosis

Published:2008-11-13 Issue:12 Volume:43 Page:1224-1232
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr. Pulmonol.

Author:

Corvol Harriet¹²³,Boelle Pierre‐Yves³⁴⁵,Brouard Jacques¹²⁶,Knauer Nicola¹²⁷,Chadelat Katarina¹²³,Henrion‐Caude Alexandra¹²³,Flamant Cyril¹²³,Muselet‐Charlier Celine¹²³,Boule Michele¹²³,Fauroux Brigitte¹²³,Vallet Christelle¹²³,Feingold Josue³⁸,Ratjen Felix⁷,Grasemann Hartmut⁷,Clement Annick¹²³

Affiliation:

1. AP‐HP, Hôpital Trousseau, Pediatric Pulmonary Department, Paris, France

2. Inserm, UMR‐S U893, Paris, France

3. Université Pierre et Marie Curie‐Paris6, Paris, France

4. AP‐HP, Hôpital St. Antoine, Biostatisitics Department, Paris, France

5. Inserm, UMR‐S U707, Paris, France

6. Department of Paediatrics, Georges Clemenceau Hospital, Caen, France

7. Children's Hospital, University of Duisburg‐Essen, Essen, Germany

8. AP‐HP, Hôpital Trousseau, Genetic Department, Paris, France

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology, and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.20935

Reference36 articles.

1. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

2. New concepts of the pathogenesis of cystic fibrosis lung disease

3. State of the Art: Why do the lungs of patients with cystic fibrosis become infected and why can't they clear the infection?

4. Cystic fibrosis

5. Distinct cytokine production by lung and blood neutrophils from children with cystic fibrosis

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3. Transforming Growth Factor ß1 and Gap Junction Protein Alpha 4 Gene Heterogeneity in Relation to the Severity of Clinical Disease in Cystic Fibrosis;Frontiers in Bioscience-Landmark;2023-07-19

4. IL1B gene variants, but not TNF, CXCL8, IL6 and IL10, modify the course of cystic fibrosis in Polish patients.;F1000Research;2022-11-22

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