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Airway Epithelium Dysfunction in Cystic Fibrosis and COPD

Airway Epithelium Dysfunction in Cystic Fibrosis and COPD

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_449956d8f973454b92325d8327f1d624

Airway Epithelium Dysfunction in Cystic Fibrosis and COPD

About this item

Full title

Airway Epithelium Dysfunction in Cystic Fibrosis and COPD

Publisher

Cairo, Egypt: Hindawi Publishing Corporation

Journal title

Mediators of inflammation, 2018-01, Vol.2018 (2018), p.1-20

Language

English

Formats

Publication information

Publisher

Cairo, Egypt: Hindawi Publishing Corporation

More information

Scope and Contents

Contents

Cystic fibrosis is a genetic disease caused by mutations in the CFTR gene, whereas chronic obstructive pulmonary disease (COPD) is mainly caused by environmental factors (mostly cigarette smoking) on a genetically susceptible background. Although the etiology and pathogenesis of these diseases are different, both are associated with progressive air...

Alternative Titles

Full title

Airway Epithelium Dysfunction in Cystic Fibrosis and COPD

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_449956d8f973454b92325d8327f1d624

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_449956d8f973454b92325d8327f1d624

Other Identifiers

ISSN

0962-9351,1466-1861

E-ISSN

1466-1861

DOI

10.1155/2018/1309746

How to access this item