A31 MECHANISMS IN CYSTIC FIBROSIS AND OTHER BRONCHIECTATIC DISEASES: Cystic Fibrosis Transmembrane C...
A31 MECHANISMS IN CYSTIC FIBROSIS AND OTHER BRONCHIECTATIC DISEASES: Cystic Fibrosis Transmembrane Conductance Regulator Channel (cftr) Controls Phosphatase And Tensin Homolog (pten)-Dependent Immunity: A Role In Cystic Fibrosis Pathology
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Full title
Author / Creator
Riquelme, S , Kitur, K , Hopkins, B , Wolfe, A , Parsons, R and Prince, A S
Publisher
New York: American Thoracic Society
Journal title
Language
English
Formats
Publication information
Publisher
New York: American Thoracic Society
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Scope and Contents
Contents
Rationale: Mutations that compromise protein levels, membrane expression or activity of the Cystic Fibrosis Transmembrane Conductance Regulator Channel (CFTR) result in progressive airway damage, recurrent bacterial infection and hyper-inflammation (Cystic Fibrosis, CF). Conclusions: Our results suggest that the inflammatory damage and the recurren...
Alternative Titles
Full title
A31 MECHANISMS IN CYSTIC FIBROSIS AND OTHER BRONCHIECTATIC DISEASES: Cystic Fibrosis Transmembrane Conductance Regulator Channel (cftr) Controls Phosphatase And Tensin Homolog (pten)-Dependent Immunity: A Role In Cystic Fibrosis Pathology
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Record Identifier
TN_cdi_proquest_journals_1926861490
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1926861490
Other Identifiers
ISSN
1073-449X
E-ISSN
1535-4970
