Expression of S100A8 correlates with inflammatory lung disease in congenic mice deficient of the cystic fibrosis transmembrane conductance regulator
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1465-993X
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Expression of S100A8 correlates with inflammatory lung disease in congenic mice deficient of the cystic fibrosis transmembrane conductance regulator ; volume:7 ; number:1 ; day:29 ; month:3 ; year:2006 ; pages:1-11 ; date:12.2006
Respiratory research ; 7, Heft 1 (29.3.2006), 1-11, 12.2006
- Creator
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Tirkos, Sam
- Contributor
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Newbigging, Susan
Nguyen, Van
Keet, Mary
Ackerley, Cameron
Kent, Geraldine
Rozmahel, Richard F.
SpringerLink (Online service)
- DOI
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10.1186/1465-9921-7-51
- URN
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urn:nbn:de:1111-201606035918
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:53 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Tirkos, Sam
- Newbigging, Susan
- Nguyen, Van
- Keet, Mary
- Ackerley, Cameron
- Kent, Geraldine
- Rozmahel, Richard F.
- SpringerLink (Online service)
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Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function
A pathogenic role for cystic fibrosis transmembrane conductance regulator in celiac disease
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Molecular dynamics study of Cl− permeation through cystic fibrosis transmembrane conductance regulator (CFTR)
Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator
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Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Glycosylation and the cystic fibrosis transmembrane conductance regulator
The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function
A pathogenic role for cystic fibrosis transmembrane conductance regulator in celiac disease
Auswirkungen von Mutationen auf die Funktion von CFTR (Cystic fibrosis transmembrane conductance regulator)
Molecular dynamics study of Cl− permeation through cystic fibrosis transmembrane conductance regulator (CFTR)
Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator
Charakterisierung der Interaktionen des CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) mit PDZ-Domänen-Proteinen
Lack of correlation between pulmonary disease and cystic fibrosis transmembrane conductance regulator dysfunction in cystic fibrosis: a case report
Kontrolle epithelialer Ionenkanäle duch Cystic fibrosis transmembrane conductance regulator (CFTR) und Beitrag anderer regulatorischer Proteine
Sphingosine-1-Phosphate is a novel regulator of cystic fibrosis transmembrane conductance regulator (CFTR) activity
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Glycosylation and the cystic fibrosis transmembrane conductance regulator
The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function
A pathogenic role for cystic fibrosis transmembrane conductance regulator in celiac disease
Auswirkungen von Mutationen auf die Funktion von CFTR (Cystic fibrosis transmembrane conductance regulator)
Molecular dynamics study of Cl− permeation through cystic fibrosis transmembrane conductance regulator (CFTR)
Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator
Charakterisierung der Interaktionen des CFTR (Cystic Fibrosis Transmembrane Conductance Regulator) mit PDZ-Domänen-Proteinen
Lack of correlation between pulmonary disease and cystic fibrosis transmembrane conductance regulator dysfunction in cystic fibrosis: a case report
Kontrolle epithelialer Ionenkanäle duch Cystic fibrosis transmembrane conductance regulator (CFTR) und Beitrag anderer regulatorischer Proteine