Differential epithelial expression of the putative innate immune molecule SPLUNC1 in Cystic Fibrosis
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1465-993X
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Differential epithelial expression of the putative innate immune molecule SPLUNC1 in Cystic Fibrosis ; volume:8 ; number:1 ; day:07 ; month:11 ; year:2007 ; pages:1-10 ; date:12.2007
Respiratory research ; 8, Heft 1 (07.11.2007), 1-10, 12.2007
- Urheber
-
Bingle, Lynne
- Beteiligte Personen und Organisationen
-
Barnes, Frances A.
Cross, Simon S.
Rassl, Doris
Wallace, William A.
Campos, Michael A.
Bingle, Colin D.
SpringerLink (Online service)
- DOI
-
10.1186/1465-9921-8-79
- URN
-
urn:nbn:de:1111-201606038503
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:54 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Bingle, Lynne
- Barnes, Frances A.
- Cross, Simon S.
- Rassl, Doris
- Wallace, William A.
- Campos, Michael A.
- Bingle, Colin D.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Cystic fibrosis
Dysregulated signalling pathways in innate immune cells with cystic fibrosis mutations
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Comparative microbiome analysis in cystic fibrosis and non-cystic fibrosis bronchiectasis
Neutrophils in cystic fibrosis
Calprotectin in Cystic Fibrosis
Characterization of human blood type-2 innate lymphoid cells in cystic fibrosis lung disease
Gene therapy-emulating small molecule treatments in cystic fibrosis airway epithelial cells and patients
Cystic fibrosis and physical activity
Stenotrophomonas maltophilia in cystic fibrosis
Nontuberculous Mycobacteria in Cystic Fibrosis
Diagnosing Cystic Fibrosis in Adults
Cystic fibrosis
Dysregulated signalling pathways in innate immune cells with cystic fibrosis mutations
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Comparative microbiome analysis in cystic fibrosis and non-cystic fibrosis bronchiectasis
Neutrophils in cystic fibrosis
Calprotectin in Cystic Fibrosis
Characterization of human blood type-2 innate lymphoid cells in cystic fibrosis lung disease
Gene therapy-emulating small molecule treatments in cystic fibrosis airway epithelial cells and patients
Cystic fibrosis and physical activity
Stenotrophomonas maltophilia in cystic fibrosis
Nontuberculous Mycobacteria in Cystic Fibrosis
Diagnosing Cystic Fibrosis in Adults
Cystic fibrosis
Dysregulated signalling pathways in innate immune cells with cystic fibrosis mutations
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Comparative microbiome analysis in cystic fibrosis and non-cystic fibrosis bronchiectasis
Neutrophils in cystic fibrosis
Calprotectin in Cystic Fibrosis
Characterization of human blood type-2 innate lymphoid cells in cystic fibrosis lung disease
Gene therapy-emulating small molecule treatments in cystic fibrosis airway epithelial cells and patients
Cystic fibrosis and physical activity
Stenotrophomonas maltophilia in cystic fibrosis
Nontuberculous Mycobacteria in Cystic Fibrosis