- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2156
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Very mild disease phenotype of congenic Cftr TgH(neoim)Hgu cystic fibrosis mice ; volume:9 ; number:1 ; day:09 ; month:4 ; year:2008 ; pages:1-11 ; date:12.2008
BMC genetics ; 9, Heft 1 (09.4.2008), 1-11, 12.2008
- Creator
-
Tóth, Balázs
- Contributor
-
Wilke, Martina
Stanke, Frauke
Dorsch, Martina
Jansen, Silke
Wedekind, Dirk
Charizopoulou, Nikoletta
Bot, Alice
Burmester, Marion
Leonhard-Marek, Sabine
de Jonge, Hugo R.
Hedrich, Hans-Jürgen
Breves, Gerhard
Tümmler, Burkhard
SpringerLink (Online service)
- DOI
-
10.1186/1471-2156-9-28
- URN
-
urn:nbn:de:1111-2016041532419
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:03 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
- Tóth, Balázs
- Wilke, Martina
- Stanke, Frauke
- Dorsch, Martina
- Jansen, Silke
- Wedekind, Dirk
- Charizopoulou, Nikoletta
- Bot, Alice
- Burmester, Marion
- Leonhard-Marek, Sabine
- de Jonge, Hugo R.
- Hedrich, Hans-Jürgen
- Breves, Gerhard
- Tümmler, Burkhard
- SpringerLink (Online service)
Other Objects (12)
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Instability of the insertional mutation in Cftr TgH(neoim)Hgu cystic fibrosis mouse model
Association between electrophysiological phenotype and genotype in the CftrTgH(neoim)Hgu mouse model
Genetic and phenotypic characterisation of the CftrTgH(neoim)Hgu cystic fibrosis mouse models : = Mausmodelle für die zystische Fibrose: geno- und phänotypische Charakterisierung der CftrTgH(neoim)Hgu-Mäusestämme
Genetic and phenotypic characterisation of the CftrTgH(neoim)Hgu cystic fibrosis mouse models : = Mausmodelle für die zystische Fibrose: geno- und phänotypische Charakterisierung der CftrTgH(neoim)Hgu-Mäusestämme
Targeted therapies to improve CFTR function in cystic fibrosis
The "Goldilocks Effect" in Cystic Fibrosis: identification of a lung phenotype in the cftr knockout and heterozygous mouse
The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability
Vectorized peptidic Inhibitors to rescue F508del-CFTR in Cystic Fibrosis
Lived experiences of individuals with cystic fibrosis on CFTR-modulators
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function
Manipulating proteostasis to repair the F508del-CFTR defect in cystic fibrosis
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Instability of the insertional mutation in Cftr TgH(neoim)Hgu cystic fibrosis mouse model
Association between electrophysiological phenotype and genotype in the CftrTgH(neoim)Hgu mouse model
Genetic and phenotypic characterisation of the CftrTgH(neoim)Hgu cystic fibrosis mouse models : = Mausmodelle für die zystische Fibrose: geno- und phänotypische Charakterisierung der CftrTgH(neoim)Hgu-Mäusestämme
Genetic and phenotypic characterisation of the CftrTgH(neoim)Hgu cystic fibrosis mouse models : = Mausmodelle für die zystische Fibrose: geno- und phänotypische Charakterisierung der CftrTgH(neoim)Hgu-Mäusestämme
Targeted therapies to improve CFTR function in cystic fibrosis
The "Goldilocks Effect" in Cystic Fibrosis: identification of a lung phenotype in the cftr knockout and heterozygous mouse
The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability
Vectorized peptidic Inhibitors to rescue F508del-CFTR in Cystic Fibrosis
Lived experiences of individuals with cystic fibrosis on CFTR-modulators
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function
Manipulating proteostasis to repair the F508del-CFTR defect in cystic fibrosis
Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis
Instability of the insertional mutation in Cftr TgH(neoim)Hgu cystic fibrosis mouse model
Association between electrophysiological phenotype and genotype in the CftrTgH(neoim)Hgu mouse model
Genetic and phenotypic characterisation of the CftrTgH(neoim)Hgu cystic fibrosis mouse models : = Mausmodelle für die zystische Fibrose: geno- und phänotypische Charakterisierung der CftrTgH(neoim)Hgu-Mäusestämme
Genetic and phenotypic characterisation of the CftrTgH(neoim)Hgu cystic fibrosis mouse models : = Mausmodelle für die zystische Fibrose: geno- und phänotypische Charakterisierung der CftrTgH(neoim)Hgu-Mäusestämme
Targeted therapies to improve CFTR function in cystic fibrosis
The "Goldilocks Effect" in Cystic Fibrosis: identification of a lung phenotype in the cftr knockout and heterozygous mouse
The cystic fibrosis transmembrane conductance regulator (CFTR) and its stability
Vectorized peptidic Inhibitors to rescue F508del-CFTR in Cystic Fibrosis
Lived experiences of individuals with cystic fibrosis on CFTR-modulators
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have differential effects on cystic fibrosis macrophage function