nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Biosynthesis of cystic fibrosis transmembrane conductance regulator
|
Pranke, Iwona M. |
|
2014 |
52 |
C |
p. 26-38 13 p. |
artikel |
2 |
CFTR structure and cystic fibrosis
|
Cant, Natasha |
|
2014 |
52 |
C |
p. 15-25 11 p. |
artikel |
3 |
Current concepts of immune dysregulation in cystic fibrosis
|
Rieber, N. |
|
2014 |
52 |
C |
p. 108-112 5 p. |
artikel |
4 |
Cx26 regulates proliferation of repairing basal airway epithelial cells
|
Crespin, S. |
|
2014 |
52 |
C |
p. 152-160 9 p. |
artikel |
5 |
Cystic fibrosis, a multi-systemic mucosal disease: 25 years after the discovery of CFTR
|
Edelman, Aleksander |
|
2014 |
52 |
C |
p. 2-4 3 p. |
artikel |
6 |
Cystic fibrosis: An inherited disease affecting mucin-producing organs
|
Ehre, Camille |
|
2014 |
52 |
C |
p. 136-145 10 p. |
artikel |
7 |
Cystic fibrosis: Evidence for gut inflammation
|
Munck, Anne |
|
2014 |
52 |
C |
p. 180-183 4 p. |
artikel |
8 |
Cystic fibrosis: From a single gene to complex pathophysiology
|
Kargul, Joanna |
|
2014 |
52 |
C |
p. 1- 1 p. |
artikel |
9 |
Cystic fibrosis: Toward personalized therapies
|
Ikpa, Pauline T. |
|
2014 |
52 |
C |
p. 192-200 9 p. |
artikel |
10 |
Cytoskeleton and CFTR
|
Edelman, Aleksander |
|
2014 |
52 |
C |
p. 68-72 5 p. |
artikel |
11 |
Early cystic fibrosis lung disease: Role of airway surface dehydration and lessons from preventive rehydration therapies in mice
|
Mall, Marcus A. |
|
2014 |
52 |
C |
p. 174-179 6 p. |
artikel |
12 |
Editorial board
|
|
|
2014 |
52 |
C |
p. CO2- 1 p. |
artikel |
13 |
Effects of airway surface liquid pH on host defense in cystic fibrosis
|
Berkebile, Abigail R. |
|
2014 |
52 |
C |
p. 124-129 6 p. |
artikel |
14 |
Functional interaction of the cystic fibrosis transmembrane conductance regulator with members of the SLC26 family of anion transporters (SLC26A8 and SLC26A9): Physiological and pathophysiological relevance
|
El Khouri, Elma |
|
2014 |
52 |
C |
p. 58-67 10 p. |
artikel |
15 |
Fungi in the cystic fibrosis lung: Bystanders or pathogens?
|
Chotirmall, Sanjay H. |
|
2014 |
52 |
C |
p. 161-173 13 p. |
artikel |
16 |
Genetics of cystic fibrosis: CFTR mutation classifications toward genotype-based CF therapies
|
Fanen, Pascale |
|
2014 |
52 |
C |
p. 94-102 9 p. |
artikel |
17 |
Gerd Döring
|
Quinton, Paul M. |
|
2014 |
52 |
C |
p. 5-6 2 p. |
artikel |
18 |
Localized lipidomics in cystic fibrosis: TOF-SIMS imaging of lungs from Pseudomonas aeruginosa-infected mice
|
Desbenoit, Nicolas |
|
2014 |
52 |
C |
p. 77-82 6 p. |
artikel |
19 |
Long noncoding RNA are aberrantly expressed in vivo in the cystic fibrosis bronchial epithelium
|
McKiernan, Paul J. |
|
2014 |
52 |
C |
p. 184-191 8 p. |
artikel |
20 |
Lung disease modifier genes in cystic fibrosis
|
Guillot, Loic |
|
2014 |
52 |
C |
p. 83-93 11 p. |
artikel |
21 |
Mammalian short palate lung and nasal epithelial clone 1 (SPLUNC1) in pH-dependent airway hydration
|
Tarran, Robert |
|
2014 |
52 |
C |
p. 130-135 6 p. |
artikel |
22 |
Molecular modelling approaches for cystic fibrosis transmembrane conductance regulator studies
|
Odolczyk, Norbert |
|
2014 |
52 |
C |
p. 39-46 8 p. |
artikel |
23 |
On the structural organization of the intracellular domains of CFTR
|
Moran, Oscar |
|
2014 |
52 |
C |
p. 7-14 8 p. |
artikel |
24 |
Phagocytic and signaling innate immune receptors: are they dysregulated in cystic fibrosis in the fight against Pseudomonas aeruginosa?
|
Sallenave, Jean-Michel |
|
2014 |
52 |
C |
p. 103-107 5 p. |
artikel |
25 |
Redox balance in Cystic Fibrosis
|
Ziady, Assem G. |
|
2014 |
52 |
C |
p. 113-123 11 p. |
artikel |
26 |
The TMEM16A chloride channel as an alternative therapeutic target in cystic fibrosis
|
Sondo, Elvira |
|
2014 |
52 |
C |
p. 73-76 4 p. |
artikel |
27 |
TPL2 signalling: From Toll-like receptors-mediated ERK1/ERK2 activation to Cystic Fibrosis lung disease
|
Martel, Guy |
|
2014 |
52 |
C |
p. 146-151 6 p. |
artikel |
28 |
Understanding how cystic fibrosis mutations disrupt CFTR function: From single molecules to animal models
|
Wang, Yiting |
|
2014 |
52 |
C |
p. 47-57 11 p. |
artikel |