nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Alternative chloride transport pathways as pharmacological targets for the treatment of cystic fibrosis
|
Quesada, Roberto |
|
|
19 |
S1 |
p. S37-S41 |
artikel |
2 |
CFTR: New insights into structure and function and implications for modulation by small molecules
|
Kleizen, Bertrand |
|
|
19 |
S1 |
p. S19-S24 |
artikel |
3 |
CFTR processing, trafficking and interactions
|
Amaral, Margarida D. |
|
|
19 |
S1 |
p. S33-S36 |
artikel |
4 |
Editorial Board
|
|
|
|
19 |
S1 |
p. ii |
artikel |
5 |
Exploring the basic mechanisms in Cystic Fibrosis: Promoting data presentation and discussion at the 16th ECFS Basic Science Conference
|
Callebaut, Isabelle |
|
|
19 |
S1 |
p. S1-S4 |
artikel |
6 |
Genetic variation in CFTR and modifier loci may modulate cystic fibrosis disease severity
|
Paranjapye, Alekh |
|
|
19 |
S1 |
p. S10-S14 |
artikel |
7 |
Interplay between host-microbe and microbe-microbe interactions in cystic fibrosis
|
Armbruster, Catherine R. |
|
|
19 |
S1 |
p. S47-S53 |
artikel |
8 |
Intestinal organoids for Cystic Fibrosis research
|
de Poel, E. |
|
|
19 |
S1 |
p. S60-S64 |
artikel |
9 |
New approaches to genetic therapies for cystic fibrosis
|
Christopher Boyd, A. |
|
|
19 |
S1 |
p. S54-S59 |
artikel |
10 |
Regeneration of airway epithelial cells to study rare cell states in cystic fibrosis
|
Barbry, Pascal |
|
|
19 |
S1 |
p. S42-S46 |
artikel |
11 |
The genetics and genomics of cystic fibrosis
|
Sharma, N. |
|
|
19 |
S1 |
p. S5-S9 |
artikel |
12 |
The influence of CFTR complex alleles on precision therapy of cystic fibrosis
|
Chevalier, Benoit |
|
|
19 |
S1 |
p. S15-S18 |
artikel |
13 |
Towards next generation therapies for cystic fibrosis: Folding, function and pharmacology of CFTR
|
Bose, Samuel J. |
|
|
19 |
S1 |
p. S25-S32 |
artikel |