TY  - JOUR 
AU  - Gianotti, Ambra
AU  - Capurro, Valeria
AU  - Delpiano, Livia
AU  - Mielczarek, Marcin
AU  - García Valverde, María
AU  - Carreira Barral, Israel
AU  - Ludovico, Alessandra
AU  - Fiore, Michele
AU  - Baroni, Debora
AU  - Moran, Óscar
AU  - Quesada Pato, Roberto
AU  - Caci, Emanuela
PY  - 2020
SN  - 1422-0067
UR  - http://hdl.handle.net/10259/8329
AB  - Cystic fibrosis (CF) is a genetic disease characterized by the lack of cystic fibrosis transmembrane conductance regulator (CFTR) protein expressed in epithelial cells. The resulting defective chloride and bicarbonate secretion and imbalance of the...
LA  - eng
PB  - MDPI
KW  - Cystic fibrosis
KW  - Anionophore
KW  - Bronchial epithelial cells culture
KW  - Ion transport
KW  - Periciliar mucus properties
KW  - Medicina
KW  - Medicine
KW  - Salud
KW  - Health
KW  - Química orgánica
KW  - Chemistry, Organic
TI  - Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia
DO  - 10.3390/ijms21041488
T2  - International Journal of Molecular Sciences
VL  - 21
M2  - 1488
ER  -