Salt and fluid absorption and secretion are two processes that are fundamental to epithelial function and whole body fluid homeostasis, and as such are tightly regulated in epithelial tissues. The CFTR anion channel plays a major role in regulating both secretion and absorption in a diverse range of epithelial tissues, including the airways, the GI and reproductive tracts, sweat and salivary glands. It is not surprising then that defects in CFTR function are linked to disease, including life-threatening secretory diarrhoeas, such as cholera, as well as the inherited disease, cystic fibrosis (CF), one of the most common life-limiting genetic diseases in Caucasian populations. More recently, CFTR dysfunction has also been implicated in the pa...
Sinonasal respiratory epithelium is a highly regulated barrier that employs mucociliary clearance (M...
Many cystic fibrosis transmembrane conductance regulator (CFTR)-expressing epithelia secrete bicarbo...
The cystic fibrosis transmembrane conductance regulator (CFTR) belongs to the family of ATP binding ...
International audienceSalt and fluid absorption and secretion are two processes that are fundamental...
is a cAMP-activated chloride and bicarbonate channel that is critical for lung homeostasis. Decrease...
Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in a gene encoding a protein...
The cystic fibrosis conductance regulator CFTR gene is found on chromosome 7 (Kerem et al., 1989; Ri...
Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in a gene encoding a protein...
Salt and fluid absorption is a shared function of many of the body’s epithelia, but its use is highl...
Cystic fibrosis is a hereditary disease that mainly affects secretory organs in humans. It is caused...
Dysfunction of CFTR in cystic fibrosis (CF) airway epithelium perturbs the normal regulation of ion ...
The secretory epithelia of the pancreatic duct and airway share the ability to generate HCO3--rich f...
Cystic fibrosis (CF) is a multi-organ autosomal recessive disease of fluid-transporting epithelia, d...
This review examines of the concept of a defective chloride channel in epithelial cells being a majo...
Chronic obstructive pulmonary disease (COPD) manifests with a variety of clinical presentations, ref...
Sinonasal respiratory epithelium is a highly regulated barrier that employs mucociliary clearance (M...
Many cystic fibrosis transmembrane conductance regulator (CFTR)-expressing epithelia secrete bicarbo...
The cystic fibrosis transmembrane conductance regulator (CFTR) belongs to the family of ATP binding ...
International audienceSalt and fluid absorption and secretion are two processes that are fundamental...
is a cAMP-activated chloride and bicarbonate channel that is critical for lung homeostasis. Decrease...
Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in a gene encoding a protein...
The cystic fibrosis conductance regulator CFTR gene is found on chromosome 7 (Kerem et al., 1989; Ri...
Cystic fibrosis (CF) is a recessive genetic disease caused by mutations in a gene encoding a protein...
Salt and fluid absorption is a shared function of many of the body’s epithelia, but its use is highl...
Cystic fibrosis is a hereditary disease that mainly affects secretory organs in humans. It is caused...
Dysfunction of CFTR in cystic fibrosis (CF) airway epithelium perturbs the normal regulation of ion ...
The secretory epithelia of the pancreatic duct and airway share the ability to generate HCO3--rich f...
Cystic fibrosis (CF) is a multi-organ autosomal recessive disease of fluid-transporting epithelia, d...
This review examines of the concept of a defective chloride channel in epithelial cells being a majo...
Chronic obstructive pulmonary disease (COPD) manifests with a variety of clinical presentations, ref...
Sinonasal respiratory epithelium is a highly regulated barrier that employs mucociliary clearance (M...
Many cystic fibrosis transmembrane conductance regulator (CFTR)-expressing epithelia secrete bicarbo...
The cystic fibrosis transmembrane conductance regulator (CFTR) belongs to the family of ATP binding ...