Sökning: "Cystisk fibros"
Visar resultat 6 - 10 av 13 avhandlingar innehållade orden Cystisk fibros.
6. Advances in Pharmacological Treatment of Cystic Fibrosis
Sammanfattning : Cystic fibrosis (CF) is an inborn, hereditary disease, due to mutations in the gene for a cAMP-activated chloride (Cl-) channel, the cystic fibrosis transmembrane conductance regulator (CFTR). As a result of impaired ion and water transport,the airway mucus is abnormally viscous, which leads to bacterial colonization. LÄS MER
7. Midkine - a host defence protein
Sammanfattning : Every day we encounter many potentially harmful microbes in our environment. The epithelial linings constitute an anatomical barrier protecting us and they also produce antimicrobial polypeptides (AMPs) that act as a chemical barrier. These AMPs are small and positively charged, killing a broad range of microbes rapidly. LÄS MER
8. Aiway Mucins: experimental models for studies of secretions
Sammanfattning : Mucins are essential components of the mucosal barrier. The complexity of the airway mucosal barrier is reflected in the lack of specific treatments to block mucin hypersecretion associated with several respiratory diseases such as chronic bronchitis, asthma and cystic fibrosis. LÄS MER
9. Microbial biofilms on peritoneal dialysis catheters
Sammanfattning : Då njurarna slutar fungera produceras ingen urin, och avfallsprodukterna stannar kvar i blodet. Detta tillstånd kallas uremi (”urin i blodet”) och leder till döden om det inte behandlas. Det finns två artificiella sätt att rena blodet på, hemodialys och peritonealdialys. LÄS MER
10. The role of exocrine pancreas for feed intake and growth. Studies in a model with exocrine pancreatic insufficient young pigs
Sammanfattning : Exocrine pancreatic insufficiency (EPI), resulting from disease (e.g. cystic fibrosis, chronic pancreatitis) or surgery (e.g. LÄS MER