Search for dissertations about: "Anca Dragomir"

Found 4 swedish dissertations containing the words Anca Dragomir.

  1. 1. Assessment of chloride transport in epithelial cells with reference to cystic fibrosis

    Author : Anca Dragomir; Uppsala universitet; []
    Keywords : ;

    Abstract : .... READ MORE

  2. 2. Approaches to Pharmacological Treatment and Gene Therapy of Cystic Fibrosis

    Author : Anca Dragomir; Godfried M. Roomans; Robert Dormer; Uppsala universitet; []
    Keywords : MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; Anatomy; airway epithelium; colchicine; cystic fibrosis; chloride transport; genotype; heparin; phenotype; transfection; X-ray microanalysis; Anatomi; Anatomy; Anatomi;

    Abstract : Cystic fibrosis (CF) is the most common lethal genetic disease in the white population. It is due to mutations in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR), a protein that functions mainly as a cAMP-activated chloride channel. READ MORE

  3. 3. Studies on Airway Surface Liquid in Connection with Cystic Fibrosis

    Author : Inna Kozlova; Godfried Roomans; Anca Dragomir; Marieann Högman; Isabelle Sermet-Gaudelus; Uppsala universitet; []
    Keywords : NATURVETENSKAP; NATURAL SCIENCES; cystic fibrosis; CFTR; airway surface liquid; ion content; anesthesia; mist tent therapy; Pseudomonas aeruginosa infection; Cell biology; Cellbiologi;

    Abstract : Cystic fibrosis (CF) is one of the most common fatal inherited diseases, most prevalent among Caucasians. CF is caused by a mutation in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR), which helps to create sweat, digestive juices, and airway surface liquid (ASL). READ MORE

  4. 4. Studies of Tight Junctions and Airway Surface Liquid in Airway Epithelium with Relevance to Cystic Fibrosis

    Author : Harriet Nilsson; Godfried M Roomans; Anca Dragomir; Marie Johannesson; Olafur Baldurson; Uppsala universitet; []
    Keywords : ;

    Abstract : Cystic fibrosis (CF) is a multi-organ autosomal recessive disease of fluid-transporting epithelia, due to a mutation in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. CFTR is a cAMP-regulated Cl-channel involved in various regulatory processes. READ MORE