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Defects of Secretion in Cystic Fibrosis
Defects in Secretion of Cystic Fibrosis presents an overview on current research from leading experts in North America and Europe. This update on cystic fibrosis provides in depth original work as well as review material on many of the relevant physiological and molecular topics in the field. Subjec...
| Clasificación: | Libro Electrónico |
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| Autor Corporativo: | |
| Otros Autores: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
New York, NY :
Springer US : Imprint: Springer,
2005.
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| Edición: | 1st ed. 2005. |
| Temas: | |
| Acceso en línea: | Texto Completo |
Tabla de Contenidos:
- Outside Neurons/Inside Epithelia: Novel Activation of CFTR Cl? and HCO3 ? Conductances
- Role of CFTR and Other Ion Channels in Cystic Fibrosis
- Ion Channels in the Apical Membrane: Role of Electrical Coupling on Transepithelial Transport
- Ion Channels in Secretory Granules of the Pancreas: Molecular Identification and Their Role in Regulated Secretion
- Epithelial Transport and Intracellular Trafficking: Physiology and Pathophysiology
- Kinases, Cell Volume, and the Regulation of Chloride Channels
- The CLCAs: Proteins with Ion Channel, Cell Adhesion and Tumor Suppressor Functions
- Is Intervention in Inositol Phosphate Signaling a Useful Therapeutic Option for Cystic Fibrosis?
- An Inositol Phosphate Analog, INO-4995, Normalizes Electrophysiology in CF Airway Epithelia
- Vitamin C and Flavonoids Potentiate CFTR Cl Transport in Human Airway Epithelia
- Airway Glycoconjugates Secreted in Cystic Fibrosis and Severe Chronic Airway Inflammation Relationship with Pseudomonas aeruginosa
- Biosynthesis and Secretion of Mucins, Especially the MUC2 Mucin, in Relation to Cystic Fibrosis.