Defects of Secretion in Cystic Fibrosis /
| Autor Corporativo: | |
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| Otros Autores: | |
| Formato: | eBook |
| Lenguaje: | English |
| Publicado: |
New York, NY :
Springer US : Imprint: Springer,
2005.
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| Edición: | 1st ed. 2005. |
| Materias: |
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.