Titlebook: Defects of Secretion in Cystic Fibrosis; Carsten Schultz Conference proceedings 2005 The Editor(s) (if applicable) and The Author(s), unde

值得赞赏

Ion Channels in the Apical Membrane: Role of Electrical Coupling on Transepithelial Transport,

唤醒

Ion Channels in Secretory Granules of the Pancreas: Molecular Identification and Their Role in Regu

摸索

相互影响

Kinases, Cell Volume, and the Regulation of Chloride Channels,

Infelicity

The CLCAs: Proteins with Ion Channel, Cell Adhesion and Tumor Suppressor Functions,

countenance

Conclave

Vitamin C and Flavonoids Potentiate CFTR Cl Transport in Human Airway Epithelia,

Ferritin

一小块

Nostalgia

Eileen K. Maziarz,John R. Perfectt on ATP hydrolysis. Evidence that these responses are properties of CFTR is derived from tissues from cystic fibrosis patients that show CFTR mutation (genotype) specific responses. The physiological role of glutamate activation remains to be defined, but we speculate that it may involve controls o