1 cular, actin brush borders, and hampered the reabsorptive and filtrative capacities of these tubular

2 hereby causing dedifferentiation and loss of reabsorptive capacity of PT cells.

3 omerulus might be mediated by changes in the reabsorptive capacity of the tubule, which can affect th

4 t these channels may contribute to the fluid-reabsorptive driving force in adult lung.

5 s has a lower secretory portion and an upper reabsorptive duct leading to the secretory pore in the s

6 onchiolar epithelia and basolaterally in the reabsorptive duct of human sweat glands.

7 of sodium-coupled acid-base transport in the reabsorptive duct of the human eccrine sweat gland, whic

8  A was as much as eightfold greater than the reabsorptive flux, indicating that net secretion is the

9 a link to protein networks implicated in the reabsorptive function of the kidney and in the trafficki

10 transporting renal (Malpighian) tubules, the reabsorptive hindgut and the endocytic nephrocytes.

11 hese data suggest that several distal sodium reabsorptive mechanisms are upregulated during vasopress

12 ntified claudin-2 as constituting the cation-reabsorptive pathway in the proximal tubule; claudin-14,

13                                   This hyper reabsorptive phenotype was rescued upon crossing with RP

14 en cephaloridine and carnitine for the renal reabsorptive process.

15  in the secretory process, separate from the reabsorptive striated ducts.

16                   OSC are known to sustain a reabsorptive transepithelial current and to contain an i

17          The new Na+- dependent, active urea reabsorptive transport process may be a basolateral Na+-

18                  In IMCD1s, this active urea reabsorptive transport process was inhibited by: (i) 0.2

19                              The basolateral reabsorptive urate transporter GLUT9a appears to be the