1 on with 40 mM potassium stimulated the PACAP secretory rate 10- to 20-fold, with concomitant increase

2 reparations, a threefold rise in the insulin secretory rate associated with increased amplitude of th

3 ned beta-cell secretory capacity and insulin secretory rates from glucose-potentiated arginine and mi

4 ne whether it is possible to obtain accurate secretory rates from the extended combined model, which

5 st 49 years of age (n = 15) (average insulin secretory rates: geometric mean [95% CI] 369 [209-652] v

6 racellular calcium levels ([Ca2+]i), and Cl- secretory rates (I(Cl-)) were quantitated in HNE cells i

7  (OCR), NAD(P)H, cytosolic Ca2+, and insulin secretory rate (ISR) were measured.

8 fect was assessed from ratios of the insulin secretory rates (ISR) during oral and isoglycemic glucos

9                                  The maximal secretory rate (nmol/min/g liver) for TC in the single p

10 roportion to Ca2+ influx with a mean initial secretory rate of 36 granule fusions s-1.

11    No abnormalities in the concentrations or secretory rates of 2 other major platelet granules, lyso

12  and have very slow passive, absorptive, and secretory rates of transport relative to transport rates

13 012), C-peptide (P = 0.004), and the insulin secretory rate (P = 0.020) compared with the control OGT

14 accurate but facile assessment of islet cell secretory rate, particularly in large group studies in w

15 gered vesicle exocytosis and accelerates its secretory rates, providing two independent, but synergis

16 nsulin had no inhibitory effect on C-peptide secretory rates under this condition.

17 acy and reliability of beta-adrenergic sweat secretory rates using an evaporimeter was assessed and c

18       C-peptide and, where possible, insulin secretory rates were measured.