1 ic genetic manipulations show that lipid can overflow from adipose tissue and is taken up by renal ce

2 ens preparation differed from the pattern of overflow from chromaffin cells and there was also some t

3 nt sensitization by regulating dopamine (DA) overflow from DA neuron terminals in the nucleus accumbe

4 es were utilized to show differences in 5-HT overflow from ex vivo ileum and colon following exposure

5 lation of H(3)R or A(1)R reduced ischemic NE overflow from H(3)R(+/+) hearts by 50%, only A(1)R, but

6                                  Coronary NE overflow from hearts subjected to ischemia/reperfusion w

7                                          NPY overflow from isolated arterioles was assessed at 0 s an

8                  Accordingly, norepinephrine overflow from isolated guinea pig hearts undergoing 20-m

9 ispersal of bacteria in rainwater runoff and overflow from open sewer systems.

10 ogenase, which in turn is driven by fumarate overflow from purine nucleotide breakdown and partial re

11 ed to conduct multisite measurements of 5-HT overflow from the entire colon.

12 LA microelectrodes were able to monitor 5-HT overflow from the ex vivo ileum tissue.

13 l in the superfusate, representing adenosine overflow from the retinas, and the adenosine level in re

14 (DeltaAd) adipocytes and the resultant lipid overflow from WAT led to marked hepatosteatosis, dyslipi