ライフサイエンスコーパス: intraportally

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1 ong with 4x basal insulin and basal glucagon intraportally.

2 x basal) and glucagon (basal) were replaced intraportally.

3 ia with similar efficacy as grafts implanted intraportally.

4 ptidase IV+ Fischer 344 rats) were delivered intraportally (2 x 10(6) cells) into the liver of retror

5 was determined by examining the function of intraportally administered islet iso- and allografts by

6 8-Br-cGMP (50 microg/kg/min) was delivered intraportally, and either the glucose load to the liver

7 p), basal insulin and glucagon were replaced intraportally, and hyperglycemia was created via a perip

8 from 0 to 90 min (P1), and 5-HT was infused intraportally at 10, 20, and 40 microg.kg(-1).min(-1) fr

9 usly, and insulin and glucagon were replaced intraportally at 4- and 3-fold basal rates, respectively

10 the experimental period, insulin was infused intraportally at a basal rate (BI, n = 6), at a fourfold

11 Fructose was infused intraportally at a rate of 1.7, 3.3, or 6.7 micromol x k

12 up; a group that received 0.4 mg/kg rPSGL-Ig intraportally at the time of harvest; and a group that r

13 ved 0.4 mg/kg rPSGL-Ig plus 1 micromol D-Exo intraportally both at the time of harvest and at the ons

14 GSH was infused intraportally by mini-osmotic pump.

15 and adipose tissue), epinephrine was infused intraportally (EPI po) or peripherally (EPI pe) into 18-

16 other group (SAL; n = 8), saline was infused intraportally from 0 to 270 min.

17 oup of dogs (SER; n = 8), saline was infused intraportally from 0 to 90 min (P1), and 5-HT was infuse

18 8.8x10(8), 96% viable human hepatocytes were intraportally infused.

19 Fluorescently labelled hMSCs were infused intraportally into CCl(4) -injured mice with and without

20 nt AAV expressing human factor IX (AAV-hFIX) intraportally into the livers of mice which had been pre

21 of recombinant human insulin (HI) delivered intraportally or peripherally were compared with an acyl

22 eceived untreated or gamma-irradiated LEW SC intraportally reacted to in vitro stimulation by LEW all

23 In the control group, saline was given intraportally (SAL; n = 10), and the hepatic glucose con

24 ds from L-[methyl-3H]methionine administered intraportally to an experimental animal; clarification o

25 sly to maintain basal concentrations (EuAA), intraportally to mimic the postmeal AA increase (PoAA),

26 sualize histologic and pathologic changes in intraportally transplanted islets and surrounding hepati

27 The very low blood perfusion of intraportally transplanted islets is likely to predispos

28 ed as a benchmark for novel agents targeting intraportally transplanted islets.

29 obe provides a method to noninvasively image intraportally transplanted islets.

30 al studies indicate low revascularization of intraportally transplanted islets.

31 e portal vein may compromise the survival of intraportally transplanted pancreatic islets.

32 We transplanted hyperglycemic rats intraportally with 2500 ferucarbotran-labeled syngeneic

33 cynomolgus monkeys underwent transplantation intraportally with 48-hr cultured 10,000 islet equivalen

34 Rats were injected intraportally with a replication-defective recombinant a

35 Allogeneic donor MSCs were cotransplanted intraportally with islets on postoperative day (POD) 0 a

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