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1 he physiological insulin balance between the hepatic portal and peripheral circulations and thereby a
2 ted from the femoral artery and vein and the hepatic, portal, and renal veins to determine total hemo
3 mediated by vagal afferents innervating the hepatic portal area (HPA), through which most water and
4 The arterial glucagon levels (ng/l) and the hepatic portal-arterial difference in plasma glucagon (n
5 The arterial glucagon level (ng/l) and the hepatic portal-arterial difference in plasma glucagon (n
7 The arterial plasma glucagon levels and the hepatic portal-arterial difference in plasma glucagon de
9 erial plasma insulin levels (pmol/l) and the hepatic portal-arterial difference in plasma insulin (pm
11 The arterial plasma insulin levels and the hepatic portal-arterial difference in plasma insulin inc
14 ned, the insulin and glucagon levels and the hepatic portal-arterial difference remained constant.
17 ive agent of schistosomiasis, resides in the hepatic portal circulation of their human host up to 30
21 ar hyperplasia along with varying degrees of hepatic portal fibrosis that is indistinguishable from t
23 that a commitment to life in the endothermic hepatic portal system favored a filiform body form for e
26 ective activation of the nerve plexus of the hepatic portal system via peripheral focused ultrasound
27 and IL21R in PBC livers (particularly in the hepatic portal tracks) support a disease mechanism in wh
29 e alveolar edema in the absence of necrosis, hepatic-portal triaditis, mononuclear-cellular infiltrat
30 ve islet transplant (n = 400 islets) via the hepatic portal vein (HPV) with fibroblast growth factor
34 ch potentially sensing glucose levels in the hepatic portal vein has recently been suggested in a mou
35 n for essential amino acids over time in the hepatic portal vein in contrast to that of the non-selec
36 luate an alternate method of administration, hepatic portal vein infusion of G207 was performed in a
42 Hepatocytes are usually infused into the hepatic portal vein with many cells rapidly cleared by t
43 dy compared insulin infusion via endogenous (hepatic portal vein) and clinical (peripheral) routes to
44 ntegrity of vagal nerve supply to the liver, hepatic portal vein, and the proximal duodenum provided
45 ecretory bursts at ~5-min intervals into the hepatic portal vein, these pulses being attenuated early